TY  - JOUR
AU  - Jović, Borka M.
AU  - Jović, Vladimir D.
AU  - Lačnjevac, Uroš
AU  - Stevanović, Sanja
AU  - Kovač, Janez
AU  - Radović, Miladin
AU  - Krstajić, Nedeljko V.
PY  - 2016
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5839
AB  - In this work, the hydrogen evolution reaction (HER) was studied on Ru coated Ti2AlC electrodes in 1.0 mol dm(-3) H2SO4 at 25 degrees C. Ti2AlC was found to be a highly stable substrate in sulfuric acid solutions due to the formation of a passivating oxide layer on the surface, which was confirmed by the X-ray photoelectron spectroscopy (XPS) analysis of as-prepared and anodically treated Ti2AlC samples. Ru films were electrodeposited onto Ti2AlC substrates by cycling the potential of Ti2AlC in the solution containing 0.01 mol dm(-3) RuCl3 + 0.1 mol dm(-3) H2SO4 between -0.5 V and 0.4 V vs. a saturated calomel electrode (SCE) at the sweep rate of 20 mV s(-1). Four Ru/Ti2AlC samples were prepared, obtained at 5, 10, 15 and 20 cycles of Ru electrodeposition. Characterization of samples was performed by scanning electron microscopy (SEM) and cyclic voltammetry (CV), while the thickness of the electrodeposited Ru layers was determined by atomic force microscopy (AFM). It was found that the most compact sample with the thickness of about 0.42 mu m was obtained after 5 cycles. Electrochemical impedance spectroscopy (EIS) and steady-state polarization measurements showed that all Ru/Ti2AlC electrodes were exceptionally active for the HER. A Tafel slope of about -60 mV dec(-1) was observed on all polarization curves in the range of high cathodic current densities. Based on formal kinetics analysis, an appropriate mechanism for the HER on Ru/Ti2AlC was suggested.
PB  - Elsevier
T2  - Journal of Electroanalytical Chemistry
T1  - Ru layers electrodeposited onto highly stable Ti2AlC substrates as cathodes for hydrogen evolution in sulfuric acid solutions
EP  - 86
SP  - 78
VL  - 766
DO  - 10.1016/j.jelechem.2016.01.038
ER  - 

@article{
author = "Jović, Borka M. and Jović, Vladimir D. and Lačnjevac, Uroš and Stevanović, Sanja and Kovač, Janez and Radović, Miladin and Krstajić, Nedeljko V.",
year = "2016",
abstract = "In this work, the hydrogen evolution reaction (HER) was studied on Ru coated Ti2AlC electrodes in 1.0 mol dm(-3) H2SO4 at 25 degrees C. Ti2AlC was found to be a highly stable substrate in sulfuric acid solutions due to the formation of a passivating oxide layer on the surface, which was confirmed by the X-ray photoelectron spectroscopy (XPS) analysis of as-prepared and anodically treated Ti2AlC samples. Ru films were electrodeposited onto Ti2AlC substrates by cycling the potential of Ti2AlC in the solution containing 0.01 mol dm(-3) RuCl3 + 0.1 mol dm(-3) H2SO4 between -0.5 V and 0.4 V vs. a saturated calomel electrode (SCE) at the sweep rate of 20 mV s(-1). Four Ru/Ti2AlC samples were prepared, obtained at 5, 10, 15 and 20 cycles of Ru electrodeposition. Characterization of samples was performed by scanning electron microscopy (SEM) and cyclic voltammetry (CV), while the thickness of the electrodeposited Ru layers was determined by atomic force microscopy (AFM). It was found that the most compact sample with the thickness of about 0.42 mu m was obtained after 5 cycles. Electrochemical impedance spectroscopy (EIS) and steady-state polarization measurements showed that all Ru/Ti2AlC electrodes were exceptionally active for the HER. A Tafel slope of about -60 mV dec(-1) was observed on all polarization curves in the range of high cathodic current densities. Based on formal kinetics analysis, an appropriate mechanism for the HER on Ru/Ti2AlC was suggested.",
publisher = "Elsevier",
journal = "Journal of Electroanalytical Chemistry",
title = "Ru layers electrodeposited onto highly stable Ti2AlC substrates as cathodes for hydrogen evolution in sulfuric acid solutions",
pages = "86-78",
volume = "766",
doi = "10.1016/j.jelechem.2016.01.038"
}

Jović, B. M., Jović, V. D., Lačnjevac, U., Stevanović, S., Kovač, J., Radović, M.,& Krstajić, N. V.. (2016). Ru layers electrodeposited onto highly stable Ti2AlC substrates as cathodes for hydrogen evolution in sulfuric acid solutions. in Journal of Electroanalytical Chemistry
Elsevier., 766, 78-86.
https://doi.org/10.1016/j.jelechem.2016.01.038

Jović BM, Jović VD, Lačnjevac U, Stevanović S, Kovač J, Radović M, Krstajić NV. Ru layers electrodeposited onto highly stable Ti2AlC substrates as cathodes for hydrogen evolution in sulfuric acid solutions. in Journal of Electroanalytical Chemistry. 2016;766:78-86.
doi:10.1016/j.jelechem.2016.01.038 .

Jović, Borka M., Jović, Vladimir D., Lačnjevac, Uroš, Stevanović, Sanja, Kovač, Janez, Radović, Miladin, Krstajić, Nedeljko V., "Ru layers electrodeposited onto highly stable Ti2AlC substrates as cathodes for hydrogen evolution in sulfuric acid solutions" in Journal of Electroanalytical Chemistry, 766 (2016):78-86,
https://doi.org/10.1016/j.jelechem.2016.01.038 . .

TY  - JOUR
AU  - Jović, Borka M.
AU  - Jović, Vladimir D.
AU  - Lačnjevac, Uroš
AU  - Stevanović, Sanja
AU  - Kovač, Janez
AU  - Radović, Miladin
AU  - Krstajić, Nedeljko V.
PY  - 2016
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4297
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/6365
AB  - In this work, the hydrogen evolution reaction (HER) was studied on Ru coated Ti2AlC electrodes in 1.0 mol dm(-3) H2SO4 at 25 degrees C. Ti2AlC was found to be a highly stable substrate in sulfuric acid solutions due to the formation of a passivating oxide layer on the surface, which was confirmed by the X-ray photoelectron spectroscopy (XPS) analysis of as-prepared and anodically treated Ti2AlC samples. Ru films were electrodeposited onto Ti2AlC substrates by cycling the potential of Ti2AlC in the solution containing 0.01 mol dm(-3) RuCl3 + 0.1 mol dm(-3) H2SO4 between -0.5 V and 0.4 V vs. a saturated calomel electrode (SCE) at the sweep rate of 20 mV s(-1). Four Ru/Ti2AlC samples were prepared, obtained at 5, 10, 15 and 20 cycles of Ru electrodeposition. Characterization of samples was performed by scanning electron microscopy (SEM) and cyclic voltammetry (CV), while the thickness of the electrodeposited Ru layers was determined by atomic force microscopy (AFM). It was found that the most compact sample with the thickness of about 0.42 mu m was obtained after 5 cycles. Electrochemical impedance spectroscopy (EIS) and steady-state polarization measurements showed that all Ru/Ti2AlC electrodes were exceptionally active for the HER. A Tafel slope of about -60 mV dec(-1) was observed on all polarization curves in the range of high cathodic current densities. Based on formal kinetics analysis, an appropriate mechanism for the HER on Ru/Ti2AlC was suggested.
PB  - Elsevier
T2  - Journal of Electroanalytical Chemistry
T1  - Ru layers electrodeposited onto highly stable Ti2AlC substrates as cathodes for hydrogen evolution in sulfuric acid solutions
EP  - 86
SP  - 78
VL  - 766
DO  - 10.1016/j.jelechem.2016.01.038
ER  - 

@article{
author = "Jović, Borka M. and Jović, Vladimir D. and Lačnjevac, Uroš and Stevanović, Sanja and Kovač, Janez and Radović, Miladin and Krstajić, Nedeljko V.",
year = "2016",
abstract = "In this work, the hydrogen evolution reaction (HER) was studied on Ru coated Ti2AlC electrodes in 1.0 mol dm(-3) H2SO4 at 25 degrees C. Ti2AlC was found to be a highly stable substrate in sulfuric acid solutions due to the formation of a passivating oxide layer on the surface, which was confirmed by the X-ray photoelectron spectroscopy (XPS) analysis of as-prepared and anodically treated Ti2AlC samples. Ru films were electrodeposited onto Ti2AlC substrates by cycling the potential of Ti2AlC in the solution containing 0.01 mol dm(-3) RuCl3 + 0.1 mol dm(-3) H2SO4 between -0.5 V and 0.4 V vs. a saturated calomel electrode (SCE) at the sweep rate of 20 mV s(-1). Four Ru/Ti2AlC samples were prepared, obtained at 5, 10, 15 and 20 cycles of Ru electrodeposition. Characterization of samples was performed by scanning electron microscopy (SEM) and cyclic voltammetry (CV), while the thickness of the electrodeposited Ru layers was determined by atomic force microscopy (AFM). It was found that the most compact sample with the thickness of about 0.42 mu m was obtained after 5 cycles. Electrochemical impedance spectroscopy (EIS) and steady-state polarization measurements showed that all Ru/Ti2AlC electrodes were exceptionally active for the HER. A Tafel slope of about -60 mV dec(-1) was observed on all polarization curves in the range of high cathodic current densities. Based on formal kinetics analysis, an appropriate mechanism for the HER on Ru/Ti2AlC was suggested.",
publisher = "Elsevier",
journal = "Journal of Electroanalytical Chemistry",
title = "Ru layers electrodeposited onto highly stable Ti2AlC substrates as cathodes for hydrogen evolution in sulfuric acid solutions",
pages = "86-78",
volume = "766",
doi = "10.1016/j.jelechem.2016.01.038"
}

Jović, B. M., Jović, V. D., Lačnjevac, U., Stevanović, S., Kovač, J., Radović, M.,& Krstajić, N. V.. (2016). Ru layers electrodeposited onto highly stable Ti2AlC substrates as cathodes for hydrogen evolution in sulfuric acid solutions. in Journal of Electroanalytical Chemistry
Elsevier., 766, 78-86.
https://doi.org/10.1016/j.jelechem.2016.01.038

Jović BM, Jović VD, Lačnjevac U, Stevanović S, Kovač J, Radović M, Krstajić NV. Ru layers electrodeposited onto highly stable Ti2AlC substrates as cathodes for hydrogen evolution in sulfuric acid solutions. in Journal of Electroanalytical Chemistry. 2016;766:78-86.
doi:10.1016/j.jelechem.2016.01.038 .

Jović, Borka M., Jović, Vladimir D., Lačnjevac, Uroš, Stevanović, Sanja, Kovač, Janez, Radović, Miladin, Krstajić, Nedeljko V., "Ru layers electrodeposited onto highly stable Ti2AlC substrates as cathodes for hydrogen evolution in sulfuric acid solutions" in Journal of Electroanalytical Chemistry, 766 (2016):78-86,
https://doi.org/10.1016/j.jelechem.2016.01.038 . .

TY  - JOUR
AU  - Elezović, Nevenka R.
AU  - Radmilović, Velimir R
AU  - Krstajić, Nedeljko V
PY  - 2016
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5834
AB  - In this manuscript a survey of the contemporary research related to platinum nanocatalysts on metal oxide based supports for low temperature fuel cell applications is presented. Different carbon based supports, used as state of the art materials, are listed and discussed, as well. Although carbon based materials possess many desirable properties, such as high surface area, high conductivity and relatively low cost and easy synthesis, the large scale commercialization is limited by instability under accelerated stability testing, simulating real fuel cell operating conditions. To overcome these disadvantages of carbon supports, different metal oxide based ones have been studied and promising results are referenced. The most often used oxide based supports for low temperature fuel cell applications are presented in this review. Suitable discussion and future research related remarks are given, as well.
PB  - Royal Soc Chemistry, Cambridge
T2  - RSC Advances
T1  - Platinum nanocatalysts on metal oxide based supports for low temperature fuel cell applications
EP  - 6801
IS  - 8
SP  - 6788
VL  - 6
DO  - 10.1039/C5RA22403A
ER  - 

@article{
author = "Elezović, Nevenka R. and Radmilović, Velimir R and Krstajić, Nedeljko V",
year = "2016",
abstract = "In this manuscript a survey of the contemporary research related to platinum nanocatalysts on metal oxide based supports for low temperature fuel cell applications is presented. Different carbon based supports, used as state of the art materials, are listed and discussed, as well. Although carbon based materials possess many desirable properties, such as high surface area, high conductivity and relatively low cost and easy synthesis, the large scale commercialization is limited by instability under accelerated stability testing, simulating real fuel cell operating conditions. To overcome these disadvantages of carbon supports, different metal oxide based ones have been studied and promising results are referenced. The most often used oxide based supports for low temperature fuel cell applications are presented in this review. Suitable discussion and future research related remarks are given, as well.",
publisher = "Royal Soc Chemistry, Cambridge",
journal = "RSC Advances",
title = "Platinum nanocatalysts on metal oxide based supports for low temperature fuel cell applications",
pages = "6801-6788",
number = "8",
volume = "6",
doi = "10.1039/C5RA22403A"
}

Elezović, N. R., Radmilović, V. R.,& Krstajić, N. V.. (2016). Platinum nanocatalysts on metal oxide based supports for low temperature fuel cell applications. in RSC Advances
Royal Soc Chemistry, Cambridge., 6(8), 6788-6801.
https://doi.org/10.1039/C5RA22403A

Elezović NR, Radmilović VR, Krstajić NV. Platinum nanocatalysts on metal oxide based supports for low temperature fuel cell applications. in RSC Advances. 2016;6(8):6788-6801.
doi:10.1039/C5RA22403A .

Elezović, Nevenka R., Radmilović, Velimir R, Krstajić, Nedeljko V, "Platinum nanocatalysts on metal oxide based supports for low temperature fuel cell applications" in RSC Advances, 6, no. 8 (2016):6788-6801,
https://doi.org/10.1039/C5RA22403A . .

TY  - JOUR
AU  - Elezović, Nevenka R.
AU  - Ercius, P.
AU  - Kovac, Janez
AU  - Radmilović, Velimir R
AU  - Babić, Biljana M.
AU  - Krstajić, Nedeljko V
PY  - 2015
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5799
AB  - Ruthenium oxide/titanium oxide, with a Ru:Ti atomic ratio of 7:3 was synthesized by modified sol-gel procedure and used as a support for platinum nanocatalyst for oxygen reduction reaction. The synthesized materials were characterized in terms of morphology, particle size distribution, chemical and phase composition by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), high angle annular dark filed scanning transmission electron microscopy (HAADF, STEM) and electron energy loss spectroscopy (EELS). XPS spectra revealed that Ru atoms were in mainly in Ru(4+) oxidation state, the Ti atoms in Ti(4+) oxidation state, whereas the Pt-atoms were in metallic state. TEM analysis proved that platinum nanoparticles nucleated at both oxide species and homogeneous distribution was observed. The average platinum nanoparticle size was 3.05 nm. Electrochemically active surface area of platinum was 32 m(2) g(-1). Kinetics of the oxygen reduction was studied at rotating disc electrode in 0.5 mol dm(-3) HClO4 solution, at 25 degrees C. The catalytic activities expressed in terms of specific activity (per electrochemically active surface area of platinum) and mass activity (per mass of platinum) were determined and compared to Pt catalyst on carbon support. The high catalytic activity was proven by electrochemical characterization.
PB  - Elsevier Science Sa, Lausanne
T2  - Journal of Electroanalytical Chemistry
T1  - Synthesis and characterization of Pt nanocatalyst on Ru0.7Ti0.3O2 support as a cathode for fuel cells application
EP  - 171
SP  - 164
VL  - 739
DO  - 10.1016/j.jelechem.2014.12.033
ER  - 

@article{
author = "Elezović, Nevenka R. and Ercius, P. and Kovac, Janez and Radmilović, Velimir R and Babić, Biljana M. and Krstajić, Nedeljko V",
year = "2015",
abstract = "Ruthenium oxide/titanium oxide, with a Ru:Ti atomic ratio of 7:3 was synthesized by modified sol-gel procedure and used as a support for platinum nanocatalyst for oxygen reduction reaction. The synthesized materials were characterized in terms of morphology, particle size distribution, chemical and phase composition by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), high angle annular dark filed scanning transmission electron microscopy (HAADF, STEM) and electron energy loss spectroscopy (EELS). XPS spectra revealed that Ru atoms were in mainly in Ru(4+) oxidation state, the Ti atoms in Ti(4+) oxidation state, whereas the Pt-atoms were in metallic state. TEM analysis proved that platinum nanoparticles nucleated at both oxide species and homogeneous distribution was observed. The average platinum nanoparticle size was 3.05 nm. Electrochemically active surface area of platinum was 32 m(2) g(-1). Kinetics of the oxygen reduction was studied at rotating disc electrode in 0.5 mol dm(-3) HClO4 solution, at 25 degrees C. The catalytic activities expressed in terms of specific activity (per electrochemically active surface area of platinum) and mass activity (per mass of platinum) were determined and compared to Pt catalyst on carbon support. The high catalytic activity was proven by electrochemical characterization.",
publisher = "Elsevier Science Sa, Lausanne",
journal = "Journal of Electroanalytical Chemistry",
title = "Synthesis and characterization of Pt nanocatalyst on Ru0.7Ti0.3O2 support as a cathode for fuel cells application",
pages = "171-164",
volume = "739",
doi = "10.1016/j.jelechem.2014.12.033"
}

Elezović, N. R., Ercius, P., Kovac, J., Radmilović, V. R., Babić, B. M.,& Krstajić, N. V.. (2015). Synthesis and characterization of Pt nanocatalyst on Ru0.7Ti0.3O2 support as a cathode for fuel cells application. in Journal of Electroanalytical Chemistry
Elsevier Science Sa, Lausanne., 739, 164-171.
https://doi.org/10.1016/j.jelechem.2014.12.033

Elezović NR, Ercius P, Kovac J, Radmilović VR, Babić BM, Krstajić NV. Synthesis and characterization of Pt nanocatalyst on Ru0.7Ti0.3O2 support as a cathode for fuel cells application. in Journal of Electroanalytical Chemistry. 2015;739:164-171.
doi:10.1016/j.jelechem.2014.12.033 .

Elezović, Nevenka R., Ercius, P., Kovac, Janez, Radmilović, Velimir R, Babić, Biljana M., Krstajić, Nedeljko V, "Synthesis and characterization of Pt nanocatalyst on Ru0.7Ti0.3O2 support as a cathode for fuel cells application" in Journal of Electroanalytical Chemistry, 739 (2015):164-171,
https://doi.org/10.1016/j.jelechem.2014.12.033 . .

TY  - JOUR
AU  - Jović, Borka M
AU  - Lačnjevac, Uroš
AU  - Jović, Vladimir D
AU  - Krstajić, Nedeljko V
PY  - 2015
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5765
AB  - In order to examine the intrinsic catalytic activity and durability of the electrodeposited NiSn alloy electrodes and the electrodeposited Ni as a reference electrode material for the oxygen evolution reaction (OER) in alkaline solutions, a comparative investigation was performed. A series of NiSn electrodes were prepared by electrodeposition of NiSn alloys at different current densities onto a Ni40 mesh substrate. The surface morphology and chemical composition were studied by scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS). The electrochemical surface characteristics were studied by cyclic voltammetry in order to find interdependence between the nickel oxyhydroxide surface electrochemistry and the activity of the electrode for the OER Quasi steady-state polarization measurements and electrochemical impedance spectroscopy (EIS) were used to determine kinetically significant parameters including the Tafel slopes and exchange current densities. Two well-defined Tafel slopes, the same for all investigated NiSn electrodes, were observed at the polarization curves, indicating that the OER was controlled by the same mechanism. It was demonstrated that any anodic polarization pretreatment led to a shift of the anodic and cathodic current peaks corresponding to the Ni(II)/Ni(III) redox transition towards cathodic potentials and, consequently, to some activation of the NiSn electrodes. The opposite behavior was obtained for the Ni electrode. Prolonged anodic polarization led to a loss of the initial catalytic activity of the Ni electrode, which was explained by the increase in the portion of gamma-NiOOH at the Ni electrode surface. Among the investigated NiSn electrodes, the NiSn100 electrode, prepared by electrodeposition at the highest cathodic current density of - 100 mAcm(-2), exhibited the highest apparent catalytic activity for the OER, entirely due to surface roughness effects. Despite the fact that the NiSn electrodes did not exhibit better intrinsic catalytic activity than Ni, their high stability during the OER and acceptable apparent activity made them promising anodes for alkaline water electrolysis.
PB  - Elsevier Science Sa, Lausanne
T2  - Journal of Electroanalytical Chemistry
T1  - Kinetics of the oxygen evolution reaction on NiSn electrodes in alkaline solutions
EP  - 108
SP  - 100
VL  - 754
DO  - 10.1016/j.jelechem.2015.07.013
ER  - 

@article{
author = "Jović, Borka M and Lačnjevac, Uroš and Jović, Vladimir D and Krstajić, Nedeljko V",
year = "2015",
abstract = "In order to examine the intrinsic catalytic activity and durability of the electrodeposited NiSn alloy electrodes and the electrodeposited Ni as a reference electrode material for the oxygen evolution reaction (OER) in alkaline solutions, a comparative investigation was performed. A series of NiSn electrodes were prepared by electrodeposition of NiSn alloys at different current densities onto a Ni40 mesh substrate. The surface morphology and chemical composition were studied by scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS). The electrochemical surface characteristics were studied by cyclic voltammetry in order to find interdependence between the nickel oxyhydroxide surface electrochemistry and the activity of the electrode for the OER Quasi steady-state polarization measurements and electrochemical impedance spectroscopy (EIS) were used to determine kinetically significant parameters including the Tafel slopes and exchange current densities. Two well-defined Tafel slopes, the same for all investigated NiSn electrodes, were observed at the polarization curves, indicating that the OER was controlled by the same mechanism. It was demonstrated that any anodic polarization pretreatment led to a shift of the anodic and cathodic current peaks corresponding to the Ni(II)/Ni(III) redox transition towards cathodic potentials and, consequently, to some activation of the NiSn electrodes. The opposite behavior was obtained for the Ni electrode. Prolonged anodic polarization led to a loss of the initial catalytic activity of the Ni electrode, which was explained by the increase in the portion of gamma-NiOOH at the Ni electrode surface. Among the investigated NiSn electrodes, the NiSn100 electrode, prepared by electrodeposition at the highest cathodic current density of - 100 mAcm(-2), exhibited the highest apparent catalytic activity for the OER, entirely due to surface roughness effects. Despite the fact that the NiSn electrodes did not exhibit better intrinsic catalytic activity than Ni, their high stability during the OER and acceptable apparent activity made them promising anodes for alkaline water electrolysis.",
publisher = "Elsevier Science Sa, Lausanne",
journal = "Journal of Electroanalytical Chemistry",
title = "Kinetics of the oxygen evolution reaction on NiSn electrodes in alkaline solutions",
pages = "108-100",
volume = "754",
doi = "10.1016/j.jelechem.2015.07.013"
}

Jović, B. M., Lačnjevac, U., Jović, V. D.,& Krstajić, N. V.. (2015). Kinetics of the oxygen evolution reaction on NiSn electrodes in alkaline solutions. in Journal of Electroanalytical Chemistry
Elsevier Science Sa, Lausanne., 754, 100-108.
https://doi.org/10.1016/j.jelechem.2015.07.013

Jović BM, Lačnjevac U, Jović VD, Krstajić NV. Kinetics of the oxygen evolution reaction on NiSn electrodes in alkaline solutions. in Journal of Electroanalytical Chemistry. 2015;754:100-108.
doi:10.1016/j.jelechem.2015.07.013 .

Jović, Borka M, Lačnjevac, Uroš, Jović, Vladimir D, Krstajić, Nedeljko V, "Kinetics of the oxygen evolution reaction on NiSn electrodes in alkaline solutions" in Journal of Electroanalytical Chemistry, 754 (2015):100-108,
https://doi.org/10.1016/j.jelechem.2015.07.013 . .

TY  - JOUR
AU  - Jović, Borka M
AU  - Lačnjevac, Uroš
AU  - Krstajić, Nedeljko V
AU  - Jović, Vladimir D
PY  - 2014
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5784
AB  - In this work the "service life test" (SLT) of the NiSn alloy coatings as cathodes for the hydrogen evolution reaction (HER), deposited onto Ni 40 mesh at different current densities from the bath containing 0.1 mol dm(-3) SnCl2 + 0.3 mol dm(-3) NiCl2 + 0.6 mol dm(-3) K4P2O7 + 0.3 mol dm(-3) NH2CH2COOH at 50 degrees C, was investigated and compared with that recorded for the commercial Ni-RuO2 De Nora's (DN) cathode. The morphology and chemical compositions of all NiSn samples were investigated by SEM and EDS techniques before and after the SLT. HER during the SLT has also been monitored by EIS technique. The chemical compositions of surfaces of all NiSn alloy samples, as well as EIS results, were found to depend on the number of cycles performed during the SLT. The decrease of their catalytic activity for the HER in 32 wt.% NaOH at 90 degrees C with increasing the number of cycles (about 20-25 mV after 25 cycles) was practically identical to that for DN cathode, while NiSn samples deposited at -30 mA cm(-2), -60 mA cm(-2) and -100 mA cm(-2) possessed lower overpotential for the HER before and after SLT in comparison with that for the DN cathode. It is confirmed by the SEM-EDS and EIS analysis of the NiSn samples that the minor loss of the catalytic activity for the HER is the consequence of the change of chemical composition of NiSn coatings and decrease of the active surface area. This decrease is ascribed to partially eroded NiSn coatings due to oxygen evolution during the SLT.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - International Journal of Hydrogen Energy
T1  - Service life test of the NiSn coatings as cathodes for hydrogen evolution in industrial chlor-alkali electrolysis
EP  - 8958
IS  - 17
SP  - 8947
VL  - 39
DO  - 10.1016/j.ijhydene.2014.04.015
ER  - 

@article{
author = "Jović, Borka M and Lačnjevac, Uroš and Krstajić, Nedeljko V and Jović, Vladimir D",
year = "2014",
abstract = "In this work the "service life test" (SLT) of the NiSn alloy coatings as cathodes for the hydrogen evolution reaction (HER), deposited onto Ni 40 mesh at different current densities from the bath containing 0.1 mol dm(-3) SnCl2 + 0.3 mol dm(-3) NiCl2 + 0.6 mol dm(-3) K4P2O7 + 0.3 mol dm(-3) NH2CH2COOH at 50 degrees C, was investigated and compared with that recorded for the commercial Ni-RuO2 De Nora's (DN) cathode. The morphology and chemical compositions of all NiSn samples were investigated by SEM and EDS techniques before and after the SLT. HER during the SLT has also been monitored by EIS technique. The chemical compositions of surfaces of all NiSn alloy samples, as well as EIS results, were found to depend on the number of cycles performed during the SLT. The decrease of their catalytic activity for the HER in 32 wt.% NaOH at 90 degrees C with increasing the number of cycles (about 20-25 mV after 25 cycles) was practically identical to that for DN cathode, while NiSn samples deposited at -30 mA cm(-2), -60 mA cm(-2) and -100 mA cm(-2) possessed lower overpotential for the HER before and after SLT in comparison with that for the DN cathode. It is confirmed by the SEM-EDS and EIS analysis of the NiSn samples that the minor loss of the catalytic activity for the HER is the consequence of the change of chemical composition of NiSn coatings and decrease of the active surface area. This decrease is ascribed to partially eroded NiSn coatings due to oxygen evolution during the SLT.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "International Journal of Hydrogen Energy",
title = "Service life test of the NiSn coatings as cathodes for hydrogen evolution in industrial chlor-alkali electrolysis",
pages = "8958-8947",
number = "17",
volume = "39",
doi = "10.1016/j.ijhydene.2014.04.015"
}

Jović, B. M., Lačnjevac, U., Krstajić, N. V.,& Jović, V. D.. (2014). Service life test of the NiSn coatings as cathodes for hydrogen evolution in industrial chlor-alkali electrolysis. in International Journal of Hydrogen Energy
Pergamon-Elsevier Science Ltd, Oxford., 39(17), 8947-8958.
https://doi.org/10.1016/j.ijhydene.2014.04.015

Jović BM, Lačnjevac U, Krstajić NV, Jović VD. Service life test of the NiSn coatings as cathodes for hydrogen evolution in industrial chlor-alkali electrolysis. in International Journal of Hydrogen Energy. 2014;39(17):8947-8958.
doi:10.1016/j.ijhydene.2014.04.015 .

Jović, Borka M, Lačnjevac, Uroš, Krstajić, Nedeljko V, Jović, Vladimir D, "Service life test of the NiSn coatings as cathodes for hydrogen evolution in industrial chlor-alkali electrolysis" in International Journal of Hydrogen Energy, 39, no. 17 (2014):8947-8958,
https://doi.org/10.1016/j.ijhydene.2014.04.015 . .

TY  - JOUR
AU  - Jović, Borka M
AU  - Lačnjevac, Uroš
AU  - Krstajić, Nedeljko V
AU  - Jović, Vladimir D
PY  - 2013
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5706
AB  - In this work the hydrogen evolution reaction (HER) at Ni-Sn alloy coatings, deposited onto Ni 40 mesh at different current densities from the bath containing 0.1 mol dm(-3) SnCl2 + 0.3 mol dm(-3) NiCl2 in the pyrophosphate-glycine solutions, was investigated by polarization and EIS measurements. The morphology and chemical compositions of all samples were investigated by the SEM and EDS techniques. It was shown that their morphologies and chemical compositions depend on the deposition current density. The increase of their catalytic activity for the HER in 6 mol dm(-3) KOH and in 1 mol dm(-3) NaOH with increasing the deposition current density was shown to be the consequence of the change of both: their chemical composition and morphology.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Electrochimica Acta
T1  - Ni-Sn coatings as cathodes for hydrogen evolution in alkaline solutions
EP  - 818
SP  - 813
VL  - 114
DO  - 10.1016/j.electacta.2013.06.024
ER  - 

@article{
author = "Jović, Borka M and Lačnjevac, Uroš and Krstajić, Nedeljko V and Jović, Vladimir D",
year = "2013",
abstract = "In this work the hydrogen evolution reaction (HER) at Ni-Sn alloy coatings, deposited onto Ni 40 mesh at different current densities from the bath containing 0.1 mol dm(-3) SnCl2 + 0.3 mol dm(-3) NiCl2 in the pyrophosphate-glycine solutions, was investigated by polarization and EIS measurements. The morphology and chemical compositions of all samples were investigated by the SEM and EDS techniques. It was shown that their morphologies and chemical compositions depend on the deposition current density. The increase of their catalytic activity for the HER in 6 mol dm(-3) KOH and in 1 mol dm(-3) NaOH with increasing the deposition current density was shown to be the consequence of the change of both: their chemical composition and morphology.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Electrochimica Acta",
title = "Ni-Sn coatings as cathodes for hydrogen evolution in alkaline solutions",
pages = "818-813",
volume = "114",
doi = "10.1016/j.electacta.2013.06.024"
}

Jović, B. M., Lačnjevac, U., Krstajić, N. V.,& Jović, V. D.. (2013). Ni-Sn coatings as cathodes for hydrogen evolution in alkaline solutions. in Electrochimica Acta
Pergamon-Elsevier Science Ltd, Oxford., 114, 813-818.
https://doi.org/10.1016/j.electacta.2013.06.024

Jović BM, Lačnjevac U, Krstajić NV, Jović VD. Ni-Sn coatings as cathodes for hydrogen evolution in alkaline solutions. in Electrochimica Acta. 2013;114:813-818.
doi:10.1016/j.electacta.2013.06.024 .

Jović, Borka M, Lačnjevac, Uroš, Krstajić, Nedeljko V, Jović, Vladimir D, "Ni-Sn coatings as cathodes for hydrogen evolution in alkaline solutions" in Electrochimica Acta, 114 (2013):813-818,
https://doi.org/10.1016/j.electacta.2013.06.024 . .

TY  - JOUR
AU  - Lačnjevac, Uroš
AU  - Jović, Borka M
AU  - Jović, Vladimir D
AU  - Radmilović, Velimir R
AU  - Krstajić, Nedeljko V
PY  - 2013
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5703
AB  - The hydrogen evolution reaction (HER) was studied on Ni, Ni-Ebonex and Ni-(Ebonex-Ru) coatings in 1 mol dm(-3) NaOH solution at 25 degrees C. The composite coatings were electro-deposited from a nickel Watts-type bath containing suspended Ebonex (chemical composition mainly Ti4O7) or Ebonex-supported Ru(10 wt.%) particles (0-10 g dm(-3)) onto Ni mesh substrate. The electrodes were investigated by cyclic voltammetry (CV), transmission electron microscopy (TEM) and scanning electron microscopy (SEM) in combination with energy dispersive X-ray spectroscopy (EDS) and electron energy loss spectroscopy (EELS), electrochemical impedance spectroscopy (EIS) and polarization measurements. These investigations showed that the roughness factor of the Ni-(Ebonex-Ru) and the Ni-Ebonex coating was 29 and 6 times higher than that of a pure Ni coating, respectively. In the whole potential range of the HER only one Tafel slope of about -120 mV was present at the polarization curves of Ni and Ni-Ebonex electrodes, with increased activity of the latter being attributed only to the increase of the electrochemically active surface area. The Ni(Ebonex-Ru) electrodes exhibited the highest intrinsic catalytic activity with two Tafel slopes, indicating also that the HER takes place exclusively. on Ru active sites.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - International Journal of Hydrogen Energy
T1  - Kinetics of the hydrogen evolution reaction on Ni-(Ebonex-supported Ru) composite coatings in alkaline solution
EP  - 10190
IS  - 25
SP  - 10178
VL  - 38
DO  - 10.1016/j.ijhydene.2013.06.037
ER  - 

@article{
author = "Lačnjevac, Uroš and Jović, Borka M and Jović, Vladimir D and Radmilović, Velimir R and Krstajić, Nedeljko V",
year = "2013",
abstract = "The hydrogen evolution reaction (HER) was studied on Ni, Ni-Ebonex and Ni-(Ebonex-Ru) coatings in 1 mol dm(-3) NaOH solution at 25 degrees C. The composite coatings were electro-deposited from a nickel Watts-type bath containing suspended Ebonex (chemical composition mainly Ti4O7) or Ebonex-supported Ru(10 wt.%) particles (0-10 g dm(-3)) onto Ni mesh substrate. The electrodes were investigated by cyclic voltammetry (CV), transmission electron microscopy (TEM) and scanning electron microscopy (SEM) in combination with energy dispersive X-ray spectroscopy (EDS) and electron energy loss spectroscopy (EELS), electrochemical impedance spectroscopy (EIS) and polarization measurements. These investigations showed that the roughness factor of the Ni-(Ebonex-Ru) and the Ni-Ebonex coating was 29 and 6 times higher than that of a pure Ni coating, respectively. In the whole potential range of the HER only one Tafel slope of about -120 mV was present at the polarization curves of Ni and Ni-Ebonex electrodes, with increased activity of the latter being attributed only to the increase of the electrochemically active surface area. The Ni(Ebonex-Ru) electrodes exhibited the highest intrinsic catalytic activity with two Tafel slopes, indicating also that the HER takes place exclusively. on Ru active sites.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "International Journal of Hydrogen Energy",
title = "Kinetics of the hydrogen evolution reaction on Ni-(Ebonex-supported Ru) composite coatings in alkaline solution",
pages = "10190-10178",
number = "25",
volume = "38",
doi = "10.1016/j.ijhydene.2013.06.037"
}

Lačnjevac, U., Jović, B. M., Jović, V. D., Radmilović, V. R.,& Krstajić, N. V.. (2013). Kinetics of the hydrogen evolution reaction on Ni-(Ebonex-supported Ru) composite coatings in alkaline solution. in International Journal of Hydrogen Energy
Pergamon-Elsevier Science Ltd, Oxford., 38(25), 10178-10190.
https://doi.org/10.1016/j.ijhydene.2013.06.037

Lačnjevac U, Jović BM, Jović VD, Radmilović VR, Krstajić NV. Kinetics of the hydrogen evolution reaction on Ni-(Ebonex-supported Ru) composite coatings in alkaline solution. in International Journal of Hydrogen Energy. 2013;38(25):10178-10190.
doi:10.1016/j.ijhydene.2013.06.037 .

Lačnjevac, Uroš, Jović, Borka M, Jović, Vladimir D, Radmilović, Velimir R, Krstajić, Nedeljko V, "Kinetics of the hydrogen evolution reaction on Ni-(Ebonex-supported Ru) composite coatings in alkaline solution" in International Journal of Hydrogen Energy, 38, no. 25 (2013):10178-10190,
https://doi.org/10.1016/j.ijhydene.2013.06.037 . .

TY  - JOUR
AU  - Jović, Vladimir D
AU  - Lačnjevac, Uroš
AU  - Jović, Borka M
AU  - Karanović, Ljiljana C.
AU  - Krstajić, Nedeljko V
PY  - 2012
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5718
AB  - In this work the hydrogen evolution reaction (HER) onto Ni-Sn alloy coatings deposited at different current densities from the bath containing 0.1 M Sn2+ and 0.1 M Ni2+ ions in the pyrophosphate-glycine solution, was investigated by polarization curves and electrochemical impedance spectroscopy (EIS) measurements. Their morphology and chemical composition were investigated by scanning electron microscopy equipped with an energy-dispersive X-ray spectroscopy (SEM-EDS), while the phase composition was investigated by X-ray powder diffraction (XRPD). It was shown that their chemical composition, phase composition and morphology depend on the deposition current density. In deposited samples all detected phases, face centered cubic (fcc) Ni, close packed (hcp) hexagonal Ni3Sn, hexagonal Ni(1-i-x)Sn (0  lt  x  lt  0.5) which adopts NiAs structure type and monoclinic Ni3Sn4 (CoSn structure type), were of low crystallinity. The increase of the Ni-Sn alloy coatings catalytic activity for HER in 6 M KOH with increasing the deposition current density was shown to be the consequence of the change of all three parameters: chemical composition, phase composition and morphology, with the effect of morphology being the most pronounced.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - International Journal of Hydrogen Energy
T1  - Ni-Sn coatings as cathodes for hydrogen evolution in alkaline solution. Chemical composition, phase composition and morphology effects
EP  - 17891
IS  - 23
SP  - 17882
VL  - 37
DO  - 10.1016/j.ijhydene.2012.09.110
ER  - 

@article{
author = "Jović, Vladimir D and Lačnjevac, Uroš and Jović, Borka M and Karanović, Ljiljana C. and Krstajić, Nedeljko V",
year = "2012",
abstract = "In this work the hydrogen evolution reaction (HER) onto Ni-Sn alloy coatings deposited at different current densities from the bath containing 0.1 M Sn2+ and 0.1 M Ni2+ ions in the pyrophosphate-glycine solution, was investigated by polarization curves and electrochemical impedance spectroscopy (EIS) measurements. Their morphology and chemical composition were investigated by scanning electron microscopy equipped with an energy-dispersive X-ray spectroscopy (SEM-EDS), while the phase composition was investigated by X-ray powder diffraction (XRPD). It was shown that their chemical composition, phase composition and morphology depend on the deposition current density. In deposited samples all detected phases, face centered cubic (fcc) Ni, close packed (hcp) hexagonal Ni3Sn, hexagonal Ni(1-i-x)Sn (0  lt  x  lt  0.5) which adopts NiAs structure type and monoclinic Ni3Sn4 (CoSn structure type), were of low crystallinity. The increase of the Ni-Sn alloy coatings catalytic activity for HER in 6 M KOH with increasing the deposition current density was shown to be the consequence of the change of all three parameters: chemical composition, phase composition and morphology, with the effect of morphology being the most pronounced.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "International Journal of Hydrogen Energy",
title = "Ni-Sn coatings as cathodes for hydrogen evolution in alkaline solution. Chemical composition, phase composition and morphology effects",
pages = "17891-17882",
number = "23",
volume = "37",
doi = "10.1016/j.ijhydene.2012.09.110"
}

Jović, V. D., Lačnjevac, U., Jović, B. M., Karanović, L. C.,& Krstajić, N. V.. (2012). Ni-Sn coatings as cathodes for hydrogen evolution in alkaline solution. Chemical composition, phase composition and morphology effects. in International Journal of Hydrogen Energy
Pergamon-Elsevier Science Ltd, Oxford., 37(23), 17882-17891.
https://doi.org/10.1016/j.ijhydene.2012.09.110

Jović VD, Lačnjevac U, Jović BM, Karanović LC, Krstajić NV. Ni-Sn coatings as cathodes for hydrogen evolution in alkaline solution. Chemical composition, phase composition and morphology effects. in International Journal of Hydrogen Energy. 2012;37(23):17882-17891.
doi:10.1016/j.ijhydene.2012.09.110 .

Jović, Vladimir D, Lačnjevac, Uroš, Jović, Borka M, Karanović, Ljiljana C., Krstajić, Nedeljko V, "Ni-Sn coatings as cathodes for hydrogen evolution in alkaline solution. Chemical composition, phase composition and morphology effects" in International Journal of Hydrogen Energy, 37, no. 23 (2012):17882-17891,
https://doi.org/10.1016/j.ijhydene.2012.09.110 . .

TY  - JOUR
AU  - Jović, Vladimir D
AU  - Lačnjevac, Uroš
AU  - Jović, Borka M
AU  - Krstajić, Nedeljko V
PY  - 2012
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5738
AB  - In this work polarization characteristics and "service life" test of the non-noble metal composite coatings Ni-MoOx and Ni-MoO2 for hydrogen evolution reaction (HER) in 32 wt.% NaOH at 90 degrees C were investigated and compared with that recorded for De Nora's commercial Ni + RuO2 cathode coating (DN). It was shown that under conditions of industrial application in the "zero-gap" membrane cells the lowest over-voltage for HER has been recorded for the Ni-MoO2 coating. At the same time the "service life" test was performed on all three electrodes in the same solution. This test was based on monitoring the current density response before and after repetitive cycling of these electrodes with 50 mV s(-1) in the potential range from hydrogen (-1.25 V vs. SCE) to oxygen (0.50 V vs. SCE) evolution. It was shown that the activity for all electrodes at the end of a "service life" test dropped to approximately 54% of the initial value, being comparable with the results obtained for Pt-based cathodes. The SEM-EDS analysis of the electrodes after the "service life" test showed that the Ni-MoO2 is much more stable than the Ni-MoOx composite coating and could be promising replacement for the commercial cathode.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Electrochimica Acta
T1  - Service life test of non-noble metal composite cathodes for hydrogen evolution in sodium hydroxide solution
EP  - 130
SP  - 124
VL  - 63
DO  - 10.1016/j.electacta.2011.12.078
ER  - 

@article{
author = "Jović, Vladimir D and Lačnjevac, Uroš and Jović, Borka M and Krstajić, Nedeljko V",
year = "2012",
abstract = "In this work polarization characteristics and "service life" test of the non-noble metal composite coatings Ni-MoOx and Ni-MoO2 for hydrogen evolution reaction (HER) in 32 wt.% NaOH at 90 degrees C were investigated and compared with that recorded for De Nora's commercial Ni + RuO2 cathode coating (DN). It was shown that under conditions of industrial application in the "zero-gap" membrane cells the lowest over-voltage for HER has been recorded for the Ni-MoO2 coating. At the same time the "service life" test was performed on all three electrodes in the same solution. This test was based on monitoring the current density response before and after repetitive cycling of these electrodes with 50 mV s(-1) in the potential range from hydrogen (-1.25 V vs. SCE) to oxygen (0.50 V vs. SCE) evolution. It was shown that the activity for all electrodes at the end of a "service life" test dropped to approximately 54% of the initial value, being comparable with the results obtained for Pt-based cathodes. The SEM-EDS analysis of the electrodes after the "service life" test showed that the Ni-MoO2 is much more stable than the Ni-MoOx composite coating and could be promising replacement for the commercial cathode.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Electrochimica Acta",
title = "Service life test of non-noble metal composite cathodes for hydrogen evolution in sodium hydroxide solution",
pages = "130-124",
volume = "63",
doi = "10.1016/j.electacta.2011.12.078"
}

Jović, V. D., Lačnjevac, U., Jović, B. M.,& Krstajić, N. V.. (2012). Service life test of non-noble metal composite cathodes for hydrogen evolution in sodium hydroxide solution. in Electrochimica Acta
Pergamon-Elsevier Science Ltd, Oxford., 63, 124-130.
https://doi.org/10.1016/j.electacta.2011.12.078

Jović VD, Lačnjevac U, Jović BM, Krstajić NV. Service life test of non-noble metal composite cathodes for hydrogen evolution in sodium hydroxide solution. in Electrochimica Acta. 2012;63:124-130.
doi:10.1016/j.electacta.2011.12.078 .

Jović, Vladimir D, Lačnjevac, Uroš, Jović, Borka M, Krstajić, Nedeljko V, "Service life test of non-noble metal composite cathodes for hydrogen evolution in sodium hydroxide solution" in Electrochimica Acta, 63 (2012):124-130,
https://doi.org/10.1016/j.electacta.2011.12.078 . .

TY  - JOUR
AU  - Lačnjevac, Uroš
AU  - Jović, Borka M
AU  - Jović, Vladimir D
AU  - Krstajić, Nedeljko V
PY  - 2012
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5680
AB  - As a result of research on the non-noble metal-based composite electrocatalysts for the hydrogen evolution reaction (HER), the Ni-MoO2 composite coating was produced by electrodeposition from an NH4Cl and NiCl2 containing solution with suspended MoO2 powder particles, exhibiting almost the identical activity for the HER as the commercial cathode in conditions of industrial application and satisfactory mechanical stability. In this work, investigations were extended to the kinetics and mechanism of the HER on the Ni-MoO2 electrode in 8 M NaOH solution at 30 degrees C. The steady-state polarization curve for the HER was characterized by only one Tafel slope of -122 mV/dec. Kinetic parameters for the HER, as well as a contribution of surface roughness to the catalytic activity, were evaluated using an electrochemical impedance spectroscopy (EIS) technique. On the basis of the presented theoretical model for the faradaic impedance of the HER, the rate constants of the individual steps were determined by simulating both polarization and EIS experimental data. It was found that the reaction equally proceeds via the Volmer-Heyrovsky and Volmer-Tafel routes at lower overpotentials, while at higher overpotentials the Volmer-Heyrovsky pathway dominates the process with the Heyrovsky step being the rate determining step (rds). A comparison of intrinsic activities of the Ni-MoO2 composite and a flat Ni electrode proved that the combination of Ni and MoO2 produced a true catalytic effect for the HER.
PB  - Elsevier Science Sa, Lausanne
T2  - Journal of Electroanalytical Chemistry
T1  - Determination of kinetic parameters for the hydrogen evolution reaction on the electrodeposited Ni-MoO2 composite coating in alkaline solution
EP  - 40
SP  - 31
VL  - 677
DO  - 10.1016/j.jelechem.2012.05.004
ER  - 

@article{
author = "Lačnjevac, Uroš and Jović, Borka M and Jović, Vladimir D and Krstajić, Nedeljko V",
year = "2012",
abstract = "As a result of research on the non-noble metal-based composite electrocatalysts for the hydrogen evolution reaction (HER), the Ni-MoO2 composite coating was produced by electrodeposition from an NH4Cl and NiCl2 containing solution with suspended MoO2 powder particles, exhibiting almost the identical activity for the HER as the commercial cathode in conditions of industrial application and satisfactory mechanical stability. In this work, investigations were extended to the kinetics and mechanism of the HER on the Ni-MoO2 electrode in 8 M NaOH solution at 30 degrees C. The steady-state polarization curve for the HER was characterized by only one Tafel slope of -122 mV/dec. Kinetic parameters for the HER, as well as a contribution of surface roughness to the catalytic activity, were evaluated using an electrochemical impedance spectroscopy (EIS) technique. On the basis of the presented theoretical model for the faradaic impedance of the HER, the rate constants of the individual steps were determined by simulating both polarization and EIS experimental data. It was found that the reaction equally proceeds via the Volmer-Heyrovsky and Volmer-Tafel routes at lower overpotentials, while at higher overpotentials the Volmer-Heyrovsky pathway dominates the process with the Heyrovsky step being the rate determining step (rds). A comparison of intrinsic activities of the Ni-MoO2 composite and a flat Ni electrode proved that the combination of Ni and MoO2 produced a true catalytic effect for the HER.",
publisher = "Elsevier Science Sa, Lausanne",
journal = "Journal of Electroanalytical Chemistry",
title = "Determination of kinetic parameters for the hydrogen evolution reaction on the electrodeposited Ni-MoO2 composite coating in alkaline solution",
pages = "40-31",
volume = "677",
doi = "10.1016/j.jelechem.2012.05.004"
}

Lačnjevac, U., Jović, B. M., Jović, V. D.,& Krstajić, N. V.. (2012). Determination of kinetic parameters for the hydrogen evolution reaction on the electrodeposited Ni-MoO2 composite coating in alkaline solution. in Journal of Electroanalytical Chemistry
Elsevier Science Sa, Lausanne., 677, 31-40.
https://doi.org/10.1016/j.jelechem.2012.05.004

Lačnjevac U, Jović BM, Jović VD, Krstajić NV. Determination of kinetic parameters for the hydrogen evolution reaction on the electrodeposited Ni-MoO2 composite coating in alkaline solution. in Journal of Electroanalytical Chemistry. 2012;677:31-40.
doi:10.1016/j.jelechem.2012.05.004 .

Lačnjevac, Uroš, Jović, Borka M, Jović, Vladimir D, Krstajić, Nedeljko V, "Determination of kinetic parameters for the hydrogen evolution reaction on the electrodeposited Ni-MoO2 composite coating in alkaline solution" in Journal of Electroanalytical Chemistry, 677 (2012):31-40,
https://doi.org/10.1016/j.jelechem.2012.05.004 . .

TY  - JOUR
AU  - Krstajić, Nedeljko V
AU  - Lačnjevac, Uroš
AU  - Jović, Borka M
AU  - Mora, S
AU  - Jović, Vladimir D
PY  - 2011
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5647
AB  - In this work the procedure of the deposition of composite Ni-MoO2 coatings onto Ni mesh from the nickel chloride-ammonium chloride electrolyte containing suspended MoO2 powder particles, under simulated industrial deposition conditions for commercial cathodes, has been presented. The morphology of the obtained coatings was investigated by SEM, the composition by EDS and the phase composition by XRD techniques. The polarization characteristics for hydrogen evolution on the obtained Ni-MoO2 coatings were investigated in the 32 wt.% NaOH at 90 degrees C and compared with the one recorded for the commercial De Nora's coating (DN). It was shown that the best Ni-MoO2 coating posses identical polarization characteristics as the commercial one. By the cross section and XRD analysis of deposited samples it was confirmed that MoO2 powder particles were occluded by the Ni deposit, being uniformly distributed in the deposit.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - International Journal of Hydrogen Energy
T1  - Non-noble metal composite cathodes for hydrogen evolution. Part II: The Ni-MoO2 coatings electrodeposited from nickel chloride-ammonium chloride bath containing MoO2 powder particles
EP  - 6461
IS  - 11
SP  - 6450
VL  - 36
DO  - 10.1016/j.ijhydene.2011.02.106
ER  - 

@article{
author = "Krstajić, Nedeljko V and Lačnjevac, Uroš and Jović, Borka M and Mora, S and Jović, Vladimir D",
year = "2011",
abstract = "In this work the procedure of the deposition of composite Ni-MoO2 coatings onto Ni mesh from the nickel chloride-ammonium chloride electrolyte containing suspended MoO2 powder particles, under simulated industrial deposition conditions for commercial cathodes, has been presented. The morphology of the obtained coatings was investigated by SEM, the composition by EDS and the phase composition by XRD techniques. The polarization characteristics for hydrogen evolution on the obtained Ni-MoO2 coatings were investigated in the 32 wt.% NaOH at 90 degrees C and compared with the one recorded for the commercial De Nora's coating (DN). It was shown that the best Ni-MoO2 coating posses identical polarization characteristics as the commercial one. By the cross section and XRD analysis of deposited samples it was confirmed that MoO2 powder particles were occluded by the Ni deposit, being uniformly distributed in the deposit.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "International Journal of Hydrogen Energy",
title = "Non-noble metal composite cathodes for hydrogen evolution. Part II: The Ni-MoO2 coatings electrodeposited from nickel chloride-ammonium chloride bath containing MoO2 powder particles",
pages = "6461-6450",
number = "11",
volume = "36",
doi = "10.1016/j.ijhydene.2011.02.106"
}

Krstajić, N. V., Lačnjevac, U., Jović, B. M., Mora, S.,& Jović, V. D.. (2011). Non-noble metal composite cathodes for hydrogen evolution. Part II: The Ni-MoO2 coatings electrodeposited from nickel chloride-ammonium chloride bath containing MoO2 powder particles. in International Journal of Hydrogen Energy
Pergamon-Elsevier Science Ltd, Oxford., 36(11), 6450-6461.
https://doi.org/10.1016/j.ijhydene.2011.02.106

Krstajić NV, Lačnjevac U, Jović BM, Mora S, Jović VD. Non-noble metal composite cathodes for hydrogen evolution. Part II: The Ni-MoO2 coatings electrodeposited from nickel chloride-ammonium chloride bath containing MoO2 powder particles. in International Journal of Hydrogen Energy. 2011;36(11):6450-6461.
doi:10.1016/j.ijhydene.2011.02.106 .

Krstajić, Nedeljko V, Lačnjevac, Uroš, Jović, Borka M, Mora, S, Jović, Vladimir D, "Non-noble metal composite cathodes for hydrogen evolution. Part II: The Ni-MoO2 coatings electrodeposited from nickel chloride-ammonium chloride bath containing MoO2 powder particles" in International Journal of Hydrogen Energy, 36, no. 11 (2011):6450-6461,
https://doi.org/10.1016/j.ijhydene.2011.02.106 . .

TY  - JOUR
AU  - Elezović, Nevenka R.
AU  - Babić, Biljana M.
AU  - Radmilović, Velimir R
AU  - Vračar, Ljiljana M
AU  - Krstajić, Nedeljko V
PY  - 2011
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5645
AB  - Platinum based nanocatalyst at home made Nb-TiO2 support was synthesized and characterized as the catalyst for oxygen reduction reaction in 0.1 mol dm(-3) NaOH, at 25 degrees C. Nb doped TiO2 catalyst support, containing 5% of Nb, has been synthesized by modified acid-catalyzed sol-gel procedure in non-aqueous medium. BET and X-ray diffraction (XRD) techniques were applied for characterization of synthesized supporting material. XRD analysis revealed only presence of anatase TiO2 phase in synthesized support powder. Existence of any peaks belonging to Nb compounds has not been observed, indicating Nb incorporated into the lattice. Nb-TiO2 supported Pt nanocatalyst synthesized, using borohydride reduction method, was characterized by TEM and HRTEM techniques. Platinum nanoparticles distribution, over Nb doped TiO2 support, was quite homogenous. Mean particle size of about 4 nm was found with no pronounced particle agglomeration. Electrochemical techniques: cyclic voltammetry and linear sweep voltammetry at rotating disc electrode were applied in order to study kinetics and estimate catalytic activity of this new catalyst for the oxygen reduction reaction in alkaline solution. Two different Tafel slopes were found: one close to -90 mV dec(-1) in low current density region and other approximately 200 my dec(-1) in high current density region, which is in good accordance with literature results for oxygen reduction at Pt single crystals, as well as Pt nanocatalysts in alkaline solutions. Similar specific catalytic activity (expressed in term of kinetic current density per real surface area) of Nb(5%)-TiO2/Pt catalyst for oxygen reduction reaction in comparison with the carbon supported platinum (Vulcan/Pt) nanocatalyst, was found.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Electrochimica Acta
T1  - Nb-TiO2 supported platinum nanocatalyst for oxygen reduction reaction in alkaline solutions
EP  - 9026
IS  - 25
SP  - 9020
VL  - 56
DO  - 10.1016/j.electacta.2011.04.075
ER  - 

@article{
author = "Elezović, Nevenka R. and Babić, Biljana M. and Radmilović, Velimir R and Vračar, Ljiljana M and Krstajić, Nedeljko V",
year = "2011",
abstract = "Platinum based nanocatalyst at home made Nb-TiO2 support was synthesized and characterized as the catalyst for oxygen reduction reaction in 0.1 mol dm(-3) NaOH, at 25 degrees C. Nb doped TiO2 catalyst support, containing 5% of Nb, has been synthesized by modified acid-catalyzed sol-gel procedure in non-aqueous medium. BET and X-ray diffraction (XRD) techniques were applied for characterization of synthesized supporting material. XRD analysis revealed only presence of anatase TiO2 phase in synthesized support powder. Existence of any peaks belonging to Nb compounds has not been observed, indicating Nb incorporated into the lattice. Nb-TiO2 supported Pt nanocatalyst synthesized, using borohydride reduction method, was characterized by TEM and HRTEM techniques. Platinum nanoparticles distribution, over Nb doped TiO2 support, was quite homogenous. Mean particle size of about 4 nm was found with no pronounced particle agglomeration. Electrochemical techniques: cyclic voltammetry and linear sweep voltammetry at rotating disc electrode were applied in order to study kinetics and estimate catalytic activity of this new catalyst for the oxygen reduction reaction in alkaline solution. Two different Tafel slopes were found: one close to -90 mV dec(-1) in low current density region and other approximately 200 my dec(-1) in high current density region, which is in good accordance with literature results for oxygen reduction at Pt single crystals, as well as Pt nanocatalysts in alkaline solutions. Similar specific catalytic activity (expressed in term of kinetic current density per real surface area) of Nb(5%)-TiO2/Pt catalyst for oxygen reduction reaction in comparison with the carbon supported platinum (Vulcan/Pt) nanocatalyst, was found.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Electrochimica Acta",
title = "Nb-TiO2 supported platinum nanocatalyst for oxygen reduction reaction in alkaline solutions",
pages = "9026-9020",
number = "25",
volume = "56",
doi = "10.1016/j.electacta.2011.04.075"
}

Elezović, N. R., Babić, B. M., Radmilović, V. R., Vračar, L. M.,& Krstajić, N. V.. (2011). Nb-TiO2 supported platinum nanocatalyst for oxygen reduction reaction in alkaline solutions. in Electrochimica Acta
Pergamon-Elsevier Science Ltd, Oxford., 56(25), 9020-9026.
https://doi.org/10.1016/j.electacta.2011.04.075

Elezović NR, Babić BM, Radmilović VR, Vračar LM, Krstajić NV. Nb-TiO2 supported platinum nanocatalyst for oxygen reduction reaction in alkaline solutions. in Electrochimica Acta. 2011;56(25):9020-9026.
doi:10.1016/j.electacta.2011.04.075 .

Elezović, Nevenka R., Babić, Biljana M., Radmilović, Velimir R, Vračar, Ljiljana M, Krstajić, Nedeljko V, "Nb-TiO2 supported platinum nanocatalyst for oxygen reduction reaction in alkaline solutions" in Electrochimica Acta, 56, no. 25 (2011):9020-9026,
https://doi.org/10.1016/j.electacta.2011.04.075 . .