TY  - JOUR
AU  - Radović, Magdalena
AU  - Mirković, Marija D.
AU  - Nikolić, Aleksandar S.
AU  - Kuraica, Milorad M.
AU  - Iskrenović, Predrag
AU  - Milanović, Zorana
AU  - Vranješ-Đurić, Sanja
AU  - Perić, Marko
PY  - 2021
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/9850
AB  - Different phosphates and phosphonates have shown excellent coating ability toward magnetic nanoparticles, improving their stability and biocompatibility which enables their biomedical application. The magnetic hyperthermia efficiency of phosphates (IDP and IHP) and phosphonates (MDP and HEDP) coated Fe3O4 magnetic nanoparticles (MNPs) were evaluated in an alternating magnetic field. For a deeper understanding of hyperthermia, the behavior of investigated MNPs in the non-alternating magnetic field was monitored by measuring the transparency of the sample. To investigate their theranostic potential coated Fe3O4-MNPs were radiolabeled with radionuclide 177Lu. Phosphate coated MNPs were radiolabeled in high radiolabeling yield (> 99%) while phosphonate coated MNPs reached maximum radiolabeling yield of 78%. Regardless lower radiolabeling yield both radiolabeled phosphonate MNPs may be further purified reaching radiochemical purity of more than 95%. In vitro stabile radiolabeled nanoparticles in saline and HSA were obtained. The high heating ability of phosphates and phosphonates coated MNPs as sine qua non for efficient in vivo hyperthermia treatment and satisfactory radiolabeling yield justifies their further research in order to develop new theranostic agents. © 2021, The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
T2  - Journal of Inorganic and Organometallic Polymers and Materials
T1  - Transmittance Measurements in Non-alternating Magnetic Field as Reliable Method for Determining of Heating Properties of Phosphate and Phosphonate Coated Fe3O4 Magnetic Nanoparticles
DO  - 10.1007/s10904-021-02059-1
ER  - 

@article{
author = "Radović, Magdalena and Mirković, Marija D. and Nikolić, Aleksandar S. and Kuraica, Milorad M. and Iskrenović, Predrag and Milanović, Zorana and Vranješ-Đurić, Sanja and Perić, Marko",
year = "2021",
abstract = "Different phosphates and phosphonates have shown excellent coating ability toward magnetic nanoparticles, improving their stability and biocompatibility which enables their biomedical application. The magnetic hyperthermia efficiency of phosphates (IDP and IHP) and phosphonates (MDP and HEDP) coated Fe3O4 magnetic nanoparticles (MNPs) were evaluated in an alternating magnetic field. For a deeper understanding of hyperthermia, the behavior of investigated MNPs in the non-alternating magnetic field was monitored by measuring the transparency of the sample. To investigate their theranostic potential coated Fe3O4-MNPs were radiolabeled with radionuclide 177Lu. Phosphate coated MNPs were radiolabeled in high radiolabeling yield (> 99%) while phosphonate coated MNPs reached maximum radiolabeling yield of 78%. Regardless lower radiolabeling yield both radiolabeled phosphonate MNPs may be further purified reaching radiochemical purity of more than 95%. In vitro stabile radiolabeled nanoparticles in saline and HSA were obtained. The high heating ability of phosphates and phosphonates coated MNPs as sine qua non for efficient in vivo hyperthermia treatment and satisfactory radiolabeling yield justifies their further research in order to develop new theranostic agents. © 2021, The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.",
journal = "Journal of Inorganic and Organometallic Polymers and Materials",
title = "Transmittance Measurements in Non-alternating Magnetic Field as Reliable Method for Determining of Heating Properties of Phosphate and Phosphonate Coated Fe3O4 Magnetic Nanoparticles",
doi = "10.1007/s10904-021-02059-1"
}

Radović, M., Mirković, M. D., Nikolić, A. S., Kuraica, M. M., Iskrenović, P., Milanović, Z., Vranješ-Đurić, S.,& Perić, M.. (2021). Transmittance Measurements in Non-alternating Magnetic Field as Reliable Method for Determining of Heating Properties of Phosphate and Phosphonate Coated Fe3O4 Magnetic Nanoparticles. in Journal of Inorganic and Organometallic Polymers and Materials.
https://doi.org/10.1007/s10904-021-02059-1

Radović M, Mirković MD, Nikolić AS, Kuraica MM, Iskrenović P, Milanović Z, Vranješ-Đurić S, Perić M. Transmittance Measurements in Non-alternating Magnetic Field as Reliable Method for Determining of Heating Properties of Phosphate and Phosphonate Coated Fe3O4 Magnetic Nanoparticles. in Journal of Inorganic and Organometallic Polymers and Materials. 2021;.
doi:10.1007/s10904-021-02059-1 .

Radović, Magdalena, Mirković, Marija D., Nikolić, Aleksandar S., Kuraica, Milorad M., Iskrenović, Predrag, Milanović, Zorana, Vranješ-Đurić, Sanja, Perić, Marko, "Transmittance Measurements in Non-alternating Magnetic Field as Reliable Method for Determining of Heating Properties of Phosphate and Phosphonate Coated Fe3O4 Magnetic Nanoparticles" in Journal of Inorganic and Organometallic Polymers and Materials (2021),
https://doi.org/10.1007/s10904-021-02059-1 . .

TY  - JOUR
AU  - Lakić, Mladen
AU  - Anđelković, Ljubica
AU  - Šuljagić, Marija
AU  - Vulić, Predrag
AU  - Perić, Marko R.
AU  - Iskrenović, Predrag
AU  - Krstić, Ivan
AU  - Kuraica, Milorad M.
AU  - Nikolić, Aleksandar S.
PY  - 2019
UR  - https://linkinghub.elsevier.com/retrieve/pii/S0925346719301995
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8114
AB  - Light-transmitting measurements of white light and a consequentially chosen laser beam of 655 nm propagating through citrate- and oleate-coated CoFe 2 O 4 , FeFe 2 O 4 and MgFe 2 O 4 nanoparticles under the influence of an external magnetic field were presented. New experimental settings were developed for the optical study of ferrites’ behavior in ferrofluid with the applied magnetic field strength within the 30–400 mT range. A magnetic field-induced change of light transmittance occurred and a precipitation of all studied samples was obtained. Optical investigations of ferrofluid suspensions revealed that, contrary to the linear aggregates of colloidal CoFe 2 O 4 and FeFe 2 O 4 , spheroidal aggregates were formed in the case of MgFe 2 O 4 . In all three cases, the surface modification resulted in decreased dipole–dipole interactions between ferrite cores, and thus, less precipitates were noticed. All oleate-coated nanoparticles have demonstrated weaker magnetic responses compared to the citrate-encapsulated samples. The aggregation of nanoparticles potentially increases cytotoxicity. Regarding non-linear clustering of MgFe 2 O 4 suspensions, it can be concluded that its excretion from the organism may likely be easier and faster when used in diagnosis and/or therapy. Therefore, more attention should be paid to the lowly toxic MgFe 2 O 4 regarding its medical application. © 2019
T2  - Optical Materials
T1  - Optical evidence of magnetic field-induced ferrofluid aggregation: Comparison of cobalt ferrite, magnetite, and magnesium ferrite
VL  - 91
SP  - 279
EP  - 285
DO  - 10.1016/j.optmat.2019.03.031
ER  - 

@article{
author = "Lakić, Mladen and Anđelković, Ljubica and Šuljagić, Marija and Vulić, Predrag and Perić, Marko R. and Iskrenović, Predrag and Krstić, Ivan and Kuraica, Milorad M. and Nikolić, Aleksandar S.",
year = "2019",
abstract = "Light-transmitting measurements of white light and a consequentially chosen laser beam of 655 nm propagating through citrate- and oleate-coated CoFe 2 O 4 , FeFe 2 O 4 and MgFe 2 O 4 nanoparticles under the influence of an external magnetic field were presented. New experimental settings were developed for the optical study of ferrites’ behavior in ferrofluid with the applied magnetic field strength within the 30–400 mT range. A magnetic field-induced change of light transmittance occurred and a precipitation of all studied samples was obtained. Optical investigations of ferrofluid suspensions revealed that, contrary to the linear aggregates of colloidal CoFe 2 O 4 and FeFe 2 O 4 , spheroidal aggregates were formed in the case of MgFe 2 O 4 . In all three cases, the surface modification resulted in decreased dipole–dipole interactions between ferrite cores, and thus, less precipitates were noticed. All oleate-coated nanoparticles have demonstrated weaker magnetic responses compared to the citrate-encapsulated samples. The aggregation of nanoparticles potentially increases cytotoxicity. Regarding non-linear clustering of MgFe 2 O 4 suspensions, it can be concluded that its excretion from the organism may likely be easier and faster when used in diagnosis and/or therapy. Therefore, more attention should be paid to the lowly toxic MgFe 2 O 4 regarding its medical application. © 2019",
journal = "Optical Materials",
title = "Optical evidence of magnetic field-induced ferrofluid aggregation: Comparison of cobalt ferrite, magnetite, and magnesium ferrite",
volume = "91",
pages = "279-285",
doi = "10.1016/j.optmat.2019.03.031"
}

Lakić, M., Anđelković, L., Šuljagić, M., Vulić, P., Perić, M. R., Iskrenović, P., Krstić, I., Kuraica, M. M.,& Nikolić, A. S.. (2019). Optical evidence of magnetic field-induced ferrofluid aggregation: Comparison of cobalt ferrite, magnetite, and magnesium ferrite. in Optical Materials, 91, 279-285.
https://doi.org/10.1016/j.optmat.2019.03.031

Lakić M, Anđelković L, Šuljagić M, Vulić P, Perić MR, Iskrenović P, Krstić I, Kuraica MM, Nikolić AS. Optical evidence of magnetic field-induced ferrofluid aggregation: Comparison of cobalt ferrite, magnetite, and magnesium ferrite. in Optical Materials. 2019;91:279-285.
doi:10.1016/j.optmat.2019.03.031 .

Lakić, Mladen, Anđelković, Ljubica, Šuljagić, Marija, Vulić, Predrag, Perić, Marko R., Iskrenović, Predrag, Krstić, Ivan, Kuraica, Milorad M., Nikolić, Aleksandar S., "Optical evidence of magnetic field-induced ferrofluid aggregation: Comparison of cobalt ferrite, magnetite, and magnesium ferrite" in Optical Materials, 91 (2019):279-285,
https://doi.org/10.1016/j.optmat.2019.03.031 . .

TY  - JOUR
AU  - Perić, Marko R.
AU  - Radović, Magdalena
AU  - Mirković, Marija D.
AU  - Nikolić, Aleksandar S.
AU  - Iskrenović, Predrag
AU  - Janković, Drina
AU  - Vranješ-Đurić, Sanja
PY  - 2019
UR  - http://xlink.rsc.org/?DOI=C8NJ06478D
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8139
AB  - The advances in nanotechnology are directed towards the development of new theranostic agents based on magnetic nanoparticles that can be used for both cancer detection and treatment. In this study, 2,3-dicarboxypropane-1,1-diphosphonic acid-coated magnetite nanoparticles (Fe3O4-DPD MNPs) were evaluated for their theranostic application using different methods. The magnetic hyperthermia efficiency of the Fe3O4-DPD MNPs was investigated in saline solution with ionic strengths between 0.05 and 1.0 mol dm(-3). For a better understanding of hyperthermia, the behavior of Fe3O4-DPD MNPs under a non-alternating magnetic field was studied, and the transparency of the sample was measured. Furthermore, the radiotracer method using the radionuclides Tc-99m and Y-90 was applied as a reliable and powerful method for evaluating the in vivo behavior of a nanoprobe; a high radiolabeling yield (>93%), in vitro and in vivo stability of the radiolabeled nanoparticles and high heating effect were observed, thus paving the way for the possible theranostic applications of Fe3O4-DPD MNPs.
T2  - New Journal of Chemistry
T1  - The analysis of 2,3-dicarboxypropane-1,1-diphosphonic acid-coated magnetite nanoparticles under an external magnetic field and their radiolabeling for possible theranostic applications
VL  - 43
IS  - 15
SP  - 5932
EP  - 5939
DO  - 10.1039/C8NJ06478D
ER  - 

@article{
author = "Perić, Marko R. and Radović, Magdalena and Mirković, Marija D. and Nikolić, Aleksandar S. and Iskrenović, Predrag and Janković, Drina and Vranješ-Đurić, Sanja",
year = "2019",
abstract = "The advances in nanotechnology are directed towards the development of new theranostic agents based on magnetic nanoparticles that can be used for both cancer detection and treatment. In this study, 2,3-dicarboxypropane-1,1-diphosphonic acid-coated magnetite nanoparticles (Fe3O4-DPD MNPs) were evaluated for their theranostic application using different methods. The magnetic hyperthermia efficiency of the Fe3O4-DPD MNPs was investigated in saline solution with ionic strengths between 0.05 and 1.0 mol dm(-3). For a better understanding of hyperthermia, the behavior of Fe3O4-DPD MNPs under a non-alternating magnetic field was studied, and the transparency of the sample was measured. Furthermore, the radiotracer method using the radionuclides Tc-99m and Y-90 was applied as a reliable and powerful method for evaluating the in vivo behavior of a nanoprobe; a high radiolabeling yield (>93%), in vitro and in vivo stability of the radiolabeled nanoparticles and high heating effect were observed, thus paving the way for the possible theranostic applications of Fe3O4-DPD MNPs.",
journal = "New Journal of Chemistry",
title = "The analysis of 2,3-dicarboxypropane-1,1-diphosphonic acid-coated magnetite nanoparticles under an external magnetic field and their radiolabeling for possible theranostic applications",
volume = "43",
number = "15",
pages = "5932-5939",
doi = "10.1039/C8NJ06478D"
}

Perić, M. R., Radović, M., Mirković, M. D., Nikolić, A. S., Iskrenović, P., Janković, D.,& Vranješ-Đurić, S.. (2019). The analysis of 2,3-dicarboxypropane-1,1-diphosphonic acid-coated magnetite nanoparticles under an external magnetic field and their radiolabeling for possible theranostic applications. in New Journal of Chemistry, 43(15), 5932-5939.
https://doi.org/10.1039/C8NJ06478D

Perić MR, Radović M, Mirković MD, Nikolić AS, Iskrenović P, Janković D, Vranješ-Đurić S. The analysis of 2,3-dicarboxypropane-1,1-diphosphonic acid-coated magnetite nanoparticles under an external magnetic field and their radiolabeling for possible theranostic applications. in New Journal of Chemistry. 2019;43(15):5932-5939.
doi:10.1039/C8NJ06478D .

Perić, Marko R., Radović, Magdalena, Mirković, Marija D., Nikolić, Aleksandar S., Iskrenović, Predrag, Janković, Drina, Vranješ-Đurić, Sanja, "The analysis of 2,3-dicarboxypropane-1,1-diphosphonic acid-coated magnetite nanoparticles under an external magnetic field and their radiolabeling for possible theranostic applications" in New Journal of Chemistry, 43, no. 15 (2019):5932-5939,
https://doi.org/10.1039/C8NJ06478D . .

TY  - JOUR
AU  - Kuraica, Milorad M.
AU  - Iskrenović, Predrag
AU  - Perić, Marko R.
AU  - Krstić, Ivan
AU  - Nikolić, Aleksandar S.
PY  - 2018
UR  - http://link.springer.com/10.1007/s11696-017-0380-8
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7711
AB  - Using simple optical measurements, the selective spectral behavior of suspended nano-particles of magnetite (Fe3O4) and cobalt-ferrite (CoFe2O4) coated with starch, was observed through switching on/off of external magnetic field. The field strength was varied in the interval 30–300 mT. In these transient regimes, the unexpected and unusually large changes of transmitted light occur. An explanation is suggested, within the model based on ordering of magnetic moments of nano-particles along the lines of magnetic field into magnetic chains and organization of magnetic chains into spatial structure—a quasi-lattice. This fact indicates the possibility of more efficient local heating of nano-particles in the fast changing magnetic field; for instance when taking magnetic nano-particles for therapeutic purposes.
T2  - Chemical Papers
T1  - External magnetic field influence on magnetite and cobalt-ferrite nano-particles in ferrofluid
VL  - 72
IS  - 6
SP  - 1535
EP  - 1542
DO  - 10.1007/s11696-017-0380-8
ER  - 

@article{
author = "Kuraica, Milorad M. and Iskrenović, Predrag and Perić, Marko R. and Krstić, Ivan and Nikolić, Aleksandar S.",
year = "2018",
abstract = "Using simple optical measurements, the selective spectral behavior of suspended nano-particles of magnetite (Fe3O4) and cobalt-ferrite (CoFe2O4) coated with starch, was observed through switching on/off of external magnetic field. The field strength was varied in the interval 30–300 mT. In these transient regimes, the unexpected and unusually large changes of transmitted light occur. An explanation is suggested, within the model based on ordering of magnetic moments of nano-particles along the lines of magnetic field into magnetic chains and organization of magnetic chains into spatial structure—a quasi-lattice. This fact indicates the possibility of more efficient local heating of nano-particles in the fast changing magnetic field; for instance when taking magnetic nano-particles for therapeutic purposes.",
journal = "Chemical Papers",
title = "External magnetic field influence on magnetite and cobalt-ferrite nano-particles in ferrofluid",
volume = "72",
number = "6",
pages = "1535-1542",
doi = "10.1007/s11696-017-0380-8"
}

Kuraica, M. M., Iskrenović, P., Perić, M. R., Krstić, I.,& Nikolić, A. S.. (2018). External magnetic field influence on magnetite and cobalt-ferrite nano-particles in ferrofluid. in Chemical Papers, 72(6), 1535-1542.
https://doi.org/10.1007/s11696-017-0380-8

Kuraica MM, Iskrenović P, Perić MR, Krstić I, Nikolić AS. External magnetic field influence on magnetite and cobalt-ferrite nano-particles in ferrofluid. in Chemical Papers. 2018;72(6):1535-1542.
doi:10.1007/s11696-017-0380-8 .

Kuraica, Milorad M., Iskrenović, Predrag, Perić, Marko R., Krstić, Ivan, Nikolić, Aleksandar S., "External magnetic field influence on magnetite and cobalt-ferrite nano-particles in ferrofluid" in Chemical Papers, 72, no. 6 (2018):1535-1542,
https://doi.org/10.1007/s11696-017-0380-8 . .

TY  - JOUR
AU  - Lakić, Mladen
AU  - Vukadinović, Aleksandar
AU  - Kalcher, Kurt
AU  - Nikolić, Aleksandar S.
AU  - Stanković, Dalibor M.
PY  - 2016
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1292
AB  - This work presents the simultaneous determination of catechol (CC) and hydroquinone (HQ), employing a modified carbon paste electrode (CPE) with ferrite nanomaterial. Ferrite nanomaterial was doped with different amount of cobalt and this was investigated toward simultaneous oxidation of CC and HQ. It was shown that this modification strongly increases electrochemical characteristics of the CPE. Also, electrocatalytic activity of such materials strongly depends on the level of substituted Co in the ferrite nanoparticles. The modified electrodes, labeled as CoFerrite/CPE, showed two pairs of well-defined redox peaks for the electrochemical processes of catechol and hydroquinone. Involving of ferrite material in the structure of CPE, cause increase in the potentials differences between redox couples of the investigated compounds, accompanied with increases in peaks currents. Several important parameters were optimized and calibration curves, with limits of detection (LOD) of 0.15 and 0.3 mu M for catechol and hydroquinone, respectively, were constructed by employing amperometric detection. Effect of possible interfering compounds was also studied, and proposed method was successfully applied for CC and HQ quantification in real samples.
T2  - Talanta
T1  - Effect of cobalt doping level of ferrites in enhancing sensitivity of analytical performances of carbon paste electrode for simultaneous determination of catechol and hydroquinone
VL  - 161
SP  - 668
EP  - 674
DO  - 10.1016/j.talanta.2016.09.029
ER  - 

@article{
author = "Lakić, Mladen and Vukadinović, Aleksandar and Kalcher, Kurt and Nikolić, Aleksandar S. and Stanković, Dalibor M.",
year = "2016",
abstract = "This work presents the simultaneous determination of catechol (CC) and hydroquinone (HQ), employing a modified carbon paste electrode (CPE) with ferrite nanomaterial. Ferrite nanomaterial was doped with different amount of cobalt and this was investigated toward simultaneous oxidation of CC and HQ. It was shown that this modification strongly increases electrochemical characteristics of the CPE. Also, electrocatalytic activity of such materials strongly depends on the level of substituted Co in the ferrite nanoparticles. The modified electrodes, labeled as CoFerrite/CPE, showed two pairs of well-defined redox peaks for the electrochemical processes of catechol and hydroquinone. Involving of ferrite material in the structure of CPE, cause increase in the potentials differences between redox couples of the investigated compounds, accompanied with increases in peaks currents. Several important parameters were optimized and calibration curves, with limits of detection (LOD) of 0.15 and 0.3 mu M for catechol and hydroquinone, respectively, were constructed by employing amperometric detection. Effect of possible interfering compounds was also studied, and proposed method was successfully applied for CC and HQ quantification in real samples.",
journal = "Talanta",
title = "Effect of cobalt doping level of ferrites in enhancing sensitivity of analytical performances of carbon paste electrode for simultaneous determination of catechol and hydroquinone",
volume = "161",
pages = "668-674",
doi = "10.1016/j.talanta.2016.09.029"
}

Lakić, M., Vukadinović, A., Kalcher, K., Nikolić, A. S.,& Stanković, D. M.. (2016). Effect of cobalt doping level of ferrites in enhancing sensitivity of analytical performances of carbon paste electrode for simultaneous determination of catechol and hydroquinone. in Talanta, 161, 668-674.
https://doi.org/10.1016/j.talanta.2016.09.029

Lakić M, Vukadinović A, Kalcher K, Nikolić AS, Stanković DM. Effect of cobalt doping level of ferrites in enhancing sensitivity of analytical performances of carbon paste electrode for simultaneous determination of catechol and hydroquinone. in Talanta. 2016;161:668-674.
doi:10.1016/j.talanta.2016.09.029 .

Lakić, Mladen, Vukadinović, Aleksandar, Kalcher, Kurt, Nikolić, Aleksandar S., Stanković, Dalibor M., "Effect of cobalt doping level of ferrites in enhancing sensitivity of analytical performances of carbon paste electrode for simultaneous determination of catechol and hydroquinone" in Talanta, 161 (2016):668-674,
https://doi.org/10.1016/j.talanta.2016.09.029 . .

TY  - JOUR
AU  - Gavrilović, Tamara V.
AU  - Jovanović, Dragana J.
AU  - Lojpur, Vesna
AU  - Nikolić, Aleksandar S.
AU  - Dramićanin, Miroslav
PY  - 2015
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/729
AB  - In this paper, we studied the effects of Er3+/Yb3+ concentration ratio on structural, morphological and luminescence properties of GdVO4:Er3+/Yb3+ green phosphors prepared by a high-temperature solid state method. The samples with different concentrations (between 0.5 to 2 mol%) of dopant Er3+ emitting ions and different concentrations (between 5 to 20 mol%) of sensitizer ions (Yb3+) were studied. The phosphors were characterized by the X-ray diffraction (XRD), scanning electron microscopy (SEM) and photoluminescence spectroscopy. For all samples, XRD diffraction patterns confirmed a formation of a pure GdVO4 phase, while the SEM showed that the materials are comprised of chunks of deformed particles with an average diameter ranging from approximately 2 mu m to 8 mu m. Both, down-conversion and up-conversion emission spectra of GdVO4: Er3+/Yb3+ samples, under near UV and IR excitations, exhibit two strong emission bands in the green spectral region at 525 nm and 552 nm wavelengths corresponding to H-2(11/2) - GT I-4(15/2) and S-4(3/2) - GT I-4(15/2) electronic transitions of Er3+ ions. The intensity of the green emission was changed by changing the Er3+/Yb3+ concentration ratio. This dual-mode luminescence makes these materials ideal as green phosphors for a wide variety of applications in the fields of bioanalysis and biomedical.
T2  - Science of Sintering
T1  - Influence of Er3+/Yb3+ Concentration Ratio on the Down-conversion and Up-conversion Luminescence and Lifetime in GdVO4:Er3+/Yb3+ Microcrystals
VL  - 47
IS  - 2
SP  - 221
EP  - 228
DO  - 10.2298/SOS1502221G
ER  - 

@article{
author = "Gavrilović, Tamara V. and Jovanović, Dragana J. and Lojpur, Vesna and Nikolić, Aleksandar S. and Dramićanin, Miroslav",
year = "2015",
abstract = "In this paper, we studied the effects of Er3+/Yb3+ concentration ratio on structural, morphological and luminescence properties of GdVO4:Er3+/Yb3+ green phosphors prepared by a high-temperature solid state method. The samples with different concentrations (between 0.5 to 2 mol%) of dopant Er3+ emitting ions and different concentrations (between 5 to 20 mol%) of sensitizer ions (Yb3+) were studied. The phosphors were characterized by the X-ray diffraction (XRD), scanning electron microscopy (SEM) and photoluminescence spectroscopy. For all samples, XRD diffraction patterns confirmed a formation of a pure GdVO4 phase, while the SEM showed that the materials are comprised of chunks of deformed particles with an average diameter ranging from approximately 2 mu m to 8 mu m. Both, down-conversion and up-conversion emission spectra of GdVO4: Er3+/Yb3+ samples, under near UV and IR excitations, exhibit two strong emission bands in the green spectral region at 525 nm and 552 nm wavelengths corresponding to H-2(11/2) - GT I-4(15/2) and S-4(3/2) - GT I-4(15/2) electronic transitions of Er3+ ions. The intensity of the green emission was changed by changing the Er3+/Yb3+ concentration ratio. This dual-mode luminescence makes these materials ideal as green phosphors for a wide variety of applications in the fields of bioanalysis and biomedical.",
journal = "Science of Sintering",
title = "Influence of Er3+/Yb3+ Concentration Ratio on the Down-conversion and Up-conversion Luminescence and Lifetime in GdVO4:Er3+/Yb3+ Microcrystals",
volume = "47",
number = "2",
pages = "221-228",
doi = "10.2298/SOS1502221G"
}

Gavrilović, T. V., Jovanović, D. J., Lojpur, V., Nikolić, A. S.,& Dramićanin, M.. (2015). Influence of Er3+/Yb3+ Concentration Ratio on the Down-conversion and Up-conversion Luminescence and Lifetime in GdVO4:Er3+/Yb3+ Microcrystals. in Science of Sintering, 47(2), 221-228.
https://doi.org/10.2298/SOS1502221G

Gavrilović TV, Jovanović DJ, Lojpur V, Nikolić AS, Dramićanin M. Influence of Er3+/Yb3+ Concentration Ratio on the Down-conversion and Up-conversion Luminescence and Lifetime in GdVO4:Er3+/Yb3+ Microcrystals. in Science of Sintering. 2015;47(2):221-228.
doi:10.2298/SOS1502221G .

Gavrilović, Tamara V., Jovanović, Dragana J., Lojpur, Vesna, Nikolić, Aleksandar S., Dramićanin, Miroslav, "Influence of Er3+/Yb3+ Concentration Ratio on the Down-conversion and Up-conversion Luminescence and Lifetime in GdVO4:Er3+/Yb3+ Microcrystals" in Science of Sintering, 47, no. 2 (2015):221-228,
https://doi.org/10.2298/SOS1502221G . .

TY  - JOUR
AU  - Nikolić, Aleksandar S.
AU  - Bošković, Marko
AU  - Spasojević, Vojislav
AU  - Jančar, Boštjan
AU  - Antić, Bratislav
PY  - 2014
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/5939
AB  - Magnetic nanocomposites can show enhanced properties compared to their single phase counterparts. Novel soft ferrite Fe3O4/soft ferrite MnFe2O4 nanocomposite, as well as pure MnFe2O4 and Fe3O4 for the sake of comparison, were synthesized by co-precipitation method. The spinel type of structure (space group Fd (3) over barm) of the samples was confirmed by XRPD and SAED. Samples are composed of spherical particles with size in the range 5-15 nm. Nanocomposite (92 wt%) MnFe2O4/(8 wt%) Fe3O4 exert single phase like magnetic behavior. Saturation magnetization (M-S) of Fe3O4/MnFe2O4 is 26% greater than M-S of MnFe2O4 and even 50% than M-S of Fe3O4. At the same time coercivity field of the nanocomposite is twice less value (H-C=180 Oe) than in binary ferrites (H-C=360 Oe). Magnetization enhancement and softening in Magnetite/Mn-ferrite is discussed related to particle interactions among two different ferrites and intrinsic properties of nanoparticles. Tailoring phase ratio and synthesis conditions can be a tool for tuning magnetic properties of nanocomposites. (C) 2014 Elsevier B.V. All rights reserved.
T2  - Materials Letters
T1  - Magnetite/Mn-ferrite nanocomposite with improved magnetic properties
VL  - 120
SP  - 86
EP  - 89
DO  - 10.1016/j.matlet.2014.01.023
ER  - 

@article{
author = "Nikolić, Aleksandar S. and Bošković, Marko and Spasojević, Vojislav and Jančar, Boštjan and Antić, Bratislav",
year = "2014",
abstract = "Magnetic nanocomposites can show enhanced properties compared to their single phase counterparts. Novel soft ferrite Fe3O4/soft ferrite MnFe2O4 nanocomposite, as well as pure MnFe2O4 and Fe3O4 for the sake of comparison, were synthesized by co-precipitation method. The spinel type of structure (space group Fd (3) over barm) of the samples was confirmed by XRPD and SAED. Samples are composed of spherical particles with size in the range 5-15 nm. Nanocomposite (92 wt%) MnFe2O4/(8 wt%) Fe3O4 exert single phase like magnetic behavior. Saturation magnetization (M-S) of Fe3O4/MnFe2O4 is 26% greater than M-S of MnFe2O4 and even 50% than M-S of Fe3O4. At the same time coercivity field of the nanocomposite is twice less value (H-C=180 Oe) than in binary ferrites (H-C=360 Oe). Magnetization enhancement and softening in Magnetite/Mn-ferrite is discussed related to particle interactions among two different ferrites and intrinsic properties of nanoparticles. Tailoring phase ratio and synthesis conditions can be a tool for tuning magnetic properties of nanocomposites. (C) 2014 Elsevier B.V. All rights reserved.",
journal = "Materials Letters",
title = "Magnetite/Mn-ferrite nanocomposite with improved magnetic properties",
volume = "120",
pages = "86-89",
doi = "10.1016/j.matlet.2014.01.023"
}

Nikolić, A. S., Bošković, M., Spasojević, V., Jančar, B.,& Antić, B.. (2014). Magnetite/Mn-ferrite nanocomposite with improved magnetic properties. in Materials Letters, 120, 86-89.
https://doi.org/10.1016/j.matlet.2014.01.023

Nikolić AS, Bošković M, Spasojević V, Jančar B, Antić B. Magnetite/Mn-ferrite nanocomposite with improved magnetic properties. in Materials Letters. 2014;120:86-89.
doi:10.1016/j.matlet.2014.01.023 .

Nikolić, Aleksandar S., Bošković, Marko, Spasojević, Vojislav, Jančar, Boštjan, Antić, Bratislav, "Magnetite/Mn-ferrite nanocomposite with improved magnetic properties" in Materials Letters, 120 (2014):86-89,
https://doi.org/10.1016/j.matlet.2014.01.023 . .

TY  - JOUR
AU  - Nikolić, Aleksandar S.
AU  - Bošković, Marko
AU  - Fabian, Martin
AU  - Božanić, Dušan K.
AU  - Vučinić-Vasić, Milica
AU  - Kremenović, Aleksandar S.
AU  - Antić, Bratislav
PY  - 2013
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/5813
AB  - Herein a comparative study of five nanocrystalline cerium oxides (CeO2-delta) synthesised by different methods and calcined at 500 degrees C is reported. XRPD analysis showed that stoichiometry parameter delta, crystallite size/strain and lattice constant were only slightly affected by the method utilized. All ceria nanoparticles are nearly spherical in shape with faceted morphology, free of defects and with a relatively uniform size distribution. The average microstrain was found to be approximately 10 times higher than that of bulk counterpart. The absorption edge of nanocrystalline materials was shifted towards a higher wavelengths (red shift) in comparison with bulk counterpart, and band gap values were in the range 2.7-3.24 eV (3.33 eV for bulk counterpart).
T2  - Journal of Nanoscience and Nanotechnology
T1  - Comparative Structural and Optical Properties of Different Ceria Nanoparticles
VL  - 13
IS  - 10
SP  - 6787
EP  - 6792
DO  - 10.1166/jnn.2013.7774
ER  - 

@article{
author = "Nikolić, Aleksandar S. and Bošković, Marko and Fabian, Martin and Božanić, Dušan K. and Vučinić-Vasić, Milica and Kremenović, Aleksandar S. and Antić, Bratislav",
year = "2013",
abstract = "Herein a comparative study of five nanocrystalline cerium oxides (CeO2-delta) synthesised by different methods and calcined at 500 degrees C is reported. XRPD analysis showed that stoichiometry parameter delta, crystallite size/strain and lattice constant were only slightly affected by the method utilized. All ceria nanoparticles are nearly spherical in shape with faceted morphology, free of defects and with a relatively uniform size distribution. The average microstrain was found to be approximately 10 times higher than that of bulk counterpart. The absorption edge of nanocrystalline materials was shifted towards a higher wavelengths (red shift) in comparison with bulk counterpart, and band gap values were in the range 2.7-3.24 eV (3.33 eV for bulk counterpart).",
journal = "Journal of Nanoscience and Nanotechnology",
title = "Comparative Structural and Optical Properties of Different Ceria Nanoparticles",
volume = "13",
number = "10",
pages = "6787-6792",
doi = "10.1166/jnn.2013.7774"
}

Nikolić, A. S., Bošković, M., Fabian, M., Božanić, D. K., Vučinić-Vasić, M., Kremenović, A. S.,& Antić, B.. (2013). Comparative Structural and Optical Properties of Different Ceria Nanoparticles. in Journal of Nanoscience and Nanotechnology, 13(10), 6787-6792.
https://doi.org/10.1166/jnn.2013.7774

Nikolić AS, Bošković M, Fabian M, Božanić DK, Vučinić-Vasić M, Kremenović AS, Antić B. Comparative Structural and Optical Properties of Different Ceria Nanoparticles. in Journal of Nanoscience and Nanotechnology. 2013;13(10):6787-6792.
doi:10.1166/jnn.2013.7774 .

Nikolić, Aleksandar S., Bošković, Marko, Fabian, Martin, Božanić, Dušan K., Vučinić-Vasić, Milica, Kremenović, Aleksandar S., Antić, Bratislav, "Comparative Structural and Optical Properties of Different Ceria Nanoparticles" in Journal of Nanoscience and Nanotechnology, 13, no. 10 (2013):6787-6792,
https://doi.org/10.1166/jnn.2013.7774 . .

TY  - JOUR
AU  - Nikolić, Aleksandar S.
AU  - Jović, Nataša G.
AU  - Rogan, Jelena R.
AU  - Kremenović, Aleksandar S.
AU  - Ristić, Mira
AU  - Meden, A.
AU  - Antić, Bratislav
PY  - 2013
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/5544
AB  - Different synthesis methods for the preparation of nanocrystalline nickel ferrites are reported: the thermal decomposition of precursors, made of: (i) metal-nitrate salts with carboxylic acids (citric, malonic and tartaric), and (ii) metal-nitrate salts and polyethylene glycol (PEG), in the presence of potassium chloride as a capping agent. The as-prepared gel precursors were characterized by TGA/DTA, while the samples obtained after annealing at 450 degrees C were investigated by FTIR, FESEM, XRD and Mossbauer spectroscopy. Regardless of the type of carboxylic acid used, nanocrystallites prepared by (i) method are similar in size (11-16 nm), while the method (ii) gives crystallites similar to 33 nm in size with negligible microstrain. The differences in the lattice parameter, ranging from 8.3369(2) to 8.3574(2) angstrom, result from cation distribution, nonstoichiometry and structural imperfections in the nickel ferrite nanoparticles. The Mossbauer spectra analysis indicates existence of large distortions of tetrahedral and octahedral sites in these spinel compounds. (C) 2013 Elsevier Ltd and Techna Group S.r.l. All rights reserved.
T2  - Ceramics International
T1  - Carboxylic acids and polyethylene glycol assisted synthesis of nanocrystalline nickel ferrites
VL  - 39
IS  - 6
SP  - 6681
EP  - 6688
DO  - 10.1016/j.ceramint.2013.01.106
ER  - 

@article{
author = "Nikolić, Aleksandar S. and Jović, Nataša G. and Rogan, Jelena R. and Kremenović, Aleksandar S. and Ristić, Mira and Meden, A. and Antić, Bratislav",
year = "2013",
abstract = "Different synthesis methods for the preparation of nanocrystalline nickel ferrites are reported: the thermal decomposition of precursors, made of: (i) metal-nitrate salts with carboxylic acids (citric, malonic and tartaric), and (ii) metal-nitrate salts and polyethylene glycol (PEG), in the presence of potassium chloride as a capping agent. The as-prepared gel precursors were characterized by TGA/DTA, while the samples obtained after annealing at 450 degrees C were investigated by FTIR, FESEM, XRD and Mossbauer spectroscopy. Regardless of the type of carboxylic acid used, nanocrystallites prepared by (i) method are similar in size (11-16 nm), while the method (ii) gives crystallites similar to 33 nm in size with negligible microstrain. The differences in the lattice parameter, ranging from 8.3369(2) to 8.3574(2) angstrom, result from cation distribution, nonstoichiometry and structural imperfections in the nickel ferrite nanoparticles. The Mossbauer spectra analysis indicates existence of large distortions of tetrahedral and octahedral sites in these spinel compounds. (C) 2013 Elsevier Ltd and Techna Group S.r.l. All rights reserved.",
journal = "Ceramics International",
title = "Carboxylic acids and polyethylene glycol assisted synthesis of nanocrystalline nickel ferrites",
volume = "39",
number = "6",
pages = "6681-6688",
doi = "10.1016/j.ceramint.2013.01.106"
}

Nikolić, A. S., Jović, N. G., Rogan, J. R., Kremenović, A. S., Ristić, M., Meden, A.,& Antić, B.. (2013). Carboxylic acids and polyethylene glycol assisted synthesis of nanocrystalline nickel ferrites. in Ceramics International, 39(6), 6681-6688.
https://doi.org/10.1016/j.ceramint.2013.01.106

Nikolić AS, Jović NG, Rogan JR, Kremenović AS, Ristić M, Meden A, Antić B. Carboxylic acids and polyethylene glycol assisted synthesis of nanocrystalline nickel ferrites. in Ceramics International. 2013;39(6):6681-6688.
doi:10.1016/j.ceramint.2013.01.106 .

Nikolić, Aleksandar S., Jović, Nataša G., Rogan, Jelena R., Kremenović, Aleksandar S., Ristić, Mira, Meden, A., Antić, Bratislav, "Carboxylic acids and polyethylene glycol assisted synthesis of nanocrystalline nickel ferrites" in Ceramics International, 39, no. 6 (2013):6681-6688,
https://doi.org/10.1016/j.ceramint.2013.01.106 . .

TY  - JOUR
AU  - Kremenović, Aleksandar S.
AU  - Božanić, Dušan K.
AU  - Welsch, A. -M.
AU  - Jančar, Boštjan
AU  - Nikolić, Aleksandar S.
AU  - Bošković, Marko
AU  - Colomban, Ph.
AU  - Fabian, Martin
AU  - Antić, Bratislav
PY  - 2012
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/5320
AB  - The 5-10 nnn Ce1-XEuXO2-delta (0 LT = x LT = 0.30) nanoparticles with fluorite structure were synthesized by thermal decomposition of Eu- and Ce-2,4-pentanedione complexes mixtures. X-ray line broadening analysis of mixed samples Ce1-XEuXO2-delta (0.05 LT = x LT = 0.30) showed that the crystallite size was lower and root mean square strain higher than in pure ceria. However, within mixed samples Ce1-XEuXO2-delta (0.05 LT = x LT = 0.30) crystallite size and root mean square strain were independent of Eu3+ concentration. Raman spectroscopy results indicated that europium ions yield disorder by breaking the phonon propagation and therefore making the non-centre Brillouin zone modes Raman active. The absorption bands in the spectra of mixed oxides were blue-shifted in comparison to pure CeO2-delta nanopowder. The samples show red emission typical for Eu ions. The biggest photoluminescent intensity was observed for the highest Eu3+ concentration (x = 0.30) and further enhanced with the increase in crystallinity.
T2  - Journal of Nanoscience and Nanotechnology
T1  - Effects of Eu3+ Concentration on Structural, Optical and Vibrational Properties of Multifunctional Ce1-X,EuXO2-delta Nanoparticles Synthesized by Thermolysis of 2,4-Pentanedione Complexes
VL  - 12
IS  - 12
SP  - 8893
EP  - 8899
DO  - 10.1166/jnn.2012.6797
ER  - 

@article{
author = "Kremenović, Aleksandar S. and Božanić, Dušan K. and Welsch, A. -M. and Jančar, Boštjan and Nikolić, Aleksandar S. and Bošković, Marko and Colomban, Ph. and Fabian, Martin and Antić, Bratislav",
year = "2012",
abstract = "The 5-10 nnn Ce1-XEuXO2-delta (0 LT = x LT = 0.30) nanoparticles with fluorite structure were synthesized by thermal decomposition of Eu- and Ce-2,4-pentanedione complexes mixtures. X-ray line broadening analysis of mixed samples Ce1-XEuXO2-delta (0.05 LT = x LT = 0.30) showed that the crystallite size was lower and root mean square strain higher than in pure ceria. However, within mixed samples Ce1-XEuXO2-delta (0.05 LT = x LT = 0.30) crystallite size and root mean square strain were independent of Eu3+ concentration. Raman spectroscopy results indicated that europium ions yield disorder by breaking the phonon propagation and therefore making the non-centre Brillouin zone modes Raman active. The absorption bands in the spectra of mixed oxides were blue-shifted in comparison to pure CeO2-delta nanopowder. The samples show red emission typical for Eu ions. The biggest photoluminescent intensity was observed for the highest Eu3+ concentration (x = 0.30) and further enhanced with the increase in crystallinity.",
journal = "Journal of Nanoscience and Nanotechnology",
title = "Effects of Eu3+ Concentration on Structural, Optical and Vibrational Properties of Multifunctional Ce1-X,EuXO2-delta Nanoparticles Synthesized by Thermolysis of 2,4-Pentanedione Complexes",
volume = "12",
number = "12",
pages = "8893-8899",
doi = "10.1166/jnn.2012.6797"
}

Kremenović, A. S., Božanić, D. K., Welsch, A. -M., Jančar, B., Nikolić, A. S., Bošković, M., Colomban, Ph., Fabian, M.,& Antić, B.. (2012). Effects of Eu3+ Concentration on Structural, Optical and Vibrational Properties of Multifunctional Ce1-X,EuXO2-delta Nanoparticles Synthesized by Thermolysis of 2,4-Pentanedione Complexes. in Journal of Nanoscience and Nanotechnology, 12(12), 8893-8899.
https://doi.org/10.1166/jnn.2012.6797

Kremenović AS, Božanić DK, Welsch A-, Jančar B, Nikolić AS, Bošković M, Colomban P, Fabian M, Antić B. Effects of Eu3+ Concentration on Structural, Optical and Vibrational Properties of Multifunctional Ce1-X,EuXO2-delta Nanoparticles Synthesized by Thermolysis of 2,4-Pentanedione Complexes. in Journal of Nanoscience and Nanotechnology. 2012;12(12):8893-8899.
doi:10.1166/jnn.2012.6797 .

Kremenović, Aleksandar S., Božanić, Dušan K., Welsch, A. -M., Jančar, Boštjan, Nikolić, Aleksandar S., Bošković, Marko, Colomban, Ph., Fabian, Martin, Antić, Bratislav, "Effects of Eu3+ Concentration on Structural, Optical and Vibrational Properties of Multifunctional Ce1-X,EuXO2-delta Nanoparticles Synthesized by Thermolysis of 2,4-Pentanedione Complexes" in Journal of Nanoscience and Nanotechnology, 12, no. 12 (2012):8893-8899,
https://doi.org/10.1166/jnn.2012.6797 . .

TY  - JOUR
AU  - Antić, Bratislav
AU  - Kremenović, Aleksandar S.
AU  - Jović, Nataša G.
AU  - Pavlović, Miodrag B.
AU  - Jovalekić, Čedomir
AU  - Nikolić, Aleksandar S.
AU  - Goya, Gerardo F.
AU  - Weidenthaler, C.
PY  - 2012
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/6946
AB  - We present a study of the structural and magnetic properties of (Mn,Fe)(3-delta)O-4 nanoparticles synthesized by soft mechanochemistry using Mn(OH)(2) x 2 H2O and Fe(OH)(3) powders as starting compounds. The resulting nanoparticles with a composition of the (Mn,Fe)(3-delta)O-4 type are found to have a core/shell structure with different Mn/Fe ratios in the core and at the surface. XPS analysis points to valences of +2, +3, and +4 for Mn and +3 for Fe at the particle surface. Combined results of XRPD, Mossbauer spectroscopy, and EDX analysis suggest that there is a deviation from stoichiometry in the nanoparticle core compared to the shell, accompanied by creation of cation polyvalence and vacancies. The value of saturation magnetization, M-S, of 73.5 emu/g at room temperature, is among the highest reported so far among nanocrystalline ferrite systems of similar composition. (C) 2012 American Institute of Physics. [http://dx.doi.org/10.1063/1.3700228]
T2  - Journal of Applied Physics
T1  - Magnetization enhancement and cation valences in nonstoichiometric (Mn,Fe)(3-delta)O-4 nanoparticles
VL  - 111
IS  - 7
DO  - 10.1063/1.3700228
ER  - 

@article{
author = "Antić, Bratislav and Kremenović, Aleksandar S. and Jović, Nataša G. and Pavlović, Miodrag B. and Jovalekić, Čedomir and Nikolić, Aleksandar S. and Goya, Gerardo F. and Weidenthaler, C.",
year = "2012",
abstract = "We present a study of the structural and magnetic properties of (Mn,Fe)(3-delta)O-4 nanoparticles synthesized by soft mechanochemistry using Mn(OH)(2) x 2 H2O and Fe(OH)(3) powders as starting compounds. The resulting nanoparticles with a composition of the (Mn,Fe)(3-delta)O-4 type are found to have a core/shell structure with different Mn/Fe ratios in the core and at the surface. XPS analysis points to valences of +2, +3, and +4 for Mn and +3 for Fe at the particle surface. Combined results of XRPD, Mossbauer spectroscopy, and EDX analysis suggest that there is a deviation from stoichiometry in the nanoparticle core compared to the shell, accompanied by creation of cation polyvalence and vacancies. The value of saturation magnetization, M-S, of 73.5 emu/g at room temperature, is among the highest reported so far among nanocrystalline ferrite systems of similar composition. (C) 2012 American Institute of Physics. [http://dx.doi.org/10.1063/1.3700228]",
journal = "Journal of Applied Physics",
title = "Magnetization enhancement and cation valences in nonstoichiometric (Mn,Fe)(3-delta)O-4 nanoparticles",
volume = "111",
number = "7",
doi = "10.1063/1.3700228"
}

Antić, B., Kremenović, A. S., Jović, N. G., Pavlović, M. B., Jovalekić, Č., Nikolić, A. S., Goya, G. F.,& Weidenthaler, C.. (2012). Magnetization enhancement and cation valences in nonstoichiometric (Mn,Fe)(3-delta)O-4 nanoparticles. in Journal of Applied Physics, 111(7).
https://doi.org/10.1063/1.3700228

Antić B, Kremenović AS, Jović NG, Pavlović MB, Jovalekić Č, Nikolić AS, Goya GF, Weidenthaler C. Magnetization enhancement and cation valences in nonstoichiometric (Mn,Fe)(3-delta)O-4 nanoparticles. in Journal of Applied Physics. 2012;111(7).
doi:10.1063/1.3700228 .

Antić, Bratislav, Kremenović, Aleksandar S., Jović, Nataša G., Pavlović, Miodrag B., Jovalekić, Čedomir, Nikolić, Aleksandar S., Goya, Gerardo F., Weidenthaler, C., "Magnetization enhancement and cation valences in nonstoichiometric (Mn,Fe)(3-delta)O-4 nanoparticles" in Journal of Applied Physics, 111, no. 7 (2012),
https://doi.org/10.1063/1.3700228 . .

TY  - JOUR
AU  - Antić, Bratislav
AU  - Rogan, Jelena R.
AU  - Kremenović, Aleksandar S.
AU  - Nikolić, Aleksandar S.
AU  - Vučinić-Vasić, Milica
AU  - Božanić, Dušan K.
AU  - Goya, Gerardo F.
AU  - Colomban, Ph
PY  - 2010
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/4008
AB  - Spherical shaped nanoparticles of series Y2-xEuxO3 (x = 0.06, 0.10, 0.20, and 2) and Gd2-xEuxO3 (x = 0.06, 0.10) were prepared by thermolysis of 2,4-pentanedione complexes of Y, Gd, and Eu. The bixbyite phase of Gd2-xEuxO3 samples was formed at 500 degrees C, whereas the thermal decomposition of Y and Eu complexes mixtures occurred at higher temperatures. Linearity in the concentration dependence on lattice parameter confirmed the formation of solid solutions. The distribution of Eu3+ in Gd2-xEuxO3 was changed with thermal annealing: in the as-prepared sample (x = 0.10) the distribution was preferential at C-3i sites while in the annealed samples, Eu3+ were distributed at both C-2 and C-3i sites. Rietveld refinement of site occupancies as well as emission spectra showed a random distribution of cations in Y2-xEuxO3. The photoluminescence (PL) measurements of the sample showed red emission with the main peak at 614 nm (D-5(0)-F-7(2)). The PL intensity increased with increasing concentration of Eu3+ in both series. Infrared excitation was required to obtain good Raman spectra. The linear dependence of the main Raman peak wavenumber offers a non-destructive method for monitoring the substitution level and its homogeneity at the micron scale.
T2  - Nanotechnology
T1  - Optimization of photoluminescence of Y2O3:Eu and Gd2O3:Eu phosphors synthesized by thermolysis of 2,4-pentanedione complexes
VL  - 21
IS  - 24
DO  - 10.1088/0957-4484/21/24/245702
ER  - 

@article{
author = "Antić, Bratislav and Rogan, Jelena R. and Kremenović, Aleksandar S. and Nikolić, Aleksandar S. and Vučinić-Vasić, Milica and Božanić, Dušan K. and Goya, Gerardo F. and Colomban, Ph",
year = "2010",
abstract = "Spherical shaped nanoparticles of series Y2-xEuxO3 (x = 0.06, 0.10, 0.20, and 2) and Gd2-xEuxO3 (x = 0.06, 0.10) were prepared by thermolysis of 2,4-pentanedione complexes of Y, Gd, and Eu. The bixbyite phase of Gd2-xEuxO3 samples was formed at 500 degrees C, whereas the thermal decomposition of Y and Eu complexes mixtures occurred at higher temperatures. Linearity in the concentration dependence on lattice parameter confirmed the formation of solid solutions. The distribution of Eu3+ in Gd2-xEuxO3 was changed with thermal annealing: in the as-prepared sample (x = 0.10) the distribution was preferential at C-3i sites while in the annealed samples, Eu3+ were distributed at both C-2 and C-3i sites. Rietveld refinement of site occupancies as well as emission spectra showed a random distribution of cations in Y2-xEuxO3. The photoluminescence (PL) measurements of the sample showed red emission with the main peak at 614 nm (D-5(0)-F-7(2)). The PL intensity increased with increasing concentration of Eu3+ in both series. Infrared excitation was required to obtain good Raman spectra. The linear dependence of the main Raman peak wavenumber offers a non-destructive method for monitoring the substitution level and its homogeneity at the micron scale.",
journal = "Nanotechnology",
title = "Optimization of photoluminescence of Y2O3:Eu and Gd2O3:Eu phosphors synthesized by thermolysis of 2,4-pentanedione complexes",
volume = "21",
number = "24",
doi = "10.1088/0957-4484/21/24/245702"
}

Antić, B., Rogan, J. R., Kremenović, A. S., Nikolić, A. S., Vučinić-Vasić, M., Božanić, D. K., Goya, G. F.,& Colomban, P.. (2010). Optimization of photoluminescence of Y2O3:Eu and Gd2O3:Eu phosphors synthesized by thermolysis of 2,4-pentanedione complexes. in Nanotechnology, 21(24).
https://doi.org/10.1088/0957-4484/21/24/245702

Antić B, Rogan JR, Kremenović AS, Nikolić AS, Vučinić-Vasić M, Božanić DK, Goya GF, Colomban P. Optimization of photoluminescence of Y2O3:Eu and Gd2O3:Eu phosphors synthesized by thermolysis of 2,4-pentanedione complexes. in Nanotechnology. 2010;21(24).
doi:10.1088/0957-4484/21/24/245702 .

Antić, Bratislav, Rogan, Jelena R., Kremenović, Aleksandar S., Nikolić, Aleksandar S., Vučinić-Vasić, Milica, Božanić, Dušan K., Goya, Gerardo F., Colomban, Ph, "Optimization of photoluminescence of Y2O3:Eu and Gd2O3:Eu phosphors synthesized by thermolysis of 2,4-pentanedione complexes" in Nanotechnology, 21, no. 24 (2010),
https://doi.org/10.1088/0957-4484/21/24/245702 . .

TY  - JOUR
AU  - Antić, Bratislav
AU  - Jović, Nataša G.
AU  - Pavlović, Miodrag B.
AU  - Kremenović, Aleksandar S.
AU  - Manojlović, Dragan D.
AU  - Vučinić-Vasić, Milica
AU  - Nikolić, Aleksandar S.
PY  - 2010
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/3921
AB  - In this paper we report results of structural, spectroscopic, and magnetic investigations of MgFe2O4 nanoparticles prepared by soft mechanochemical synthesis. MgFe2O4 nanoparticles crystallize in Fd3m space group with mixed cation distribution and reduced percentage of Fe3+ at tetrahedral (8a) sites. Discrepancy in the cation distribution compared to that in the bulk Mg-ferrite is one of the highest known. X-ray line broadening analysis reveals crystallite size and strain anisotropy. The saturation magnetization, M-sat=62 emu/g measured at 5 K is twice higher than that found in the bulk counterparts. Such high value of M-sat is attributed to the low value of cation inversion parameter (delta=0.69), to the core/shell structure of the nanoparticles and to the surface/volume ratio. Moumlssbauer spectrum collected at room temperature reveals ferrimagnetic ordering between Fe3+ ions in 8a and 16d sites, while zero-field-cooled (ZFC) and field-cooled (FC) M(T) measurements were shown superparamagnetic state above 350 K.
T2  - Journal of Applied Physics
T1  - Magnetization enhancement in nanostructured random type MgFe2O4 spinel prepared by soft mechanochemical route
VL  - 107
IS  - 4
DO  - 10.1063/1.3319563
ER  - 

@article{
author = "Antić, Bratislav and Jović, Nataša G. and Pavlović, Miodrag B. and Kremenović, Aleksandar S. and Manojlović, Dragan D. and Vučinić-Vasić, Milica and Nikolić, Aleksandar S.",
year = "2010",
abstract = "In this paper we report results of structural, spectroscopic, and magnetic investigations of MgFe2O4 nanoparticles prepared by soft mechanochemical synthesis. MgFe2O4 nanoparticles crystallize in Fd3m space group with mixed cation distribution and reduced percentage of Fe3+ at tetrahedral (8a) sites. Discrepancy in the cation distribution compared to that in the bulk Mg-ferrite is one of the highest known. X-ray line broadening analysis reveals crystallite size and strain anisotropy. The saturation magnetization, M-sat=62 emu/g measured at 5 K is twice higher than that found in the bulk counterparts. Such high value of M-sat is attributed to the low value of cation inversion parameter (delta=0.69), to the core/shell structure of the nanoparticles and to the surface/volume ratio. Moumlssbauer spectrum collected at room temperature reveals ferrimagnetic ordering between Fe3+ ions in 8a and 16d sites, while zero-field-cooled (ZFC) and field-cooled (FC) M(T) measurements were shown superparamagnetic state above 350 K.",
journal = "Journal of Applied Physics",
title = "Magnetization enhancement in nanostructured random type MgFe2O4 spinel prepared by soft mechanochemical route",
volume = "107",
number = "4",
doi = "10.1063/1.3319563"
}

Antić, B., Jović, N. G., Pavlović, M. B., Kremenović, A. S., Manojlović, D. D., Vučinić-Vasić, M.,& Nikolić, A. S.. (2010). Magnetization enhancement in nanostructured random type MgFe2O4 spinel prepared by soft mechanochemical route. in Journal of Applied Physics, 107(4).
https://doi.org/10.1063/1.3319563

Antić B, Jović NG, Pavlović MB, Kremenović AS, Manojlović DD, Vučinić-Vasić M, Nikolić AS. Magnetization enhancement in nanostructured random type MgFe2O4 spinel prepared by soft mechanochemical route. in Journal of Applied Physics. 2010;107(4).
doi:10.1063/1.3319563 .

Antić, Bratislav, Jović, Nataša G., Pavlović, Miodrag B., Kremenović, Aleksandar S., Manojlović, Dragan D., Vučinić-Vasić, Milica, Nikolić, Aleksandar S., "Magnetization enhancement in nanostructured random type MgFe2O4 spinel prepared by soft mechanochemical route" in Journal of Applied Physics, 107, no. 4 (2010),
https://doi.org/10.1063/1.3319563 . .

TY  - JOUR
AU  - Antić, Bratislav
AU  - Kremenović, Aleksandar S.
AU  - Vučinić-Vasić, Milica
AU  - Dohcevic-Mitrovic, Z.
AU  - Nikolić, Aleksandar S.
AU  - Gruden-Pavlović, Maja
AU  - Jančar, Boštjan
AU  - Meden, A.
PY  - 2010
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/4015
AB  - After controlled thermal degradation of acetylacetonato (AA) complexes, mixtures of monodisperse similar to 5 nm large isometric particles of Y2-xYbxO3 (x = 0.06, 0.10, 0.20, 0.40) were synthesized. Detailed information on nanoparticles microstructure and core crystal structure is reported. The Yb3+ ions occupy preferently C-3i sites for low Yb3+ concentrations, while for 20 at.% Yb3+, a random distribution was found. It was shown that the particle/crystallite size and strain as well as Raman modes positions and widths are influenced by Yb3+ concentration. Crystallographic and Raman spectroscopy results indicate that the particles are core/shell structured with cubic crystalline core and monoclinic-like disordered shell. Most probable particles shell/core volume ratio decreased with annealing at 500 degrees C and the shell disappeared when annealed at 1000 degrees C. (C) 2010 Elsevier B.V. All rights reserved.
T2  - Materials Chemistry and Physics
T1  - Composition related properties of (Yb,Y)(2)O-3 nanoparticles synthesized by controlled thermal degradation of AA complexes
VL  - 122
IS  - 2-3
SP  - 386
EP  - 391
DO  - 10.1016/j.matchemphys.2010.03.010
ER  - 

@article{
author = "Antić, Bratislav and Kremenović, Aleksandar S. and Vučinić-Vasić, Milica and Dohcevic-Mitrovic, Z. and Nikolić, Aleksandar S. and Gruden-Pavlović, Maja and Jančar, Boštjan and Meden, A.",
year = "2010",
abstract = "After controlled thermal degradation of acetylacetonato (AA) complexes, mixtures of monodisperse similar to 5 nm large isometric particles of Y2-xYbxO3 (x = 0.06, 0.10, 0.20, 0.40) were synthesized. Detailed information on nanoparticles microstructure and core crystal structure is reported. The Yb3+ ions occupy preferently C-3i sites for low Yb3+ concentrations, while for 20 at.% Yb3+, a random distribution was found. It was shown that the particle/crystallite size and strain as well as Raman modes positions and widths are influenced by Yb3+ concentration. Crystallographic and Raman spectroscopy results indicate that the particles are core/shell structured with cubic crystalline core and monoclinic-like disordered shell. Most probable particles shell/core volume ratio decreased with annealing at 500 degrees C and the shell disappeared when annealed at 1000 degrees C. (C) 2010 Elsevier B.V. All rights reserved.",
journal = "Materials Chemistry and Physics",
title = "Composition related properties of (Yb,Y)(2)O-3 nanoparticles synthesized by controlled thermal degradation of AA complexes",
volume = "122",
number = "2-3",
pages = "386-391",
doi = "10.1016/j.matchemphys.2010.03.010"
}

Antić, B., Kremenović, A. S., Vučinić-Vasić, M., Dohcevic-Mitrovic, Z., Nikolić, A. S., Gruden-Pavlović, M., Jančar, B.,& Meden, A.. (2010). Composition related properties of (Yb,Y)(2)O-3 nanoparticles synthesized by controlled thermal degradation of AA complexes. in Materials Chemistry and Physics, 122(2-3), 386-391.
https://doi.org/10.1016/j.matchemphys.2010.03.010

Antić B, Kremenović AS, Vučinić-Vasić M, Dohcevic-Mitrovic Z, Nikolić AS, Gruden-Pavlović M, Jančar B, Meden A. Composition related properties of (Yb,Y)(2)O-3 nanoparticles synthesized by controlled thermal degradation of AA complexes. in Materials Chemistry and Physics. 2010;122(2-3):386-391.
doi:10.1016/j.matchemphys.2010.03.010 .

Antić, Bratislav, Kremenović, Aleksandar S., Vučinić-Vasić, Milica, Dohcevic-Mitrovic, Z., Nikolić, Aleksandar S., Gruden-Pavlović, Maja, Jančar, Boštjan, Meden, A., "Composition related properties of (Yb,Y)(2)O-3 nanoparticles synthesized by controlled thermal degradation of AA complexes" in Materials Chemistry and Physics, 122, no. 2-3 (2010):386-391,
https://doi.org/10.1016/j.matchemphys.2010.03.010 . .

TY  - JOUR
AU  - Vučinić-Vasić, Milica
AU  - Kremenović, Aleksandar S.
AU  - Nikolić, Aleksandar S.
AU  - Colomban, Philippe
AU  - Mazzerolles, Leo
AU  - Kahlenberg, Volker
AU  - Antić, Bratislav
PY  - 2010
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/4055
AB  - This paper reports results concerning the crystal structure of core and shell as well as microstructure of 25 nm-ytterbium sesquioxide (Yb(2)O(3)) nanoparticles synthesized using a unique method based on thermal decomposition of a 2,4 pentadione complex. Used Raman spectroscopy measurements indicate core/shell structure, with monoclinic or a mixture of monoclinic and cubic symmetry of the particle shell. In addition, XRPD and SAED confirmed bixbyite structure type for the core (space group Ia (3) over bar). Broadening of the observed Raman bands indicates structural distortions in the nanocrystalline sample. The size/strain analysis was done on XRPD data using Fullprof/MarqX approach. Anisotropy of X-ray line broadening is caused by size effects only. The resulting mean microstrain (6 x 10(-4)) points to a low concentration of defects within the crystallites. (C) 2010 Elsevier B.V. All rights reserved.
T2  - Journal of Alloys and Compounds
T1  - Core and shell structure of ytterbium sesquioxide nanoparticles
VL  - 502
IS  - 1
SP  - 107
EP  - 111
DO  - 10.1016/j.jallcom.2010.03.158
ER  - 

@article{
author = "Vučinić-Vasić, Milica and Kremenović, Aleksandar S. and Nikolić, Aleksandar S. and Colomban, Philippe and Mazzerolles, Leo and Kahlenberg, Volker and Antić, Bratislav",
year = "2010",
abstract = "This paper reports results concerning the crystal structure of core and shell as well as microstructure of 25 nm-ytterbium sesquioxide (Yb(2)O(3)) nanoparticles synthesized using a unique method based on thermal decomposition of a 2,4 pentadione complex. Used Raman spectroscopy measurements indicate core/shell structure, with monoclinic or a mixture of monoclinic and cubic symmetry of the particle shell. In addition, XRPD and SAED confirmed bixbyite structure type for the core (space group Ia (3) over bar). Broadening of the observed Raman bands indicates structural distortions in the nanocrystalline sample. The size/strain analysis was done on XRPD data using Fullprof/MarqX approach. Anisotropy of X-ray line broadening is caused by size effects only. The resulting mean microstrain (6 x 10(-4)) points to a low concentration of defects within the crystallites. (C) 2010 Elsevier B.V. All rights reserved.",
journal = "Journal of Alloys and Compounds",
title = "Core and shell structure of ytterbium sesquioxide nanoparticles",
volume = "502",
number = "1",
pages = "107-111",
doi = "10.1016/j.jallcom.2010.03.158"
}

Vučinić-Vasić, M., Kremenović, A. S., Nikolić, A. S., Colomban, P., Mazzerolles, L., Kahlenberg, V.,& Antić, B.. (2010). Core and shell structure of ytterbium sesquioxide nanoparticles. in Journal of Alloys and Compounds, 502(1), 107-111.
https://doi.org/10.1016/j.jallcom.2010.03.158

Vučinić-Vasić M, Kremenović AS, Nikolić AS, Colomban P, Mazzerolles L, Kahlenberg V, Antić B. Core and shell structure of ytterbium sesquioxide nanoparticles. in Journal of Alloys and Compounds. 2010;502(1):107-111.
doi:10.1016/j.jallcom.2010.03.158 .

Vučinić-Vasić, Milica, Kremenović, Aleksandar S., Nikolić, Aleksandar S., Colomban, Philippe, Mazzerolles, Leo, Kahlenberg, Volker, Antić, Bratislav, "Core and shell structure of ytterbium sesquioxide nanoparticles" in Journal of Alloys and Compounds, 502, no. 1 (2010):107-111,
https://doi.org/10.1016/j.jallcom.2010.03.158 . .

TY  - JOUR
AU  - Vučinić-Vasić, Milica
AU  - Antić, Bratislav
AU  - Kremenović, Aleksandar S.
AU  - Nikolić, Aleksandar S.
AU  - Blanuša, Jovan
AU  - Rakić, Srđan
AU  - Spasojević, Vojislav
AU  - Kapor, Agneš
PY  - 2007
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/3146
AB  - Applying a new synthesis route based on the thermal decomposition of a mixture acetylacetonato complexes, Li(AA), La(AA)(3) and Fe(AA)(3), Li, La ferrite (Li0.5La0.08Fe2.42O4) was formed. The element analysis performed by ICP technique and the Rietveld refinement data indicate that the sample is composed of three phases: Li0.5La0.008Fe2.42O4 (69%, SG P4(3)32, a = 8.3445(3) angstrom), La0.14Fe3O4 (16%, SG Fd (3) over barm, a = 8.403(1) angstrom) and LiFeO2 (15%, SG Fm (3) over barm, a = 4.2291(8) angstrom). A partial substitution Fe3+ - GT La3+ in Li ferrite and La insertion at 16c site in Fe3O4 occur at low concentrations. A partial cation ordering at 4b and 12d octahedral sites in Li0.5La0.08Fe2.42O4 was noticed. TEM micrograph shows that the nanoparticles are spherically shaped and that the particle distribution is in the range between 7 and 33 nm. The sample exhibits superparamagnetic behavior, thus the composite has potential industrial applications. (c) 2006 Elsevier B.V. All rights reserved.
T2  - Journal of Alloys and Compounds
T1  - Investigation of nanocrystalline phases in Li-La-Fe-O system formed by the decomposition of acetylacetonato complexes
VL  - 428
IS  - 1-2
SP  - 322
EP  - 326
DO  - 10.1016/j.jallcom.2006.03.042
ER  - 

@article{
author = "Vučinić-Vasić, Milica and Antić, Bratislav and Kremenović, Aleksandar S. and Nikolić, Aleksandar S. and Blanuša, Jovan and Rakić, Srđan and Spasojević, Vojislav and Kapor, Agneš",
year = "2007",
abstract = "Applying a new synthesis route based on the thermal decomposition of a mixture acetylacetonato complexes, Li(AA), La(AA)(3) and Fe(AA)(3), Li, La ferrite (Li0.5La0.08Fe2.42O4) was formed. The element analysis performed by ICP technique and the Rietveld refinement data indicate that the sample is composed of three phases: Li0.5La0.008Fe2.42O4 (69%, SG P4(3)32, a = 8.3445(3) angstrom), La0.14Fe3O4 (16%, SG Fd (3) over barm, a = 8.403(1) angstrom) and LiFeO2 (15%, SG Fm (3) over barm, a = 4.2291(8) angstrom). A partial substitution Fe3+ - GT La3+ in Li ferrite and La insertion at 16c site in Fe3O4 occur at low concentrations. A partial cation ordering at 4b and 12d octahedral sites in Li0.5La0.08Fe2.42O4 was noticed. TEM micrograph shows that the nanoparticles are spherically shaped and that the particle distribution is in the range between 7 and 33 nm. The sample exhibits superparamagnetic behavior, thus the composite has potential industrial applications. (c) 2006 Elsevier B.V. All rights reserved.",
journal = "Journal of Alloys and Compounds",
title = "Investigation of nanocrystalline phases in Li-La-Fe-O system formed by the decomposition of acetylacetonato complexes",
volume = "428",
number = "1-2",
pages = "322-326",
doi = "10.1016/j.jallcom.2006.03.042"
}

Vučinić-Vasić, M., Antić, B., Kremenović, A. S., Nikolić, A. S., Blanuša, J., Rakić, S., Spasojević, V.,& Kapor, A.. (2007). Investigation of nanocrystalline phases in Li-La-Fe-O system formed by the decomposition of acetylacetonato complexes. in Journal of Alloys and Compounds, 428(1-2), 322-326.
https://doi.org/10.1016/j.jallcom.2006.03.042

Vučinić-Vasić M, Antić B, Kremenović AS, Nikolić AS, Blanuša J, Rakić S, Spasojević V, Kapor A. Investigation of nanocrystalline phases in Li-La-Fe-O system formed by the decomposition of acetylacetonato complexes. in Journal of Alloys and Compounds. 2007;428(1-2):322-326.
doi:10.1016/j.jallcom.2006.03.042 .

Vučinić-Vasić, Milica, Antić, Bratislav, Kremenović, Aleksandar S., Nikolić, Aleksandar S., Blanuša, Jovan, Rakić, Srđan, Spasojević, Vojislav, Kapor, Agneš, "Investigation of nanocrystalline phases in Li-La-Fe-O system formed by the decomposition of acetylacetonato complexes" in Journal of Alloys and Compounds, 428, no. 1-2 (2007):322-326,
https://doi.org/10.1016/j.jallcom.2006.03.042 . .

TY  - JOUR
AU  - Kremenović, Aleksandar S.
AU  - Antić, Bratislav
AU  - Nikolić, Aleksandar S.
AU  - Blanuša, Jovan
AU  - Jančar, Boštjan
AU  - Meden, A.
AU  - Mentus, Slavko V.
PY  - 2007
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/3308
AB  - A novel synthesis route based on thermal decomposition of yttrium and gadolinium complexes with 2,4-pentanedione ligand has been used to synthesize 5 nn size (Y0.9Gd0.1)(2)O-3 powder. Refinement of occupancy parameters revealed that Gd3+ ions preferably occupy C-3i sites in host Y2O3, forming a material with a metastable cation distribution. The average crystallite size was found to increase, and the average microstrain to decrease, as the annealing temperature is increased, while the Gd3+ ion distribution remained metastable in nature. Small anisotropic X-ray powder diffraction pattern line broadening due to crystallite size effects was observed. The inverse susceptibility of the 5 nn sample exhibits unusual break in slope to a smaller value below 2.7 K. (C) 2007 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
T2  - Scripta Materialia
T1  - The dependence of cation distribution, microstrain and magnetic susceptibility on particle size in nanocrystalline Gd2O3/Y2O3
VL  - 57
IS  - 12
SP  - 1061
EP  - 1064
DO  - 10.1016/j.scriptamat.2007.09.002
ER  - 

@article{
author = "Kremenović, Aleksandar S. and Antić, Bratislav and Nikolić, Aleksandar S. and Blanuša, Jovan and Jančar, Boštjan and Meden, A. and Mentus, Slavko V.",
year = "2007",
abstract = "A novel synthesis route based on thermal decomposition of yttrium and gadolinium complexes with 2,4-pentanedione ligand has been used to synthesize 5 nn size (Y0.9Gd0.1)(2)O-3 powder. Refinement of occupancy parameters revealed that Gd3+ ions preferably occupy C-3i sites in host Y2O3, forming a material with a metastable cation distribution. The average crystallite size was found to increase, and the average microstrain to decrease, as the annealing temperature is increased, while the Gd3+ ion distribution remained metastable in nature. Small anisotropic X-ray powder diffraction pattern line broadening due to crystallite size effects was observed. The inverse susceptibility of the 5 nn sample exhibits unusual break in slope to a smaller value below 2.7 K. (C) 2007 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.",
journal = "Scripta Materialia",
title = "The dependence of cation distribution, microstrain and magnetic susceptibility on particle size in nanocrystalline Gd2O3/Y2O3",
volume = "57",
number = "12",
pages = "1061-1064",
doi = "10.1016/j.scriptamat.2007.09.002"
}

Kremenović, A. S., Antić, B., Nikolić, A. S., Blanuša, J., Jančar, B., Meden, A.,& Mentus, S. V.. (2007). The dependence of cation distribution, microstrain and magnetic susceptibility on particle size in nanocrystalline Gd2O3/Y2O3. in Scripta Materialia, 57(12), 1061-1064.
https://doi.org/10.1016/j.scriptamat.2007.09.002

Kremenović AS, Antić B, Nikolić AS, Blanuša J, Jančar B, Meden A, Mentus SV. The dependence of cation distribution, microstrain and magnetic susceptibility on particle size in nanocrystalline Gd2O3/Y2O3. in Scripta Materialia. 2007;57(12):1061-1064.
doi:10.1016/j.scriptamat.2007.09.002 .

Kremenović, Aleksandar S., Antić, Bratislav, Nikolić, Aleksandar S., Blanuša, Jovan, Jančar, Boštjan, Meden, A., Mentus, Slavko V., "The dependence of cation distribution, microstrain and magnetic susceptibility on particle size in nanocrystalline Gd2O3/Y2O3" in Scripta Materialia, 57, no. 12 (2007):1061-1064,
https://doi.org/10.1016/j.scriptamat.2007.09.002 . .

TY  - JOUR
AU  - Blanuša, Jovan
AU  - Antić, Bratislav
AU  - Kremenović, Aleksandar S.
AU  - Nikolić, Aleksandar S.
AU  - Mazzerolles, L.
AU  - Mentus, Slavko V.
AU  - Spasojević, Vojislav
PY  - 2007
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/3321
AB  - New synthesis routine based on thermal decomposition of an erbium complex with acetylacetonato ligand (2, 4-pentadione) was used to prepare nanosized Er2O3 with a particle size of 5 nm and a narrow size distribution. For the sake of comparison, the ultrafine-Er2O3 powder was prepared by precipitation and subsequent sintering. The magnetic susceptibility of nanosized Er2O3 indicates the antiferromagnetic LT - GT paramagnetic transition at 1.8 K or lower, while in ultrafine such as in a bulk counterpart the transition was observed at noticeably higher temperature of similar to 3.4 K. The decrease in Neel temperature, observed in the case of nanosized Er2O3 sample, was attributed to both particle surface and core effects. (c) 2007 Elsevier Ltd. All rights reserved.
T2  - Solid State Communications
T1  - Particle size effect on Neel temperature in Er2O3 nanopowder synthesized by thermolysis of 2, 4-pentadione complex
VL  - 144
IS  - 7-8
SP  - 310
EP  - 314
DO  - 10.1016/j.ssc.2007.09.003
ER  - 

@article{
author = "Blanuša, Jovan and Antić, Bratislav and Kremenović, Aleksandar S. and Nikolić, Aleksandar S. and Mazzerolles, L. and Mentus, Slavko V. and Spasojević, Vojislav",
year = "2007",
abstract = "New synthesis routine based on thermal decomposition of an erbium complex with acetylacetonato ligand (2, 4-pentadione) was used to prepare nanosized Er2O3 with a particle size of 5 nm and a narrow size distribution. For the sake of comparison, the ultrafine-Er2O3 powder was prepared by precipitation and subsequent sintering. The magnetic susceptibility of nanosized Er2O3 indicates the antiferromagnetic LT - GT paramagnetic transition at 1.8 K or lower, while in ultrafine such as in a bulk counterpart the transition was observed at noticeably higher temperature of similar to 3.4 K. The decrease in Neel temperature, observed in the case of nanosized Er2O3 sample, was attributed to both particle surface and core effects. (c) 2007 Elsevier Ltd. All rights reserved.",
journal = "Solid State Communications",
title = "Particle size effect on Neel temperature in Er2O3 nanopowder synthesized by thermolysis of 2, 4-pentadione complex",
volume = "144",
number = "7-8",
pages = "310-314",
doi = "10.1016/j.ssc.2007.09.003"
}

Blanuša, J., Antić, B., Kremenović, A. S., Nikolić, A. S., Mazzerolles, L., Mentus, S. V.,& Spasojević, V.. (2007). Particle size effect on Neel temperature in Er2O3 nanopowder synthesized by thermolysis of 2, 4-pentadione complex. in Solid State Communications, 144(7-8), 310-314.
https://doi.org/10.1016/j.ssc.2007.09.003

Blanuša J, Antić B, Kremenović AS, Nikolić AS, Mazzerolles L, Mentus SV, Spasojević V. Particle size effect on Neel temperature in Er2O3 nanopowder synthesized by thermolysis of 2, 4-pentadione complex. in Solid State Communications. 2007;144(7-8):310-314.
doi:10.1016/j.ssc.2007.09.003 .

Blanuša, Jovan, Antić, Bratislav, Kremenović, Aleksandar S., Nikolić, Aleksandar S., Mazzerolles, L., Mentus, Slavko V., Spasojević, Vojislav, "Particle size effect on Neel temperature in Er2O3 nanopowder synthesized by thermolysis of 2, 4-pentadione complex" in Solid State Communications, 144, no. 7-8 (2007):310-314,
https://doi.org/10.1016/j.ssc.2007.09.003 . .

TY  - JOUR
AU  - Vučinić-Vasić, Milica
AU  - Antić, Bratislav
AU  - Blanuša, Jovan
AU  - Rakić, Srđan
AU  - Kremenović, Aleksandar S.
AU  - Nikolić, Aleksandar S.
AU  - Kapor, Agneš
PY  - 2006
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/2955
AB  - Nanosize Li-ferrites were synthesised by the thermal decomposition of an appropriate mixture of complex compounds with acetylacetone - (2,4 pentadione) ligands ([M(AA)(x)]; M = Li and Fe) at 500 degrees C. The obtained sample is composed of three phases determined by the standard Rietveld procedure: Li0.5Fe2.5O4 (S. G. P4(3)32), Li1.16Fe3O4 (S.G. Fd (3) over barm) and LiFeO2 (S.G. Fm (3) over barm). Cation distribution in nanosize ordered spinel Li0.5Fe2.5O4 deviates from that of the bulk counterpart. Microstructure parameters (crystallite size of similar to 23 nm and strain of 3.2526(9) x 10(3)) were determined by the Rietveld refinement of the TCH-pV parameters. SEM microphotographs show a particle size of similar to 50-60 nm. An order disorder phase transition in ordered spinel Li0.5Fe2.5O4 was studied by DSC measurements and in situ XRPD technique. The temperature of phase transition was found to be 762 degrees C ( DSC) and (745 +/- 5) degrees C ( XRPD).
T2  - Applied Physics. A: Materials Science and Processing
T1  - Formation of nanosize Li-ferrites from acetylacetonato complexes and their crystal structure, microstructure and order-disorder phase transition
VL  - 82
IS  - 1
SP  - 49
EP  - 54
DO  - 10.1007/s00339-005-3378-y
ER  - 

@article{
author = "Vučinić-Vasić, Milica and Antić, Bratislav and Blanuša, Jovan and Rakić, Srđan and Kremenović, Aleksandar S. and Nikolić, Aleksandar S. and Kapor, Agneš",
year = "2006",
abstract = "Nanosize Li-ferrites were synthesised by the thermal decomposition of an appropriate mixture of complex compounds with acetylacetone - (2,4 pentadione) ligands ([M(AA)(x)]; M = Li and Fe) at 500 degrees C. The obtained sample is composed of three phases determined by the standard Rietveld procedure: Li0.5Fe2.5O4 (S. G. P4(3)32), Li1.16Fe3O4 (S.G. Fd (3) over barm) and LiFeO2 (S.G. Fm (3) over barm). Cation distribution in nanosize ordered spinel Li0.5Fe2.5O4 deviates from that of the bulk counterpart. Microstructure parameters (crystallite size of similar to 23 nm and strain of 3.2526(9) x 10(3)) were determined by the Rietveld refinement of the TCH-pV parameters. SEM microphotographs show a particle size of similar to 50-60 nm. An order disorder phase transition in ordered spinel Li0.5Fe2.5O4 was studied by DSC measurements and in situ XRPD technique. The temperature of phase transition was found to be 762 degrees C ( DSC) and (745 +/- 5) degrees C ( XRPD).",
journal = "Applied Physics. A: Materials Science and Processing",
title = "Formation of nanosize Li-ferrites from acetylacetonato complexes and their crystal structure, microstructure and order-disorder phase transition",
volume = "82",
number = "1",
pages = "49-54",
doi = "10.1007/s00339-005-3378-y"
}

Vučinić-Vasić, M., Antić, B., Blanuša, J., Rakić, S., Kremenović, A. S., Nikolić, A. S.,& Kapor, A.. (2006). Formation of nanosize Li-ferrites from acetylacetonato complexes and their crystal structure, microstructure and order-disorder phase transition. in Applied Physics. A: Materials Science and Processing, 82(1), 49-54.
https://doi.org/10.1007/s00339-005-3378-y

Vučinić-Vasić M, Antić B, Blanuša J, Rakić S, Kremenović AS, Nikolić AS, Kapor A. Formation of nanosize Li-ferrites from acetylacetonato complexes and their crystal structure, microstructure and order-disorder phase transition. in Applied Physics. A: Materials Science and Processing. 2006;82(1):49-54.
doi:10.1007/s00339-005-3378-y .

Vučinić-Vasić, Milica, Antić, Bratislav, Blanuša, Jovan, Rakić, Srđan, Kremenović, Aleksandar S., Nikolić, Aleksandar S., Kapor, Agneš, "Formation of nanosize Li-ferrites from acetylacetonato complexes and their crystal structure, microstructure and order-disorder phase transition" in Applied Physics. A: Materials Science and Processing, 82, no. 1 (2006):49-54,
https://doi.org/10.1007/s00339-005-3378-y . .

TY  - CONF
AU  - Vučinić-Vasić, Milica
AU  - Antić, Bratislav
AU  - Nikolić, Aleksandar S.
AU  - Kremenović, Aleksandar S.
AU  - Rakić, Srđan
AU  - Blanuša, Jovan
AU  - Cvjetićanin, Nikola
AU  - Kapor, Agneš
PY  - 2004
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/9536
AB  - An order-disorder phase transition of nanosize Li-ferrite (Li0.50Fe2.50O4) was studied by DSC measurements and in situ XRPD technique. The phase transition temperature is found to be 762 °C (DSC) and (745±5) °C (XRPD).
PB  - Society of Physical Chemists of Serbia
C3  - Physical chemistry 2004: 7th international conference on fundemental and applied aspract of physical chemistry
T1  - In situ XRPD and DSC study of order-disorder phase transition in nanosize Li-ferrite
VL  - 2
SP  - 508
EP  - 510
UR  - https://hdl.handle.net/21.15107/rcub_vinar_9536
ER  - 

@conference{
author = "Vučinić-Vasić, Milica and Antić, Bratislav and Nikolić, Aleksandar S. and Kremenović, Aleksandar S. and Rakić, Srđan and Blanuša, Jovan and Cvjetićanin, Nikola and Kapor, Agneš",
year = "2004",
abstract = "An order-disorder phase transition of nanosize Li-ferrite (Li0.50Fe2.50O4) was studied by DSC measurements and in situ XRPD technique. The phase transition temperature is found to be 762 °C (DSC) and (745±5) °C (XRPD).",
publisher = "Society of Physical Chemists of Serbia",
journal = "Physical chemistry 2004: 7th international conference on fundemental and applied aspract of physical chemistry",
title = "In situ XRPD and DSC study of order-disorder phase transition in nanosize Li-ferrite",
volume = "2",
pages = "508-510",
url = "https://hdl.handle.net/21.15107/rcub_vinar_9536"
}

Vučinić-Vasić, M., Antić, B., Nikolić, A. S., Kremenović, A. S., Rakić, S., Blanuša, J., Cvjetićanin, N.,& Kapor, A.. (2004). In situ XRPD and DSC study of order-disorder phase transition in nanosize Li-ferrite. in Physical chemistry 2004: 7th international conference on fundemental and applied aspract of physical chemistry
Society of Physical Chemists of Serbia., 2, 508-510.
https://hdl.handle.net/21.15107/rcub_vinar_9536

Vučinić-Vasić M, Antić B, Nikolić AS, Kremenović AS, Rakić S, Blanuša J, Cvjetićanin N, Kapor A. In situ XRPD and DSC study of order-disorder phase transition in nanosize Li-ferrite. in Physical chemistry 2004: 7th international conference on fundemental and applied aspract of physical chemistry. 2004;2:508-510.
https://hdl.handle.net/21.15107/rcub_vinar_9536 .

Vučinić-Vasić, Milica, Antić, Bratislav, Nikolić, Aleksandar S., Kremenović, Aleksandar S., Rakić, Srđan, Blanuša, Jovan, Cvjetićanin, Nikola, Kapor, Agneš, "In situ XRPD and DSC study of order-disorder phase transition in nanosize Li-ferrite" in Physical chemistry 2004: 7th international conference on fundemental and applied aspract of physical chemistry, 2 (2004):508-510,
https://hdl.handle.net/21.15107/rcub_vinar_9536 .

TY  - JOUR
AU  - Blanuša, Jovan
AU  - Antić, Bratislav
AU  - Nikolić, Aleksandar S.
AU  - Rakić, Srđan
AU  - Jović, Nataša G.
AU  - Sreckovic, M
PY  - 2004
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/6406
AB  - The ultrafine spinel NiFe1.9M0.1O4 powders (M=Al, Y, Cr, Fe) were synthesized by thermal decomposition of appropriate mixtures of complex compounds with acetylacetone - (2,4 pentadione) ligands ([M(AA)(x)]) at 500 degreesC. Samples were annealed in the temperature range 600-1000 degreesC and the crystallization process was followed by XRD. The largest crystallite size and the highest crystallization rate are observed for NiFe1.9Al0.1O4, while the opposite was found for NiFe1.9Y0.1O4. Strain value in NiFe1.9Y0.1O4 changes sign at temperatures between 700-800 degreesC, while for NiFe1.9M0.1O4 (M=Al, Cr) it has a positive sign and reaches the maximum value at 700 degreesC. The crystal structure of the Samples annealed at 1000 degreesC was refined using the Rietveld profile method. Cation substitution in Ni-ferrite changes its structural and microstructural parameters, and can also significantly influence other physical properties.
T2  - Materials Science Forum
T1  - Synthesis and characterization of Al, Y, Co and Cr substituted ultrafine powder of NiFe2O4
VL  - 443-4
SP  - 283
EP  - 286
DO  - 10.4028/www.scientific.net/MSF.443-444.283
ER  - 

@article{
author = "Blanuša, Jovan and Antić, Bratislav and Nikolić, Aleksandar S. and Rakić, Srđan and Jović, Nataša G. and Sreckovic, M",
year = "2004",
abstract = "The ultrafine spinel NiFe1.9M0.1O4 powders (M=Al, Y, Cr, Fe) were synthesized by thermal decomposition of appropriate mixtures of complex compounds with acetylacetone - (2,4 pentadione) ligands ([M(AA)(x)]) at 500 degreesC. Samples were annealed in the temperature range 600-1000 degreesC and the crystallization process was followed by XRD. The largest crystallite size and the highest crystallization rate are observed for NiFe1.9Al0.1O4, while the opposite was found for NiFe1.9Y0.1O4. Strain value in NiFe1.9Y0.1O4 changes sign at temperatures between 700-800 degreesC, while for NiFe1.9M0.1O4 (M=Al, Cr) it has a positive sign and reaches the maximum value at 700 degreesC. The crystal structure of the Samples annealed at 1000 degreesC was refined using the Rietveld profile method. Cation substitution in Ni-ferrite changes its structural and microstructural parameters, and can also significantly influence other physical properties.",
journal = "Materials Science Forum",
title = "Synthesis and characterization of Al, Y, Co and Cr substituted ultrafine powder of NiFe2O4",
volume = "443-4",
pages = "283-286",
doi = "10.4028/www.scientific.net/MSF.443-444.283"
}

Blanuša, J., Antić, B., Nikolić, A. S., Rakić, S., Jović, N. G.,& Sreckovic, M.. (2004). Synthesis and characterization of Al, Y, Co and Cr substituted ultrafine powder of NiFe2O4. in Materials Science Forum, 443-4, 283-286.
https://doi.org/10.4028/www.scientific.net/MSF.443-444.283

Blanuša J, Antić B, Nikolić AS, Rakić S, Jović NG, Sreckovic M. Synthesis and characterization of Al, Y, Co and Cr substituted ultrafine powder of NiFe2O4. in Materials Science Forum. 2004;443-4:283-286.
doi:10.4028/www.scientific.net/MSF.443-444.283 .

Blanuša, Jovan, Antić, Bratislav, Nikolić, Aleksandar S., Rakić, Srđan, Jović, Nataša G., Sreckovic, M, "Synthesis and characterization of Al, Y, Co and Cr substituted ultrafine powder of NiFe2O4" in Materials Science Forum, 443-4 (2004):283-286,
https://doi.org/10.4028/www.scientific.net/MSF.443-444.283 . .

TY  - JOUR
AU  - Nikolić, Aleksandar S.
AU  - Likar-Smiljanic, V
AU  - Jovalekić, Čedomir
AU  - Cajkovski, T
AU  - Biljic, R
AU  - Lazarević, Zorica Ž.
AU  - Pavlović, Miodrag B.
PY  - 2004
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/6437
AB  - Nickel and nickel-zinc ferrites are ones of the most abundant members of the soft magnetic materials. In the last few years, the interest in new methods of their preparation increases, because it is well known that the physical and chemical properties of these materials strongly depend on the preparing conditions. Powder samples of soft ferrites of NiFe2O4 and NixZn1-xFC2O4 were synthesized by a classical sintering procedure, planetary mill synthesis, and by a chemical procedure from complex compounds with acetylacetonato-ligands. Average particle sizes were 1 mum, 40 nm and 20x20x4 nm (slabs), respectively. All of the obtained materials were measured ill the frequency range of 7 - 12 GHz for the real and the imaginary part of permittivity and permeability, and the absorption coefficients were calculated. A concurrent analysis of the obtained values showed the influence of the method of synthesis, as well as the particle size on the absorption coefficients in the applied frequency range.
T2  - Materials Science Forum
T1  - Nicolson-Ross analysis of absorption coefficients of nickel and nickel-zinc ferrite powders prepared using a novel method
VL  - 453-454
SP  - 405
EP  - 410
DO  - 10.4028/www.scientific.net/MSF.453-454.405
ER  - 

@article{
author = "Nikolić, Aleksandar S. and Likar-Smiljanic, V and Jovalekić, Čedomir and Cajkovski, T and Biljic, R and Lazarević, Zorica Ž. and Pavlović, Miodrag B.",
year = "2004",
abstract = "Nickel and nickel-zinc ferrites are ones of the most abundant members of the soft magnetic materials. In the last few years, the interest in new methods of their preparation increases, because it is well known that the physical and chemical properties of these materials strongly depend on the preparing conditions. Powder samples of soft ferrites of NiFe2O4 and NixZn1-xFC2O4 were synthesized by a classical sintering procedure, planetary mill synthesis, and by a chemical procedure from complex compounds with acetylacetonato-ligands. Average particle sizes were 1 mum, 40 nm and 20x20x4 nm (slabs), respectively. All of the obtained materials were measured ill the frequency range of 7 - 12 GHz for the real and the imaginary part of permittivity and permeability, and the absorption coefficients were calculated. A concurrent analysis of the obtained values showed the influence of the method of synthesis, as well as the particle size on the absorption coefficients in the applied frequency range.",
journal = "Materials Science Forum",
title = "Nicolson-Ross analysis of absorption coefficients of nickel and nickel-zinc ferrite powders prepared using a novel method",
volume = "453-454",
pages = "405-410",
doi = "10.4028/www.scientific.net/MSF.453-454.405"
}

Nikolić, A. S., Likar-Smiljanic, V., Jovalekić, Č., Cajkovski, T., Biljic, R., Lazarević, Z. Ž.,& Pavlović, M. B.. (2004). Nicolson-Ross analysis of absorption coefficients of nickel and nickel-zinc ferrite powders prepared using a novel method. in Materials Science Forum, 453-454, 405-410.
https://doi.org/10.4028/www.scientific.net/MSF.453-454.405

Nikolić AS, Likar-Smiljanic V, Jovalekić Č, Cajkovski T, Biljic R, Lazarević ZŽ, Pavlović MB. Nicolson-Ross analysis of absorption coefficients of nickel and nickel-zinc ferrite powders prepared using a novel method. in Materials Science Forum. 2004;453-454:405-410.
doi:10.4028/www.scientific.net/MSF.453-454.405 .

Nikolić, Aleksandar S., Likar-Smiljanic, V, Jovalekić, Čedomir, Cajkovski, T, Biljic, R, Lazarević, Zorica Ž., Pavlović, Miodrag B., "Nicolson-Ross analysis of absorption coefficients of nickel and nickel-zinc ferrite powders prepared using a novel method" in Materials Science Forum, 453-454 (2004):405-410,
https://doi.org/10.4028/www.scientific.net/MSF.453-454.405 . .

TY  - JOUR
AU  - Antić, Bratislav
AU  - Kremenović, Aleksandar S.
AU  - Nikolić, Aleksandar S.
AU  - Stoiljković, Milovan
PY  - 2004
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/2798
AB  - The ultrafine ZnFe2O4, MnFe2O4, and cation deficit Zn-Mn ferrites were obtained by thermal decomposition of appropriate mixed complex compounds with acetylacetone (2,4-pentadione) ligands ([M(AA),]) at 500 degreesC. In ZnFe2O4 cation distribution is partially inverse with 14% of Zn2+ ions at octahedral 16d sites, while MnFe2O4 is a normal spinel. Cation distribution in nonstoichiometric (Zn,Mn,Fe)(3-delta)O-4 (delta = 0.18-0.30) is found to be (Zn(x)Mn(y)square(epsilon))(8a)[Fe(z)square(v)](16d), with a random distribution of vacancies. Nonstoichiometry in Zn-Mn ferrites is accompanied by a cation valence change, i.e., partial oxidation of Mn2+ to Mn4+. Microstructure size-strain analysis shows isotropic X-ray line broadening due to the crystallite size effect and anisotropic X-ray line broadening due to the crystallite strain effect. In binary ferrites anisotropic X-ray line broadening due to the strain effect is higher in ZnFe2O4 than in MnFe2O4, while in ternary cation-deficient Zn-Mn ferrites it decreases as the vacancy concentration delta increases.
T2  - Journal of Physical Chemistry. Part B: Condensed Matter, Materials, Surfaces, Interfaces and Biophysical
T1  - Cation distribution and size-strain microstructure analysis in ultrarine Zn-Mn ferrites obtained from acetylacetonato complexes
VL  - 108
IS  - 34
SP  - 12646
EP  - 12651
DO  - 10.1021/jp036214v
ER  - 

@article{
author = "Antić, Bratislav and Kremenović, Aleksandar S. and Nikolić, Aleksandar S. and Stoiljković, Milovan",
year = "2004",
abstract = "The ultrafine ZnFe2O4, MnFe2O4, and cation deficit Zn-Mn ferrites were obtained by thermal decomposition of appropriate mixed complex compounds with acetylacetone (2,4-pentadione) ligands ([M(AA),]) at 500 degreesC. In ZnFe2O4 cation distribution is partially inverse with 14% of Zn2+ ions at octahedral 16d sites, while MnFe2O4 is a normal spinel. Cation distribution in nonstoichiometric (Zn,Mn,Fe)(3-delta)O-4 (delta = 0.18-0.30) is found to be (Zn(x)Mn(y)square(epsilon))(8a)[Fe(z)square(v)](16d), with a random distribution of vacancies. Nonstoichiometry in Zn-Mn ferrites is accompanied by a cation valence change, i.e., partial oxidation of Mn2+ to Mn4+. Microstructure size-strain analysis shows isotropic X-ray line broadening due to the crystallite size effect and anisotropic X-ray line broadening due to the crystallite strain effect. In binary ferrites anisotropic X-ray line broadening due to the strain effect is higher in ZnFe2O4 than in MnFe2O4, while in ternary cation-deficient Zn-Mn ferrites it decreases as the vacancy concentration delta increases.",
journal = "Journal of Physical Chemistry. Part B: Condensed Matter, Materials, Surfaces, Interfaces and Biophysical",
title = "Cation distribution and size-strain microstructure analysis in ultrarine Zn-Mn ferrites obtained from acetylacetonato complexes",
volume = "108",
number = "34",
pages = "12646-12651",
doi = "10.1021/jp036214v"
}

Antić, B., Kremenović, A. S., Nikolić, A. S.,& Stoiljković, M.. (2004). Cation distribution and size-strain microstructure analysis in ultrarine Zn-Mn ferrites obtained from acetylacetonato complexes. in Journal of Physical Chemistry. Part B: Condensed Matter, Materials, Surfaces, Interfaces and Biophysical, 108(34), 12646-12651.
https://doi.org/10.1021/jp036214v

Antić B, Kremenović AS, Nikolić AS, Stoiljković M. Cation distribution and size-strain microstructure analysis in ultrarine Zn-Mn ferrites obtained from acetylacetonato complexes. in Journal of Physical Chemistry. Part B: Condensed Matter, Materials, Surfaces, Interfaces and Biophysical. 2004;108(34):12646-12651.
doi:10.1021/jp036214v .

Antić, Bratislav, Kremenović, Aleksandar S., Nikolić, Aleksandar S., Stoiljković, Milovan, "Cation distribution and size-strain microstructure analysis in ultrarine Zn-Mn ferrites obtained from acetylacetonato complexes" in Journal of Physical Chemistry. Part B: Condensed Matter, Materials, Surfaces, Interfaces and Biophysical, 108, no. 34 (2004):12646-12651,
https://doi.org/10.1021/jp036214v . .

TY  - JOUR
AU  - Antić, Bratislav
AU  - Rodić, Dubravko
AU  - Nikolić, Aleksandar S.
AU  - Kačarević-Popović, Zorica M.
AU  - Karanović, Ljiljana
PY  - 2002
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/2507
AB  - In this work we present results of synthesis and structural investigation of the spinels with general formula LixMg1-2xFe2+xO4, where 0.00less than or equal toxless than or equal to0.50. Ultrafine powder of MgFe2O4 (x=0.00) was prepared by thermal decomposition of a mixture of complex compounds [Mg(AA)(2)] and [Fe(AA)(3)] at 500degreesC (AA=acetylacetone). The solid solutions of LixMg1-2xFe2+xO4 (0.10less than or equal toxless than or equal to0.45) were synthesized by conventional ceramic method. The samples with xgreater than or equal to0.40 belong to ordered spinels with primitive cubic cell, space group P4(3)32 and the samples with xgreater than or equal to0.35 are spinels with face-centered cubic cell, space group Fd-3m. Crystal structures of samples with x=0.00, 0.40 and 0.45 were refined by the Rietveld method using DBWS-9411 software package. In ordered spinels (x=0.40, 0.45) Li+ ions occupy both 4b (preferentially) and 12d octahedral sites. At tetrahedral 8c positions Li+ ions were not found (within the experimental error). Mg2+ ions occupy octahedral 12d and tetrahedral 8c sites and Fe3+ ions occupy all three different cationic sites. Cation ordering in 1:3 type ordered spinel (the occupancy ratio of the Wyckoffs positions 4b and 12d) of Li+ and Fe3(+) at octahedral sites is not complete as in Li0.5Fe2.5O4, In MgFe2O4 spinel, cation distribution in the tetrahedral sites was determined and given by occupation numbers N: N(Mg-8a(2+))=0.183(7) and N(Fe-8a(3+))=0.817(7). (C) 2002 Elsevier Science BY All rights reserved.
T2  - Journal of Alloys and Compounds
T1  - The change of crystal symmetry and cation ordering in Li-Mg ferrites
VL  - 336
IS  - 1-2
SP  - 286
EP  - 291
DO  - 10.1016/S0925-8388(01)01885-0
ER  - 

@article{
author = "Antić, Bratislav and Rodić, Dubravko and Nikolić, Aleksandar S. and Kačarević-Popović, Zorica M. and Karanović, Ljiljana",
year = "2002",
abstract = "In this work we present results of synthesis and structural investigation of the spinels with general formula LixMg1-2xFe2+xO4, where 0.00less than or equal toxless than or equal to0.50. Ultrafine powder of MgFe2O4 (x=0.00) was prepared by thermal decomposition of a mixture of complex compounds [Mg(AA)(2)] and [Fe(AA)(3)] at 500degreesC (AA=acetylacetone). The solid solutions of LixMg1-2xFe2+xO4 (0.10less than or equal toxless than or equal to0.45) were synthesized by conventional ceramic method. The samples with xgreater than or equal to0.40 belong to ordered spinels with primitive cubic cell, space group P4(3)32 and the samples with xgreater than or equal to0.35 are spinels with face-centered cubic cell, space group Fd-3m. Crystal structures of samples with x=0.00, 0.40 and 0.45 were refined by the Rietveld method using DBWS-9411 software package. In ordered spinels (x=0.40, 0.45) Li+ ions occupy both 4b (preferentially) and 12d octahedral sites. At tetrahedral 8c positions Li+ ions were not found (within the experimental error). Mg2+ ions occupy octahedral 12d and tetrahedral 8c sites and Fe3+ ions occupy all three different cationic sites. Cation ordering in 1:3 type ordered spinel (the occupancy ratio of the Wyckoffs positions 4b and 12d) of Li+ and Fe3(+) at octahedral sites is not complete as in Li0.5Fe2.5O4, In MgFe2O4 spinel, cation distribution in the tetrahedral sites was determined and given by occupation numbers N: N(Mg-8a(2+))=0.183(7) and N(Fe-8a(3+))=0.817(7). (C) 2002 Elsevier Science BY All rights reserved.",
journal = "Journal of Alloys and Compounds",
title = "The change of crystal symmetry and cation ordering in Li-Mg ferrites",
volume = "336",
number = "1-2",
pages = "286-291",
doi = "10.1016/S0925-8388(01)01885-0"
}

Antić, B., Rodić, D., Nikolić, A. S., Kačarević-Popović, Z. M.,& Karanović, L.. (2002). The change of crystal symmetry and cation ordering in Li-Mg ferrites. in Journal of Alloys and Compounds, 336(1-2), 286-291.
https://doi.org/10.1016/S0925-8388(01)01885-0

Antić B, Rodić D, Nikolić AS, Kačarević-Popović ZM, Karanović L. The change of crystal symmetry and cation ordering in Li-Mg ferrites. in Journal of Alloys and Compounds. 2002;336(1-2):286-291.
doi:10.1016/S0925-8388(01)01885-0 .

Antić, Bratislav, Rodić, Dubravko, Nikolić, Aleksandar S., Kačarević-Popović, Zorica M., Karanović, Ljiljana, "The change of crystal symmetry and cation ordering in Li-Mg ferrites" in Journal of Alloys and Compounds, 336, no. 1-2 (2002):286-291,
https://doi.org/10.1016/S0925-8388(01)01885-0 . .