TY  - JOUR
AU  - Đurđić, Slađana
AU  - Vlahović, Filip
AU  - Ognjanović, Miloš
AU  - Gemeiner, Pavol
AU  - Sarakhman, Olha
AU  - Stanković, Vesna
AU  - Mutić, Jelena
AU  - Stanković, Dalibor
AU  - Švorc, Lubomír
PY  - 2024
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/12205
AB  - In the present work, a nanocomposite, based on embedding Co-doped CeO2 nanoparticles into graphitic carbon nitride (g-C3N4), was applied to functionalize commercial glassy carbon paste. This is the first application of the electrochemical sensor, developed through the proposed procedure, in electrochemical sensing. The sensor was utilized for the electrochemical determination of organophosphate pesticide fenitrothion (FNT). Cyclic voltammetry identified reversible oxidation of FNT (oxidation at 0.18 V and reduction at 0.13 V) and additional reduction at 0.62 V vs. Ag/AgCl in HCl solution (pH =1). Theoretical calculations were carried out to model and elucidate experimentally observed redox processes. Special attention was devoted to modeling experimental conditions, and based on the obtained results, a detailed redox mechanism of the investigated analyte was proposed. This represents the first complete and unambiguous elucidation of the FNT redox mechanism, supported by joined experimental and theoretical data. Square wave voltammetry (SWV) was utilized for quantification, whereby the FNT oxidation peak was chosen for monitoring the analyte concentration. The developed sensor provided a nanomolar detection limit (3.2 nmol L 1), a wide linear concentration range (from 0.01 to 13.7 μmol L 1), and good precision, repeatability, and selectivity towards FNT. Practical application possibility was explored by testing the sensor performance for examining tap water and apple samples. Recovery tests, conducted during the FNT-spiked sample assays, showed a great application capability of the developed sensor for real-time monitoring of FNT traces in environmental samples.
T2  - Science of The Total Environment
T1  - Nano-size cobalt-doped cerium oxide particles embedded into graphitic carbon nitride for enhanced electrochemical sensing of insecticide fenitrothion in environmental samples: An experimental study with the theoretical elucidation of redox events
VL  - 909
SP  - 168483
DO  - 10.1016/j.scitotenv.2023.168483
ER  - 

@article{
author = "Đurđić, Slađana and Vlahović, Filip and Ognjanović, Miloš and Gemeiner, Pavol and Sarakhman, Olha and Stanković, Vesna and Mutić, Jelena and Stanković, Dalibor and Švorc, Lubomír",
year = "2024",
abstract = "In the present work, a nanocomposite, based on embedding Co-doped CeO2 nanoparticles into graphitic carbon nitride (g-C3N4), was applied to functionalize commercial glassy carbon paste. This is the first application of the electrochemical sensor, developed through the proposed procedure, in electrochemical sensing. The sensor was utilized for the electrochemical determination of organophosphate pesticide fenitrothion (FNT). Cyclic voltammetry identified reversible oxidation of FNT (oxidation at 0.18 V and reduction at 0.13 V) and additional reduction at 0.62 V vs. Ag/AgCl in HCl solution (pH =1). Theoretical calculations were carried out to model and elucidate experimentally observed redox processes. Special attention was devoted to modeling experimental conditions, and based on the obtained results, a detailed redox mechanism of the investigated analyte was proposed. This represents the first complete and unambiguous elucidation of the FNT redox mechanism, supported by joined experimental and theoretical data. Square wave voltammetry (SWV) was utilized for quantification, whereby the FNT oxidation peak was chosen for monitoring the analyte concentration. The developed sensor provided a nanomolar detection limit (3.2 nmol L 1), a wide linear concentration range (from 0.01 to 13.7 μmol L 1), and good precision, repeatability, and selectivity towards FNT. Practical application possibility was explored by testing the sensor performance for examining tap water and apple samples. Recovery tests, conducted during the FNT-spiked sample assays, showed a great application capability of the developed sensor for real-time monitoring of FNT traces in environmental samples.",
journal = "Science of The Total Environment",
title = "Nano-size cobalt-doped cerium oxide particles embedded into graphitic carbon nitride for enhanced electrochemical sensing of insecticide fenitrothion in environmental samples: An experimental study with the theoretical elucidation of redox events",
volume = "909",
pages = "168483",
doi = "10.1016/j.scitotenv.2023.168483"
}

Đurđić, S., Vlahović, F., Ognjanović, M., Gemeiner, P., Sarakhman, O., Stanković, V., Mutić, J., Stanković, D.,& Švorc, L.. (2024). Nano-size cobalt-doped cerium oxide particles embedded into graphitic carbon nitride for enhanced electrochemical sensing of insecticide fenitrothion in environmental samples: An experimental study with the theoretical elucidation of redox events. in Science of The Total Environment, 909, 168483.
https://doi.org/10.1016/j.scitotenv.2023.168483

Đurđić S, Vlahović F, Ognjanović M, Gemeiner P, Sarakhman O, Stanković V, Mutić J, Stanković D, Švorc L. Nano-size cobalt-doped cerium oxide particles embedded into graphitic carbon nitride for enhanced electrochemical sensing of insecticide fenitrothion in environmental samples: An experimental study with the theoretical elucidation of redox events. in Science of The Total Environment. 2024;909:168483.
doi:10.1016/j.scitotenv.2023.168483 .

Đurđić, Slađana, Vlahović, Filip, Ognjanović, Miloš, Gemeiner, Pavol, Sarakhman, Olha, Stanković, Vesna, Mutić, Jelena, Stanković, Dalibor, Švorc, Lubomír, "Nano-size cobalt-doped cerium oxide particles embedded into graphitic carbon nitride for enhanced electrochemical sensing of insecticide fenitrothion in environmental samples: An experimental study with the theoretical elucidation of redox events" in Science of The Total Environment, 909 (2024):168483,
https://doi.org/10.1016/j.scitotenv.2023.168483 . .

TY  - JOUR
AU  - Stanković, Vesna
AU  - Đurđić, Slađana
AU  - Ognjanović, Miloš
AU  - Zlatić, Gloria
AU  - Stanković, Dalibor
PY  - 2024
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/12670
AB  - In this study, we propose an eco-friendly method for synthesizing cerium tungstate nanoparticles using hydrothermal techniques. We used scanning, transmission electron microscopy, and X-ray diffraction to analyze the morphology of the synthesized nanoparticles. The results showed that the synthesized nanoparticles were uniform and highly crystalline, with a particle size of about 50 nm. The electrocatalytic properties of the nanoparticles were then investigated using cyclic voltammetry and electrochemical impedance spectroscopy. We further used the synthesized nanoparticles to develop an electrochemical sensor based on a carbon paste electrode that can detect hydroquinone. By optimizing the differential pulse voltammetric method, a wide linearity range of 0.4 to 45 µM and a low detection limit of 0.06 µM were obtained. The developed sensor also expressed excellent repeatability (RSD up to 3.8%) and reproducibility (RSD below 5%). Interferences had an insignificant impact on the determination of analytes, making it possible to use this method for monitoring hydroquinone concentrations in tap water. This study introduces a new approach to the chemistry of materials and the environment and demonstrates that a careful selection of components can lead to new horizons in analytical chemistry.
T2  - Sensors
T1  - Triangle-Shaped Cerium Tungstate Nanoparticles Used to Modify Carbon Paste Electrode for Sensitive Hydroquinone Detection in Water Samples
VL  - 24
IS  - 2
SP  - 705
DO  - 10.3390/s24020705
ER  - 

@article{
author = "Stanković, Vesna and Đurđić, Slađana and Ognjanović, Miloš and Zlatić, Gloria and Stanković, Dalibor",
year = "2024",
abstract = "In this study, we propose an eco-friendly method for synthesizing cerium tungstate nanoparticles using hydrothermal techniques. We used scanning, transmission electron microscopy, and X-ray diffraction to analyze the morphology of the synthesized nanoparticles. The results showed that the synthesized nanoparticles were uniform and highly crystalline, with a particle size of about 50 nm. The electrocatalytic properties of the nanoparticles were then investigated using cyclic voltammetry and electrochemical impedance spectroscopy. We further used the synthesized nanoparticles to develop an electrochemical sensor based on a carbon paste electrode that can detect hydroquinone. By optimizing the differential pulse voltammetric method, a wide linearity range of 0.4 to 45 µM and a low detection limit of 0.06 µM were obtained. The developed sensor also expressed excellent repeatability (RSD up to 3.8%) and reproducibility (RSD below 5%). Interferences had an insignificant impact on the determination of analytes, making it possible to use this method for monitoring hydroquinone concentrations in tap water. This study introduces a new approach to the chemistry of materials and the environment and demonstrates that a careful selection of components can lead to new horizons in analytical chemistry.",
journal = "Sensors",
title = "Triangle-Shaped Cerium Tungstate Nanoparticles Used to Modify Carbon Paste Electrode for Sensitive Hydroquinone Detection in Water Samples",
volume = "24",
number = "2",
pages = "705",
doi = "10.3390/s24020705"
}

Stanković, V., Đurđić, S., Ognjanović, M., Zlatić, G.,& Stanković, D.. (2024). Triangle-Shaped Cerium Tungstate Nanoparticles Used to Modify Carbon Paste Electrode for Sensitive Hydroquinone Detection in Water Samples. in Sensors, 24(2), 705.
https://doi.org/10.3390/s24020705

Stanković V, Đurđić S, Ognjanović M, Zlatić G, Stanković D. Triangle-Shaped Cerium Tungstate Nanoparticles Used to Modify Carbon Paste Electrode for Sensitive Hydroquinone Detection in Water Samples. in Sensors. 2024;24(2):705.
doi:10.3390/s24020705 .

Stanković, Vesna, Đurđić, Slađana, Ognjanović, Miloš, Zlatić, Gloria, Stanković, Dalibor, "Triangle-Shaped Cerium Tungstate Nanoparticles Used to Modify Carbon Paste Electrode for Sensitive Hydroquinone Detection in Water Samples" in Sensors, 24, no. 2 (2024):705,
https://doi.org/10.3390/s24020705 . .

TY  - JOUR
AU  - Korina, Elena
AU  - Karaberova, Arina
AU  - Bol’shakov, Oleg
AU  - Bulatova, Ekaterina
AU  - Golovin, Mikhail
AU  - Abramyan, Anton
AU  - Stanković, Dalibor M.
PY  - 2024
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/12875
AB  - Electrochemical sensing is an excellent analytical means with multiple applications. Most of the electrochemical developments are based on the novel electrochemically active substrates. A lot of them have been adopted from other fields of material science. Every new class of functional materials has impacted on the development of electroanalytical chemistry. In this view, lanthanide cuprates, a well recognized high temperature superconducting materials were considered for adrenaline sensing. Obtained from corresponding oxides, a highly crystalline La2CuO4 found to be a suitable substrate for analytical method development. It inherited sponge-like morphology common for the most of the previously reported lanthanum cuprates with narrow pore size distribution at 400–700 nm. Excellent charge mobility and low resistivity provided a carbon paste electrode with improved linearity range and low limit of detection. Repeatability and stability of the developed sensor were at satisfactory level. Sensor functionality was verified on the real samples with excellent recovery rates. With this work we suggest further development of electroanalytical methods with application of lanthanide cuprates.
T2  - Journal of The Electrochemical Society
T1  - Enhancing Adrenaline Sensing with Lanthanum Cuprate: A Promising Approach for a Novel Sensor
VL  - 171
IS  - 1
SP  - 017513
DO  - 10.1149/1945-7111/ad1ecb
ER  - 

@article{
author = "Korina, Elena and Karaberova, Arina and Bol’shakov, Oleg and Bulatova, Ekaterina and Golovin, Mikhail and Abramyan, Anton and Stanković, Dalibor M.",
year = "2024",
abstract = "Electrochemical sensing is an excellent analytical means with multiple applications. Most of the electrochemical developments are based on the novel electrochemically active substrates. A lot of them have been adopted from other fields of material science. Every new class of functional materials has impacted on the development of electroanalytical chemistry. In this view, lanthanide cuprates, a well recognized high temperature superconducting materials were considered for adrenaline sensing. Obtained from corresponding oxides, a highly crystalline La2CuO4 found to be a suitable substrate for analytical method development. It inherited sponge-like morphology common for the most of the previously reported lanthanum cuprates with narrow pore size distribution at 400–700 nm. Excellent charge mobility and low resistivity provided a carbon paste electrode with improved linearity range and low limit of detection. Repeatability and stability of the developed sensor were at satisfactory level. Sensor functionality was verified on the real samples with excellent recovery rates. With this work we suggest further development of electroanalytical methods with application of lanthanide cuprates.",
journal = "Journal of The Electrochemical Society",
title = "Enhancing Adrenaline Sensing with Lanthanum Cuprate: A Promising Approach for a Novel Sensor",
volume = "171",
number = "1",
pages = "017513",
doi = "10.1149/1945-7111/ad1ecb"
}

Korina, E., Karaberova, A., Bol’shakov, O., Bulatova, E., Golovin, M., Abramyan, A.,& Stanković, D. M.. (2024). Enhancing Adrenaline Sensing with Lanthanum Cuprate: A Promising Approach for a Novel Sensor. in Journal of The Electrochemical Society, 171(1), 017513.
https://doi.org/10.1149/1945-7111/ad1ecb

Korina E, Karaberova A, Bol’shakov O, Bulatova E, Golovin M, Abramyan A, Stanković DM. Enhancing Adrenaline Sensing with Lanthanum Cuprate: A Promising Approach for a Novel Sensor. in Journal of The Electrochemical Society. 2024;171(1):017513.
doi:10.1149/1945-7111/ad1ecb .

Korina, Elena, Karaberova, Arina, Bol’shakov, Oleg, Bulatova, Ekaterina, Golovin, Mikhail, Abramyan, Anton, Stanković, Dalibor M., "Enhancing Adrenaline Sensing with Lanthanum Cuprate: A Promising Approach for a Novel Sensor" in Journal of The Electrochemical Society, 171, no. 1 (2024):017513,
https://doi.org/10.1149/1945-7111/ad1ecb . .

TY  - JOUR
AU  - Mijajlović, Aleksandar
AU  - Stanković, Vesna
AU  - Vlahović, Filip
AU  - Đurđić, Slađana
AU  - Manojlović, Dragan
AU  - Stanković, Dalibor
PY  - 2024
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/13021
AB  - Excessive pesticide use can harm human health, making it essential to develop new techniques to monitor hazardous pesticides in food. Our study focuses on detecting mesotrione (MST) using an unmodified boron-doped diamond (BDD) electrode. This was the first application of cathodically pretreated BDD electrode for the detection of MST, based on its oxidation at a high potential value of +1.4 V. We theoretically examined the oxidation mechanism of MST trough the utilization of density functional theory (DFT) methodology. The utilized DPV method achieved a detection limit of 0.45 μM and showed satisfactory selectivity. The practical application of this method was demonstrated by examining corn-based food products. To ensure practical application of the method, MST was deliberately added to the samples to evaluate the accuracy of the proposed method. The effectiveness of the method was confirmed by using HPLC method. This environmentally-friendly approach can establish a solid foundation for future use in food analysis.
T2  - Food Chemistry
T1  - The cathodically pretreated boron-doped diamond electrode as an environmentally friendly electrochemical tool for the detection and monitoring of mesotrione in food samples
VL  - 447
SP  - 138993
DO  - 10.1016/j.foodchem.2024.138993
ER  - 

@article{
author = "Mijajlović, Aleksandar and Stanković, Vesna and Vlahović, Filip and Đurđić, Slađana and Manojlović, Dragan and Stanković, Dalibor",
year = "2024",
abstract = "Excessive pesticide use can harm human health, making it essential to develop new techniques to monitor hazardous pesticides in food. Our study focuses on detecting mesotrione (MST) using an unmodified boron-doped diamond (BDD) electrode. This was the first application of cathodically pretreated BDD electrode for the detection of MST, based on its oxidation at a high potential value of +1.4 V. We theoretically examined the oxidation mechanism of MST trough the utilization of density functional theory (DFT) methodology. The utilized DPV method achieved a detection limit of 0.45 μM and showed satisfactory selectivity. The practical application of this method was demonstrated by examining corn-based food products. To ensure practical application of the method, MST was deliberately added to the samples to evaluate the accuracy of the proposed method. The effectiveness of the method was confirmed by using HPLC method. This environmentally-friendly approach can establish a solid foundation for future use in food analysis.",
journal = "Food Chemistry",
title = "The cathodically pretreated boron-doped diamond electrode as an environmentally friendly electrochemical tool for the detection and monitoring of mesotrione in food samples",
volume = "447",
pages = "138993",
doi = "10.1016/j.foodchem.2024.138993"
}

Mijajlović, A., Stanković, V., Vlahović, F., Đurđić, S., Manojlović, D.,& Stanković, D.. (2024). The cathodically pretreated boron-doped diamond electrode as an environmentally friendly electrochemical tool for the detection and monitoring of mesotrione in food samples. in Food Chemistry, 447, 138993.
https://doi.org/10.1016/j.foodchem.2024.138993

Mijajlović A, Stanković V, Vlahović F, Đurđić S, Manojlović D, Stanković D. The cathodically pretreated boron-doped diamond electrode as an environmentally friendly electrochemical tool for the detection and monitoring of mesotrione in food samples. in Food Chemistry. 2024;447:138993.
doi:10.1016/j.foodchem.2024.138993 .

Mijajlović, Aleksandar, Stanković, Vesna, Vlahović, Filip, Đurđić, Slađana, Manojlović, Dragan, Stanković, Dalibor, "The cathodically pretreated boron-doped diamond electrode as an environmentally friendly electrochemical tool for the detection and monitoring of mesotrione in food samples" in Food Chemistry, 447 (2024):138993,
https://doi.org/10.1016/j.foodchem.2024.138993 . .

TY  - JOUR
AU  - Mutić, Tijana
AU  - Ognjanović, Miloš
AU  - Ivković, Đurđa
AU  - Nikolić, Vladimir
AU  - Stanković, Vesna
AU  - Ristivojević, Petar
AU  - Stanković, Dalibor
PY  - 2024
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/13031
AB  - In this study, we successfully prepared a modified nickel oxide (NiO) carbon paste electrode to detect gallic acid (GA). NiO nanoparticles were synthesized by the simple, organic solvent-free chemical coprecipitation method, and the electrochemical properties of the electrode and GA were thoroughly investigated using CV, SWV, and EIS, while morphological properties were examined using ICP-OES, TEM, SEM, and XRD. Excellent catalytic characteristics are displayed by the developed material which facilitates the interaction of the target with the electrode surface. The obtained electrochemical information showed that the incorporation of NiO nanoparticles to the carbon paste electrode effectively facilitates electron transfer processes and enriches the catalytic response of the carbon paste electrode. The fabricated NiO/CPE sensor showed a satisfactory linear relationship between peak current and GA concentration in the broad range of 0.2–100 μM and 100–200 μM with a low detection limit of 0.04 μM and limit of quantification of 0.12 μM at pH 3 of BRBS as supporting electrolyte. The selectivity of the proposed method was satisfactory, with acceptable stability, considerable repeatability, and accurate reproducibility. Moreover, the good practicability performance could be effectuated at the NiO/CPE sensor for the quantitative analysis of GA in bourtree, walnut, primrose, and chamomile tea samples. The results were compared with the standard DPPH test and statistical processing of the results was performed, which confirmed the excellent agreement between the two methods. The developed method can provide a cost-effective, rapid, selective, and sensitive means for GA monitoring. When compared to other works, the developed technique has a wider linear range and lower LOD and LOQ, which makes this work a very important reference for the highly sensitive analysis of GA in the field of food safety.
T2  - Journal of Electroanalytical Chemistry
T1  - Improving gallic acid detection in plant samples: Fabrication and optimization of a sensitive and selective NiO-supported carbon paste electrode
VL  - 960
SP  - 118213
DO  - 10.1016/j.jelechem.2024.118213
ER  - 

@article{
author = "Mutić, Tijana and Ognjanović, Miloš and Ivković, Đurđa and Nikolić, Vladimir and Stanković, Vesna and Ristivojević, Petar and Stanković, Dalibor",
year = "2024",
abstract = "In this study, we successfully prepared a modified nickel oxide (NiO) carbon paste electrode to detect gallic acid (GA). NiO nanoparticles were synthesized by the simple, organic solvent-free chemical coprecipitation method, and the electrochemical properties of the electrode and GA were thoroughly investigated using CV, SWV, and EIS, while morphological properties were examined using ICP-OES, TEM, SEM, and XRD. Excellent catalytic characteristics are displayed by the developed material which facilitates the interaction of the target with the electrode surface. The obtained electrochemical information showed that the incorporation of NiO nanoparticles to the carbon paste electrode effectively facilitates electron transfer processes and enriches the catalytic response of the carbon paste electrode. The fabricated NiO/CPE sensor showed a satisfactory linear relationship between peak current and GA concentration in the broad range of 0.2–100 μM and 100–200 μM with a low detection limit of 0.04 μM and limit of quantification of 0.12 μM at pH 3 of BRBS as supporting electrolyte. The selectivity of the proposed method was satisfactory, with acceptable stability, considerable repeatability, and accurate reproducibility. Moreover, the good practicability performance could be effectuated at the NiO/CPE sensor for the quantitative analysis of GA in bourtree, walnut, primrose, and chamomile tea samples. The results were compared with the standard DPPH test and statistical processing of the results was performed, which confirmed the excellent agreement between the two methods. The developed method can provide a cost-effective, rapid, selective, and sensitive means for GA monitoring. When compared to other works, the developed technique has a wider linear range and lower LOD and LOQ, which makes this work a very important reference for the highly sensitive analysis of GA in the field of food safety.",
journal = "Journal of Electroanalytical Chemistry",
title = "Improving gallic acid detection in plant samples: Fabrication and optimization of a sensitive and selective NiO-supported carbon paste electrode",
volume = "960",
pages = "118213",
doi = "10.1016/j.jelechem.2024.118213"
}

Mutić, T., Ognjanović, M., Ivković, Đ., Nikolić, V., Stanković, V., Ristivojević, P.,& Stanković, D.. (2024). Improving gallic acid detection in plant samples: Fabrication and optimization of a sensitive and selective NiO-supported carbon paste electrode. in Journal of Electroanalytical Chemistry, 960, 118213.
https://doi.org/10.1016/j.jelechem.2024.118213

Mutić T, Ognjanović M, Ivković Đ, Nikolić V, Stanković V, Ristivojević P, Stanković D. Improving gallic acid detection in plant samples: Fabrication and optimization of a sensitive and selective NiO-supported carbon paste electrode. in Journal of Electroanalytical Chemistry. 2024;960:118213.
doi:10.1016/j.jelechem.2024.118213 .

Mutić, Tijana, Ognjanović, Miloš, Ivković, Đurđa, Nikolić, Vladimir, Stanković, Vesna, Ristivojević, Petar, Stanković, Dalibor, "Improving gallic acid detection in plant samples: Fabrication and optimization of a sensitive and selective NiO-supported carbon paste electrode" in Journal of Electroanalytical Chemistry, 960 (2024):118213,
https://doi.org/10.1016/j.jelechem.2024.118213 . .

TY  - JOUR
AU  - Mutić, Tijana
AU  - Stanković, Dalibor M.
AU  - Manojlović, Dragan
AU  - Petrić, Đorđe
AU  - Pastor, Ferenc
AU  - Avdin, Vyacheslav V.
AU  - Ognjanović, Miloš
AU  - Stanković, Vesna
PY  - 2024
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/13122
AB  - In this work, we successfully prepared a modified cobalt oxide (Co3O4) carbon paste electrode to detect Levofloxacin (LEV). By synthesizing Co3O4 nanoparticles through the chemical coprecipitation method, the electrochemical properties of the electrode and LEV were thoroughly investigated using CV, SWV, and EIS, while material properties were scrutinized using ICP-OES, TEM, SEM, and XRD. The results showed that the prepared electrode displayed a better electrocatalytic response than the bare carbon paste electrode. After optimizing SWV, the electrode exhibited a wide linear working range from 1 to 85 μM at pH 5 of BRBS as the supporting electrolyte. The selectivity of the proposed method was satisfactory, with good repeatability and reproducibility, strongly suggesting a potential application for determining LEV in real samples, particularly in pharmaceutical formulations. The practicality of the approach was demonstrated through good recoveries, and the morphology of the materials was found to be closely related to other parameters, indicating that the developed method can provide a cost-effective, rapid, selective, and sensitive means for LEV monitoring. Overall, this project has made significant progress towards developing a reliable method for detecting LEV and has opened up new opportunities for future research in this field.
T2  - Electrochem
T1  - Micromolar Levofloxacin Sensor by Incorporating Highly Crystalline Co3O4 into a Carbon Paste Electrode Structure
VL  - 5
IS  - 1
SP  - 45
EP  - 56
DO  - 10.3390/electrochem5010003
ER  - 

@article{
author = "Mutić, Tijana and Stanković, Dalibor M. and Manojlović, Dragan and Petrić, Đorđe and Pastor, Ferenc and Avdin, Vyacheslav V. and Ognjanović, Miloš and Stanković, Vesna",
year = "2024",
abstract = "In this work, we successfully prepared a modified cobalt oxide (Co3O4) carbon paste electrode to detect Levofloxacin (LEV). By synthesizing Co3O4 nanoparticles through the chemical coprecipitation method, the electrochemical properties of the electrode and LEV were thoroughly investigated using CV, SWV, and EIS, while material properties were scrutinized using ICP-OES, TEM, SEM, and XRD. The results showed that the prepared electrode displayed a better electrocatalytic response than the bare carbon paste electrode. After optimizing SWV, the electrode exhibited a wide linear working range from 1 to 85 μM at pH 5 of BRBS as the supporting electrolyte. The selectivity of the proposed method was satisfactory, with good repeatability and reproducibility, strongly suggesting a potential application for determining LEV in real samples, particularly in pharmaceutical formulations. The practicality of the approach was demonstrated through good recoveries, and the morphology of the materials was found to be closely related to other parameters, indicating that the developed method can provide a cost-effective, rapid, selective, and sensitive means for LEV monitoring. Overall, this project has made significant progress towards developing a reliable method for detecting LEV and has opened up new opportunities for future research in this field.",
journal = "Electrochem",
title = "Micromolar Levofloxacin Sensor by Incorporating Highly Crystalline Co3O4 into a Carbon Paste Electrode Structure",
volume = "5",
number = "1",
pages = "45-56",
doi = "10.3390/electrochem5010003"
}

Mutić, T., Stanković, D. M., Manojlović, D., Petrić, Đ., Pastor, F., Avdin, V. V., Ognjanović, M.,& Stanković, V.. (2024). Micromolar Levofloxacin Sensor by Incorporating Highly Crystalline Co3O4 into a Carbon Paste Electrode Structure. in Electrochem, 5(1), 45-56.
https://doi.org/10.3390/electrochem5010003

Mutić T, Stanković DM, Manojlović D, Petrić Đ, Pastor F, Avdin VV, Ognjanović M, Stanković V. Micromolar Levofloxacin Sensor by Incorporating Highly Crystalline Co3O4 into a Carbon Paste Electrode Structure. in Electrochem. 2024;5(1):45-56.
doi:10.3390/electrochem5010003 .

Mutić, Tijana, Stanković, Dalibor M., Manojlović, Dragan, Petrić, Đorđe, Pastor, Ferenc, Avdin, Vyacheslav V., Ognjanović, Miloš, Stanković, Vesna, "Micromolar Levofloxacin Sensor by Incorporating Highly Crystalline Co3O4 into a Carbon Paste Electrode Structure" in Electrochem, 5, no. 1 (2024):45-56,
https://doi.org/10.3390/electrochem5010003 . .

TY  - JOUR
AU  - Milikić, Jadranka
AU  - Nastasić, Ana
AU  - Rakočević, Lazar
AU  - Radinović, Kristina
AU  - Stojadinović, Stevan
AU  - Stanković, Dalibor
AU  - Šljukić, Biljana
PY  - 2024
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/13174
AB  - Three different iron-based electrocatalysts deposited on reduced graphene oxide (Fe/rGO, FeNi/rGO, and FeCu/ rGO) were synthesized and examined for oxygen reduction and evolution reactions (ORR and OER, respectively) in alkaline media. X-ray powder diffraction analysis, Fourier transform infrared spectroscopy, scanning electron microscopy with energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, and transmission electron microscopy were used for a thorough investigation of physico-chemical properties of FeM/rGO electrocatalysts. XPS analysis indicated the presence of transition metals in higher oxidation states. Onset potentials during OER were found to be 1.51, 1.64, and 1.71 V for FeNi/rGO, FeCu/rGO, and Fe/rGO, respectively. Moreover, FeNi/rGO showed the highest OER current density (~40 mA cm benchmark OER electrocatalyst, IrO 2 2 at 2 V), two times higher than the -1 , and the lowest Tafel slope (88 mV dec ), lower than IrO . The somewhat better catalytic activity of Fe/rGO for ORR in alkaline media compared to FeNi/rGO and FeCu/rGO was noticed. Tafel slopes of 105, 112, and 113 mV dec 2-1 during ORR were found for Fe/rGO, FeCu/rGO, and FeNi/rGO, respectively. Almost constant ORR current densities during chronoamperometric measurements were noticed for Fe/rGO and FeCu/rGO indicating stable performance.
T2  - Fuel
T1  - FeM/rGO (M = Ni and Cu) as bifunctional oxygen electrode
VL  - 368
SP  - 131654
DO  - 10.1016/j.fuel.2024.131654
ER  - 

@article{
author = "Milikić, Jadranka and Nastasić, Ana and Rakočević, Lazar and Radinović, Kristina and Stojadinović, Stevan and Stanković, Dalibor and Šljukić, Biljana",
year = "2024",
abstract = "Three different iron-based electrocatalysts deposited on reduced graphene oxide (Fe/rGO, FeNi/rGO, and FeCu/ rGO) were synthesized and examined for oxygen reduction and evolution reactions (ORR and OER, respectively) in alkaline media. X-ray powder diffraction analysis, Fourier transform infrared spectroscopy, scanning electron microscopy with energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, and transmission electron microscopy were used for a thorough investigation of physico-chemical properties of FeM/rGO electrocatalysts. XPS analysis indicated the presence of transition metals in higher oxidation states. Onset potentials during OER were found to be 1.51, 1.64, and 1.71 V for FeNi/rGO, FeCu/rGO, and Fe/rGO, respectively. Moreover, FeNi/rGO showed the highest OER current density (~40 mA cm benchmark OER electrocatalyst, IrO 2 2 at 2 V), two times higher than the -1 , and the lowest Tafel slope (88 mV dec ), lower than IrO . The somewhat better catalytic activity of Fe/rGO for ORR in alkaline media compared to FeNi/rGO and FeCu/rGO was noticed. Tafel slopes of 105, 112, and 113 mV dec 2-1 during ORR were found for Fe/rGO, FeCu/rGO, and FeNi/rGO, respectively. Almost constant ORR current densities during chronoamperometric measurements were noticed for Fe/rGO and FeCu/rGO indicating stable performance.",
journal = "Fuel",
title = "FeM/rGO (M = Ni and Cu) as bifunctional oxygen electrode",
volume = "368",
pages = "131654",
doi = "10.1016/j.fuel.2024.131654"
}

Milikić, J., Nastasić, A., Rakočević, L., Radinović, K., Stojadinović, S., Stanković, D.,& Šljukić, B.. (2024). FeM/rGO (M = Ni and Cu) as bifunctional oxygen electrode. in Fuel, 368, 131654.
https://doi.org/10.1016/j.fuel.2024.131654

Milikić J, Nastasić A, Rakočević L, Radinović K, Stojadinović S, Stanković D, Šljukić B. FeM/rGO (M = Ni and Cu) as bifunctional oxygen electrode. in Fuel. 2024;368:131654.
doi:10.1016/j.fuel.2024.131654 .

Milikić, Jadranka, Nastasić, Ana, Rakočević, Lazar, Radinović, Kristina, Stojadinović, Stevan, Stanković, Dalibor, Šljukić, Biljana, "FeM/rGO (M = Ni and Cu) as bifunctional oxygen electrode" in Fuel, 368 (2024):131654,
https://doi.org/10.1016/j.fuel.2024.131654 . .

TY  - JOUR
AU  - Anđelković, Ljubica
AU  - Šuljagić, Marija
AU  - Pavlović, Vladimir
AU  - Mirković, Miljana
AU  - Vrbica, Boško
AU  - Novaković, Irena
AU  - Stanković, Dalibor
AU  - Kremenović, Aleksandar
AU  - Uskoković, Vuk
PY  - 2024
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/13175
AB  - Metals and metal oxides have subpar antibacterial activities compared to those of small-molecule antibiotics, yet there are hopes that with proper compositional and structural adjustments this gap might be bridged. In this study, titanium dioxide (TiO2) nanoparticles were mechanically activated and combined with particulate silver through simple reduction process elicited by UV irradiation and assisted with the ultrasound. The resulting powders in various combinations (Ag vs. no Ag, activated vs. non-activated) were characterized using a range of experimental techniques and assessed for their antibacterial activities. The preparation procedure presented in this work prevails over the disadvantages of many chemical routes, most critically by avoiding the use of toxic substances. The mechanical activation did not reduce the particle size or crystallinity of TiO2 nor did it consistently alter the bandgap, yet it enabled the doubling of the amount of silver incorporable into the material. Further, while both mechanical activation and the addition of silver in the amount not exceeding 0.5 wt% produced barely detectable structural changes in the material, they both augmented its antibacterial activity. The precursor TiO2 powder produced no inhibition zone against any of the four bacterial species tested, while the mechanical activation of TiO2 led to the formation of distinct inhibition zones against each of the four bacterial species tested. The addition of silver to activated TiO2 further widened the inhibition zones and it also imparted the antibacterial activity to non-activated TiO2. The boost in the antibacterial activity achieved by the short mechanical activation was of a similar magnitude as the boost obtained after the addition of silver. The antibacterial activity was not different for different species when no silver was added to the system. However, with the addition of silver, species selectivity was obtained, as the composites were more effective against the two Gram-negative species (Escherichia coli and Klebsiella pneumoniae) than against the two Gram-positive ones (Staphylococcus aureus and Bacillus subtilis). The antibacterial activity increased with the addition of silver in the broth assay, but it was mediocre compared to that detected in the agar assay, attesting to the poor dispersability of the powders and their best performance when the bacterial cells migrate to the composite surface than vice versa. The findings of this study give hope that with appropriate microstructural or compositional alterations, the antibacterial activity of metal oxide powders and inorganic materials in general can be made comparable to that of small-molecule antibiotics.
T2  - Colloids and Surfaces A: Physicochemical and Engineering Aspects
T1  - Mechanical activation and silver supplementation as determinants of the antibacterial activity of titanium dioxide nanoparticles
VL  - 691
SP  - 133890
DO  - 10.1016/j.colsurfa.2024.133890
ER  - 

@article{
author = "Anđelković, Ljubica and Šuljagić, Marija and Pavlović, Vladimir and Mirković, Miljana and Vrbica, Boško and Novaković, Irena and Stanković, Dalibor and Kremenović, Aleksandar and Uskoković, Vuk",
year = "2024",
abstract = "Metals and metal oxides have subpar antibacterial activities compared to those of small-molecule antibiotics, yet there are hopes that with proper compositional and structural adjustments this gap might be bridged. In this study, titanium dioxide (TiO2) nanoparticles were mechanically activated and combined with particulate silver through simple reduction process elicited by UV irradiation and assisted with the ultrasound. The resulting powders in various combinations (Ag vs. no Ag, activated vs. non-activated) were characterized using a range of experimental techniques and assessed for their antibacterial activities. The preparation procedure presented in this work prevails over the disadvantages of many chemical routes, most critically by avoiding the use of toxic substances. The mechanical activation did not reduce the particle size or crystallinity of TiO2 nor did it consistently alter the bandgap, yet it enabled the doubling of the amount of silver incorporable into the material. Further, while both mechanical activation and the addition of silver in the amount not exceeding 0.5 wt% produced barely detectable structural changes in the material, they both augmented its antibacterial activity. The precursor TiO2 powder produced no inhibition zone against any of the four bacterial species tested, while the mechanical activation of TiO2 led to the formation of distinct inhibition zones against each of the four bacterial species tested. The addition of silver to activated TiO2 further widened the inhibition zones and it also imparted the antibacterial activity to non-activated TiO2. The boost in the antibacterial activity achieved by the short mechanical activation was of a similar magnitude as the boost obtained after the addition of silver. The antibacterial activity was not different for different species when no silver was added to the system. However, with the addition of silver, species selectivity was obtained, as the composites were more effective against the two Gram-negative species (Escherichia coli and Klebsiella pneumoniae) than against the two Gram-positive ones (Staphylococcus aureus and Bacillus subtilis). The antibacterial activity increased with the addition of silver in the broth assay, but it was mediocre compared to that detected in the agar assay, attesting to the poor dispersability of the powders and their best performance when the bacterial cells migrate to the composite surface than vice versa. The findings of this study give hope that with appropriate microstructural or compositional alterations, the antibacterial activity of metal oxide powders and inorganic materials in general can be made comparable to that of small-molecule antibiotics.",
journal = "Colloids and Surfaces A: Physicochemical and Engineering Aspects",
title = "Mechanical activation and silver supplementation as determinants of the antibacterial activity of titanium dioxide nanoparticles",
volume = "691",
pages = "133890",
doi = "10.1016/j.colsurfa.2024.133890"
}

Anđelković, L., Šuljagić, M., Pavlović, V., Mirković, M., Vrbica, B., Novaković, I., Stanković, D., Kremenović, A.,& Uskoković, V.. (2024). Mechanical activation and silver supplementation as determinants of the antibacterial activity of titanium dioxide nanoparticles. in Colloids and Surfaces A: Physicochemical and Engineering Aspects, 691, 133890.
https://doi.org/10.1016/j.colsurfa.2024.133890

Anđelković L, Šuljagić M, Pavlović V, Mirković M, Vrbica B, Novaković I, Stanković D, Kremenović A, Uskoković V. Mechanical activation and silver supplementation as determinants of the antibacterial activity of titanium dioxide nanoparticles. in Colloids and Surfaces A: Physicochemical and Engineering Aspects. 2024;691:133890.
doi:10.1016/j.colsurfa.2024.133890 .

Anđelković, Ljubica, Šuljagić, Marija, Pavlović, Vladimir, Mirković, Miljana, Vrbica, Boško, Novaković, Irena, Stanković, Dalibor, Kremenović, Aleksandar, Uskoković, Vuk, "Mechanical activation and silver supplementation as determinants of the antibacterial activity of titanium dioxide nanoparticles" in Colloids and Surfaces A: Physicochemical and Engineering Aspects, 691 (2024):133890,
https://doi.org/10.1016/j.colsurfa.2024.133890 . .

TY  - JOUR
AU  - Mušović, Jasmina
AU  - Tekić, Danijela
AU  - Marić, Slađana
AU  - Jocić, Ana
AU  - Stanković, Dalibor
AU  - Dimitrijević, Aleksandra
PY  - 2024
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/13218
AB  - The consistent expansion of the lithium-ion battery (LIB) market, coupled with their relatively brief lifespan, necessitates the development of efficient and sustainable LIB recycling strategies. Recycling is crucial not only for the recovery of critical metals like Co(II) and Li(I) from the cathode material as a secondary resource but also from an environmental perspective. This study explores the use of a series of aqueous biphasic systems (ABS) with synthesized tetrabutylphosphonium ionic liquids (ILs) and ammonium sulfate as extraction platforms for metals from LIB cathode. Firstly, liquid–liquid equilibrium phase diagrams for each ABS were established, and partitioning experiments were conducted to assess the Co(II), Ni(II), Mn(II), and Li(I) recovery efficiencies. We observed distinct partitioning behaviors for the metals, with tetrabutylphosphonium diethylenetriaminepentaacetate, [TBP][DTPA], showing recovery efficiencies exceeding 98% for Co(II), Ni(II), and Mn(II). At the same time, Li(I) was predominantly retained in the aqueous salt-rich phase. By fine-tuning ABS operational parameters such as pH, temperature, system composition, and phase ratio, we identified optimal conditions for extracting metals from the cathode material of lithium-cobalt-oxide (LCO) batteries using sulfate lixiviate. Introducing [TBP][DTPA] after the leaching process induced ABS, achieving remarkable recovery efficiency over 95% for Co(II) in the IL-rich phase, with all Li(I) remaining in the lower phase. Cobalt was subsequently extracted using oxalic acid to precipitate as Co-oxalate from concentrate, while Li(I) was isolated from the aqueous phase using ammonium carbonate. After the “cleaning” of the IL-rich phase, the [TBP][DTPA] was recovered and reused in four consecutive cycles, with small detected losses on the recovery efficiency of Co(II) and Li(I). Therefore, our innovative strategy combines sulfate-based lixiviants with IL-ABS technology, thereby enhancing selectivity and sustainability within one of the most efficient lixiviant systems widely employed in the industry. This technological advancement presents a promising pathway for the recycling of spent batteries, offering substantial environmental advantages within the well-established and extensively utilized realm of metal recovery technology in the industry.
T2  - Separation and Purification Technology
T1  - Sustainable recovery of cobalt and lithium from lithium-ion battery cathode material by combining sulfate leachates and aqueous biphasic systems based on tetrabutylphosphonium-ionic liquids
VL  - 348
SP  - 127707
DO  - 10.1016/j.seppur.2024.127707
ER  - 

@article{
author = "Mušović, Jasmina and Tekić, Danijela and Marić, Slađana and Jocić, Ana and Stanković, Dalibor and Dimitrijević, Aleksandra",
year = "2024",
abstract = "The consistent expansion of the lithium-ion battery (LIB) market, coupled with their relatively brief lifespan, necessitates the development of efficient and sustainable LIB recycling strategies. Recycling is crucial not only for the recovery of critical metals like Co(II) and Li(I) from the cathode material as a secondary resource but also from an environmental perspective. This study explores the use of a series of aqueous biphasic systems (ABS) with synthesized tetrabutylphosphonium ionic liquids (ILs) and ammonium sulfate as extraction platforms for metals from LIB cathode. Firstly, liquid–liquid equilibrium phase diagrams for each ABS were established, and partitioning experiments were conducted to assess the Co(II), Ni(II), Mn(II), and Li(I) recovery efficiencies. We observed distinct partitioning behaviors for the metals, with tetrabutylphosphonium diethylenetriaminepentaacetate, [TBP][DTPA], showing recovery efficiencies exceeding 98% for Co(II), Ni(II), and Mn(II). At the same time, Li(I) was predominantly retained in the aqueous salt-rich phase. By fine-tuning ABS operational parameters such as pH, temperature, system composition, and phase ratio, we identified optimal conditions for extracting metals from the cathode material of lithium-cobalt-oxide (LCO) batteries using sulfate lixiviate. Introducing [TBP][DTPA] after the leaching process induced ABS, achieving remarkable recovery efficiency over 95% for Co(II) in the IL-rich phase, with all Li(I) remaining in the lower phase. Cobalt was subsequently extracted using oxalic acid to precipitate as Co-oxalate from concentrate, while Li(I) was isolated from the aqueous phase using ammonium carbonate. After the “cleaning” of the IL-rich phase, the [TBP][DTPA] was recovered and reused in four consecutive cycles, with small detected losses on the recovery efficiency of Co(II) and Li(I). Therefore, our innovative strategy combines sulfate-based lixiviants with IL-ABS technology, thereby enhancing selectivity and sustainability within one of the most efficient lixiviant systems widely employed in the industry. This technological advancement presents a promising pathway for the recycling of spent batteries, offering substantial environmental advantages within the well-established and extensively utilized realm of metal recovery technology in the industry.",
journal = "Separation and Purification Technology",
title = "Sustainable recovery of cobalt and lithium from lithium-ion battery cathode material by combining sulfate leachates and aqueous biphasic systems based on tetrabutylphosphonium-ionic liquids",
volume = "348",
pages = "127707",
doi = "10.1016/j.seppur.2024.127707"
}

Mušović, J., Tekić, D., Marić, S., Jocić, A., Stanković, D.,& Dimitrijević, A.. (2024). Sustainable recovery of cobalt and lithium from lithium-ion battery cathode material by combining sulfate leachates and aqueous biphasic systems based on tetrabutylphosphonium-ionic liquids. in Separation and Purification Technology, 348, 127707.
https://doi.org/10.1016/j.seppur.2024.127707

Mušović J, Tekić D, Marić S, Jocić A, Stanković D, Dimitrijević A. Sustainable recovery of cobalt and lithium from lithium-ion battery cathode material by combining sulfate leachates and aqueous biphasic systems based on tetrabutylphosphonium-ionic liquids. in Separation and Purification Technology. 2024;348:127707.
doi:10.1016/j.seppur.2024.127707 .

Mušović, Jasmina, Tekić, Danijela, Marić, Slađana, Jocić, Ana, Stanković, Dalibor, Dimitrijević, Aleksandra, "Sustainable recovery of cobalt and lithium from lithium-ion battery cathode material by combining sulfate leachates and aqueous biphasic systems based on tetrabutylphosphonium-ionic liquids" in Separation and Purification Technology, 348 (2024):127707,
https://doi.org/10.1016/j.seppur.2024.127707 . .

TY  - JOUR
AU  - Gusmão, Filipe M.B.
AU  - Đurić, Teodora
AU  - Milikić, Jadranka
AU  - Radinović, Kristina
AU  - Santos, Diogo M.F.
AU  - Stanković, Dalibor
AU  - Šljukić, Biljana
PY  - 2024
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/13294
AB  - The potential of polyoxometalates (POMs) as alternatives to noble metal-based bifunctional electrocatalysts for air electrode, i.e., for oxygen evolution reaction (OER) and oxygen reduction reaction (ORR), was analyzed herein. Five POMs containing transition metal (Mn, Fe, Co, Ni, or Cu) were prepared and combined with reduced graphene oxide (rGO). Kenning structure of POMs with nanolamellae-like morphology and multi-layered graphene sheets of rGO were confirmed by X-ray diffraction, Fourier-transform infrared spectroscopy, scanning electron microscopy with energy dispersive X-ray spectroscopy, transmission electron microscopy and Raman spectroscopy analysis. Different POM:rGO ratios were tested to optimize the composition, and a ratio of 1:5 Ni- POM:rGO was found to be the most electrocatalytically active for OER (Tafel slope as low as 42 mV dec 1, overpotential at 10 mA cm2 of 354 mV and current density at 400 mV overpotential as high as 83.4 mA cm2), notably better than IrO2. As for ORR, Co-POM/rGO carried the lowest Tafel slope of 165 mV dec 1, half-wave potential of 0.711 V and a mixed 2- and 4-electron ORR mechanism. Moreover, these non-precious metal electrocatalysts showed stability in alkaline media with no change in their structure.
T2  - International Journal of Hydrogen Energy
T1  - Transition metal polyoxometalates with reduced graphene oxide for high-performance air-electrode of metal-air batteries
VL  - 71
SP  - 763
EP  - 774
DO  - 10.1016/j.ijhydene.2024.05.229
ER  - 

@article{
author = "Gusmão, Filipe M.B. and Đurić, Teodora and Milikić, Jadranka and Radinović, Kristina and Santos, Diogo M.F. and Stanković, Dalibor and Šljukić, Biljana",
year = "2024",
abstract = "The potential of polyoxometalates (POMs) as alternatives to noble metal-based bifunctional electrocatalysts for air electrode, i.e., for oxygen evolution reaction (OER) and oxygen reduction reaction (ORR), was analyzed herein. Five POMs containing transition metal (Mn, Fe, Co, Ni, or Cu) were prepared and combined with reduced graphene oxide (rGO). Kenning structure of POMs with nanolamellae-like morphology and multi-layered graphene sheets of rGO were confirmed by X-ray diffraction, Fourier-transform infrared spectroscopy, scanning electron microscopy with energy dispersive X-ray spectroscopy, transmission electron microscopy and Raman spectroscopy analysis. Different POM:rGO ratios were tested to optimize the composition, and a ratio of 1:5 Ni- POM:rGO was found to be the most electrocatalytically active for OER (Tafel slope as low as 42 mV dec 1, overpotential at 10 mA cm2 of 354 mV and current density at 400 mV overpotential as high as 83.4 mA cm2), notably better than IrO2. As for ORR, Co-POM/rGO carried the lowest Tafel slope of 165 mV dec 1, half-wave potential of 0.711 V and a mixed 2- and 4-electron ORR mechanism. Moreover, these non-precious metal electrocatalysts showed stability in alkaline media with no change in their structure.",
journal = "International Journal of Hydrogen Energy",
title = "Transition metal polyoxometalates with reduced graphene oxide for high-performance air-electrode of metal-air batteries",
volume = "71",
pages = "763-774",
doi = "10.1016/j.ijhydene.2024.05.229"
}

Gusmão, F. M.B., Đurić, T., Milikić, J., Radinović, K., Santos, D. M.F., Stanković, D.,& Šljukić, B.. (2024). Transition metal polyoxometalates with reduced graphene oxide for high-performance air-electrode of metal-air batteries. in International Journal of Hydrogen Energy, 71, 763-774.
https://doi.org/10.1016/j.ijhydene.2024.05.229

Gusmão FM, Đurić T, Milikić J, Radinović K, Santos DM, Stanković D, Šljukić B. Transition metal polyoxometalates with reduced graphene oxide for high-performance air-electrode of metal-air batteries. in International Journal of Hydrogen Energy. 2024;71:763-774.
doi:10.1016/j.ijhydene.2024.05.229 .

Gusmão, Filipe M.B., Đurić, Teodora, Milikić, Jadranka, Radinović, Kristina, Santos, Diogo M.F., Stanković, Dalibor, Šljukić, Biljana, "Transition metal polyoxometalates with reduced graphene oxide for high-performance air-electrode of metal-air batteries" in International Journal of Hydrogen Energy, 71 (2024):763-774,
https://doi.org/10.1016/j.ijhydene.2024.05.229 . .

TY  - JOUR
AU  - Simić, Marija
AU  - Savić, Branislava
AU  - Ognjanović, Miloš
AU  - Stanković, Dalibor M.
AU  - Relić, Dubravka J.
AU  - Aćimović, Danka D.
AU  - Brdarić, Tanja
PY  - 2023
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/10549
AB  - Bisphenol A (BPA) is an organic pollutant that is widely spread in waterbody with effluents as a result of its extensive use in the plastics industry. It posses to the class of compounds that are endocrine disruptors and has a great negative impact on living organisms. Therefore, the progress in development of green technology for BPA removal from the aquatic media is crucial for environmental protection. This paper presents BPA removal by electrochemical oxidation on SnO2-MWCNT (tin dioxide-multi walled carbon nanotube) nanocomposite anode. The nanocomposite was structural and morphological characterized by X-ray powder diffraction and transmission electron microscopy. Electrochemical properties of the SnO2-MWCNT anode were investigated using cyclic voltammetry, linear sweep voltammetry and electrical impedance spectroscopy. The electrochemical behavior of anodes toward BPA in sodium sulfate solutions has shown that BPA is oxidized by indirectly mechanism via hydroxyl radicals (verified by quenching tests). Electrolysis of BPA has been done in galvanostatic regime at current densities 2.5, 5.0, 10.0, 15.0 and 20.0 mA cm−2 in 0.1 M sodium sulfate supported electrolyte pH 4.0. Complete degradation of BPA was accomplished after 5 h of electrolysis at a current density of 20 mA cm−2. The proposed electrochemical technology using a low-cost SnO2-MWCNT electrode is promising for wastewater BPA removal.
T2  - Journal of Water Process Engineering
T1  - Degradation of bisphenol A on SnO2-MWCNT electrode using electrochemical oxidation
VL  - 51
SP  - 103416
DO  - 10.1016/j.jwpe.2022.103416
ER  - 

@article{
author = "Simić, Marija and Savić, Branislava and Ognjanović, Miloš and Stanković, Dalibor M. and Relić, Dubravka J. and Aćimović, Danka D. and Brdarić, Tanja",
year = "2023",
abstract = "Bisphenol A (BPA) is an organic pollutant that is widely spread in waterbody with effluents as a result of its extensive use in the plastics industry. It posses to the class of compounds that are endocrine disruptors and has a great negative impact on living organisms. Therefore, the progress in development of green technology for BPA removal from the aquatic media is crucial for environmental protection. This paper presents BPA removal by electrochemical oxidation on SnO2-MWCNT (tin dioxide-multi walled carbon nanotube) nanocomposite anode. The nanocomposite was structural and morphological characterized by X-ray powder diffraction and transmission electron microscopy. Electrochemical properties of the SnO2-MWCNT anode were investigated using cyclic voltammetry, linear sweep voltammetry and electrical impedance spectroscopy. The electrochemical behavior of anodes toward BPA in sodium sulfate solutions has shown that BPA is oxidized by indirectly mechanism via hydroxyl radicals (verified by quenching tests). Electrolysis of BPA has been done in galvanostatic regime at current densities 2.5, 5.0, 10.0, 15.0 and 20.0 mA cm−2 in 0.1 M sodium sulfate supported electrolyte pH 4.0. Complete degradation of BPA was accomplished after 5 h of electrolysis at a current density of 20 mA cm−2. The proposed electrochemical technology using a low-cost SnO2-MWCNT electrode is promising for wastewater BPA removal.",
journal = "Journal of Water Process Engineering",
title = "Degradation of bisphenol A on SnO2-MWCNT electrode using electrochemical oxidation",
volume = "51",
pages = "103416",
doi = "10.1016/j.jwpe.2022.103416"
}

Simić, M., Savić, B., Ognjanović, M., Stanković, D. M., Relić, D. J., Aćimović, D. D.,& Brdarić, T.. (2023). Degradation of bisphenol A on SnO2-MWCNT electrode using electrochemical oxidation. in Journal of Water Process Engineering, 51, 103416.
https://doi.org/10.1016/j.jwpe.2022.103416

Simić M, Savić B, Ognjanović M, Stanković DM, Relić DJ, Aćimović DD, Brdarić T. Degradation of bisphenol A on SnO2-MWCNT electrode using electrochemical oxidation. in Journal of Water Process Engineering. 2023;51:103416.
doi:10.1016/j.jwpe.2022.103416 .

Simić, Marija, Savić, Branislava, Ognjanović, Miloš, Stanković, Dalibor M., Relić, Dubravka J., Aćimović, Danka D., Brdarić, Tanja, "Degradation of bisphenol A on SnO2-MWCNT electrode using electrochemical oxidation" in Journal of Water Process Engineering, 51 (2023):103416,
https://doi.org/10.1016/j.jwpe.2022.103416 . .

TY  - JOUR
AU  - Đurđić, Slađana
AU  - Vlahović, Filip
AU  - Markićević, Milan
AU  - Mutić, Jelena
AU  - Manojlović, Dragan
AU  - Stanković, Vesna
AU  - Švorc, Lubomír
AU  - Stanković, Dalibor M.
PY  - 2023
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/10618
AB  - Herein, a screen–printed diamond electrode (SPDE) coupled with a “point-of-care” platform (30 µL-drop concepts, single-drop-detection approach) was successfully applied for the electrochemical determination of pterostilbene (PTS). Cyclic voltammetry identified irreversible oxidation of PTS, where oxidation peak was shown to be strongly dependent on the pH of the working environmental. Although the proposition of the detailed electrochemical oxidation mechanism of PTS goes out of the scope of the present research, we have determined the most probable reactive site of our analyte, by utilizing DFT-based reactivity descriptors (Fukui functions). For electrochemical quantification of PTS, oxidation peak at 0.32 V (vs. Ag/AgCl) was followed in presence of 0.5 mol L−1 of Briton–Robinson buffer solution (pH = 9). Coupled with the optimized parameters of differential pulse voltammetry (DPV), SPDE detected PTS in two linear ranges (first range was from 0.011 to 0.912 µmol L−1; second range was from 0.912 to 4.420 µmol L−1), providing the LOD and LOQ on a nanomolar level (3.1 nmol L−1 and 10.0 nmol L−1, respectively). The selectivity of the optimized DPV method was found to be excellent, with the current changes of less than 7%, in the presence of ten times higher concentrations of the certain interferences. The practical applicability of the SPDE and single-drop-detection approach in dietary supplements (with a declared PTS content of 50 mg/tablet), with the recovery values ranging from 95 to 102%, shows that the developed method has high potential for precise and accurate PTS detection, as well as exceptional miniaturization possibilities of relevant equipment for on-site sensing.
T2  - Chemosensors
T1  - Application of Screen Printed Diamond Electrode, Coupled with “Point-of-Care” Platform, for Nanomolar Quantification of Phytonutrient Pterostilbene in Dietary Supplements: An Experimental Study Supported by Theory
VL  - 11
IS  - 1
SP  - 15
DO  - 10.3390/chemosensors11010015
ER  - 

@article{
author = "Đurđić, Slađana and Vlahović, Filip and Markićević, Milan and Mutić, Jelena and Manojlović, Dragan and Stanković, Vesna and Švorc, Lubomír and Stanković, Dalibor M.",
year = "2023",
abstract = "Herein, a screen–printed diamond electrode (SPDE) coupled with a “point-of-care” platform (30 µL-drop concepts, single-drop-detection approach) was successfully applied for the electrochemical determination of pterostilbene (PTS). Cyclic voltammetry identified irreversible oxidation of PTS, where oxidation peak was shown to be strongly dependent on the pH of the working environmental. Although the proposition of the detailed electrochemical oxidation mechanism of PTS goes out of the scope of the present research, we have determined the most probable reactive site of our analyte, by utilizing DFT-based reactivity descriptors (Fukui functions). For electrochemical quantification of PTS, oxidation peak at 0.32 V (vs. Ag/AgCl) was followed in presence of 0.5 mol L−1 of Briton–Robinson buffer solution (pH = 9). Coupled with the optimized parameters of differential pulse voltammetry (DPV), SPDE detected PTS in two linear ranges (first range was from 0.011 to 0.912 µmol L−1; second range was from 0.912 to 4.420 µmol L−1), providing the LOD and LOQ on a nanomolar level (3.1 nmol L−1 and 10.0 nmol L−1, respectively). The selectivity of the optimized DPV method was found to be excellent, with the current changes of less than 7%, in the presence of ten times higher concentrations of the certain interferences. The practical applicability of the SPDE and single-drop-detection approach in dietary supplements (with a declared PTS content of 50 mg/tablet), with the recovery values ranging from 95 to 102%, shows that the developed method has high potential for precise and accurate PTS detection, as well as exceptional miniaturization possibilities of relevant equipment for on-site sensing.",
journal = "Chemosensors",
title = "Application of Screen Printed Diamond Electrode, Coupled with “Point-of-Care” Platform, for Nanomolar Quantification of Phytonutrient Pterostilbene in Dietary Supplements: An Experimental Study Supported by Theory",
volume = "11",
number = "1",
pages = "15",
doi = "10.3390/chemosensors11010015"
}

Đurđić, S., Vlahović, F., Markićević, M., Mutić, J., Manojlović, D., Stanković, V., Švorc, L.,& Stanković, D. M.. (2023). Application of Screen Printed Diamond Electrode, Coupled with “Point-of-Care” Platform, for Nanomolar Quantification of Phytonutrient Pterostilbene in Dietary Supplements: An Experimental Study Supported by Theory. in Chemosensors, 11(1), 15.
https://doi.org/10.3390/chemosensors11010015

Đurđić S, Vlahović F, Markićević M, Mutić J, Manojlović D, Stanković V, Švorc L, Stanković DM. Application of Screen Printed Diamond Electrode, Coupled with “Point-of-Care” Platform, for Nanomolar Quantification of Phytonutrient Pterostilbene in Dietary Supplements: An Experimental Study Supported by Theory. in Chemosensors. 2023;11(1):15.
doi:10.3390/chemosensors11010015 .

Đurđić, Slađana, Vlahović, Filip, Markićević, Milan, Mutić, Jelena, Manojlović, Dragan, Stanković, Vesna, Švorc, Lubomír, Stanković, Dalibor M., "Application of Screen Printed Diamond Electrode, Coupled with “Point-of-Care” Platform, for Nanomolar Quantification of Phytonutrient Pterostilbene in Dietary Supplements: An Experimental Study Supported by Theory" in Chemosensors, 11, no. 1 (2023):15,
https://doi.org/10.3390/chemosensors11010015 . .

TY  - JOUR
AU  - Korina, Elena
AU  - Abramyan, Anton
AU  - Bol’shakov, Oleg
AU  - Avdin, Vyacheslav V.
AU  - Savić, Slađana
AU  - Manojlović, Dragan D.
AU  - Stanković, Vesna
AU  - Stanković, Dalibor M.
PY  - 2023
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/10621
AB  - Stable, water-soluble titanium complexed with mandelic acid was used as a precursor for titanium phosphorus double oxide obtained in hydrothermal conditions in the presence of phosphoric acid. Surprisingly, hydrolysis of organic complexes provided a microstructured sphere with narrow size distribution, low aggregation and a small fraction of morphological irregularities. Obtained microspheres had a complex structure comprised of flakes, whose size could be manipulated with temperature conditions. Samples were found to be electrochemically active against sulcotrione, a well-recognized herbicide. Electrochemical sensors based on the synthesized microspheres were successfully adapted for natural water reservoir analysis and exhibited low levels of detection of 0.61 µM, limit of quantification of 1.86 µM, wide dynamic linear range from 2 to 200 µM, good selectivity, excellent reproducibility and in-time stability.
T2  - Sensors
T1  - Microspherical Titanium-Phosphorus Double Oxide: Hierarchical Structure Development for Sensing Applications
VL  - 23
IS  - 2
SP  - 933
DO  - 10.3390/s23020933
ER  - 

@article{
author = "Korina, Elena and Abramyan, Anton and Bol’shakov, Oleg and Avdin, Vyacheslav V. and Savić, Slađana and Manojlović, Dragan D. and Stanković, Vesna and Stanković, Dalibor M.",
year = "2023",
abstract = "Stable, water-soluble titanium complexed with mandelic acid was used as a precursor for titanium phosphorus double oxide obtained in hydrothermal conditions in the presence of phosphoric acid. Surprisingly, hydrolysis of organic complexes provided a microstructured sphere with narrow size distribution, low aggregation and a small fraction of morphological irregularities. Obtained microspheres had a complex structure comprised of flakes, whose size could be manipulated with temperature conditions. Samples were found to be electrochemically active against sulcotrione, a well-recognized herbicide. Electrochemical sensors based on the synthesized microspheres were successfully adapted for natural water reservoir analysis and exhibited low levels of detection of 0.61 µM, limit of quantification of 1.86 µM, wide dynamic linear range from 2 to 200 µM, good selectivity, excellent reproducibility and in-time stability.",
journal = "Sensors",
title = "Microspherical Titanium-Phosphorus Double Oxide: Hierarchical Structure Development for Sensing Applications",
volume = "23",
number = "2",
pages = "933",
doi = "10.3390/s23020933"
}

Korina, E., Abramyan, A., Bol’shakov, O., Avdin, V. V., Savić, S., Manojlović, D. D., Stanković, V.,& Stanković, D. M.. (2023). Microspherical Titanium-Phosphorus Double Oxide: Hierarchical Structure Development for Sensing Applications. in Sensors, 23(2), 933.
https://doi.org/10.3390/s23020933

Korina E, Abramyan A, Bol’shakov O, Avdin VV, Savić S, Manojlović DD, Stanković V, Stanković DM. Microspherical Titanium-Phosphorus Double Oxide: Hierarchical Structure Development for Sensing Applications. in Sensors. 2023;23(2):933.
doi:10.3390/s23020933 .

Korina, Elena, Abramyan, Anton, Bol’shakov, Oleg, Avdin, Vyacheslav V., Savić, Slađana, Manojlović, Dragan D., Stanković, Vesna, Stanković, Dalibor M., "Microspherical Titanium-Phosphorus Double Oxide: Hierarchical Structure Development for Sensing Applications" in Sensors, 23, no. 2 (2023):933,
https://doi.org/10.3390/s23020933 . .

TY  - JOUR
AU  - Marković, Aleksandar
AU  - Savić, Slađana
AU  - Kukuruzar, Andrej J.
AU  - Konya, Zoltan
AU  - Manojlović, Dragan D.
AU  - Ognjanović, Miloš
AU  - Stanković, Dalibor M.
PY  - 2023
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/10689
AB  - In this paper, electrochemical degradation of Reactive Black 5 (RB5) textile azo dye was examined in regard to different synthesis procedures for making PbO2–graphitic carbon nitride (g-C3N4) electrode. The reaction of with ClO− in the presence of different surfactants, i.e., cetyltrimethylammonium bromide (CTAB) and tetrabutylammonium phosphate (TBAP), under conventional conditions, resulted in the formation of PbO2 with varying morphology. The obtained materials were combined with g-C3N4 for the preparation of the final composite materials, which were then characterized morphologically and electrochemically. After optimizing the degradation method, it was shown that an anode comprising a steel electrode coated with the composite of PbO2 synthesized using CTAB as template and g-C3N4, and using 0.15 M Na2SO4 as the supporting electrolyte, gave the best performance for RB5 dye removal from a 35 mg/L solution. The treatment duration was 60 min, applying a current of 0.17 A (electrode surface 4 cm2, current density of 42.5 mA/cm2), while the initial pH of the testing solution was 2. The reusability and longevity of the electrode surface (which showed no significant change in activity throughout the study) may suggest that this approach is a promising candidate for wastewater treatment and pollutant removal.
T2  - Catalysts
T1  - Differently prepared PbO2/graphitic carbon nitride composites for efficient electrochemical removal of Reactive Black 5 dye
VL  - 13
IS  - 2
SP  - 328
DO  - 10.3390/catal13020328
ER  - 

@article{
author = "Marković, Aleksandar and Savić, Slađana and Kukuruzar, Andrej J. and Konya, Zoltan and Manojlović, Dragan D. and Ognjanović, Miloš and Stanković, Dalibor M.",
year = "2023",
abstract = "In this paper, electrochemical degradation of Reactive Black 5 (RB5) textile azo dye was examined in regard to different synthesis procedures for making PbO2–graphitic carbon nitride (g-C3N4) electrode. The reaction of with ClO− in the presence of different surfactants, i.e., cetyltrimethylammonium bromide (CTAB) and tetrabutylammonium phosphate (TBAP), under conventional conditions, resulted in the formation of PbO2 with varying morphology. The obtained materials were combined with g-C3N4 for the preparation of the final composite materials, which were then characterized morphologically and electrochemically. After optimizing the degradation method, it was shown that an anode comprising a steel electrode coated with the composite of PbO2 synthesized using CTAB as template and g-C3N4, and using 0.15 M Na2SO4 as the supporting electrolyte, gave the best performance for RB5 dye removal from a 35 mg/L solution. The treatment duration was 60 min, applying a current of 0.17 A (electrode surface 4 cm2, current density of 42.5 mA/cm2), while the initial pH of the testing solution was 2. The reusability and longevity of the electrode surface (which showed no significant change in activity throughout the study) may suggest that this approach is a promising candidate for wastewater treatment and pollutant removal.",
journal = "Catalysts",
title = "Differently prepared PbO2/graphitic carbon nitride composites for efficient electrochemical removal of Reactive Black 5 dye",
volume = "13",
number = "2",
pages = "328",
doi = "10.3390/catal13020328"
}

Marković, A., Savić, S., Kukuruzar, A. J., Konya, Z., Manojlović, D. D., Ognjanović, M.,& Stanković, D. M.. (2023). Differently prepared PbO2/graphitic carbon nitride composites for efficient electrochemical removal of Reactive Black 5 dye. in Catalysts, 13(2), 328.
https://doi.org/10.3390/catal13020328

Marković A, Savić S, Kukuruzar AJ, Konya Z, Manojlović DD, Ognjanović M, Stanković DM. Differently prepared PbO2/graphitic carbon nitride composites for efficient electrochemical removal of Reactive Black 5 dye. in Catalysts. 2023;13(2):328.
doi:10.3390/catal13020328 .

Marković, Aleksandar, Savić, Slađana, Kukuruzar, Andrej J., Konya, Zoltan, Manojlović, Dragan D., Ognjanović, Miloš, Stanković, Dalibor M., "Differently prepared PbO2/graphitic carbon nitride composites for efficient electrochemical removal of Reactive Black 5 dye" in Catalysts, 13, no. 2 (2023):328,
https://doi.org/10.3390/catal13020328 . .

TY  - JOUR
AU  - Mijajlović, Aleksandar
AU  - Ognjanović, Miloš
AU  - Manojlović, Dragan
AU  - Vlahović, Filip
AU  - Ðurđić, Slađana
AU  - Stanković, Vesna
AU  - Stanković, Dalibor M.
PY  - 2023
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/10692
AB  - There are ten million people in the world who have Parkinson’s disease. The most potent medicine for Parkinson’s disease is levodopa (L-DOPA). However, long-term consumption of L-DOPA leads to the appearance of side effects, as a result of which the control and monitoring of its concentrations are of great importance. In this work, we have designed a new electrochemical sensor for detecting L-DOPA using a carbon paste electrode (CPE) modified with Eu2O3@Cr2O3 composite nanoparticles. Rare earth elements, including Eu, are increasingly used to design new electrode nanocomposites with enhanced electrocatalytic properties. Europium has been considered a significant lanthanide element with greater redox reaction behavior. We conducted a hydrothermal synthesis of Eu2O3@Cr2O3 and, for the first time, the acquired nanoparticles were used to modify CPE. The proposed Eu2O3@Cr2O3/CPE electrode was investigated in terms of its electrocatalytic properties and then used to develop an analytical method for detecting and quantifying L-DOPA. The proposed sensor offers a wide linear range (1–100 µM), high sensitivity (1.38 µA µM−1 cm−2) and a low detection limit (0.72 µM). The practical application of the proposed sensor was investigated by analyzing commercially available pharmaceutical tablets of L-DOPA. The corresponding results indicate the excellent potential of the Eu2O3@Cr2O3/CPE sensor for application in real-time L-DOPA detection.
T2  - Biosensors
T1  - Eu2O3@Cr2O3 Nanoparticles-Modified Carbon Paste Electrode for Efficient Electrochemical Sensing of Neurotransmitters Precursor L-DOPA
VL  - 13
IS  - 2
SP  - 201
DO  - 10.3390/bios13020201
ER  - 

@article{
author = "Mijajlović, Aleksandar and Ognjanović, Miloš and Manojlović, Dragan and Vlahović, Filip and Ðurđić, Slađana and Stanković, Vesna and Stanković, Dalibor M.",
year = "2023",
abstract = "There are ten million people in the world who have Parkinson’s disease. The most potent medicine for Parkinson’s disease is levodopa (L-DOPA). However, long-term consumption of L-DOPA leads to the appearance of side effects, as a result of which the control and monitoring of its concentrations are of great importance. In this work, we have designed a new electrochemical sensor for detecting L-DOPA using a carbon paste electrode (CPE) modified with Eu2O3@Cr2O3 composite nanoparticles. Rare earth elements, including Eu, are increasingly used to design new electrode nanocomposites with enhanced electrocatalytic properties. Europium has been considered a significant lanthanide element with greater redox reaction behavior. We conducted a hydrothermal synthesis of Eu2O3@Cr2O3 and, for the first time, the acquired nanoparticles were used to modify CPE. The proposed Eu2O3@Cr2O3/CPE electrode was investigated in terms of its electrocatalytic properties and then used to develop an analytical method for detecting and quantifying L-DOPA. The proposed sensor offers a wide linear range (1–100 µM), high sensitivity (1.38 µA µM−1 cm−2) and a low detection limit (0.72 µM). The practical application of the proposed sensor was investigated by analyzing commercially available pharmaceutical tablets of L-DOPA. The corresponding results indicate the excellent potential of the Eu2O3@Cr2O3/CPE sensor for application in real-time L-DOPA detection.",
journal = "Biosensors",
title = "Eu2O3@Cr2O3 Nanoparticles-Modified Carbon Paste Electrode for Efficient Electrochemical Sensing of Neurotransmitters Precursor L-DOPA",
volume = "13",
number = "2",
pages = "201",
doi = "10.3390/bios13020201"
}

Mijajlović, A., Ognjanović, M., Manojlović, D., Vlahović, F., Ðurđić, S., Stanković, V.,& Stanković, D. M.. (2023). Eu2O3@Cr2O3 Nanoparticles-Modified Carbon Paste Electrode for Efficient Electrochemical Sensing of Neurotransmitters Precursor L-DOPA. in Biosensors, 13(2), 201.
https://doi.org/10.3390/bios13020201

Mijajlović A, Ognjanović M, Manojlović D, Vlahović F, Ðurđić S, Stanković V, Stanković DM. Eu2O3@Cr2O3 Nanoparticles-Modified Carbon Paste Electrode for Efficient Electrochemical Sensing of Neurotransmitters Precursor L-DOPA. in Biosensors. 2023;13(2):201.
doi:10.3390/bios13020201 .

Mijajlović, Aleksandar, Ognjanović, Miloš, Manojlović, Dragan, Vlahović, Filip, Ðurđić, Slađana, Stanković, Vesna, Stanković, Dalibor M., "Eu2O3@Cr2O3 Nanoparticles-Modified Carbon Paste Electrode for Efficient Electrochemical Sensing of Neurotransmitters Precursor L-DOPA" in Biosensors, 13, no. 2 (2023):201,
https://doi.org/10.3390/bios13020201 . .

TY  - JOUR
AU  - Ognjanović, Miloš
AU  - Jaćimović, Željko
AU  - Kosović-Perutović, Milica
AU  - Besu Žižak, Irina
AU  - Stanojković, Tatjana
AU  - Žižak, Željko
AU  - Dojčinović, Biljana
AU  - Stanković, Dalibor M.
AU  - Antić, Bratislav
PY  - 2023
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/10733
AB  - Partial cation substitution can significantly change the physical properties of parent compounds. By controlling the chemical composition and knowing the mutual relationship between composition and physical properties, it is possible to tailor the properties of materials to those that are superior for desired technological application. Using the polyol synthesis procedure, a series of yttrium-substituted iron oxide nanoconstructs, γ-Fe2−xYxO3 (YIONs), was prepared. It was found that Y3+ could substitute Fe3+ in the crystal structures of maghemite (γ-Fe2O3) up to a limited concentration of ~1.5% (γ-Fe1.969Y0.031O3). Analysis of TEM micrographs showed that crystallites or particles were aggregated in flower-like structures with diameters from 53.7 ± 6.2 nm to 97.3 ± 37.0 nm, depending on yttrium concentration. To be investigated for potential applications as magnetic hyperthermia agents, YIONs were tested twice: their heating efficiency was tested and their toxicity was investigated. The Specific Absorption Rate (SAR) values were in the range of 32.6 W/g to 513 W/g and significantly decreased with increased yttrium concentration in the samples. Intrinsic loss power (ILP) for γ-Fe2O3 and γ-Fe1.995Y0.005O3 were ~8–9 nH·m2/Kg, which pointed to their excellent heating efficiency. IC50 values of investigated samples against cancer (HeLa) and normal (MRC-5) cells decreased with increased yttrium concentration and were higher than ~300 μg/mL. The samples of γ-Fe2−xYxO3 did not show a genotoxic effect. The results of toxicity studies show that YIONs are suitable for further in vitro/in vivo studies toward to their potential medical applications, while results of heat generation point to their potential use in magnetic hyperthermia cancer treatment or use as self-heating systems for other technological applications such as catalysis.
T2  - Nanomaterials
T1  - Self-Heating Flower-like Nanoconstructs with Limited Incorporation of Yttrium in Maghemite: Effect of Chemical Composition on Heating Efficiency, Cytotoxicity and Genotoxicity
VL  - 13
IS  - 5
SP  - 870
DO  - 10.3390/nano13050870
ER  - 

@article{
author = "Ognjanović, Miloš and Jaćimović, Željko and Kosović-Perutović, Milica and Besu Žižak, Irina and Stanojković, Tatjana and Žižak, Željko and Dojčinović, Biljana and Stanković, Dalibor M. and Antić, Bratislav",
year = "2023",
abstract = "Partial cation substitution can significantly change the physical properties of parent compounds. By controlling the chemical composition and knowing the mutual relationship between composition and physical properties, it is possible to tailor the properties of materials to those that are superior for desired technological application. Using the polyol synthesis procedure, a series of yttrium-substituted iron oxide nanoconstructs, γ-Fe2−xYxO3 (YIONs), was prepared. It was found that Y3+ could substitute Fe3+ in the crystal structures of maghemite (γ-Fe2O3) up to a limited concentration of ~1.5% (γ-Fe1.969Y0.031O3). Analysis of TEM micrographs showed that crystallites or particles were aggregated in flower-like structures with diameters from 53.7 ± 6.2 nm to 97.3 ± 37.0 nm, depending on yttrium concentration. To be investigated for potential applications as magnetic hyperthermia agents, YIONs were tested twice: their heating efficiency was tested and their toxicity was investigated. The Specific Absorption Rate (SAR) values were in the range of 32.6 W/g to 513 W/g and significantly decreased with increased yttrium concentration in the samples. Intrinsic loss power (ILP) for γ-Fe2O3 and γ-Fe1.995Y0.005O3 were ~8–9 nH·m2/Kg, which pointed to their excellent heating efficiency. IC50 values of investigated samples against cancer (HeLa) and normal (MRC-5) cells decreased with increased yttrium concentration and were higher than ~300 μg/mL. The samples of γ-Fe2−xYxO3 did not show a genotoxic effect. The results of toxicity studies show that YIONs are suitable for further in vitro/in vivo studies toward to their potential medical applications, while results of heat generation point to their potential use in magnetic hyperthermia cancer treatment or use as self-heating systems for other technological applications such as catalysis.",
journal = "Nanomaterials",
title = "Self-Heating Flower-like Nanoconstructs with Limited Incorporation of Yttrium in Maghemite: Effect of Chemical Composition on Heating Efficiency, Cytotoxicity and Genotoxicity",
volume = "13",
number = "5",
pages = "870",
doi = "10.3390/nano13050870"
}

Ognjanović, M., Jaćimović, Ž., Kosović-Perutović, M., Besu Žižak, I., Stanojković, T., Žižak, Ž., Dojčinović, B., Stanković, D. M.,& Antić, B.. (2023). Self-Heating Flower-like Nanoconstructs with Limited Incorporation of Yttrium in Maghemite: Effect of Chemical Composition on Heating Efficiency, Cytotoxicity and Genotoxicity. in Nanomaterials, 13(5), 870.
https://doi.org/10.3390/nano13050870

Ognjanović M, Jaćimović Ž, Kosović-Perutović M, Besu Žižak I, Stanojković T, Žižak Ž, Dojčinović B, Stanković DM, Antić B. Self-Heating Flower-like Nanoconstructs with Limited Incorporation of Yttrium in Maghemite: Effect of Chemical Composition on Heating Efficiency, Cytotoxicity and Genotoxicity. in Nanomaterials. 2023;13(5):870.
doi:10.3390/nano13050870 .

Ognjanović, Miloš, Jaćimović, Željko, Kosović-Perutović, Milica, Besu Žižak, Irina, Stanojković, Tatjana, Žižak, Željko, Dojčinović, Biljana, Stanković, Dalibor M., Antić, Bratislav, "Self-Heating Flower-like Nanoconstructs with Limited Incorporation of Yttrium in Maghemite: Effect of Chemical Composition on Heating Efficiency, Cytotoxicity and Genotoxicity" in Nanomaterials, 13, no. 5 (2023):870,
https://doi.org/10.3390/nano13050870 . .

TY  - JOUR
AU  - Mutić, Tijana
AU  - Ognjanović, Miloš
AU  - Kodranov, Igor
AU  - Robić, Marko
AU  - Savić, Slađana
AU  - Krehula, Stjepko
AU  - Stanković, Dalibor M.
PY  - 2023
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/10737
AB  - In this work, we investigated the morphological and electrochemical properties of gallium/bismuth mixed oxide. The bismuth concentration was varied from 0 to 100%. The correct ratio was determined with inductively coupled plasma-optical emission spectroscopy (ICP-OES), while surface characteristics were determined using scanning electron microscopy (SEM) and X-ray diffraction (XRD) measurement. Electrochemical characteristics were studied using electrochemical impedance spectroscopy (EIS) in the Fe2+/3+ couple. The obtained materials were tested for adrenaline detection. After square wave voltammetry (SWV) optimization, the best electrode showed a wide linear working range from 7 to 100 µM at pH 6 of the Britton–Robinson buffer solution (BRBS) supporting electrolyte. The limit of detection (LOD) for the proposed method was calculated as 1.9 µM, with a limit of quantification (LOQ) of 5.8 µM. The excellent selectivity of the proposed method, with good repeatability and reproducibility, strongly suggests the possible application of the procedure for the determination of adrenaline in artificially prepared real samples. The practical applicability with good recovery values indicates that the morphology of the materials is closely connected with other parameters, which further suggests that the developed approach can offer a low-cost, rapid, selective, and sensitive method for adrenaline monitoring. Graphical abstract: [Figure not available: see fulltext.] © 2023, Springer-Verlag GmbH Germany, part of Springer Nature.
T2  - Analytical and Bioanalytical Chemistry
T1  - The influence of bismuth participation on the morphological and electrochemical characteristics of gallium oxide for the detection of adrenaline
VL  - 415
SP  - 4445
EP  - 4458
DO  - 10.1007/s00216-023-04617-7
ER  - 

@article{
author = "Mutić, Tijana and Ognjanović, Miloš and Kodranov, Igor and Robić, Marko and Savić, Slađana and Krehula, Stjepko and Stanković, Dalibor M.",
year = "2023",
abstract = "In this work, we investigated the morphological and electrochemical properties of gallium/bismuth mixed oxide. The bismuth concentration was varied from 0 to 100%. The correct ratio was determined with inductively coupled plasma-optical emission spectroscopy (ICP-OES), while surface characteristics were determined using scanning electron microscopy (SEM) and X-ray diffraction (XRD) measurement. Electrochemical characteristics were studied using electrochemical impedance spectroscopy (EIS) in the Fe2+/3+ couple. The obtained materials were tested for adrenaline detection. After square wave voltammetry (SWV) optimization, the best electrode showed a wide linear working range from 7 to 100 µM at pH 6 of the Britton–Robinson buffer solution (BRBS) supporting electrolyte. The limit of detection (LOD) for the proposed method was calculated as 1.9 µM, with a limit of quantification (LOQ) of 5.8 µM. The excellent selectivity of the proposed method, with good repeatability and reproducibility, strongly suggests the possible application of the procedure for the determination of adrenaline in artificially prepared real samples. The practical applicability with good recovery values indicates that the morphology of the materials is closely connected with other parameters, which further suggests that the developed approach can offer a low-cost, rapid, selective, and sensitive method for adrenaline monitoring. Graphical abstract: [Figure not available: see fulltext.] © 2023, Springer-Verlag GmbH Germany, part of Springer Nature.",
journal = "Analytical and Bioanalytical Chemistry",
title = "The influence of bismuth participation on the morphological and electrochemical characteristics of gallium oxide for the detection of adrenaline",
volume = "415",
pages = "4445-4458",
doi = "10.1007/s00216-023-04617-7"
}

Mutić, T., Ognjanović, M., Kodranov, I., Robić, M., Savić, S., Krehula, S.,& Stanković, D. M.. (2023). The influence of bismuth participation on the morphological and electrochemical characteristics of gallium oxide for the detection of adrenaline. in Analytical and Bioanalytical Chemistry, 415, 4445-4458.
https://doi.org/10.1007/s00216-023-04617-7

Mutić T, Ognjanović M, Kodranov I, Robić M, Savić S, Krehula S, Stanković DM. The influence of bismuth participation on the morphological and electrochemical characteristics of gallium oxide for the detection of adrenaline. in Analytical and Bioanalytical Chemistry. 2023;415:4445-4458.
doi:10.1007/s00216-023-04617-7 .

Mutić, Tijana, Ognjanović, Miloš, Kodranov, Igor, Robić, Marko, Savić, Slađana, Krehula, Stjepko, Stanković, Dalibor M., "The influence of bismuth participation on the morphological and electrochemical characteristics of gallium oxide for the detection of adrenaline" in Analytical and Bioanalytical Chemistry, 415 (2023):4445-4458,
https://doi.org/10.1007/s00216-023-04617-7 . .

TY  - JOUR
AU  - Mutić, Tijana
AU  - Ognjanović, Miloš
AU  - Kodranov, Igor
AU  - Robić, Marko
AU  - Savić, Slađana
AU  - Krehula, Stjepko
AU  - Stanković, Dalibor M.
PY  - 2023
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/10855
AB  - Author Tijana Mutić should be afliated to afliation 4.
Afliation 4 should be added: Faculty of Pharmacy University of Belgrade – Department of Analytical Chemistry, Vojvode Stepe 450, 11,221 Belgrade, Serbia
T2  - Analytical and Bioanalytical Chemistry
T1  - Correction to: The influence of bismuth participation on the morphological and electrochemical characteristics of gallium oxide for the detection of adrenaline
DO  - 10.1007/s00216-023-04674-y
ER  - 

@article{
author = "Mutić, Tijana and Ognjanović, Miloš and Kodranov, Igor and Robić, Marko and Savić, Slađana and Krehula, Stjepko and Stanković, Dalibor M.",
year = "2023",
abstract = "Author Tijana Mutić should be afliated to afliation 4.
Afliation 4 should be added: Faculty of Pharmacy University of Belgrade – Department of Analytical Chemistry, Vojvode Stepe 450, 11,221 Belgrade, Serbia",
journal = "Analytical and Bioanalytical Chemistry",
title = "Correction to: The influence of bismuth participation on the morphological and electrochemical characteristics of gallium oxide for the detection of adrenaline",
doi = "10.1007/s00216-023-04674-y"
}

Mutić, T., Ognjanović, M., Kodranov, I., Robić, M., Savić, S., Krehula, S.,& Stanković, D. M.. (2023). Correction to: The influence of bismuth participation on the morphological and electrochemical characteristics of gallium oxide for the detection of adrenaline. in Analytical and Bioanalytical Chemistry.
https://doi.org/10.1007/s00216-023-04674-y

Mutić T, Ognjanović M, Kodranov I, Robić M, Savić S, Krehula S, Stanković DM. Correction to: The influence of bismuth participation on the morphological and electrochemical characteristics of gallium oxide for the detection of adrenaline. in Analytical and Bioanalytical Chemistry. 2023;.
doi:10.1007/s00216-023-04674-y .

Mutić, Tijana, Ognjanović, Miloš, Kodranov, Igor, Robić, Marko, Savić, Slađana, Krehula, Stjepko, Stanković, Dalibor M., "Correction to: The influence of bismuth participation on the morphological and electrochemical characteristics of gallium oxide for the detection of adrenaline" in Analytical and Bioanalytical Chemistry (2023),
https://doi.org/10.1007/s00216-023-04674-y . .

TY  - JOUR
AU  - Milikić, Jadranka
AU  - Knežević, Sara
AU  - Ognjanović, Miloš
AU  - Stanković, Dalibor M.
AU  - Rakočević, Lazar
AU  - Šljukić, Biljana
PY  - 2023
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/10860
AB  - Porous cobalt (III) oxide (Co3O4) and mixed cobalt (III) oxide - tin oxide (Co3O4/SnO2) were prepared by a novel template-based hydrothermal method resulting in their spherical morphology as confirmed by thorough physico-chemical characterisation. Two oxides were systematically examined as bifunctional electrocatalysts for oxygen reduction (ORR) and evolution (OER) reaction in alkaline media by voltammetry with rotating disk electrode, electrochemical impedance spectroscopy, and chronoamperometry. Low-cost Co3O4 and Co3O4/SnO2 electrocatalysts showed excellent ORR performance with low onset and half-wave potential, low Tafel slope, and the number of exchange electrons near 4, comparable to the commercial Pt/C electrocatalyst. Low OER onset potential of 1.52 and 1.57 V was observed for Co3O4 and Co3O4/SnO2, respectively, with low charge transfer resistance under anodic polarization conditions. Finally, to test bifunctional activity and durability of the two electrocatalyst, switch OER/ORR test was carried out.
T2  - International Journal of Hydrogen Energy
T1  - Template-based synthesis of Co3O4 and Co3O4/SnO2 bifunctional catalysts with enhanced electrocatalytic properties for reversible oxygen evolution and reduction reaction
IS  - InPress
DO  - 10.1016/j.ijhydene.2023.03.433
ER  - 

@article{
author = "Milikić, Jadranka and Knežević, Sara and Ognjanović, Miloš and Stanković, Dalibor M. and Rakočević, Lazar and Šljukić, Biljana",
year = "2023",
abstract = "Porous cobalt (III) oxide (Co3O4) and mixed cobalt (III) oxide - tin oxide (Co3O4/SnO2) were prepared by a novel template-based hydrothermal method resulting in their spherical morphology as confirmed by thorough physico-chemical characterisation. Two oxides were systematically examined as bifunctional electrocatalysts for oxygen reduction (ORR) and evolution (OER) reaction in alkaline media by voltammetry with rotating disk electrode, electrochemical impedance spectroscopy, and chronoamperometry. Low-cost Co3O4 and Co3O4/SnO2 electrocatalysts showed excellent ORR performance with low onset and half-wave potential, low Tafel slope, and the number of exchange electrons near 4, comparable to the commercial Pt/C electrocatalyst. Low OER onset potential of 1.52 and 1.57 V was observed for Co3O4 and Co3O4/SnO2, respectively, with low charge transfer resistance under anodic polarization conditions. Finally, to test bifunctional activity and durability of the two electrocatalyst, switch OER/ORR test was carried out.",
journal = "International Journal of Hydrogen Energy",
title = "Template-based synthesis of Co3O4 and Co3O4/SnO2 bifunctional catalysts with enhanced electrocatalytic properties for reversible oxygen evolution and reduction reaction",
number = "InPress",
doi = "10.1016/j.ijhydene.2023.03.433"
}

Milikić, J., Knežević, S., Ognjanović, M., Stanković, D. M., Rakočević, L.,& Šljukić, B.. (2023). Template-based synthesis of Co3O4 and Co3O4/SnO2 bifunctional catalysts with enhanced electrocatalytic properties for reversible oxygen evolution and reduction reaction. in International Journal of Hydrogen Energy(InPress).
https://doi.org/10.1016/j.ijhydene.2023.03.433

Milikić J, Knežević S, Ognjanović M, Stanković DM, Rakočević L, Šljukić B. Template-based synthesis of Co3O4 and Co3O4/SnO2 bifunctional catalysts with enhanced electrocatalytic properties for reversible oxygen evolution and reduction reaction. in International Journal of Hydrogen Energy. 2023;(InPress).
doi:10.1016/j.ijhydene.2023.03.433 .

Milikić, Jadranka, Knežević, Sara, Ognjanović, Miloš, Stanković, Dalibor M., Rakočević, Lazar, Šljukić, Biljana, "Template-based synthesis of Co3O4 and Co3O4/SnO2 bifunctional catalysts with enhanced electrocatalytic properties for reversible oxygen evolution and reduction reaction" in International Journal of Hydrogen Energy, no. InPress (2023),
https://doi.org/10.1016/j.ijhydene.2023.03.433 . .

TY  - JOUR
AU  - Vlahović, Filip
AU  - Ognjanović, Miloš
AU  - Đurđić, Slađana
AU  - Kukuruzar, Andrej
AU  - Antić, Bratislav
AU  - Dojčinović, Biljana
AU  - Stanković, Dalibor M.
PY  - 2023
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/10919
AB  - We have set-up an electrochemical advanced oxidation process for ethidium bromide (1), based on the Eu-doped MnWO4 (Eu:MnWO4), obtained through a template-driven synthesis, along with developing a suitable monitoring method. Under galvanostatic conditions, Eu:MnWO4-coated graphite electrode serves as anode, applicable for removal of 1. To go further and augment the catalytic method, we have applied a modified carbon paste electrode for the monitoring of 1 with the limit of detection (LOD) of 54 nM. Enhancement of the hydrogen evolution reaction is an indication of electrocatalytic properties of the material, whereby developed method emerges as a candidate for straightforward application in electrochemical advanced oxidation processes (EAOPs). We have enriched experimental data with theoretical insights, provided by Density Functional Theory (DFT), and proposed oxidation mechanism of 1. Based on obtained results, we propose the new nanomaterial as a potent electrochemical modifier, suitable for catalytic treatment and process monitoring of the 1-polluted waters.
T2  - Applied Catalysis B: Environmental
T1  - Design of an ethidium bromide control circuit supported by deep theoretical insight
VL  - 334
SP  - 122819
DO  - 10.1016/j.apcatb.2023.122819
ER  - 

@article{
author = "Vlahović, Filip and Ognjanović, Miloš and Đurđić, Slađana and Kukuruzar, Andrej and Antić, Bratislav and Dojčinović, Biljana and Stanković, Dalibor M.",
year = "2023",
abstract = "We have set-up an electrochemical advanced oxidation process for ethidium bromide (1), based on the Eu-doped MnWO4 (Eu:MnWO4), obtained through a template-driven synthesis, along with developing a suitable monitoring method. Under galvanostatic conditions, Eu:MnWO4-coated graphite electrode serves as anode, applicable for removal of 1. To go further and augment the catalytic method, we have applied a modified carbon paste electrode for the monitoring of 1 with the limit of detection (LOD) of 54 nM. Enhancement of the hydrogen evolution reaction is an indication of electrocatalytic properties of the material, whereby developed method emerges as a candidate for straightforward application in electrochemical advanced oxidation processes (EAOPs). We have enriched experimental data with theoretical insights, provided by Density Functional Theory (DFT), and proposed oxidation mechanism of 1. Based on obtained results, we propose the new nanomaterial as a potent electrochemical modifier, suitable for catalytic treatment and process monitoring of the 1-polluted waters.",
journal = "Applied Catalysis B: Environmental",
title = "Design of an ethidium bromide control circuit supported by deep theoretical insight",
volume = "334",
pages = "122819",
doi = "10.1016/j.apcatb.2023.122819"
}

Vlahović, F., Ognjanović, M., Đurđić, S., Kukuruzar, A., Antić, B., Dojčinović, B.,& Stanković, D. M.. (2023). Design of an ethidium bromide control circuit supported by deep theoretical insight. in Applied Catalysis B: Environmental, 334, 122819.
https://doi.org/10.1016/j.apcatb.2023.122819

Vlahović F, Ognjanović M, Đurđić S, Kukuruzar A, Antić B, Dojčinović B, Stanković DM. Design of an ethidium bromide control circuit supported by deep theoretical insight. in Applied Catalysis B: Environmental. 2023;334:122819.
doi:10.1016/j.apcatb.2023.122819 .

Vlahović, Filip, Ognjanović, Miloš, Đurđić, Slađana, Kukuruzar, Andrej, Antić, Bratislav, Dojčinović, Biljana, Stanković, Dalibor M., "Design of an ethidium bromide control circuit supported by deep theoretical insight" in Applied Catalysis B: Environmental, 334 (2023):122819,
https://doi.org/10.1016/j.apcatb.2023.122819 . .

TY  - JOUR
AU  - Anđelković, Ljubica
AU  - Šuljagić, Marija
AU  - Mirković, Miljana
AU  - Pavlović, Vera P.
AU  - Petronijević, Ivan
AU  - Stanković, Dalibor M.
AU  - Jeremić, Dejan
AU  - Uskoković, Vuk
PY  - 2023
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/10935
AB  - The combination of an intense absorption of visible light and p-type semiconducting nature makes spinel cobalt oxide (Co3O4) a very attractive material for various optoelectronic applications. However, the traditional methods for its synthesis have been either time- and energy-consuming or relying on toxic chemicals. To solve this issue, a simple, facile, and eco-friendly method of synthesis was successfully developed to obtain spinel Co3O4 nanoparticles. The novel method for obtaining pure and monophasic Co3O4 reported here is based on the thermal decomposition of hexaaquacobalt(II) D-camphor10-sulfonate at 900 °C. This fast solid-state synthesis route overcomes the disadvantages of many combustion methods, most critically by avoiding the use of toxic organic solvents. The synthesized material was subjected to a detailed characterization to assess its potential for use as a nanocatalyst. The band gap measurements indicated the presence of two band gaps, one at 2.10 eV and another at 1.22 eV, confirming the purity and semiconducting properties of the sample. The electrochemical studies demonstrated a significant enhancement in the electron transfer kinetics with the addition of the synthesized Co3O4 to the carbon-paste electrode, leading to an enhanced electrocatalytic performance. These prominent functional properties, suitable for a wide range of technological applications, pave way for the implementation of the reported method for the synthesis of Co3O4 on a larger industrial scale. © 2023 Elsevier Ltd and Techna Group S.r.l.
T2  - Ceramics International
T1  - Semiconducting cobalt oxide nanocatalyst obtained through an eco-friendly thermal decomposition
VL  - 49
IS  - 14, Part A
SP  - 23491
EP  - 23498
DO  - 10.1016/j.ceramint.2023.04.182
ER  - 

@article{
author = "Anđelković, Ljubica and Šuljagić, Marija and Mirković, Miljana and Pavlović, Vera P. and Petronijević, Ivan and Stanković, Dalibor M. and Jeremić, Dejan and Uskoković, Vuk",
year = "2023",
abstract = "The combination of an intense absorption of visible light and p-type semiconducting nature makes spinel cobalt oxide (Co3O4) a very attractive material for various optoelectronic applications. However, the traditional methods for its synthesis have been either time- and energy-consuming or relying on toxic chemicals. To solve this issue, a simple, facile, and eco-friendly method of synthesis was successfully developed to obtain spinel Co3O4 nanoparticles. The novel method for obtaining pure and monophasic Co3O4 reported here is based on the thermal decomposition of hexaaquacobalt(II) D-camphor10-sulfonate at 900 °C. This fast solid-state synthesis route overcomes the disadvantages of many combustion methods, most critically by avoiding the use of toxic organic solvents. The synthesized material was subjected to a detailed characterization to assess its potential for use as a nanocatalyst. The band gap measurements indicated the presence of two band gaps, one at 2.10 eV and another at 1.22 eV, confirming the purity and semiconducting properties of the sample. The electrochemical studies demonstrated a significant enhancement in the electron transfer kinetics with the addition of the synthesized Co3O4 to the carbon-paste electrode, leading to an enhanced electrocatalytic performance. These prominent functional properties, suitable for a wide range of technological applications, pave way for the implementation of the reported method for the synthesis of Co3O4 on a larger industrial scale. © 2023 Elsevier Ltd and Techna Group S.r.l.",
journal = "Ceramics International",
title = "Semiconducting cobalt oxide nanocatalyst obtained through an eco-friendly thermal decomposition",
volume = "49",
number = "14, Part A",
pages = "23491-23498",
doi = "10.1016/j.ceramint.2023.04.182"
}

Anđelković, L., Šuljagić, M., Mirković, M., Pavlović, V. P., Petronijević, I., Stanković, D. M., Jeremić, D.,& Uskoković, V.. (2023). Semiconducting cobalt oxide nanocatalyst obtained through an eco-friendly thermal decomposition. in Ceramics International, 49(14, Part A), 23491-23498.
https://doi.org/10.1016/j.ceramint.2023.04.182

Anđelković L, Šuljagić M, Mirković M, Pavlović VP, Petronijević I, Stanković DM, Jeremić D, Uskoković V. Semiconducting cobalt oxide nanocatalyst obtained through an eco-friendly thermal decomposition. in Ceramics International. 2023;49(14, Part A):23491-23498.
doi:10.1016/j.ceramint.2023.04.182 .

Anđelković, Ljubica, Šuljagić, Marija, Mirković, Miljana, Pavlović, Vera P., Petronijević, Ivan, Stanković, Dalibor M., Jeremić, Dejan, Uskoković, Vuk, "Semiconducting cobalt oxide nanocatalyst obtained through an eco-friendly thermal decomposition" in Ceramics International, 49, no. 14, Part A (2023):23491-23498,
https://doi.org/10.1016/j.ceramint.2023.04.182 . .

TY  - JOUR
AU  - Knežević, Sanja
AU  - Ivanović, Marija
AU  - Stanković, Dalibor M.
AU  - Kisić, Danilo
AU  - Nenadović, Snežana
AU  - Potočnik, Jelena
AU  - Nenadović, Miloš
PY  - 2023
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/11074
AB  - The following investigation presents the thermal treatment of geopolymer at 300 °C, 600 °C and 900 °C. We investigated what happens to the geopolymer base when incorporated with 1% and 5% of neodymium in the form Nd2O3. A total of six samples were synthesized. Geopolymer 1 contained 1% and geopolymer 2 contained 5% Nd2O3, and these samples were treated at 300 °C; then, samples geopolymer 3 and geopolymer 4 also had the same percentage composition of Nd2O3 and were treated at 600 °C, while samples geopolymer 5 and geopolymer 6were treated at 900 °C. Physical and chemical changes in the aluminosilicate geopolymer matrix were monitored. The incorporation of rare earths into the polymer network of aluminosilicates has been proven to disrupt the basic structure of geopolymers; however, with increased temperatures, these materials show even more unusual properties. Diffuse reflectance infrared Fourier transform (DRIFT) analysis showed that the intensity of the vibrational band decreases with the increase in temperature during thermal treatment, suggesting alterations in the chemical structure of the geopolymers. Transmission electron microscopy (TEM) analysis showed that the diameter of the nanoparticles containing Al2O3 is in the range 5–10 nm, while larger crystallites range from 30 to 80 nm. Scanning electron microscopy (SEM) analysis revealed that the temperature of the thermal treatment increases to 300 °C and 600 °C; the porosity of geopolymer increases in the form of the appearance of large pores and cracks in material. X-ray photoelectron spectroscopy (XPS) analysis was used to investigate the surface chemistry of geopolymers, including the chemical composition of the surface, the oxidation state of the elements, and the presence of functional groups. The UV/Vis spectra of the synthesized geopolymers doped with Nd3+ show interesting optical properties at 900 °C; the geopolymer matrix completely disintegrates and an amorphous phase with a rare-earth precipitate appears.
T2  - Nanomaterials
T1  - Microstructural Analysis of Thermally Treated Geopolymer Incorporated with Neodymium
VL  - 13
IS  - 10
SP  - 1663
DO  - 10.3390/nano13101663
ER  - 

@article{
author = "Knežević, Sanja and Ivanović, Marija and Stanković, Dalibor M. and Kisić, Danilo and Nenadović, Snežana and Potočnik, Jelena and Nenadović, Miloš",
year = "2023",
abstract = "The following investigation presents the thermal treatment of geopolymer at 300 °C, 600 °C and 900 °C. We investigated what happens to the geopolymer base when incorporated with 1% and 5% of neodymium in the form Nd2O3. A total of six samples were synthesized. Geopolymer 1 contained 1% and geopolymer 2 contained 5% Nd2O3, and these samples were treated at 300 °C; then, samples geopolymer 3 and geopolymer 4 also had the same percentage composition of Nd2O3 and were treated at 600 °C, while samples geopolymer 5 and geopolymer 6were treated at 900 °C. Physical and chemical changes in the aluminosilicate geopolymer matrix were monitored. The incorporation of rare earths into the polymer network of aluminosilicates has been proven to disrupt the basic structure of geopolymers; however, with increased temperatures, these materials show even more unusual properties. Diffuse reflectance infrared Fourier transform (DRIFT) analysis showed that the intensity of the vibrational band decreases with the increase in temperature during thermal treatment, suggesting alterations in the chemical structure of the geopolymers. Transmission electron microscopy (TEM) analysis showed that the diameter of the nanoparticles containing Al2O3 is in the range 5–10 nm, while larger crystallites range from 30 to 80 nm. Scanning electron microscopy (SEM) analysis revealed that the temperature of the thermal treatment increases to 300 °C and 600 °C; the porosity of geopolymer increases in the form of the appearance of large pores and cracks in material. X-ray photoelectron spectroscopy (XPS) analysis was used to investigate the surface chemistry of geopolymers, including the chemical composition of the surface, the oxidation state of the elements, and the presence of functional groups. The UV/Vis spectra of the synthesized geopolymers doped with Nd3+ show interesting optical properties at 900 °C; the geopolymer matrix completely disintegrates and an amorphous phase with a rare-earth precipitate appears.",
journal = "Nanomaterials",
title = "Microstructural Analysis of Thermally Treated Geopolymer Incorporated with Neodymium",
volume = "13",
number = "10",
pages = "1663",
doi = "10.3390/nano13101663"
}

Knežević, S., Ivanović, M., Stanković, D. M., Kisić, D., Nenadović, S., Potočnik, J.,& Nenadović, M.. (2023). Microstructural Analysis of Thermally Treated Geopolymer Incorporated with Neodymium. in Nanomaterials, 13(10), 1663.
https://doi.org/10.3390/nano13101663

Knežević S, Ivanović M, Stanković DM, Kisić D, Nenadović S, Potočnik J, Nenadović M. Microstructural Analysis of Thermally Treated Geopolymer Incorporated with Neodymium. in Nanomaterials. 2023;13(10):1663.
doi:10.3390/nano13101663 .

Knežević, Sanja, Ivanović, Marija, Stanković, Dalibor M., Kisić, Danilo, Nenadović, Snežana, Potočnik, Jelena, Nenadović, Miloš, "Microstructural Analysis of Thermally Treated Geopolymer Incorporated with Neodymium" in Nanomaterials, 13, no. 10 (2023):1663,
https://doi.org/10.3390/nano13101663 . .

TY  - JOUR
AU  - Haššo, Marek
AU  - Sarakhman, Olha
AU  - Đurđić, Slađana
AU  - Stanković, Dalibor M.
AU  - Švorc, Lubomir
PY  - 2023
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/11089
AB  - In this work, an advanced electrochemical platform was developed for the simple, rapid and sensitive determination of the polyphenolic compound tannic acid in various beverages using the combination of batch injection analysis with amperometric detection on a screen-printed carbon electrode. Several experimental parameters (pH of supporting electrolyte, detection potential, dispensing rate, injected volume, stirring) were consistently evaluated. The most favorable analytical performance in terms of sensitivity, selectivity, repeatability and sampling frequency was obtained in Britton-Robinson buffer pH 5.0 at a detection potential of +0.6 V vs. Ag/AgCl, a dispensing rate of 204 µL/s and an injected volume of 80 µL under stirring condition (1500 r.p.m.). The presented platform has advantages for routine analysis including portable and small-scale experimental setup, low sample consumption (∼100 µL), simple sample preparation (dilution in supporting electrolyte), high sampling frequency (180 injections per hour), low limit of detection (80 nM) and suitable precision (RSD = 4.2% for 10 μM tannic acid, n = 20). The applicability of the method was verified by analyzing several beverage samples (tea, wine) in spike-recovery assay with the recovery values for tannic acid ranging from 94 to 101 %. © 2023 Elsevier B.V.
T2  - Journal of Electroanalytical Chemistry
T1  - Advanced electrochemical platform for simple and rapid quantification of tannic acid in beverages using batch injection analysis with amperometric detection
VL  - 942
SP  - 117578
DO  - 10.1016/j.jelechem.2023.117578
ER  - 

@article{
author = "Haššo, Marek and Sarakhman, Olha and Đurđić, Slađana and Stanković, Dalibor M. and Švorc, Lubomir",
year = "2023",
abstract = "In this work, an advanced electrochemical platform was developed for the simple, rapid and sensitive determination of the polyphenolic compound tannic acid in various beverages using the combination of batch injection analysis with amperometric detection on a screen-printed carbon electrode. Several experimental parameters (pH of supporting electrolyte, detection potential, dispensing rate, injected volume, stirring) were consistently evaluated. The most favorable analytical performance in terms of sensitivity, selectivity, repeatability and sampling frequency was obtained in Britton-Robinson buffer pH 5.0 at a detection potential of +0.6 V vs. Ag/AgCl, a dispensing rate of 204 µL/s and an injected volume of 80 µL under stirring condition (1500 r.p.m.). The presented platform has advantages for routine analysis including portable and small-scale experimental setup, low sample consumption (∼100 µL), simple sample preparation (dilution in supporting electrolyte), high sampling frequency (180 injections per hour), low limit of detection (80 nM) and suitable precision (RSD = 4.2% for 10 μM tannic acid, n = 20). The applicability of the method was verified by analyzing several beverage samples (tea, wine) in spike-recovery assay with the recovery values for tannic acid ranging from 94 to 101 %. © 2023 Elsevier B.V.",
journal = "Journal of Electroanalytical Chemistry",
title = "Advanced electrochemical platform for simple and rapid quantification of tannic acid in beverages using batch injection analysis with amperometric detection",
volume = "942",
pages = "117578",
doi = "10.1016/j.jelechem.2023.117578"
}

Haššo, M., Sarakhman, O., Đurđić, S., Stanković, D. M.,& Švorc, L.. (2023). Advanced electrochemical platform for simple and rapid quantification of tannic acid in beverages using batch injection analysis with amperometric detection. in Journal of Electroanalytical Chemistry, 942, 117578.
https://doi.org/10.1016/j.jelechem.2023.117578

Haššo M, Sarakhman O, Đurđić S, Stanković DM, Švorc L. Advanced electrochemical platform for simple and rapid quantification of tannic acid in beverages using batch injection analysis with amperometric detection. in Journal of Electroanalytical Chemistry. 2023;942:117578.
doi:10.1016/j.jelechem.2023.117578 .

Haššo, Marek, Sarakhman, Olha, Đurđić, Slađana, Stanković, Dalibor M., Švorc, Lubomir, "Advanced electrochemical platform for simple and rapid quantification of tannic acid in beverages using batch injection analysis with amperometric detection" in Journal of Electroanalytical Chemistry, 942 (2023):117578,
https://doi.org/10.1016/j.jelechem.2023.117578 . .

TY  - JOUR
AU  - Mutić, Sanja
AU  - Stanković, Dalibor
AU  - Konya, Zoltan
AU  - Anojčić, Jasmina
PY  - 2023
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/11370
AB  - In present work, the enzyme cholesterol oxidase (ChOx) was immobilized by Nafion® (Naf) on Pt,Ru–C nanocomposite and an ionic liquid (IL)–modified carbon paste electrode (CPE) in order to create cholesterol biosensor (Naf/ChOx/Pt,Ru–C/IL-CPE). The prepared working electrodes were characterized using scanning electron microscopy–energy-dispersive spectrometry, while their electrochemical performance was evaluated using electrochemical impedance spectroscopic, cyclic voltammetric, and amperometric techniques. Excellent synergism between IL 1-allyl-3-methylimidazolium dicyanamide ([AMIM][DCA]), Pt,Ru–C, and ChOx, as modifiers of CPE, offers the most pronounced analytical performance for improved cholesterol amperometric determination in phosphate buffer solution pH 7.50 at a working potential of 0.60 V. Under optimized experimental conditions, a linear relationship between oxidation current and cholesterol concentration was found for the range from 0.31 to 2.46 µM, with an estimated detection limit of 0.13 µM and relative standard deviation (RSD) below 5.5%. The optimized amperometric method in combination with the developed Naf/ChOx/Pt,Ru–C/IL-CPE biosensor showed good repeatability and high selectivity towards cholesterol biosensing. The proposed biosensor was successfully applied to determine free cholesterol in a human blood serum sample via its enzymatic reaction product hydrogen peroxide despite the presence of possible interferences. The percentage recovery ranged from 99.08 to 102.81%, while RSD was below 2.0% for the unspiked as well as the spiked human blood serum sample. The obtained results indicated excellent accuracy and precision of the method, concluding that the developed biosensor can be a promising alternative to existing commercial cholesterol tests used in medical practice. Graphical abstract: [Figure not available: see fulltext.]. © 2023, The Author(s), under exclusive licence to Springer-Verlag GmbH, DE part of Springer Nature.
T2  - Analytical and Bioanalytical Chemistry
T1  - Facile immobilization of cholesterol oxidase on Pt,Ru–C nanocomposite and ionic liquid–modified carbon paste electrode for an efficient amperometric free cholesterol biosensing
DO  - 10.1007/s00216-023-04847-9
ER  - 

@article{
author = "Mutić, Sanja and Stanković, Dalibor and Konya, Zoltan and Anojčić, Jasmina",
year = "2023",
abstract = "In present work, the enzyme cholesterol oxidase (ChOx) was immobilized by Nafion® (Naf) on Pt,Ru–C nanocomposite and an ionic liquid (IL)–modified carbon paste electrode (CPE) in order to create cholesterol biosensor (Naf/ChOx/Pt,Ru–C/IL-CPE). The prepared working electrodes were characterized using scanning electron microscopy–energy-dispersive spectrometry, while their electrochemical performance was evaluated using electrochemical impedance spectroscopic, cyclic voltammetric, and amperometric techniques. Excellent synergism between IL 1-allyl-3-methylimidazolium dicyanamide ([AMIM][DCA]), Pt,Ru–C, and ChOx, as modifiers of CPE, offers the most pronounced analytical performance for improved cholesterol amperometric determination in phosphate buffer solution pH 7.50 at a working potential of 0.60 V. Under optimized experimental conditions, a linear relationship between oxidation current and cholesterol concentration was found for the range from 0.31 to 2.46 µM, with an estimated detection limit of 0.13 µM and relative standard deviation (RSD) below 5.5%. The optimized amperometric method in combination with the developed Naf/ChOx/Pt,Ru–C/IL-CPE biosensor showed good repeatability and high selectivity towards cholesterol biosensing. The proposed biosensor was successfully applied to determine free cholesterol in a human blood serum sample via its enzymatic reaction product hydrogen peroxide despite the presence of possible interferences. The percentage recovery ranged from 99.08 to 102.81%, while RSD was below 2.0% for the unspiked as well as the spiked human blood serum sample. The obtained results indicated excellent accuracy and precision of the method, concluding that the developed biosensor can be a promising alternative to existing commercial cholesterol tests used in medical practice. Graphical abstract: [Figure not available: see fulltext.]. © 2023, The Author(s), under exclusive licence to Springer-Verlag GmbH, DE part of Springer Nature.",
journal = "Analytical and Bioanalytical Chemistry",
title = "Facile immobilization of cholesterol oxidase on Pt,Ru–C nanocomposite and ionic liquid–modified carbon paste electrode for an efficient amperometric free cholesterol biosensing",
doi = "10.1007/s00216-023-04847-9"
}

Mutić, S., Stanković, D., Konya, Z.,& Anojčić, J.. (2023). Facile immobilization of cholesterol oxidase on Pt,Ru–C nanocomposite and ionic liquid–modified carbon paste electrode for an efficient amperometric free cholesterol biosensing. in Analytical and Bioanalytical Chemistry.
https://doi.org/10.1007/s00216-023-04847-9

Mutić S, Stanković D, Konya Z, Anojčić J. Facile immobilization of cholesterol oxidase on Pt,Ru–C nanocomposite and ionic liquid–modified carbon paste electrode for an efficient amperometric free cholesterol biosensing. in Analytical and Bioanalytical Chemistry. 2023;.
doi:10.1007/s00216-023-04847-9 .

Mutić, Sanja, Stanković, Dalibor, Konya, Zoltan, Anojčić, Jasmina, "Facile immobilization of cholesterol oxidase on Pt,Ru–C nanocomposite and ionic liquid–modified carbon paste electrode for an efficient amperometric free cholesterol biosensing" in Analytical and Bioanalytical Chemistry (2023),
https://doi.org/10.1007/s00216-023-04847-9 . .

TY  - JOUR
AU  - Knežević, Sara
AU  - Terzić Jovanović, Nataša
AU  - Vlahović, Filip
AU  - Ajdačić, Vladimir
AU  - Costache, Vlad
AU  - Vidić, Jasmina
AU  - Opsenica, Igor
AU  - Stanković, Dalibor
PY  - 2023
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/11546
AB  - Covalent organic frameworks (COFs) are emerging as promising sensing materials due to their controllable structure and function properties, as well as excellent physicochemical characteristics. Here, specific interactions between a triazine-based COF and a mass-used herbicide – glyphosate (GLY) have been utilized to design a disposable sensing platform for GLY detection. This herbicide has been extensively used for decades, however, its harmful environmental impact and toxicity to humans have been recently proven, conditioning the necessity for the strict control and monitoring of its use and its presence in soil, water, and food. Glyphosate is an organophosphorus compound, and its detection in complex matrices usually requires laborious pretreatment. Here, we developed a direct, miniaturized, robust, and green approach for disposable electrochemical sensing of glyphosate, utilizing COF’s ability to selectively capture and concentrate negatively charged glyphosate molecules inside its nanopores. This process generates the concentration gradient of GLY, accelerating its diffusion towards the electrode surface. Simultaneously, specific COF-glyphosate binding catalyses the oxidative cleavage of the C–P bond and, together with pore nanoconfinement, enables sensitive glyphosate detection. Detailed sensing principles and selectiveness were scrutinized using DFT-based modelling. The proposed electrochemical method has a linear working range from 0.1 μM to 10 μM, a low limit of detection of 96 nM, and a limit of quantification of 320 nM. The elaborated sensing approach is viable for use in real sample matrices and tested for GLY determination in soil and water samples, without pretreatment, preparation, or purification. The results showed the practical usefulness of the sensor in the real sample analysis and suggested its suitability for possible out-oflaboratory sensing.
T2  - Chemosphere
T1  - Direct glyphosate soil monitoring at the triazine-based covalent organic framework with the theoretical study of sensing principle
VL  - 341
SP  - 139930
DO  - 10.1016/j.chemosphere.2023.139930
ER  - 

@article{
author = "Knežević, Sara and Terzić Jovanović, Nataša and Vlahović, Filip and Ajdačić, Vladimir and Costache, Vlad and Vidić, Jasmina and Opsenica, Igor and Stanković, Dalibor",
year = "2023",
abstract = "Covalent organic frameworks (COFs) are emerging as promising sensing materials due to their controllable structure and function properties, as well as excellent physicochemical characteristics. Here, specific interactions between a triazine-based COF and a mass-used herbicide – glyphosate (GLY) have been utilized to design a disposable sensing platform for GLY detection. This herbicide has been extensively used for decades, however, its harmful environmental impact and toxicity to humans have been recently proven, conditioning the necessity for the strict control and monitoring of its use and its presence in soil, water, and food. Glyphosate is an organophosphorus compound, and its detection in complex matrices usually requires laborious pretreatment. Here, we developed a direct, miniaturized, robust, and green approach for disposable electrochemical sensing of glyphosate, utilizing COF’s ability to selectively capture and concentrate negatively charged glyphosate molecules inside its nanopores. This process generates the concentration gradient of GLY, accelerating its diffusion towards the electrode surface. Simultaneously, specific COF-glyphosate binding catalyses the oxidative cleavage of the C–P bond and, together with pore nanoconfinement, enables sensitive glyphosate detection. Detailed sensing principles and selectiveness were scrutinized using DFT-based modelling. The proposed electrochemical method has a linear working range from 0.1 μM to 10 μM, a low limit of detection of 96 nM, and a limit of quantification of 320 nM. The elaborated sensing approach is viable for use in real sample matrices and tested for GLY determination in soil and water samples, without pretreatment, preparation, or purification. The results showed the practical usefulness of the sensor in the real sample analysis and suggested its suitability for possible out-oflaboratory sensing.",
journal = "Chemosphere",
title = "Direct glyphosate soil monitoring at the triazine-based covalent organic framework with the theoretical study of sensing principle",
volume = "341",
pages = "139930",
doi = "10.1016/j.chemosphere.2023.139930"
}

Knežević, S., Terzić Jovanović, N., Vlahović, F., Ajdačić, V., Costache, V., Vidić, J., Opsenica, I.,& Stanković, D.. (2023). Direct glyphosate soil monitoring at the triazine-based covalent organic framework with the theoretical study of sensing principle. in Chemosphere, 341, 139930.
https://doi.org/10.1016/j.chemosphere.2023.139930

Knežević S, Terzić Jovanović N, Vlahović F, Ajdačić V, Costache V, Vidić J, Opsenica I, Stanković D. Direct glyphosate soil monitoring at the triazine-based covalent organic framework with the theoretical study of sensing principle. in Chemosphere. 2023;341:139930.
doi:10.1016/j.chemosphere.2023.139930 .

Knežević, Sara, Terzić Jovanović, Nataša, Vlahović, Filip, Ajdačić, Vladimir, Costache, Vlad, Vidić, Jasmina, Opsenica, Igor, Stanković, Dalibor, "Direct glyphosate soil monitoring at the triazine-based covalent organic framework with the theoretical study of sensing principle" in Chemosphere, 341 (2023):139930,
https://doi.org/10.1016/j.chemosphere.2023.139930 . .