TY  - JOUR
AU  - Rakočević, Lazar
AU  - Štrbac, Svetlana
AU  - Potočnik, Jelena
AU  - Popović, Maja
AU  - Jugović, Dragana
AU  - Stojković-Simatović, Ivana
PY  - 2021
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/10203
AB  - Cathodic material for sodium-ion rechargeable batteries based on NaxMnO2 were synthesized by glycine nitrate method and subsequent annealing at high temperatures. Different crystal structures with different morphologies were obtained depending on the annealing temperature: hexagonal layeredα-Na0.7MnO2.05 nanoplates were obtained at 850 ◦C, while 3-D tunnel structured Na0⋅4MnO2 and Na0⋅44MnO2, both with rod-like morphology, were obtained at 800 ◦C and 900 ◦C, respectively. The investigations of the electrochemical behavior of obtained cathodic materials in aqueous NaNO3 solution have shown that Na0⋅44MnO2 obtained at 900 ◦C has shown the best battery performance. Its initial discharge capacities are 123.5 mA h/g, 113.2 mA h/g, and 102.0 mA h/g at the high current densities of 1000, 2000 and 5000 mA/g, respectively.
T2  - Ceramics International
T1  - The NaxMnO2 materials prepared by a glycine-nitrate method as advanced cathode materials for aqueous sodium-ion rechargeable batteries
VL  - 47
IS  - 4
SP  - 4595
EP  - 4603
DO  - 10.1016/j.ceramint.2020.10.025
UR  - https://hdl.handle.net/21.15107/rcub_dais_11229
ER  - 

@article{
author = "Rakočević, Lazar and Štrbac, Svetlana and Potočnik, Jelena and Popović, Maja and Jugović, Dragana and Stojković-Simatović, Ivana",
year = "2021",
abstract = "Cathodic material for sodium-ion rechargeable batteries based on NaxMnO2 were synthesized by glycine nitrate method and subsequent annealing at high temperatures. Different crystal structures with different morphologies were obtained depending on the annealing temperature: hexagonal layeredα-Na0.7MnO2.05 nanoplates were obtained at 850 ◦C, while 3-D tunnel structured Na0⋅4MnO2 and Na0⋅44MnO2, both with rod-like morphology, were obtained at 800 ◦C and 900 ◦C, respectively. The investigations of the electrochemical behavior of obtained cathodic materials in aqueous NaNO3 solution have shown that Na0⋅44MnO2 obtained at 900 ◦C has shown the best battery performance. Its initial discharge capacities are 123.5 mA h/g, 113.2 mA h/g, and 102.0 mA h/g at the high current densities of 1000, 2000 and 5000 mA/g, respectively.",
journal = "Ceramics International",
title = "The NaxMnO2 materials prepared by a glycine-nitrate method as advanced cathode materials for aqueous sodium-ion rechargeable batteries",
volume = "47",
number = "4",
pages = "4595-4603",
doi = "10.1016/j.ceramint.2020.10.025",
url = "https://hdl.handle.net/21.15107/rcub_dais_11229"
}

Rakočević, L., Štrbac, S., Potočnik, J., Popović, M., Jugović, D.,& Stojković-Simatović, I.. (2021). The NaxMnO2 materials prepared by a glycine-nitrate method as advanced cathode materials for aqueous sodium-ion rechargeable batteries. in Ceramics International, 47(4), 4595-4603.
https://doi.org/10.1016/j.ceramint.2020.10.025
https://hdl.handle.net/21.15107/rcub_dais_11229

Rakočević L, Štrbac S, Potočnik J, Popović M, Jugović D, Stojković-Simatović I. The NaxMnO2 materials prepared by a glycine-nitrate method as advanced cathode materials for aqueous sodium-ion rechargeable batteries. in Ceramics International. 2021;47(4):4595-4603.
doi:10.1016/j.ceramint.2020.10.025
https://hdl.handle.net/21.15107/rcub_dais_11229 .

Rakočević, Lazar, Štrbac, Svetlana, Potočnik, Jelena, Popović, Maja, Jugović, Dragana, Stojković-Simatović, Ivana, "The NaxMnO2 materials prepared by a glycine-nitrate method as advanced cathode materials for aqueous sodium-ion rechargeable batteries" in Ceramics International, 47, no. 4 (2021):4595-4603,
https://doi.org/10.1016/j.ceramint.2020.10.025 .,
https://hdl.handle.net/21.15107/rcub_dais_11229 .

TY  - JOUR
AU  - Rakočević, Lazar
AU  - Štrbac, Svetlana
AU  - Potočnik, Jelena
AU  - Popović, Maja
AU  - Jugović, Dragana
AU  - Stojković-Simatović, Ivana
PY  - 2021
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/10202
AB  - Cathodic material for sodium-ion rechargeable batteries based on NaxMnO2 were synthesized by glycine nitrate method and subsequent annealing at high temperatures. Different crystal structures with different morphologies were obtained depending on the annealing temperature: hexagonal layeredα-Na0.7MnO2.05 nanoplates were obtained at 850 ◦C, while 3-D tunnel structured Na0⋅4MnO2 and Na0⋅44MnO2, both with rod-like morphology, were obtained at 800 ◦C and 900 ◦C, respectively. The investigations of the electrochemical behavior of obtained cathodic materials in aqueous NaNO3 solution have shown that Na0⋅44MnO2 obtained at 900 ◦C has shown the best battery performance. Its initial discharge capacities are 123.5 mA h/g, 113.2 mA h/g, and 102.0 mA h/g at the high current densities of 1000, 2000 and 5000 mA/g, respectively.
T2  - Ceramics International
T1  - The NaxMnO2 materials prepared by a glycine-nitrate method as advanced cathode materials for aqueous sodium-ion rechargeable batteries
VL  - 47
IS  - 4
SP  - 4595
EP  - 4603
DO  - 10.1016/j.ceramint.2020.10.025
UR  - https://hdl.handle.net/21.15107/rcub_dais_11229
ER  - 

@article{
author = "Rakočević, Lazar and Štrbac, Svetlana and Potočnik, Jelena and Popović, Maja and Jugović, Dragana and Stojković-Simatović, Ivana",
year = "2021",
abstract = "Cathodic material for sodium-ion rechargeable batteries based on NaxMnO2 were synthesized by glycine nitrate method and subsequent annealing at high temperatures. Different crystal structures with different morphologies were obtained depending on the annealing temperature: hexagonal layeredα-Na0.7MnO2.05 nanoplates were obtained at 850 ◦C, while 3-D tunnel structured Na0⋅4MnO2 and Na0⋅44MnO2, both with rod-like morphology, were obtained at 800 ◦C and 900 ◦C, respectively. The investigations of the electrochemical behavior of obtained cathodic materials in aqueous NaNO3 solution have shown that Na0⋅44MnO2 obtained at 900 ◦C has shown the best battery performance. Its initial discharge capacities are 123.5 mA h/g, 113.2 mA h/g, and 102.0 mA h/g at the high current densities of 1000, 2000 and 5000 mA/g, respectively.",
journal = "Ceramics International",
title = "The NaxMnO2 materials prepared by a glycine-nitrate method as advanced cathode materials for aqueous sodium-ion rechargeable batteries",
volume = "47",
number = "4",
pages = "4595-4603",
doi = "10.1016/j.ceramint.2020.10.025",
url = "https://hdl.handle.net/21.15107/rcub_dais_11229"
}

Rakočević, L., Štrbac, S., Potočnik, J., Popović, M., Jugović, D.,& Stojković-Simatović, I.. (2021). The NaxMnO2 materials prepared by a glycine-nitrate method as advanced cathode materials for aqueous sodium-ion rechargeable batteries. in Ceramics International, 47(4), 4595-4603.
https://doi.org/10.1016/j.ceramint.2020.10.025
https://hdl.handle.net/21.15107/rcub_dais_11229

Rakočević L, Štrbac S, Potočnik J, Popović M, Jugović D, Stojković-Simatović I. The NaxMnO2 materials prepared by a glycine-nitrate method as advanced cathode materials for aqueous sodium-ion rechargeable batteries. in Ceramics International. 2021;47(4):4595-4603.
doi:10.1016/j.ceramint.2020.10.025
https://hdl.handle.net/21.15107/rcub_dais_11229 .

Rakočević, Lazar, Štrbac, Svetlana, Potočnik, Jelena, Popović, Maja, Jugović, Dragana, Stojković-Simatović, Ivana, "The NaxMnO2 materials prepared by a glycine-nitrate method as advanced cathode materials for aqueous sodium-ion rechargeable batteries" in Ceramics International, 47, no. 4 (2021):4595-4603,
https://doi.org/10.1016/j.ceramint.2020.10.025 .,
https://hdl.handle.net/21.15107/rcub_dais_11229 .

TY  - JOUR
AU  - Rakočević, Lazar
AU  - Srejić, Irina
AU  - Maksić, Aleksandar
AU  - Golubović, Jelena
AU  - Štrbac, Svetlana
PY  - 2021
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/9626
AB  - Hydrogen evolution reaction (HER) was investigated on reduced graphene oxide (rGO)-supported Au and PdAu nanoparticles in acid solution. The graphene spread over glassy carbon (rGO/GC) was used as a support for the spontaneous deposition of Au and Pd. The resulting Au/rGO and PdAu/rGO electrodes were characterized using atomic force microscopy (AFM) and X-ray photoelectron spectroscopy (XPS) techniques. Phase AFM images have shown that the edges of the rGO sheets were active sites for the deposition of both Au and Pd. XPS analysis revealed that the atomic percentages of both Au and PdAu nanoparticles were slightly higher than 1%. The activity of the PdAu/rGO electrode for the HER was remarkably high, with the overpotential close to zero. HER activity was stable over a 3 h testing time, with a low Tafel slope of approx. −46 mV/dec achieved after prolonged hydrogen evolution at a constant potential.
T2  - Catalysts
T1  - Hydrogen Evolution on Reduced Graphene Oxide-Supported PdAu Nanoparticles
VL  - 11
IS  - 4
SP  - 481
DO  - 10.3390/catal11040481
ER  - 

@article{
author = "Rakočević, Lazar and Srejić, Irina and Maksić, Aleksandar and Golubović, Jelena and Štrbac, Svetlana",
year = "2021",
abstract = "Hydrogen evolution reaction (HER) was investigated on reduced graphene oxide (rGO)-supported Au and PdAu nanoparticles in acid solution. The graphene spread over glassy carbon (rGO/GC) was used as a support for the spontaneous deposition of Au and Pd. The resulting Au/rGO and PdAu/rGO electrodes were characterized using atomic force microscopy (AFM) and X-ray photoelectron spectroscopy (XPS) techniques. Phase AFM images have shown that the edges of the rGO sheets were active sites for the deposition of both Au and Pd. XPS analysis revealed that the atomic percentages of both Au and PdAu nanoparticles were slightly higher than 1%. The activity of the PdAu/rGO electrode for the HER was remarkably high, with the overpotential close to zero. HER activity was stable over a 3 h testing time, with a low Tafel slope of approx. −46 mV/dec achieved after prolonged hydrogen evolution at a constant potential.",
journal = "Catalysts",
title = "Hydrogen Evolution on Reduced Graphene Oxide-Supported PdAu Nanoparticles",
volume = "11",
number = "4",
pages = "481",
doi = "10.3390/catal11040481"
}

Rakočević, L., Srejić, I., Maksić, A., Golubović, J.,& Štrbac, S.. (2021). Hydrogen Evolution on Reduced Graphene Oxide-Supported PdAu Nanoparticles. in Catalysts, 11(4), 481.
https://doi.org/10.3390/catal11040481

Rakočević L, Srejić I, Maksić A, Golubović J, Štrbac S. Hydrogen Evolution on Reduced Graphene Oxide-Supported PdAu Nanoparticles. in Catalysts. 2021;11(4):481.
doi:10.3390/catal11040481 .

Rakočević, Lazar, Srejić, Irina, Maksić, Aleksandar, Golubović, Jelena, Štrbac, Svetlana, "Hydrogen Evolution on Reduced Graphene Oxide-Supported PdAu Nanoparticles" in Catalysts, 11, no. 4 (2021):481,
https://doi.org/10.3390/catal11040481 . .

TY  - JOUR
AU  - Rakočević, Lazar
AU  - Štrbac, Svetlana
AU  - Srejić, Irina
PY  - 2021
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/9544
AB  - HER was examined on various glassy carbon-supported Au and PdAu electrodes in acid solution. The Au/GC electrodes were obtained after Au was electrodeposited on a GC substrate by holding the potential for various times in 0.5 M H2SO4 solution containing AuCl4− ions. PdAu/GC electrodes were obtained after Pd has been added by a spontaneous deposition on previously prepared Au/GC electrodes. Surface morphology and chemical analysis of Au/GC and PdAu/GC electrodes were performed by atomic force microscopy and X-ray photoemission spectroscopy. Electrochemical characterization was performed by cyclic voltammetry in 0.5 M H2SO4 solution, while the linear sweep voltammetry was used to gain insight into the electrocatalytic activity of these electrodes for HER. 30minPd/10minAu/GC electrode consisting of 48% Pd and 65% Au, with the total coverage of the GC substrate with PdAu islands of 70%, showed the best catalytic activity for HER. A remarkable high activity and stability of this electrode makes it a promising catalyst for HER in acid solution. © 2021 Hydrogen Energy Publications LLC
T2  - International Journal of Hydrogen Energy
T1  - Hydrogen evolution on Au/GC and PdAu/GC nanostructures in acid solution: AFM, XPS, and electrochemical study
VL  - 46
IS  - 13
SP  - 9052
EP  - 9063
DO  - 10.1016/j.ijhydene.2021.01.001
ER  - 

@article{
author = "Rakočević, Lazar and Štrbac, Svetlana and Srejić, Irina",
year = "2021",
abstract = "HER was examined on various glassy carbon-supported Au and PdAu electrodes in acid solution. The Au/GC electrodes were obtained after Au was electrodeposited on a GC substrate by holding the potential for various times in 0.5 M H2SO4 solution containing AuCl4− ions. PdAu/GC electrodes were obtained after Pd has been added by a spontaneous deposition on previously prepared Au/GC electrodes. Surface morphology and chemical analysis of Au/GC and PdAu/GC electrodes were performed by atomic force microscopy and X-ray photoemission spectroscopy. Electrochemical characterization was performed by cyclic voltammetry in 0.5 M H2SO4 solution, while the linear sweep voltammetry was used to gain insight into the electrocatalytic activity of these electrodes for HER. 30minPd/10minAu/GC electrode consisting of 48% Pd and 65% Au, with the total coverage of the GC substrate with PdAu islands of 70%, showed the best catalytic activity for HER. A remarkable high activity and stability of this electrode makes it a promising catalyst for HER in acid solution. © 2021 Hydrogen Energy Publications LLC",
journal = "International Journal of Hydrogen Energy",
title = "Hydrogen evolution on Au/GC and PdAu/GC nanostructures in acid solution: AFM, XPS, and electrochemical study",
volume = "46",
number = "13",
pages = "9052-9063",
doi = "10.1016/j.ijhydene.2021.01.001"
}

Rakočević, L., Štrbac, S.,& Srejić, I.. (2021). Hydrogen evolution on Au/GC and PdAu/GC nanostructures in acid solution: AFM, XPS, and electrochemical study. in International Journal of Hydrogen Energy, 46(13), 9052-9063.
https://doi.org/10.1016/j.ijhydene.2021.01.001

Rakočević L, Štrbac S, Srejić I. Hydrogen evolution on Au/GC and PdAu/GC nanostructures in acid solution: AFM, XPS, and electrochemical study. in International Journal of Hydrogen Energy. 2021;46(13):9052-9063.
doi:10.1016/j.ijhydene.2021.01.001 .

Rakočević, Lazar, Štrbac, Svetlana, Srejić, Irina, "Hydrogen evolution on Au/GC and PdAu/GC nanostructures in acid solution: AFM, XPS, and electrochemical study" in International Journal of Hydrogen Energy, 46, no. 13 (2021):9052-9063,
https://doi.org/10.1016/j.ijhydene.2021.01.001 . .

TY  - JOUR
AU  - Štrbac, Svetlana
AU  - Smiljanić, Milutin Lj.
AU  - Wakelin, Thomas
AU  - Potočnik, Jelena
AU  - Rakočević, Zlatko Lj.
PY  - 2019
UR  - https://linkinghub.elsevier.com/retrieve/pii/S001346861930516X
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8126
AB  - Hydrogen evolution reaction (HER) was studied in alkaline solution on Pt(poly) electrode modified by spontaneously deposited Ir nanoislands. Comprehensive insight into the characteristics of the bimetallic Ir/Pt(poly) catalysts was obtained by a combination of Atomic Force Microscopy (AFM), Field Emission Scanning Electron Microscopy (FESEM), X-ray Photoelectron Spectroscopy (XPS) and classical electrochemical techniques. HER investigations have shown that the presence of spontaneously deposited Ir enhances the activity of bare Pt(poly) in alkaline solution. This was attributed to the heterogeneity of the active surface sites and to the electronic interaction between two metals in close contact which together facilitated the adsorption of the H intermediate species. © 2019 Elsevier Ltd
T2  - Electrochimica Acta
T1  - Hydrogen evolution reaction on bimetallic Ir/Pt(poly) electrodes in alkaline solution
VL  - 306
SP  - 18
EP  - 27
DO  - 10.1016/j.electacta.2019.03.100
ER  - 

@article{
author = "Štrbac, Svetlana and Smiljanić, Milutin Lj. and Wakelin, Thomas and Potočnik, Jelena and Rakočević, Zlatko Lj.",
year = "2019",
abstract = "Hydrogen evolution reaction (HER) was studied in alkaline solution on Pt(poly) electrode modified by spontaneously deposited Ir nanoislands. Comprehensive insight into the characteristics of the bimetallic Ir/Pt(poly) catalysts was obtained by a combination of Atomic Force Microscopy (AFM), Field Emission Scanning Electron Microscopy (FESEM), X-ray Photoelectron Spectroscopy (XPS) and classical electrochemical techniques. HER investigations have shown that the presence of spontaneously deposited Ir enhances the activity of bare Pt(poly) in alkaline solution. This was attributed to the heterogeneity of the active surface sites and to the electronic interaction between two metals in close contact which together facilitated the adsorption of the H intermediate species. © 2019 Elsevier Ltd",
journal = "Electrochimica Acta",
title = "Hydrogen evolution reaction on bimetallic Ir/Pt(poly) electrodes in alkaline solution",
volume = "306",
pages = "18-27",
doi = "10.1016/j.electacta.2019.03.100"
}

Štrbac, S., Smiljanić, M. Lj., Wakelin, T., Potočnik, J.,& Rakočević, Z. Lj.. (2019). Hydrogen evolution reaction on bimetallic Ir/Pt(poly) electrodes in alkaline solution. in Electrochimica Acta, 306, 18-27.
https://doi.org/10.1016/j.electacta.2019.03.100

Štrbac S, Smiljanić ML, Wakelin T, Potočnik J, Rakočević ZL. Hydrogen evolution reaction on bimetallic Ir/Pt(poly) electrodes in alkaline solution. in Electrochimica Acta. 2019;306:18-27.
doi:10.1016/j.electacta.2019.03.100 .

Štrbac, Svetlana, Smiljanić, Milutin Lj., Wakelin, Thomas, Potočnik, Jelena, Rakočević, Zlatko Lj., "Hydrogen evolution reaction on bimetallic Ir/Pt(poly) electrodes in alkaline solution" in Electrochimica Acta, 306 (2019):18-27,
https://doi.org/10.1016/j.electacta.2019.03.100 . .

TY  - JOUR
AU  - Smiljanić, Milutin Lj.
AU  - Rakočević, Zlatko Lj.
AU  - Potočnik, Jelena
AU  - Štrbac, Svetlana
PY  - 2019
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8504
AB  - Hydrogen evolution reaction (HER) was studied on polycrystalline Pd, Pd(poly), decorated by spontaneously deposited Ru nanoislands below full coverage. Surface features of as-prepared bimetallic Ru/Pd(poly) electrodes were explored by Field Emission Scanning Electron Microscopy with Energy Dispersive X-ray Spectrometer. Electrochemical properties and hydrogen evolution activities of obtained electrodes were investigated in an alkaline electrolyte by Cyclic and Linear Sweep Voltammetry, respectively. It was found that the activities of bimetallic Ru/Pd(poly) electrodes for HER significantly exceeded the activity of bare Pd(poly) and approached the activity of Pt, which is the most active material for this reaction. This enhancement was explained by the favorable influence of the electronic interaction between Pd substrate and Ru nanoislands on the adsorption of the reactive H species. © 2019 The Authors.
T2  - International Journal of Electrochemical Science
T1  - Enhanced Activity of Polycrystalline Palladium Decorated by Ru Nanoislands for Hydrogen Evolution in Alkaline Medium
VL  - 14
IS  - 7
SP  - 5938
EP  - 5949
DO  - 10.20964/2019.07.34
ER  - 

@article{
author = "Smiljanić, Milutin Lj. and Rakočević, Zlatko Lj. and Potočnik, Jelena and Štrbac, Svetlana",
year = "2019",
abstract = "Hydrogen evolution reaction (HER) was studied on polycrystalline Pd, Pd(poly), decorated by spontaneously deposited Ru nanoislands below full coverage. Surface features of as-prepared bimetallic Ru/Pd(poly) electrodes were explored by Field Emission Scanning Electron Microscopy with Energy Dispersive X-ray Spectrometer. Electrochemical properties and hydrogen evolution activities of obtained electrodes were investigated in an alkaline electrolyte by Cyclic and Linear Sweep Voltammetry, respectively. It was found that the activities of bimetallic Ru/Pd(poly) electrodes for HER significantly exceeded the activity of bare Pd(poly) and approached the activity of Pt, which is the most active material for this reaction. This enhancement was explained by the favorable influence of the electronic interaction between Pd substrate and Ru nanoislands on the adsorption of the reactive H species. © 2019 The Authors.",
journal = "International Journal of Electrochemical Science",
title = "Enhanced Activity of Polycrystalline Palladium Decorated by Ru Nanoislands for Hydrogen Evolution in Alkaline Medium",
volume = "14",
number = "7",
pages = "5938-5949",
doi = "10.20964/2019.07.34"
}

Smiljanić, M. Lj., Rakočević, Z. Lj., Potočnik, J.,& Štrbac, S.. (2019). Enhanced Activity of Polycrystalline Palladium Decorated by Ru Nanoislands for Hydrogen Evolution in Alkaline Medium. in International Journal of Electrochemical Science, 14(7), 5938-5949.
https://doi.org/10.20964/2019.07.34

Smiljanić ML, Rakočević ZL, Potočnik J, Štrbac S. Enhanced Activity of Polycrystalline Palladium Decorated by Ru Nanoislands for Hydrogen Evolution in Alkaline Medium. in International Journal of Electrochemical Science. 2019;14(7):5938-5949.
doi:10.20964/2019.07.34 .

Smiljanić, Milutin Lj., Rakočević, Zlatko Lj., Potočnik, Jelena, Štrbac, Svetlana, "Enhanced Activity of Polycrystalline Palladium Decorated by Ru Nanoislands for Hydrogen Evolution in Alkaline Medium" in International Journal of Electrochemical Science, 14, no. 7 (2019):5938-5949,
https://doi.org/10.20964/2019.07.34 . .

TY  - JOUR
AU  - Štrbac, Svetlana
AU  - Maksić, Aleksandar
AU  - Rakočević, Zlatko Lj.
PY  - 2018
UR  - https://linkinghub.elsevier.com/retrieve/pii/S1572665718304259
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7946
AB  - Polycrystalline Pd electrode, Pd(poly), is modified by Ru nanoislands using spontaneous deposition method. Coverage of Pd(poly) electrode with the deposited Ru are approx. 20, 30 and 50% as estimated from phase atomic force microscopy images. The oxidation state of Pd substrate and the deposited Ru is determined by X-ray spectroscopy (XPS). Electrocatalytic activity of obtained Ru/Pd(poly) bimetallic electrodes is tested towards methanol oxidation in alkaline medium. Cyclic voltammetry and chronoamperometry experiments show the enhanced activity of Ru/Pd(poly) electrodes towards methanol electrooxidation with respect to bare Pd(poly). This is explained by the presence of Ru islands, which provided RuOH and Pd-RuOH sites, necessary for the oxidation of CO as the main intermediate during the oxidation of methanol at lower potentials. 30% Ru/Pd(poly) is the most active of all examined electrodes.
T2  - Journal of Electroanalytical Chemistry
T1  - Methanol oxidation on Ru/Pd(poly) in alkaline solution
VL  - 823
SP  - 161
EP  - 170
DO  - 10.1016/j.jelechem.2018.06.011
ER  - 

@article{
author = "Štrbac, Svetlana and Maksić, Aleksandar and Rakočević, Zlatko Lj.",
year = "2018",
abstract = "Polycrystalline Pd electrode, Pd(poly), is modified by Ru nanoislands using spontaneous deposition method. Coverage of Pd(poly) electrode with the deposited Ru are approx. 20, 30 and 50% as estimated from phase atomic force microscopy images. The oxidation state of Pd substrate and the deposited Ru is determined by X-ray spectroscopy (XPS). Electrocatalytic activity of obtained Ru/Pd(poly) bimetallic electrodes is tested towards methanol oxidation in alkaline medium. Cyclic voltammetry and chronoamperometry experiments show the enhanced activity of Ru/Pd(poly) electrodes towards methanol electrooxidation with respect to bare Pd(poly). This is explained by the presence of Ru islands, which provided RuOH and Pd-RuOH sites, necessary for the oxidation of CO as the main intermediate during the oxidation of methanol at lower potentials. 30% Ru/Pd(poly) is the most active of all examined electrodes.",
journal = "Journal of Electroanalytical Chemistry",
title = "Methanol oxidation on Ru/Pd(poly) in alkaline solution",
volume = "823",
pages = "161-170",
doi = "10.1016/j.jelechem.2018.06.011"
}

Štrbac, S., Maksić, A.,& Rakočević, Z. Lj.. (2018). Methanol oxidation on Ru/Pd(poly) in alkaline solution. in Journal of Electroanalytical Chemistry, 823, 161-170.
https://doi.org/10.1016/j.jelechem.2018.06.011

Štrbac S, Maksić A, Rakočević ZL. Methanol oxidation on Ru/Pd(poly) in alkaline solution. in Journal of Electroanalytical Chemistry. 2018;823:161-170.
doi:10.1016/j.jelechem.2018.06.011 .

Štrbac, Svetlana, Maksić, Aleksandar, Rakočević, Zlatko Lj., "Methanol oxidation on Ru/Pd(poly) in alkaline solution" in Journal of Electroanalytical Chemistry, 823 (2018):161-170,
https://doi.org/10.1016/j.jelechem.2018.06.011 . .

TY  - JOUR
AU  - Štrbac, Svetlana
AU  - Srejić, Irina
AU  - Rakočević, Zlatko Lj.
PY  - 2018
UR  - http://jes.ecsdl.org/lookup/doi/10.1149/2.0441815jes
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8065
AB  - Iridium nanoislands are spontaneously deposited on Au(111) from (1 mMIrCl(3) center dot xH(2)O + 0.5 MH2SO4) depositing solution. Atomic Force Microscopy images of the obtained Ir/Au(111) bimetallic surfaces show that gold surface is fully covered with nanosized Ir islands after only 3 min of deposition. X-Ray Photoelectron Spectroscopy analysis shows that the deposit consists of a mixture of adsorbed hydrated IrCl3 and to a lesser extent of Ir(OH)(3). Cyclic Voltammetry characterization in 0.5 M H2SO4 solution does not show clear Hupd region prior to hydrogen evolution reaction (HER). Linear Sweep Voltammetry measurements show pronounced catalysis of HER on Ir modified Au(111) surface compared to bare Au(111). With prolonged Ir deposition, the observed limited increasing activity for HER of Ir/Au(111) surfaces is in accordance with the limited Ir/Au(111) surface morphology changes. (c) The Author(s) 2018. Published by ECS.
T2  - Journal of The Electrochemical Society
T1  - Electrocatalysis of Hydrogen Evolution Reaction on Au(111) by Spontaneously Deposited Iridium in Acid Solution
VL  - 165
IS  - 15
SP  - J3335
EP  - J3341
DO  - 10.1149/2.0441815jes
ER  - 

@article{
author = "Štrbac, Svetlana and Srejić, Irina and Rakočević, Zlatko Lj.",
year = "2018",
abstract = "Iridium nanoislands are spontaneously deposited on Au(111) from (1 mMIrCl(3) center dot xH(2)O + 0.5 MH2SO4) depositing solution. Atomic Force Microscopy images of the obtained Ir/Au(111) bimetallic surfaces show that gold surface is fully covered with nanosized Ir islands after only 3 min of deposition. X-Ray Photoelectron Spectroscopy analysis shows that the deposit consists of a mixture of adsorbed hydrated IrCl3 and to a lesser extent of Ir(OH)(3). Cyclic Voltammetry characterization in 0.5 M H2SO4 solution does not show clear Hupd region prior to hydrogen evolution reaction (HER). Linear Sweep Voltammetry measurements show pronounced catalysis of HER on Ir modified Au(111) surface compared to bare Au(111). With prolonged Ir deposition, the observed limited increasing activity for HER of Ir/Au(111) surfaces is in accordance with the limited Ir/Au(111) surface morphology changes. (c) The Author(s) 2018. Published by ECS.",
journal = "Journal of The Electrochemical Society",
title = "Electrocatalysis of Hydrogen Evolution Reaction on Au(111) by Spontaneously Deposited Iridium in Acid Solution",
volume = "165",
number = "15",
pages = "J3335-J3341",
doi = "10.1149/2.0441815jes"
}

Štrbac, S., Srejić, I.,& Rakočević, Z. Lj.. (2018). Electrocatalysis of Hydrogen Evolution Reaction on Au(111) by Spontaneously Deposited Iridium in Acid Solution. in Journal of The Electrochemical Society, 165(15), J3335-J3341.
https://doi.org/10.1149/2.0441815jes

Štrbac S, Srejić I, Rakočević ZL. Electrocatalysis of Hydrogen Evolution Reaction on Au(111) by Spontaneously Deposited Iridium in Acid Solution. in Journal of The Electrochemical Society. 2018;165(15):J3335-J3341.
doi:10.1149/2.0441815jes .

Štrbac, Svetlana, Srejić, Irina, Rakočević, Zlatko Lj., "Electrocatalysis of Hydrogen Evolution Reaction on Au(111) by Spontaneously Deposited Iridium in Acid Solution" in Journal of The Electrochemical Society, 165, no. 15 (2018):J3335-J3341,
https://doi.org/10.1149/2.0441815jes . .

TY  - JOUR
AU  - Smiljanić, Milutin Lj.
AU  - Srejić, Irina
AU  - Potočnik, Jelena
AU  - Mitrić, Miodrag
AU  - Rakočević, Zlatko Lj.
AU  - Štrbac, Svetlana
PY  - 2018
UR  - https://linkinghub.elsevier.com/retrieve/pii/S0360319918326909
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7893
AB  - Hydrogen evolution reaction (HER) was explored on tri-metallic Rh@Pd/Au(poly) and bimetallic Pd/Au(poly) and Rh/Au(poly) electrodes in alkaline solution. Electrodes were prepared by the spontaneous deposition of either Pd or Rh and by co-deposition of both Rh and Pd on polycrystalline gold electrode. Characterization of modified electrodes was performed by cyclic voltammetry in alkaline solution, while additional information about phase analysis, chemical composition and surface morphology of tri-metallic Rh@Pd/Au(poly) electrode were acquired using X-ray diffraction, X-ray photoelectron spectroscopy, field emission scanning electron microscopy and atomic force microscopy. Investigations of HER catalysis have shown that the activity of tri-metallic Rh@Pd/Au(poly) electrode exceeds the activities of both Pd/Au(poly) and Rh/Au(poly) electrodes, meaning that the synergism between co-deposited Pd and Rh islands is achieved. Moreover, Rh@Pd/Au(poly) electrode showed significant approach to the activities of bulk Pd and Rh electrodes for HER, especially when taking into account low activity of bare Au substrate. Synergistic effect of co-deposited Pd and Rh islands is a consequence of the strong electronic interaction between three metals in a close contact, which promotes the activity for HER by lowering the adsorption energy of Hads intermediate. © 2018 Hydrogen Energy Publications LLC
T2  - International Journal of Hydrogen Energy
T1  - Synergistic electrocatalytic effect of Pd and Rh nanoislands co-deposited on Au(poly) on HER in alkaline solution
VL  - 43
IS  - 42
SP  - 19420
EP  - 19431
DO  - 10.1016/j.ijhydene.2018.08.117
ER  - 

@article{
author = "Smiljanić, Milutin Lj. and Srejić, Irina and Potočnik, Jelena and Mitrić, Miodrag and Rakočević, Zlatko Lj. and Štrbac, Svetlana",
year = "2018",
abstract = "Hydrogen evolution reaction (HER) was explored on tri-metallic Rh@Pd/Au(poly) and bimetallic Pd/Au(poly) and Rh/Au(poly) electrodes in alkaline solution. Electrodes were prepared by the spontaneous deposition of either Pd or Rh and by co-deposition of both Rh and Pd on polycrystalline gold electrode. Characterization of modified electrodes was performed by cyclic voltammetry in alkaline solution, while additional information about phase analysis, chemical composition and surface morphology of tri-metallic Rh@Pd/Au(poly) electrode were acquired using X-ray diffraction, X-ray photoelectron spectroscopy, field emission scanning electron microscopy and atomic force microscopy. Investigations of HER catalysis have shown that the activity of tri-metallic Rh@Pd/Au(poly) electrode exceeds the activities of both Pd/Au(poly) and Rh/Au(poly) electrodes, meaning that the synergism between co-deposited Pd and Rh islands is achieved. Moreover, Rh@Pd/Au(poly) electrode showed significant approach to the activities of bulk Pd and Rh electrodes for HER, especially when taking into account low activity of bare Au substrate. Synergistic effect of co-deposited Pd and Rh islands is a consequence of the strong electronic interaction between three metals in a close contact, which promotes the activity for HER by lowering the adsorption energy of Hads intermediate. © 2018 Hydrogen Energy Publications LLC",
journal = "International Journal of Hydrogen Energy",
title = "Synergistic electrocatalytic effect of Pd and Rh nanoislands co-deposited on Au(poly) on HER in alkaline solution",
volume = "43",
number = "42",
pages = "19420-19431",
doi = "10.1016/j.ijhydene.2018.08.117"
}

Smiljanić, M. Lj., Srejić, I., Potočnik, J., Mitrić, M., Rakočević, Z. Lj.,& Štrbac, S.. (2018). Synergistic electrocatalytic effect of Pd and Rh nanoislands co-deposited on Au(poly) on HER in alkaline solution. in International Journal of Hydrogen Energy, 43(42), 19420-19431.
https://doi.org/10.1016/j.ijhydene.2018.08.117

Smiljanić ML, Srejić I, Potočnik J, Mitrić M, Rakočević ZL, Štrbac S. Synergistic electrocatalytic effect of Pd and Rh nanoislands co-deposited on Au(poly) on HER in alkaline solution. in International Journal of Hydrogen Energy. 2018;43(42):19420-19431.
doi:10.1016/j.ijhydene.2018.08.117 .

Smiljanić, Milutin Lj., Srejić, Irina, Potočnik, Jelena, Mitrić, Miodrag, Rakočević, Zlatko Lj., Štrbac, Svetlana, "Synergistic electrocatalytic effect of Pd and Rh nanoislands co-deposited on Au(poly) on HER in alkaline solution" in International Journal of Hydrogen Energy, 43, no. 42 (2018):19420-19431,
https://doi.org/10.1016/j.ijhydene.2018.08.117 . .

TY  - JOUR
AU  - Smiljanić, Milutin Lj.
AU  - Rakočević, Zlatko Lj.
AU  - Štrbac, Svetlana
PY  - 2018
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7658
AB  - Hydrogen evolution reaction (HER) was investigated in alkaline solution on tri-metallic Rh@Pd/Pt(poly) electrode, prepared by spontaneous deposition of Rh on top of Pd/Pt(poly) electrode with intermediate Pd coverage of 35%. Characterization of tri-metallic catalyst was performed by electrochemical methods of cyclic voltammetry and CO stripping voltammetry, while its activity for HER was tested by linear sweep voltammetry in 0.1 M NaOH. Rh@Pd/Pt(poly) catalyst has shown superior catalytic activity for HER with respect to initial Pt(poly) and both corresponding bimetallic Pd/Pt(poly) and Rh/Pt(poly) electrodes. This was explained by a strong synergistic electronic interaction between three metals in close contact induced at a number of different active sites across the surface of tri-metallic catalyst, which results with lowering of the binding energy for the adsorption of H intermediate species. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
T2  - International Journal of Hydrogen Energy
T1  - Electrocatalysis of hydrogen evolution reaction on tri-metallic Rh@Pd/Pt(poly) electrode
VL  - 43
IS  - 5
SP  - 2763
EP  - 2771
DO  - 10.1016/j.ijhydene.2017.12.112
ER  - 

@article{
author = "Smiljanić, Milutin Lj. and Rakočević, Zlatko Lj. and Štrbac, Svetlana",
year = "2018",
abstract = "Hydrogen evolution reaction (HER) was investigated in alkaline solution on tri-metallic Rh@Pd/Pt(poly) electrode, prepared by spontaneous deposition of Rh on top of Pd/Pt(poly) electrode with intermediate Pd coverage of 35%. Characterization of tri-metallic catalyst was performed by electrochemical methods of cyclic voltammetry and CO stripping voltammetry, while its activity for HER was tested by linear sweep voltammetry in 0.1 M NaOH. Rh@Pd/Pt(poly) catalyst has shown superior catalytic activity for HER with respect to initial Pt(poly) and both corresponding bimetallic Pd/Pt(poly) and Rh/Pt(poly) electrodes. This was explained by a strong synergistic electronic interaction between three metals in close contact induced at a number of different active sites across the surface of tri-metallic catalyst, which results with lowering of the binding energy for the adsorption of H intermediate species. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.",
journal = "International Journal of Hydrogen Energy",
title = "Electrocatalysis of hydrogen evolution reaction on tri-metallic Rh@Pd/Pt(poly) electrode",
volume = "43",
number = "5",
pages = "2763-2771",
doi = "10.1016/j.ijhydene.2017.12.112"
}

Smiljanić, M. Lj., Rakočević, Z. Lj.,& Štrbac, S.. (2018). Electrocatalysis of hydrogen evolution reaction on tri-metallic Rh@Pd/Pt(poly) electrode. in International Journal of Hydrogen Energy, 43(5), 2763-2771.
https://doi.org/10.1016/j.ijhydene.2017.12.112

Smiljanić ML, Rakočević ZL, Štrbac S. Electrocatalysis of hydrogen evolution reaction on tri-metallic Rh@Pd/Pt(poly) electrode. in International Journal of Hydrogen Energy. 2018;43(5):2763-2771.
doi:10.1016/j.ijhydene.2017.12.112 .

Smiljanić, Milutin Lj., Rakočević, Zlatko Lj., Štrbac, Svetlana, "Electrocatalysis of hydrogen evolution reaction on tri-metallic Rh@Pd/Pt(poly) electrode" in International Journal of Hydrogen Energy, 43, no. 5 (2018):2763-2771,
https://doi.org/10.1016/j.ijhydene.2017.12.112 . .

TY  - JOUR
AU  - Potočnik, Jelena
AU  - Popović, Maja
AU  - Rakočević, Zlatko Lj.
AU  - Štrbac, Svetlana
PY  - 2017
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1636
AB  - Nanostructured nickel thin films were deposited on glass using glancing angle deposition (GLAD) technique. Cross-sectional field emission scanning electron microscopy images have shown that obtained Ni thin films consist of vertical, tilted or zigzag nano-scaled columns, while X-ray diffraction have shown that (111) orientation prevailed. X-ray photoelectron spectroscopy revealed that apart from metallic nickel, NiO and Ni(OH)(2) were also present in lower amount. Cyclic voltammetry in alkaline solution has shown that hydrogen evolution reaction (HER) was significantly catalyzed on all columnar nanostructures compared to Ni(poly). This was ascribed to the high electroactive surface area (EASA) of porous nickel columns. EASAs for vertical, tilted and zigzag Ni thin layers were higher 32, 25.3, and 24.9 times, respectively, than their geommetric areas. Accordingly, Ni thin films with vertical columns have shown the highest activity for HER.
T2  - International Journal of Electrochemical Science
T1  - Hydrogen Evolution on Columnar Ni Thin Films Obtained by GLAD
VL  - 12
IS  - 6
SP  - 4692
EP  - 4701
DO  - 10.20964/2017.06.89
ER  - 

@article{
author = "Potočnik, Jelena and Popović, Maja and Rakočević, Zlatko Lj. and Štrbac, Svetlana",
year = "2017",
abstract = "Nanostructured nickel thin films were deposited on glass using glancing angle deposition (GLAD) technique. Cross-sectional field emission scanning electron microscopy images have shown that obtained Ni thin films consist of vertical, tilted or zigzag nano-scaled columns, while X-ray diffraction have shown that (111) orientation prevailed. X-ray photoelectron spectroscopy revealed that apart from metallic nickel, NiO and Ni(OH)(2) were also present in lower amount. Cyclic voltammetry in alkaline solution has shown that hydrogen evolution reaction (HER) was significantly catalyzed on all columnar nanostructures compared to Ni(poly). This was ascribed to the high electroactive surface area (EASA) of porous nickel columns. EASAs for vertical, tilted and zigzag Ni thin layers were higher 32, 25.3, and 24.9 times, respectively, than their geommetric areas. Accordingly, Ni thin films with vertical columns have shown the highest activity for HER.",
journal = "International Journal of Electrochemical Science",
title = "Hydrogen Evolution on Columnar Ni Thin Films Obtained by GLAD",
volume = "12",
number = "6",
pages = "4692-4701",
doi = "10.20964/2017.06.89"
}

Potočnik, J., Popović, M., Rakočević, Z. Lj.,& Štrbac, S.. (2017). Hydrogen Evolution on Columnar Ni Thin Films Obtained by GLAD. in International Journal of Electrochemical Science, 12(6), 4692-4701.
https://doi.org/10.20964/2017.06.89

Potočnik J, Popović M, Rakočević ZL, Štrbac S. Hydrogen Evolution on Columnar Ni Thin Films Obtained by GLAD. in International Journal of Electrochemical Science. 2017;12(6):4692-4701.
doi:10.20964/2017.06.89 .

Potočnik, Jelena, Popović, Maja, Rakočević, Zlatko Lj., Štrbac, Svetlana, "Hydrogen Evolution on Columnar Ni Thin Films Obtained by GLAD" in International Journal of Electrochemical Science, 12, no. 6 (2017):4692-4701,
https://doi.org/10.20964/2017.06.89 . .

TY  - JOUR
AU  - Đolić, Maja B.
AU  - Rajaković-Ognjanović, Vladana N.
AU  - Štrbac, Svetlana
AU  - Dimitrijević, Suzana I.
AU  - Mitrić, Miodrag
AU  - Onjia, Antonije E.
AU  - Rajaković, Ljubinka V.
PY  - 2017
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1728
AB  - The objective of this study was to investigate the modification of materials used in wastewater treatment for possible antimicrobial application(s). Granulated activated carbon (GAC) and natural clinoptilolite (CLI) were activated using Cu2+-and Zn2+-ions and the disinfection ability of the resulting materials was tested. Studies of the sorption and desorption kinetics were performed in order to determine and clarify the antimicrobial activity of the metal-activated sorbents. The exact sorption capacities of the selected sorbents, GAC and CLI, activated through use of Cu2+-ions, were 15.90 and 3.60 mg/g, respectively, while for the materials activated by Zn2+-ions, the corresponding capacities were 14.00 and 4.72 mg/g,. The desorption rates were 2 and 3 orders of magnitude lower than their sorption efficacy for the Cu2+-, and Zn2+-activated sorbents, respectively. The intermediate sorption capacity and low desorption rate indicated that the overall antimicrobial activity of the metal-modified sorbents was a result of metal ions immobilized onto surface sites. The effect of antimicrobial activity of free ions desorbed from the metal-activated surface may thus be disregarded. The antimicrobial activities of Cu/GAC, Zn/GAC, Cu/CLI and Zn/ CLI were also tested against Escherichia coli, Staphylococcus aureus, and Candida albicans. After 15 min exposure, the highest levels of cell inactivation were obtained through the Cu/CLI and the Cu/GAC against E. coli, 100.0 and 98.24%, respectively. However, for S. aureus and yeast cell inactivation, all Cu2+-and Zn2+-activated sorbents proved to be unsatisfactory. A characterization of the sorbents was performed by Xray diffraction (XRD), X-ray photo electron spectroscopy (XPS), and field emission scanning electron microscopy (FE-SEM). A concentration of the adsorbed and released ions was determined by inductively coupled plasma-optical emission spectroscopy (ICP-OES) and mass spectrometry (ICP-MS). The results showed that the antimicrobial performance of the activated sorbents depended on the surface characteristics of the material, which itself designates the distribution and the bioavailability of the activating agent. (C) 2017 Elsevier B. V. All rights reserved.
T2  - New Biotechnology
T1  - Natural sorbents modified by divalent Cu2+- and Zn2+- ions and their corresponding antimicrobial activity
VL  - 39
SP  - 150
EP  - 159
DO  - 10.1016/j.nbt.2017.03.001
ER  - 

@article{
author = "Đolić, Maja B. and Rajaković-Ognjanović, Vladana N. and Štrbac, Svetlana and Dimitrijević, Suzana I. and Mitrić, Miodrag and Onjia, Antonije E. and Rajaković, Ljubinka V.",
year = "2017",
abstract = "The objective of this study was to investigate the modification of materials used in wastewater treatment for possible antimicrobial application(s). Granulated activated carbon (GAC) and natural clinoptilolite (CLI) were activated using Cu2+-and Zn2+-ions and the disinfection ability of the resulting materials was tested. Studies of the sorption and desorption kinetics were performed in order to determine and clarify the antimicrobial activity of the metal-activated sorbents. The exact sorption capacities of the selected sorbents, GAC and CLI, activated through use of Cu2+-ions, were 15.90 and 3.60 mg/g, respectively, while for the materials activated by Zn2+-ions, the corresponding capacities were 14.00 and 4.72 mg/g,. The desorption rates were 2 and 3 orders of magnitude lower than their sorption efficacy for the Cu2+-, and Zn2+-activated sorbents, respectively. The intermediate sorption capacity and low desorption rate indicated that the overall antimicrobial activity of the metal-modified sorbents was a result of metal ions immobilized onto surface sites. The effect of antimicrobial activity of free ions desorbed from the metal-activated surface may thus be disregarded. The antimicrobial activities of Cu/GAC, Zn/GAC, Cu/CLI and Zn/ CLI were also tested against Escherichia coli, Staphylococcus aureus, and Candida albicans. After 15 min exposure, the highest levels of cell inactivation were obtained through the Cu/CLI and the Cu/GAC against E. coli, 100.0 and 98.24%, respectively. However, for S. aureus and yeast cell inactivation, all Cu2+-and Zn2+-activated sorbents proved to be unsatisfactory. A characterization of the sorbents was performed by Xray diffraction (XRD), X-ray photo electron spectroscopy (XPS), and field emission scanning electron microscopy (FE-SEM). A concentration of the adsorbed and released ions was determined by inductively coupled plasma-optical emission spectroscopy (ICP-OES) and mass spectrometry (ICP-MS). The results showed that the antimicrobial performance of the activated sorbents depended on the surface characteristics of the material, which itself designates the distribution and the bioavailability of the activating agent. (C) 2017 Elsevier B. V. All rights reserved.",
journal = "New Biotechnology",
title = "Natural sorbents modified by divalent Cu2+- and Zn2+- ions and their corresponding antimicrobial activity",
volume = "39",
pages = "150-159",
doi = "10.1016/j.nbt.2017.03.001"
}

Đolić, M. B., Rajaković-Ognjanović, V. N., Štrbac, S., Dimitrijević, S. I., Mitrić, M., Onjia, A. E.,& Rajaković, L. V.. (2017). Natural sorbents modified by divalent Cu2+- and Zn2+- ions and their corresponding antimicrobial activity. in New Biotechnology, 39, 150-159.
https://doi.org/10.1016/j.nbt.2017.03.001

Đolić MB, Rajaković-Ognjanović VN, Štrbac S, Dimitrijević SI, Mitrić M, Onjia AE, Rajaković LV. Natural sorbents modified by divalent Cu2+- and Zn2+- ions and their corresponding antimicrobial activity. in New Biotechnology. 2017;39:150-159.
doi:10.1016/j.nbt.2017.03.001 .

Đolić, Maja B., Rajaković-Ognjanović, Vladana N., Štrbac, Svetlana, Dimitrijević, Suzana I., Mitrić, Miodrag, Onjia, Antonije E., Rajaković, Ljubinka V., "Natural sorbents modified by divalent Cu2+- and Zn2+- ions and their corresponding antimicrobial activity" in New Biotechnology, 39 (2017):150-159,
https://doi.org/10.1016/j.nbt.2017.03.001 . .

TY  - JOUR
AU  - Štrbac, Svetlana
AU  - Srejić, Irina
AU  - Rakočević, Zlatko Lj.
PY  - 2017
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1484
AB  - Catalytic properties of electrochemically activated polycrystalline gold, Au(poly), modified by spontaneously deposited palladium nanoislands with the coverage below a monolayer were examined for the oxygen reduction reaction (ORR) in alkaline solution using the rotating disc electrode (RDE) technique. Atomic force microscopy (AFM) images have shown that the coverage of randomly distributed nanosized Pd islands ranged from 18% to 77%. Cyclic voltammetry characterization involved hydrogen adsorption/desorption on the deposited Pd islands, as well as their oxidation/reduction at more positive potentials. RDE measurements have shown that, although ORR on Au(poly) proceeds partly through 4e-reduction pathway, in the presence of Pd islands it turns completely to 4e-pathway, exceeding the activity of bare Pd(poly). Among different Pd/Au(poly) nanostructures, the ones with Pd coverage of 18% and 30% have shown the highest activity for ORR in alkaline solution.
T2  - Journal of Electroanalytical Chemistry
T1  - Catalysis of oxygen reduction on electrochemically activated polycrystalline gold by Pd nanoislands in alkaline solution
VL  - 789
SP  - 76
EP  - 84
DO  - 10.1016/j.jelechem.2017.02.034
ER  - 

@article{
author = "Štrbac, Svetlana and Srejić, Irina and Rakočević, Zlatko Lj.",
year = "2017",
abstract = "Catalytic properties of electrochemically activated polycrystalline gold, Au(poly), modified by spontaneously deposited palladium nanoislands with the coverage below a monolayer were examined for the oxygen reduction reaction (ORR) in alkaline solution using the rotating disc electrode (RDE) technique. Atomic force microscopy (AFM) images have shown that the coverage of randomly distributed nanosized Pd islands ranged from 18% to 77%. Cyclic voltammetry characterization involved hydrogen adsorption/desorption on the deposited Pd islands, as well as their oxidation/reduction at more positive potentials. RDE measurements have shown that, although ORR on Au(poly) proceeds partly through 4e-reduction pathway, in the presence of Pd islands it turns completely to 4e-pathway, exceeding the activity of bare Pd(poly). Among different Pd/Au(poly) nanostructures, the ones with Pd coverage of 18% and 30% have shown the highest activity for ORR in alkaline solution.",
journal = "Journal of Electroanalytical Chemistry",
title = "Catalysis of oxygen reduction on electrochemically activated polycrystalline gold by Pd nanoislands in alkaline solution",
volume = "789",
pages = "76-84",
doi = "10.1016/j.jelechem.2017.02.034"
}

Štrbac, S., Srejić, I.,& Rakočević, Z. Lj.. (2017). Catalysis of oxygen reduction on electrochemically activated polycrystalline gold by Pd nanoislands in alkaline solution. in Journal of Electroanalytical Chemistry, 789, 76-84.
https://doi.org/10.1016/j.jelechem.2017.02.034

Štrbac S, Srejić I, Rakočević ZL. Catalysis of oxygen reduction on electrochemically activated polycrystalline gold by Pd nanoislands in alkaline solution. in Journal of Electroanalytical Chemistry. 2017;789:76-84.
doi:10.1016/j.jelechem.2017.02.034 .

Štrbac, Svetlana, Srejić, Irina, Rakočević, Zlatko Lj., "Catalysis of oxygen reduction on electrochemically activated polycrystalline gold by Pd nanoislands in alkaline solution" in Journal of Electroanalytical Chemistry, 789 (2017):76-84,
https://doi.org/10.1016/j.jelechem.2017.02.034 . .

TY  - JOUR
AU  - Srejić, Irina
AU  - Smiljanić, Milutin Lj.
AU  - Rakočević, Zlatko Lj.
AU  - Štrbac, Svetlana
PY  - 2016
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1374
AB  - Catalytic properties of polycrystalline gold, Au(poly), were examined for the oxygen reduction reaction in alkaline solution using the rotating disc electrode technique. On electrochemically prepared Au(poly), oxygen reduction proceeds partly through 4e-reaction pathway resembling the activity of bare Au(100) in alkaline solution. Electrochemical behavior of such Au(100)-like polycrystalline gold electrode was compared with bare Au(100) surface, as well as with stepped Au(210)=Au[2(100)x(110)] and Au(533)=Au[4(111)x(100)] surfaces. It is shown that polycrystalline gold electrode behaved in a similar manner as stepped Au[n(111)x(100)] surfaces, meaning that the enrichment in (111)x(100) steps, rather than in (100) orientation is responsible for a partial 4e-reaction pathway in alkaline solution.
T2  - International Journal of Electrochemical Science
T1  - Oxygen Reduction on Au(100)-like Polycrystalline Gold Electrode in Alkaline Solution
VL  - 11
IS  - 12
SP  - 10436
EP  - 10448
DO  - 10.20964/2016.12.51
ER  - 

@article{
author = "Srejić, Irina and Smiljanić, Milutin Lj. and Rakočević, Zlatko Lj. and Štrbac, Svetlana",
year = "2016",
abstract = "Catalytic properties of polycrystalline gold, Au(poly), were examined for the oxygen reduction reaction in alkaline solution using the rotating disc electrode technique. On electrochemically prepared Au(poly), oxygen reduction proceeds partly through 4e-reaction pathway resembling the activity of bare Au(100) in alkaline solution. Electrochemical behavior of such Au(100)-like polycrystalline gold electrode was compared with bare Au(100) surface, as well as with stepped Au(210)=Au[2(100)x(110)] and Au(533)=Au[4(111)x(100)] surfaces. It is shown that polycrystalline gold electrode behaved in a similar manner as stepped Au[n(111)x(100)] surfaces, meaning that the enrichment in (111)x(100) steps, rather than in (100) orientation is responsible for a partial 4e-reaction pathway in alkaline solution.",
journal = "International Journal of Electrochemical Science",
title = "Oxygen Reduction on Au(100)-like Polycrystalline Gold Electrode in Alkaline Solution",
volume = "11",
number = "12",
pages = "10436-10448",
doi = "10.20964/2016.12.51"
}

Srejić, I., Smiljanić, M. Lj., Rakočević, Z. Lj.,& Štrbac, S.. (2016). Oxygen Reduction on Au(100)-like Polycrystalline Gold Electrode in Alkaline Solution. in International Journal of Electrochemical Science, 11(12), 10436-10448.
https://doi.org/10.20964/2016.12.51

Srejić I, Smiljanić ML, Rakočević ZL, Štrbac S. Oxygen Reduction on Au(100)-like Polycrystalline Gold Electrode in Alkaline Solution. in International Journal of Electrochemical Science. 2016;11(12):10436-10448.
doi:10.20964/2016.12.51 .

Srejić, Irina, Smiljanić, Milutin Lj., Rakočević, Zlatko Lj., Štrbac, Svetlana, "Oxygen Reduction on Au(100)-like Polycrystalline Gold Electrode in Alkaline Solution" in International Journal of Electrochemical Science, 11, no. 12 (2016):10436-10448,
https://doi.org/10.20964/2016.12.51 . .

TY  - JOUR
AU  - Štrbac, Svetlana
AU  - Smiljanić, Milutin Lj.
AU  - Rakočević, Zlatko Lj.
PY  - 2016
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1325
AB  - Rhodium nanoislands were spontaneously deposited on Au(111) up to a full coverage. Obtained Rh/Au(111) bimetallic surface was characterized ex situ by Atomic Force Microscopy imaging and by X-Ray Photoelectron Microscopy, while in situ characterization was performed by Cyclic Voltammetry in 0.1 M NaOH solution. Pronounced catalysis of hydrogen evolution reaction has been observed on Rh modified Au(111) surface compared to bare Au(111). This is ascribed to the suitable geometry of obtained Rh/Au(111) nanostructured electrode surface providing large number of active sites and to the electronic interaction between Au(111) substrate and Rh deposit. (C) 2016 The Electrochemical Society. All rights reserved.
T2  - Journal of the Electrochemical Society
T1  - Spontaneously Deposited Rh on Au(111) Observed by AFM and XPS: Electrocatalysis of Hydrogen Evolution
VL  - 163
IS  - 12
SP  - D3027
EP  - D3033
DO  - 10.1149/2.0041612jes
ER  - 

@article{
author = "Štrbac, Svetlana and Smiljanić, Milutin Lj. and Rakočević, Zlatko Lj.",
year = "2016",
abstract = "Rhodium nanoislands were spontaneously deposited on Au(111) up to a full coverage. Obtained Rh/Au(111) bimetallic surface was characterized ex situ by Atomic Force Microscopy imaging and by X-Ray Photoelectron Microscopy, while in situ characterization was performed by Cyclic Voltammetry in 0.1 M NaOH solution. Pronounced catalysis of hydrogen evolution reaction has been observed on Rh modified Au(111) surface compared to bare Au(111). This is ascribed to the suitable geometry of obtained Rh/Au(111) nanostructured electrode surface providing large number of active sites and to the electronic interaction between Au(111) substrate and Rh deposit. (C) 2016 The Electrochemical Society. All rights reserved.",
journal = "Journal of the Electrochemical Society",
title = "Spontaneously Deposited Rh on Au(111) Observed by AFM and XPS: Electrocatalysis of Hydrogen Evolution",
volume = "163",
number = "12",
pages = "D3027-D3033",
doi = "10.1149/2.0041612jes"
}

Štrbac, S., Smiljanić, M. Lj.,& Rakočević, Z. Lj.. (2016). Spontaneously Deposited Rh on Au(111) Observed by AFM and XPS: Electrocatalysis of Hydrogen Evolution. in Journal of the Electrochemical Society, 163(12), D3027-D3033.
https://doi.org/10.1149/2.0041612jes

Štrbac S, Smiljanić ML, Rakočević ZL. Spontaneously Deposited Rh on Au(111) Observed by AFM and XPS: Electrocatalysis of Hydrogen Evolution. in Journal of the Electrochemical Society. 2016;163(12):D3027-D3033.
doi:10.1149/2.0041612jes .

Štrbac, Svetlana, Smiljanić, Milutin Lj., Rakočević, Zlatko Lj., "Spontaneously Deposited Rh on Au(111) Observed by AFM and XPS: Electrocatalysis of Hydrogen Evolution" in Journal of the Electrochemical Society, 163, no. 12 (2016):D3027-D3033,
https://doi.org/10.1149/2.0041612jes . .

TY  - JOUR
AU  - Maksić, Aleksandar
AU  - Smiljanić, Milutin Lj.
AU  - Miljanić, Šćepan S.
AU  - Rakočević, Zlatko Lj.
AU  - Štrbac, Svetlana
PY  - 2016
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1169
AB  - Bimetallic electrodes prepared by Rh nanoislands spontaneously deposited on polycrystalline palladium, Pd(poly), at submonolayer coverage were explored for ethanol oxidation in alkaline media. Characterization of obtained Rh/Pd(poly) nanostructures was performed ex situ by AFM imaging and by X-ray photoelectron spectroscopy. In situ characterization of the obtained electrodes and subsequent ethanol oxidation measurements were performed by cyclic voltammetry in 0.1 M KOH. Palladium surface with 50% Rh coverage exhibited the highest catalytic activity for ethanol oxidation in alkaline media. The origin of the enhanced catalysis of Rh/Pd(poly) surfaces with respect to bare Pd was explained by the electronic effect. Possible reaction pathways for ethanol oxidation were discussed taking into account the activity of obtained bimetallic electrodes for the oxidation of CO and acetaldehyde, as the most probable reaction intermediates. (C) 2016 Elsevier Ltd. All rights reserved.
T2  - Electrochimica Acta
T1  - Ethanol Oxidation on Rh/Pd(poly) in Alkaline Solution
VL  - 209
SP  - 323
EP  - 331
DO  - 10.1016/j.electacta.2016.05.096
ER  - 

@article{
author = "Maksić, Aleksandar and Smiljanić, Milutin Lj. and Miljanić, Šćepan S. and Rakočević, Zlatko Lj. and Štrbac, Svetlana",
year = "2016",
abstract = "Bimetallic electrodes prepared by Rh nanoislands spontaneously deposited on polycrystalline palladium, Pd(poly), at submonolayer coverage were explored for ethanol oxidation in alkaline media. Characterization of obtained Rh/Pd(poly) nanostructures was performed ex situ by AFM imaging and by X-ray photoelectron spectroscopy. In situ characterization of the obtained electrodes and subsequent ethanol oxidation measurements were performed by cyclic voltammetry in 0.1 M KOH. Palladium surface with 50% Rh coverage exhibited the highest catalytic activity for ethanol oxidation in alkaline media. The origin of the enhanced catalysis of Rh/Pd(poly) surfaces with respect to bare Pd was explained by the electronic effect. Possible reaction pathways for ethanol oxidation were discussed taking into account the activity of obtained bimetallic electrodes for the oxidation of CO and acetaldehyde, as the most probable reaction intermediates. (C) 2016 Elsevier Ltd. All rights reserved.",
journal = "Electrochimica Acta",
title = "Ethanol Oxidation on Rh/Pd(poly) in Alkaline Solution",
volume = "209",
pages = "323-331",
doi = "10.1016/j.electacta.2016.05.096"
}

Maksić, A., Smiljanić, M. Lj., Miljanić, Š. S., Rakočević, Z. Lj.,& Štrbac, S.. (2016). Ethanol Oxidation on Rh/Pd(poly) in Alkaline Solution. in Electrochimica Acta, 209, 323-331.
https://doi.org/10.1016/j.electacta.2016.05.096

Maksić A, Smiljanić ML, Miljanić ŠS, Rakočević ZL, Štrbac S. Ethanol Oxidation on Rh/Pd(poly) in Alkaline Solution. in Electrochimica Acta. 2016;209:323-331.
doi:10.1016/j.electacta.2016.05.096 .

Maksić, Aleksandar, Smiljanić, Milutin Lj., Miljanić, Šćepan S., Rakočević, Zlatko Lj., Štrbac, Svetlana, "Ethanol Oxidation on Rh/Pd(poly) in Alkaline Solution" in Electrochimica Acta, 209 (2016):323-331,
https://doi.org/10.1016/j.electacta.2016.05.096 . .

TY  - JOUR
AU  - Đolić, Maja B.
AU  - Rajaković-Ognjanović, Vladana N.
AU  - Štrbac, Svetlana
AU  - Rakočević, Zlatko Lj.
AU  - Veljović, Đorđe N.
AU  - Dimitrijević, Suzana I.
AU  - Rajaković, Ljubinka V.
PY  - 2015
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/849
AB  - This study is focused on the surface modifications of the materials that are used for antimicrobial water treatment. Sorbents of different origin were activated by Ag+-ions. The selection of the most appropriate materials and the most effective activation agents was done according to the results of the sorption and desorption kinetic studies. Sorption capacities of selected sorbents: granulated activated carbon (GAC), zeolite (Z), and titanium dioxide (T), activated by Ag+-ions were following: 42.06, 13.51 and 17.53 mg/g, respectively. The antimicrobial activity of Ag/Z, Ag/GAC and Ag/T sorbents were tested against Gram-negative bacteria E. coli, Gram-positive bacteria S. aureus and yeast C. albicans. After 15 min of exposure period, the highest cell removal was obtained using Ag/Z against S. aureus and E. coli, 98.8 and 93.5%, respectively. Yeast cell inactivation was unsatisfactory for all three activated sorbents. The antimicrobial pathway of the activated sorbents has been examined by two separate tests - Ag+-ions desorbed from the activated surface to the aqueous phase and microbial cell removal caused by the Ag+-ions from the solid phase (activated surface sites). The results indicated that disinfection process significantly depended on the microbial-activated sites interactions on the modified surface. The chemical state of the activating agent had crucial impact to the inhibition rate. The characterization of the native and modified sorbents was performed by X-ray diffraction technique, X-ray photoelectron spectroscopy and scanning electron microscope. The concentration of adsorbed and released ions was determined by inductively coupled plasma optical emission spectroscopy and mass spectrometry. The antimicrobial efficiency of activated sorbents was related not only to the concentration of the activating agent, but moreover on the surface characteristics of the material, which affects the distribution and the accessibility of the activating agent. (C) 2015 Elsevier B.V. All rights reserved.
PB  - Elsevier
T2  - Applied Surface Science
T1  - The antimicrobial efficiency of silver activated sorbents
VL  - 357
SP  - 819
EP  - 831
DO  - 10.1016/j.apsusc.2015.09.032
ER  - 

@article{
author = "Đolić, Maja B. and Rajaković-Ognjanović, Vladana N. and Štrbac, Svetlana and Rakočević, Zlatko Lj. and Veljović, Đorđe N. and Dimitrijević, Suzana I. and Rajaković, Ljubinka V.",
year = "2015",
abstract = "This study is focused on the surface modifications of the materials that are used for antimicrobial water treatment. Sorbents of different origin were activated by Ag+-ions. The selection of the most appropriate materials and the most effective activation agents was done according to the results of the sorption and desorption kinetic studies. Sorption capacities of selected sorbents: granulated activated carbon (GAC), zeolite (Z), and titanium dioxide (T), activated by Ag+-ions were following: 42.06, 13.51 and 17.53 mg/g, respectively. The antimicrobial activity of Ag/Z, Ag/GAC and Ag/T sorbents were tested against Gram-negative bacteria E. coli, Gram-positive bacteria S. aureus and yeast C. albicans. After 15 min of exposure period, the highest cell removal was obtained using Ag/Z against S. aureus and E. coli, 98.8 and 93.5%, respectively. Yeast cell inactivation was unsatisfactory for all three activated sorbents. The antimicrobial pathway of the activated sorbents has been examined by two separate tests - Ag+-ions desorbed from the activated surface to the aqueous phase and microbial cell removal caused by the Ag+-ions from the solid phase (activated surface sites). The results indicated that disinfection process significantly depended on the microbial-activated sites interactions on the modified surface. The chemical state of the activating agent had crucial impact to the inhibition rate. The characterization of the native and modified sorbents was performed by X-ray diffraction technique, X-ray photoelectron spectroscopy and scanning electron microscope. The concentration of adsorbed and released ions was determined by inductively coupled plasma optical emission spectroscopy and mass spectrometry. The antimicrobial efficiency of activated sorbents was related not only to the concentration of the activating agent, but moreover on the surface characteristics of the material, which affects the distribution and the accessibility of the activating agent. (C) 2015 Elsevier B.V. All rights reserved.",
publisher = "Elsevier",
journal = "Applied Surface Science",
title = "The antimicrobial efficiency of silver activated sorbents",
volume = "357",
pages = "819-831",
doi = "10.1016/j.apsusc.2015.09.032"
}

Đolić, M. B., Rajaković-Ognjanović, V. N., Štrbac, S., Rakočević, Z. Lj., Veljović, Đ. N., Dimitrijević, S. I.,& Rajaković, L. V.. (2015). The antimicrobial efficiency of silver activated sorbents. in Applied Surface Science
Elsevier., 357, 819-831.
https://doi.org/10.1016/j.apsusc.2015.09.032

Đolić MB, Rajaković-Ognjanović VN, Štrbac S, Rakočević ZL, Veljović ĐN, Dimitrijević SI, Rajaković LV. The antimicrobial efficiency of silver activated sorbents. in Applied Surface Science. 2015;357:819-831.
doi:10.1016/j.apsusc.2015.09.032 .

Đolić, Maja B., Rajaković-Ognjanović, Vladana N., Štrbac, Svetlana, Rakočević, Zlatko Lj., Veljović, Đorđe N., Dimitrijević, Suzana I., Rajaković, Ljubinka V., "The antimicrobial efficiency of silver activated sorbents" in Applied Surface Science, 357 (2015):819-831,
https://doi.org/10.1016/j.apsusc.2015.09.032 . .

TY  - JOUR
AU  - Maksić, Aleksandar
AU  - Rakočević, Zlatko Lj.
AU  - Smiljanić, Milutin Lj.
AU  - Nenadović, Miloš
AU  - Štrbac, Svetlana
PY  - 2015
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/244
AB  - Bimetallic electrodes prepared by Pd nanoislands spontaneously deposited on polycrystalline platinum, Pt(poly), at submonolayer coverage were explored for methanol oxidation in alkaline media. Characterization of obtained Pd/Pt(poly) nanostructures was performed ex situ by AFM imaging, spectroscopic ellipsometry and by X-ray photoelectron spectroscopy. In situ characterization of the obtained electrodes and subsequent methanol oxidation measurements were performed by cyclic voltammetry in 0.1 M KOH. Platinum surface with 35% Pd coverage exhibited the highest catalytic activity for methanol oxidation in alkaline media, exceeding those of bare Pt and Pd. Both synergistic and electronic effects are responsible for such enhanced catalysis. The origin of the synergistic effect and possible reaction pathways for methanol oxidation were discussed taking into account the activity of obtained bimetallic electrodes for the oxidation of CO and formaldehyde, as the most probable reaction intermediates. (C) 2014 Elsevier B.V. All rights reserved.
T2  - Journal of Power Sources
T1  - Methanol oxidation on Pd/Pt(poly) in alkaline solution
VL  - 273
SP  - 724
EP  - 734
DO  - 10.1016/j.jpowsour.2014.09.138
ER  - 

@article{
author = "Maksić, Aleksandar and Rakočević, Zlatko Lj. and Smiljanić, Milutin Lj. and Nenadović, Miloš and Štrbac, Svetlana",
year = "2015",
abstract = "Bimetallic electrodes prepared by Pd nanoislands spontaneously deposited on polycrystalline platinum, Pt(poly), at submonolayer coverage were explored for methanol oxidation in alkaline media. Characterization of obtained Pd/Pt(poly) nanostructures was performed ex situ by AFM imaging, spectroscopic ellipsometry and by X-ray photoelectron spectroscopy. In situ characterization of the obtained electrodes and subsequent methanol oxidation measurements were performed by cyclic voltammetry in 0.1 M KOH. Platinum surface with 35% Pd coverage exhibited the highest catalytic activity for methanol oxidation in alkaline media, exceeding those of bare Pt and Pd. Both synergistic and electronic effects are responsible for such enhanced catalysis. The origin of the synergistic effect and possible reaction pathways for methanol oxidation were discussed taking into account the activity of obtained bimetallic electrodes for the oxidation of CO and formaldehyde, as the most probable reaction intermediates. (C) 2014 Elsevier B.V. All rights reserved.",
journal = "Journal of Power Sources",
title = "Methanol oxidation on Pd/Pt(poly) in alkaline solution",
volume = "273",
pages = "724-734",
doi = "10.1016/j.jpowsour.2014.09.138"
}

Maksić, A., Rakočević, Z. Lj., Smiljanić, M. Lj., Nenadović, M.,& Štrbac, S.. (2015). Methanol oxidation on Pd/Pt(poly) in alkaline solution. in Journal of Power Sources, 273, 724-734.
https://doi.org/10.1016/j.jpowsour.2014.09.138

Maksić A, Rakočević ZL, Smiljanić ML, Nenadović M, Štrbac S. Methanol oxidation on Pd/Pt(poly) in alkaline solution. in Journal of Power Sources. 2015;273:724-734.
doi:10.1016/j.jpowsour.2014.09.138 .

Maksić, Aleksandar, Rakočević, Zlatko Lj., Smiljanić, Milutin Lj., Nenadović, Miloš, Štrbac, Svetlana, "Methanol oxidation on Pd/Pt(poly) in alkaline solution" in Journal of Power Sources, 273 (2015):724-734,
https://doi.org/10.1016/j.jpowsour.2014.09.138 . .

TY  - JOUR
AU  - Štrbac, Svetlana
AU  - Smiljanić, Milutin Lj.
AU  - Rakočević, Zlatko Lj.
PY  - 2015
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/770
AB  - Hydrogen evolution reaction (HER) was investigated on bimetallic Rh/Pd(poly) electrodes in alkaline solution. Bimetallic electrodes were obtained by a spontaneous deposition of rhodium on polycrystalline Pd. Characterization of obtained electrodes was performed ex situ by atomic force microscopy and by spectroscopic ellipsometry. The results have shown that the coverage of palladium substrate with the deposited Rh nanoislands was up to 50%, depending on the chosen deposition time. Electrochemical properties and catalytic activity of Rh/Pd(poly) nanostructures for HER were examined in 0.1 M NaOH solution by cyclic voltammetry and linear sweep voltammetry. Rh/Pd(poly) electrodes have shown an enhanced activity for HER with respect to bare Pd(poly), which was ascribed to the strong electronic interaction between palladium substrate and the deposited rhodium islands. The enhanced catalytic activity of 50% Rh/Pd(poly) for HER in alkaline solution is comparable to that of bare Pt(poly). (C) 2015 Elsevier B.V. All rights reserved.
T2  - Journal of Electroanalytical Chemistry
T1  - Electrocatalysis of hydrogen evolution on polycrystalline palladium by rhodium nanoislands in alkaline solution
VL  - 755
SP  - 115
EP  - 121
DO  - 10.1016/j.jelechem.2015.07.044
ER  - 

@article{
author = "Štrbac, Svetlana and Smiljanić, Milutin Lj. and Rakočević, Zlatko Lj.",
year = "2015",
abstract = "Hydrogen evolution reaction (HER) was investigated on bimetallic Rh/Pd(poly) electrodes in alkaline solution. Bimetallic electrodes were obtained by a spontaneous deposition of rhodium on polycrystalline Pd. Characterization of obtained electrodes was performed ex situ by atomic force microscopy and by spectroscopic ellipsometry. The results have shown that the coverage of palladium substrate with the deposited Rh nanoislands was up to 50%, depending on the chosen deposition time. Electrochemical properties and catalytic activity of Rh/Pd(poly) nanostructures for HER were examined in 0.1 M NaOH solution by cyclic voltammetry and linear sweep voltammetry. Rh/Pd(poly) electrodes have shown an enhanced activity for HER with respect to bare Pd(poly), which was ascribed to the strong electronic interaction between palladium substrate and the deposited rhodium islands. The enhanced catalytic activity of 50% Rh/Pd(poly) for HER in alkaline solution is comparable to that of bare Pt(poly). (C) 2015 Elsevier B.V. All rights reserved.",
journal = "Journal of Electroanalytical Chemistry",
title = "Electrocatalysis of hydrogen evolution on polycrystalline palladium by rhodium nanoislands in alkaline solution",
volume = "755",
pages = "115-121",
doi = "10.1016/j.jelechem.2015.07.044"
}

Štrbac, S., Smiljanić, M. Lj.,& Rakočević, Z. Lj.. (2015). Electrocatalysis of hydrogen evolution on polycrystalline palladium by rhodium nanoislands in alkaline solution. in Journal of Electroanalytical Chemistry, 755, 115-121.
https://doi.org/10.1016/j.jelechem.2015.07.044

Štrbac S, Smiljanić ML, Rakočević ZL. Electrocatalysis of hydrogen evolution on polycrystalline palladium by rhodium nanoislands in alkaline solution. in Journal of Electroanalytical Chemistry. 2015;755:115-121.
doi:10.1016/j.jelechem.2015.07.044 .

Štrbac, Svetlana, Smiljanić, Milutin Lj., Rakočević, Zlatko Lj., "Electrocatalysis of hydrogen evolution on polycrystalline palladium by rhodium nanoislands in alkaline solution" in Journal of Electroanalytical Chemistry, 755 (2015):115-121,
https://doi.org/10.1016/j.jelechem.2015.07.044 . .

TY  - JOUR
AU  - Srejić, Irina
AU  - Rakočević, Zlatko Lj.
AU  - Nenadović, Miloš
AU  - Štrbac, Svetlana
PY  - 2015
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/559
AB  - Oxygen reduction reaction (ORR) was investigated on polycrystalline palladium, Pd(poly), in acid and alkaline solutions using rotating-disc electrode technique. Pd(poly) was prepared in non-aqueous media which provided surface with good quality and reproducibility. According to cyclic voltammetry curves and to the analysis of polarization curves for ORR and of ones obtained separately for hydrogen peroxide reduction/oxidation reactions, ORR in both media proceeds mainly through 4e-series pathway in the potential regions where Pd surface is either oxide free or oxidized to PdOH. ORR occurs partly through 2e-reduction in the potential region where PdO is present on the surface. As revealed by cyclic voltammetry, spectroscopic ellipsometry and by atomic force microscopy, Pd(poly) surface undergoes both topography and chemical changes during ORR. Pd surface roughness as well as the degree of its oxidation increase during ORR. (C) 2015 Elsevier Ltd. All rights reserved.
T2  - Electrochimica Acta
T1  - Oxygen reduction on polycrystalline palladium in acid and alkaline solutions: topographical and chemical Pd surface changes
VL  - 169
SP  - 22
EP  - 31
DO  - 10.1016/j.electacta.2015.04.032
ER  - 

@article{
author = "Srejić, Irina and Rakočević, Zlatko Lj. and Nenadović, Miloš and Štrbac, Svetlana",
year = "2015",
abstract = "Oxygen reduction reaction (ORR) was investigated on polycrystalline palladium, Pd(poly), in acid and alkaline solutions using rotating-disc electrode technique. Pd(poly) was prepared in non-aqueous media which provided surface with good quality and reproducibility. According to cyclic voltammetry curves and to the analysis of polarization curves for ORR and of ones obtained separately for hydrogen peroxide reduction/oxidation reactions, ORR in both media proceeds mainly through 4e-series pathway in the potential regions where Pd surface is either oxide free or oxidized to PdOH. ORR occurs partly through 2e-reduction in the potential region where PdO is present on the surface. As revealed by cyclic voltammetry, spectroscopic ellipsometry and by atomic force microscopy, Pd(poly) surface undergoes both topography and chemical changes during ORR. Pd surface roughness as well as the degree of its oxidation increase during ORR. (C) 2015 Elsevier Ltd. All rights reserved.",
journal = "Electrochimica Acta",
title = "Oxygen reduction on polycrystalline palladium in acid and alkaline solutions: topographical and chemical Pd surface changes",
volume = "169",
pages = "22-31",
doi = "10.1016/j.electacta.2015.04.032"
}

Srejić, I., Rakočević, Z. Lj., Nenadović, M.,& Štrbac, S.. (2015). Oxygen reduction on polycrystalline palladium in acid and alkaline solutions: topographical and chemical Pd surface changes. in Electrochimica Acta, 169, 22-31.
https://doi.org/10.1016/j.electacta.2015.04.032

Srejić I, Rakočević ZL, Nenadović M, Štrbac S. Oxygen reduction on polycrystalline palladium in acid and alkaline solutions: topographical and chemical Pd surface changes. in Electrochimica Acta. 2015;169:22-31.
doi:10.1016/j.electacta.2015.04.032 .

Srejić, Irina, Rakočević, Zlatko Lj., Nenadović, Miloš, Štrbac, Svetlana, "Oxygen reduction on polycrystalline palladium in acid and alkaline solutions: topographical and chemical Pd surface changes" in Electrochimica Acta, 169 (2015):22-31,
https://doi.org/10.1016/j.electacta.2015.04.032 . .

TY  - JOUR
AU  - Kisić, Danilo
AU  - Nenadović, Miloš
AU  - Štrbac, Svetlana
AU  - Adnađević, Borivoj
AU  - Rakočević, Zlatko Lj.
PY  - 2014
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/6015
AB  - The effect of ultraviolet (UV) ozone treatment on the surface properties of gold implanted high density polyethylene (HDPE) was investigated at a nanoscale using Atomic Force Microscopy (AFM). HDPE samples were modified by the implantation of gold ions at a dose of 5 x 10(15) ions/cm(2), using energies of 50, 100, 150, and 200 keV, and subsequently treated with UV/ozone. AFM surface topography images revealed that after UV/ozone treatment, the surface roughness of all Au/HDPE samples increased, while Power Spectral Density function increased only for samples implanted using higher energies, with a maximum for 150 keV. The chemical surface composition was homogenous in all cases, which was evidenced by appearance of single peaks in the histograms obtained from the phase AFM images. For UV/ozone treated samples, the shift of the peaks positions in the histograms to the higher values of the phase lag with respect to untreated ones indicated the decrease of surface hardness. Besides, a significant change of fractal dimension of surface grains is observed after UV/ozone treatment. (C) 2014 Elsevier B.V. All rights reserved.
T2  - Applied Surface Science
T1  - Effect of UV/ozone treatment on the nanoscale surface properties of gold implanted polyethylene
VL  - 307
SP  - 311
EP  - 318
DO  - 10.1016/j.apsusc.2014.04.032
ER  - 

@article{
author = "Kisić, Danilo and Nenadović, Miloš and Štrbac, Svetlana and Adnađević, Borivoj and Rakočević, Zlatko Lj.",
year = "2014",
abstract = "The effect of ultraviolet (UV) ozone treatment on the surface properties of gold implanted high density polyethylene (HDPE) was investigated at a nanoscale using Atomic Force Microscopy (AFM). HDPE samples were modified by the implantation of gold ions at a dose of 5 x 10(15) ions/cm(2), using energies of 50, 100, 150, and 200 keV, and subsequently treated with UV/ozone. AFM surface topography images revealed that after UV/ozone treatment, the surface roughness of all Au/HDPE samples increased, while Power Spectral Density function increased only for samples implanted using higher energies, with a maximum for 150 keV. The chemical surface composition was homogenous in all cases, which was evidenced by appearance of single peaks in the histograms obtained from the phase AFM images. For UV/ozone treated samples, the shift of the peaks positions in the histograms to the higher values of the phase lag with respect to untreated ones indicated the decrease of surface hardness. Besides, a significant change of fractal dimension of surface grains is observed after UV/ozone treatment. (C) 2014 Elsevier B.V. All rights reserved.",
journal = "Applied Surface Science",
title = "Effect of UV/ozone treatment on the nanoscale surface properties of gold implanted polyethylene",
volume = "307",
pages = "311-318",
doi = "10.1016/j.apsusc.2014.04.032"
}

Kisić, D., Nenadović, M., Štrbac, S., Adnađević, B.,& Rakočević, Z. Lj.. (2014). Effect of UV/ozone treatment on the nanoscale surface properties of gold implanted polyethylene. in Applied Surface Science, 307, 311-318.
https://doi.org/10.1016/j.apsusc.2014.04.032

Kisić D, Nenadović M, Štrbac S, Adnađević B, Rakočević ZL. Effect of UV/ozone treatment on the nanoscale surface properties of gold implanted polyethylene. in Applied Surface Science. 2014;307:311-318.
doi:10.1016/j.apsusc.2014.04.032 .

Kisić, Danilo, Nenadović, Miloš, Štrbac, Svetlana, Adnađević, Borivoj, Rakočević, Zlatko Lj., "Effect of UV/ozone treatment on the nanoscale surface properties of gold implanted polyethylene" in Applied Surface Science, 307 (2014):311-318,
https://doi.org/10.1016/j.apsusc.2014.04.032 . .

TY  - JOUR
AU  - Smiljanić, Milutin Lj.
AU  - Rakočević, Zlatko Lj.
AU  - Maksić, Aleksandar
AU  - Štrbac, Svetlana
PY  - 2014
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/5925
AB  - Pd/Pt(poly) and Rh/Pt(poly) bimetallic electrodes prepared by spontaneous deposition of Pd and Rh nanoislands on Pt(poly) at submonolayer coverage were explored as catalysts for hydrogen evolution reaction (HER) in alkaline media. Characterization of bimetallic surfaces was performed ex situ by height and phase AFM imaging and in situ by cyclic voltammetry. HER was investigated by linear sweep voltammetry in 0.1 M NaOH. Both Pd/Pt(poly) and Rh/Pt(poly) surfaces exhibited an enhanced catalysis for HER with respect to bare Pt(poly), which is explained by a strong synergistic electronic effect of platinum substrate on the deposited Pd or Rh nanoislands. This electronic effect leads to the lowering of a binding energy of adsorbed hydrogen intermediate and consequently to the lowering of the overpotential for HER. (C) 2013 Elsevier Ltd. All rights reserved.
T2  - Electrochimica Acta
T1  - Hydrogen Evolution Reaction on Platinum Catalyzed by Palladium and Rhodium Nanoislands
VL  - 117
SP  - 336
EP  - 343
DO  - 10.1016/j.electacta.2013.11.142
ER  - 

@article{
author = "Smiljanić, Milutin Lj. and Rakočević, Zlatko Lj. and Maksić, Aleksandar and Štrbac, Svetlana",
year = "2014",
abstract = "Pd/Pt(poly) and Rh/Pt(poly) bimetallic electrodes prepared by spontaneous deposition of Pd and Rh nanoislands on Pt(poly) at submonolayer coverage were explored as catalysts for hydrogen evolution reaction (HER) in alkaline media. Characterization of bimetallic surfaces was performed ex situ by height and phase AFM imaging and in situ by cyclic voltammetry. HER was investigated by linear sweep voltammetry in 0.1 M NaOH. Both Pd/Pt(poly) and Rh/Pt(poly) surfaces exhibited an enhanced catalysis for HER with respect to bare Pt(poly), which is explained by a strong synergistic electronic effect of platinum substrate on the deposited Pd or Rh nanoislands. This electronic effect leads to the lowering of a binding energy of adsorbed hydrogen intermediate and consequently to the lowering of the overpotential for HER. (C) 2013 Elsevier Ltd. All rights reserved.",
journal = "Electrochimica Acta",
title = "Hydrogen Evolution Reaction on Platinum Catalyzed by Palladium and Rhodium Nanoislands",
volume = "117",
pages = "336-343",
doi = "10.1016/j.electacta.2013.11.142"
}

Smiljanić, M. Lj., Rakočević, Z. Lj., Maksić, A.,& Štrbac, S.. (2014). Hydrogen Evolution Reaction on Platinum Catalyzed by Palladium and Rhodium Nanoislands. in Electrochimica Acta, 117, 336-343.
https://doi.org/10.1016/j.electacta.2013.11.142

Smiljanić ML, Rakočević ZL, Maksić A, Štrbac S. Hydrogen Evolution Reaction on Platinum Catalyzed by Palladium and Rhodium Nanoislands. in Electrochimica Acta. 2014;117:336-343.
doi:10.1016/j.electacta.2013.11.142 .

Smiljanić, Milutin Lj., Rakočević, Zlatko Lj., Maksić, Aleksandar, Štrbac, Svetlana, "Hydrogen Evolution Reaction on Platinum Catalyzed by Palladium and Rhodium Nanoislands" in Electrochimica Acta, 117 (2014):336-343,
https://doi.org/10.1016/j.electacta.2013.11.142 . .

TY  - JOUR
AU  - Potočnik, Jelena
AU  - Nenadović, Miloš
AU  - Jokić, Bojan M.
AU  - Štrbac, Svetlana
AU  - Rakočević, Zlatko Lj.
PY  - 2013
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/5470
AB  - In this work, a columnar structure of nickel thin film has been obtained using an advanced deposition technique known as Glancing Angle Deposition. Nickel thin film was deposited on glass sample at the constant emission current of 100 mA. Glass sample was positioned 15 degrees with respect to the nickel vapor flux. The obtained nickel thin film was characterized by Force Modulation Atomic Force Microscopy and by Scanning Electron Microscopy. Analysis indicated that the formation of the columnar structure occurred at the film thickness of 1 mu m, which was achieved for the deposition time of 3 hours.
AB  - У овом раду, стубичаста структура танког слоја никла је добијена коришћењем напредне технике депоновања при малим угловима. Танки слој никла је депонован на стаклу, при константној емисионој струји која је износила 100 mA. Подлога од стакла је постављена, у односу на флукс паре никла, под углом од 15 степени. Добијени танки слој никла је карактерисан помоћу микроскопа у пољу атомских сила и сканирајућег електронског микроскопа. Анализа указује да се формирање стубичасте структуре јавља при дебљини слоја никла од 1 μm, а та дебљина је добијена након 3 сата депоновања.
T2  - Science of Sintering
T1  - Structural Characterization of the Nickel Thin Film Deposited by GLAD Technique
VL  - 45
IS  - 1
SP  - 61
EP  - 67
DO  - 10.2298/SOS1301061P
ER  - 

@article{
author = "Potočnik, Jelena and Nenadović, Miloš and Jokić, Bojan M. and Štrbac, Svetlana and Rakočević, Zlatko Lj.",
year = "2013",
abstract = "In this work, a columnar structure of nickel thin film has been obtained using an advanced deposition technique known as Glancing Angle Deposition. Nickel thin film was deposited on glass sample at the constant emission current of 100 mA. Glass sample was positioned 15 degrees with respect to the nickel vapor flux. The obtained nickel thin film was characterized by Force Modulation Atomic Force Microscopy and by Scanning Electron Microscopy. Analysis indicated that the formation of the columnar structure occurred at the film thickness of 1 mu m, which was achieved for the deposition time of 3 hours., У овом раду, стубичаста структура танког слоја никла је добијена коришћењем напредне технике депоновања при малим угловима. Танки слој никла је депонован на стаклу, при константној емисионој струји која је износила 100 mA. Подлога од стакла је постављена, у односу на флукс паре никла, под углом од 15 степени. Добијени танки слој никла је карактерисан помоћу микроскопа у пољу атомских сила и сканирајућег електронског микроскопа. Анализа указује да се формирање стубичасте структуре јавља при дебљини слоја никла од 1 μm, а та дебљина је добијена након 3 сата депоновања.",
journal = "Science of Sintering",
title = "Structural Characterization of the Nickel Thin Film Deposited by GLAD Technique",
volume = "45",
number = "1",
pages = "61-67",
doi = "10.2298/SOS1301061P"
}

Potočnik, J., Nenadović, M., Jokić, B. M., Štrbac, S.,& Rakočević, Z. Lj.. (2013). Structural Characterization of the Nickel Thin Film Deposited by GLAD Technique. in Science of Sintering, 45(1), 61-67.
https://doi.org/10.2298/SOS1301061P

Potočnik J, Nenadović M, Jokić BM, Štrbac S, Rakočević ZL. Structural Characterization of the Nickel Thin Film Deposited by GLAD Technique. in Science of Sintering. 2013;45(1):61-67.
doi:10.2298/SOS1301061P .

Potočnik, Jelena, Nenadović, Miloš, Jokić, Bojan M., Štrbac, Svetlana, Rakočević, Zlatko Lj., "Structural Characterization of the Nickel Thin Film Deposited by GLAD Technique" in Science of Sintering, 45, no. 1 (2013):61-67,
https://doi.org/10.2298/SOS1301061P . .

TY  - JOUR
AU  - Nenadović, Miloš
AU  - Potočnik, Jelena
AU  - Mitrić, Miodrag
AU  - Štrbac, Svetlana
AU  - Rakočević, Zlatko Lj.
PY  - 2013
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/5754
AB  - High density polyethylene (HDPE) samples were modified by Au+ ion implantation at a dose of 5 x 10(15) ions cm(-2), using energies of 50, 100, 150 and 200 keV. The existence of implanted gold in the near-surface region of HDPE samples was confirmed by X-ray diffraction analysis. Surface roughness and Power Spectral Density analyses based on Atomic Force Microscopy (AFM) images of the surface topography revealed that the mechanism of HDPE modification during gold ion implantation depended on the energy of gold ions. Histograms obtained from phase AFM images indicated a qualitative change in the chemical composition of the surface during implantation with gold ions with different energies. Depth profiles obtained experimentally from cross-sectional Force Modulation Microscopy images and ones obtained from a theoretical simulation are in agreement for gold ions energies lower than 100 keV. The deviation that was observed for higher energies of the gold ions is explained by carbon precipitation in the near surface region of the HDPE, which prevented the penetration of gold ions further into the depth of the sample. (C) 2013 Elsevier B.V. All rights reserved.
T2  - Materials Chemistry and Physics
T1  - Modification of high density polyethylene by gold implantation using different ion energies
VL  - 142
IS  - 2-3
SP  - 633
EP  - 639
DO  - 10.1016/j.matchemphys.2013.08.013
ER  - 

@article{
author = "Nenadović, Miloš and Potočnik, Jelena and Mitrić, Miodrag and Štrbac, Svetlana and Rakočević, Zlatko Lj.",
year = "2013",
abstract = "High density polyethylene (HDPE) samples were modified by Au+ ion implantation at a dose of 5 x 10(15) ions cm(-2), using energies of 50, 100, 150 and 200 keV. The existence of implanted gold in the near-surface region of HDPE samples was confirmed by X-ray diffraction analysis. Surface roughness and Power Spectral Density analyses based on Atomic Force Microscopy (AFM) images of the surface topography revealed that the mechanism of HDPE modification during gold ion implantation depended on the energy of gold ions. Histograms obtained from phase AFM images indicated a qualitative change in the chemical composition of the surface during implantation with gold ions with different energies. Depth profiles obtained experimentally from cross-sectional Force Modulation Microscopy images and ones obtained from a theoretical simulation are in agreement for gold ions energies lower than 100 keV. The deviation that was observed for higher energies of the gold ions is explained by carbon precipitation in the near surface region of the HDPE, which prevented the penetration of gold ions further into the depth of the sample. (C) 2013 Elsevier B.V. All rights reserved.",
journal = "Materials Chemistry and Physics",
title = "Modification of high density polyethylene by gold implantation using different ion energies",
volume = "142",
number = "2-3",
pages = "633-639",
doi = "10.1016/j.matchemphys.2013.08.013"
}

Nenadović, M., Potočnik, J., Mitrić, M., Štrbac, S.,& Rakočević, Z. Lj.. (2013). Modification of high density polyethylene by gold implantation using different ion energies. in Materials Chemistry and Physics, 142(2-3), 633-639.
https://doi.org/10.1016/j.matchemphys.2013.08.013

Nenadović M, Potočnik J, Mitrić M, Štrbac S, Rakočević ZL. Modification of high density polyethylene by gold implantation using different ion energies. in Materials Chemistry and Physics. 2013;142(2-3):633-639.
doi:10.1016/j.matchemphys.2013.08.013 .

Nenadović, Miloš, Potočnik, Jelena, Mitrić, Miodrag, Štrbac, Svetlana, Rakočević, Zlatko Lj., "Modification of high density polyethylene by gold implantation using different ion energies" in Materials Chemistry and Physics, 142, no. 2-3 (2013):633-639,
https://doi.org/10.1016/j.matchemphys.2013.08.013 . .

TY  - JOUR
AU  - Smiljanić, Milutin Lj.
AU  - Srejić, Irina
AU  - Grgur, Branimir
AU  - Rakočević, Zlatko Lj.
AU  - Štrbac, Svetlana
PY  - 2013
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/5316
AB  - Hydrogen evolution reaction (HER) was studied on Pd/Au(1 1 1) bimetallic surfaces in alkaline solution. Au(1 1 1) was modified by palladium nanoislands spontaneously deposited using PdSO4 center dot 2H(2)O and PdCl2 salts. As revealed from both surface topography Atomic Force Microscopy (AFM) and phase AFM images, for the same deposition conditions, the obtained Pd/Au(1 1 1) nanostructures differ depending on the counter anion in the depositing palladium salt. These differences are reflected on their catalytic activity toward HER, which occurs between the potentials for pure consisting metals. HER proceeded with the same mechanism, but it is shifted to more positive potentials for Pd/Au(1 1 1) nanostructures obtained using PdCl2 salt with respect to ones obtained using PdSO4 salt. Better catalytic activity of Pd/Au(1 1 1) nanostructures obtained using PdCl2 salt can be explained by their surface structure consisting of smaller and thinner Pd nanoislands, preferentially deposited at steps, which provides more Pd and Pd/Au sites suitable for hydrogen evolution reaction. (C) 2012 Elsevier Ltd. All rights reserved.
T2  - Electrochimica Acta
T1  - Catalysis of hydrogen evolution on different Pd/Au(111) nanostructures in alkaline solution
VL  - 88
SP  - 589
EP  - 596
DO  - 10.1016/j.electacta.2012.10.128
ER  - 

@article{
author = "Smiljanić, Milutin Lj. and Srejić, Irina and Grgur, Branimir and Rakočević, Zlatko Lj. and Štrbac, Svetlana",
year = "2013",
abstract = "Hydrogen evolution reaction (HER) was studied on Pd/Au(1 1 1) bimetallic surfaces in alkaline solution. Au(1 1 1) was modified by palladium nanoislands spontaneously deposited using PdSO4 center dot 2H(2)O and PdCl2 salts. As revealed from both surface topography Atomic Force Microscopy (AFM) and phase AFM images, for the same deposition conditions, the obtained Pd/Au(1 1 1) nanostructures differ depending on the counter anion in the depositing palladium salt. These differences are reflected on their catalytic activity toward HER, which occurs between the potentials for pure consisting metals. HER proceeded with the same mechanism, but it is shifted to more positive potentials for Pd/Au(1 1 1) nanostructures obtained using PdCl2 salt with respect to ones obtained using PdSO4 salt. Better catalytic activity of Pd/Au(1 1 1) nanostructures obtained using PdCl2 salt can be explained by their surface structure consisting of smaller and thinner Pd nanoislands, preferentially deposited at steps, which provides more Pd and Pd/Au sites suitable for hydrogen evolution reaction. (C) 2012 Elsevier Ltd. All rights reserved.",
journal = "Electrochimica Acta",
title = "Catalysis of hydrogen evolution on different Pd/Au(111) nanostructures in alkaline solution",
volume = "88",
pages = "589-596",
doi = "10.1016/j.electacta.2012.10.128"
}

Smiljanić, M. Lj., Srejić, I., Grgur, B., Rakočević, Z. Lj.,& Štrbac, S.. (2013). Catalysis of hydrogen evolution on different Pd/Au(111) nanostructures in alkaline solution. in Electrochimica Acta, 88, 589-596.
https://doi.org/10.1016/j.electacta.2012.10.128

Smiljanić ML, Srejić I, Grgur B, Rakočević ZL, Štrbac S. Catalysis of hydrogen evolution on different Pd/Au(111) nanostructures in alkaline solution. in Electrochimica Acta. 2013;88:589-596.
doi:10.1016/j.electacta.2012.10.128 .

Smiljanić, Milutin Lj., Srejić, Irina, Grgur, Branimir, Rakočević, Zlatko Lj., Štrbac, Svetlana, "Catalysis of hydrogen evolution on different Pd/Au(111) nanostructures in alkaline solution" in Electrochimica Acta, 88 (2013):589-596,
https://doi.org/10.1016/j.electacta.2012.10.128 . .