Obradović, Maja D.

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Palladium-copper bimetallic surfaces as electrocatalysts for the ethanol oxidation in an alkaline medium

Obradović, Maja D.; Lačnjevac, Uroš Č.; Radmilović, Vuk V.; Gavrilović-Wohlmuther, Aleksandra; Kovač, Janez; Rogan, Jelena R.; Radmilović, Velimir R.; Gojković, Snežana Lj.

(Elsevier B.V., 2023)

TY  - JOUR
AU  - Obradović, Maja D.
AU  - Lačnjevac, Uroš Č.
AU  - Radmilović, Vuk V.
AU  - Gavrilović-Wohlmuther, Aleksandra
AU  - Kovač, Janez
AU  - Rogan, Jelena R.
AU  - Radmilović, Velimir R.
AU  - Gojković, Snežana Lj.
PY  - 2023
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/6587
AB  - Two types of Cu-modified Pd catalysts supported on high area carbon were prepared: Pd nanoparticles modified with a sub-monolayer of underpotentially deposited Cu (Cu@Pd/C) and Pd-Cu alloy nanoparticles (Pd-Cu/C), and examined for the ethanol oxidation reaction (EOR) in alkaline solution. The catalysts were characterized by energy-dispersive X-ray spectroscopy, X-ray diffraction, transmission electron microscopy and X-ray photoelectron spectroscopy, as well as cyclic voltammetry. As reference catalysts, Pd/C and Pt/C were used. The electrochemically active surface area of all samples was determined from COads and Cuupd desorption and Pd oxide reduction, and used to assess their intrinsic activity for EOR. Intimate contact of Pd with Cu atoms enhanced its activity, regardless of the type of bimetal catalyst. The atomic Pd:Cu ratio between 2:1 and 4:1 appears to be optimal for high activity. The most active catalyst under the potentiodynamic conditions was Cu@Pd/C with θ(Cu) = 0.21,although Pd-Cu/C was superior during the potentiostatic test. All bimetallic catalysts surpassed Pd/C in mass activity. The EOR activity of Pt/C was higher compared to Pd-based catalysts at low potentials, both in terms of specific and mass activity, but with a significant decline over a 30-min potentiostatic stability test.
PB  - Elsevier B.V.
T2  - Journal of Electroanalytical Chemistry
T1  - Palladium-copper bimetallic surfaces as electrocatalysts for the ethanol oxidation in an alkaline medium
SP  - 117673
VL  - 944
DO  - 10.1016/j.jelechem.2023.117673
ER  - 
@article{
author = "Obradović, Maja D. and Lačnjevac, Uroš Č. and Radmilović, Vuk V. and Gavrilović-Wohlmuther, Aleksandra and Kovač, Janez and Rogan, Jelena R. and Radmilović, Velimir R. and Gojković, Snežana Lj.",
year = "2023",
abstract = "Two types of Cu-modified Pd catalysts supported on high area carbon were prepared: Pd nanoparticles modified with a sub-monolayer of underpotentially deposited Cu (Cu@Pd/C) and Pd-Cu alloy nanoparticles (Pd-Cu/C), and examined for the ethanol oxidation reaction (EOR) in alkaline solution. The catalysts were characterized by energy-dispersive X-ray spectroscopy, X-ray diffraction, transmission electron microscopy and X-ray photoelectron spectroscopy, as well as cyclic voltammetry. As reference catalysts, Pd/C and Pt/C were used. The electrochemically active surface area of all samples was determined from COads and Cuupd desorption and Pd oxide reduction, and used to assess their intrinsic activity for EOR. Intimate contact of Pd with Cu atoms enhanced its activity, regardless of the type of bimetal catalyst. The atomic Pd:Cu ratio between 2:1 and 4:1 appears to be optimal for high activity. The most active catalyst under the potentiodynamic conditions was Cu@Pd/C with θ(Cu) = 0.21,although Pd-Cu/C was superior during the potentiostatic test. All bimetallic catalysts surpassed Pd/C in mass activity. The EOR activity of Pt/C was higher compared to Pd-based catalysts at low potentials, both in terms of specific and mass activity, but with a significant decline over a 30-min potentiostatic stability test.",
publisher = "Elsevier B.V.",
journal = "Journal of Electroanalytical Chemistry",
title = "Palladium-copper bimetallic surfaces as electrocatalysts for the ethanol oxidation in an alkaline medium",
pages = "117673",
volume = "944",
doi = "10.1016/j.jelechem.2023.117673"
}
Obradović, M. D., Lačnjevac, U. Č., Radmilović, V. V., Gavrilović-Wohlmuther, A., Kovač, J., Rogan, J. R., Radmilović, V. R.,& Gojković, S. Lj.. (2023). Palladium-copper bimetallic surfaces as electrocatalysts for the ethanol oxidation in an alkaline medium. in Journal of Electroanalytical Chemistry
Elsevier B.V.., 944, 117673.
https://doi.org/10.1016/j.jelechem.2023.117673
Obradović MD, Lačnjevac UČ, Radmilović VV, Gavrilović-Wohlmuther A, Kovač J, Rogan JR, Radmilović VR, Gojković SL. Palladium-copper bimetallic surfaces as electrocatalysts for the ethanol oxidation in an alkaline medium. in Journal of Electroanalytical Chemistry. 2023;944:117673.
doi:10.1016/j.jelechem.2023.117673 .
Obradović, Maja D., Lačnjevac, Uroš Č., Radmilović, Vuk V., Gavrilović-Wohlmuther, Aleksandra, Kovač, Janez, Rogan, Jelena R., Radmilović, Velimir R., Gojković, Snežana Lj., "Palladium-copper bimetallic surfaces as electrocatalysts for the ethanol oxidation in an alkaline medium" in Journal of Electroanalytical Chemistry, 944 (2023):117673,
https://doi.org/10.1016/j.jelechem.2023.117673 . .
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Challenges in determining the electrochemically active surface area of Ni-oxides in the oxygen evolution reaction

Obradović, Maja D.; Gojković, Snežana Lj.

(Elsevier B.V., 2022)

TY  - JOUR
AU  - Obradović, Maja D.
AU  - Gojković, Snežana Lj.
PY  - 2022
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5154
AB  - Thin films of Ni-oxy-hydroxides of different composition and thickness were electrochemically grown on Ni foil electrode: hydrated α-phase, anhydrous β-phase, and two mixed α- and β-phase electrodeposited by potential cycling. The characterization of bare Ni and the deposited films by cycling voltammetry (CV) and electrochemical impedance spectroscopy (EIS) provided data of the initial electrochemically active surface area (ECSA), an amount of Ni-active oxide species, double-layer capacitance, ionic adsorption capacitance and the adsorption pseudocapacitance in the oxygen evolution reaction (OER) potential range. Ni-oxy-hydroxide films were deposited with loading up to 18 monolayers or 25 nmol cm−2. The specific pseudocapacitance was calculated from a linear correlation of the capacitance and the film thickness. Steady-state polarization curves of OER were presented as specific activity obtained by normalization of the currents by ECSA derived from the maximum adsorption pseudocapacitance. Also, polarization curves were given as turnover frequency calculated from the amount of Ni-active oxide species derived from CV. Both method of evaluation of intrinsic activity of Ni-oxy-hydroxide films towards OER gave consistent results and can be used to compare the activity of similar Ni-oxide catalysts.
PB  - Elsevier B.V.
T2  - Journal of Electroanalytical Chemistry
T1  - Challenges in determining the electrochemically active surface area of Ni-oxides in the oxygen evolution reaction
SP  - 116479
VL  - 918
DO  - 10.1016/j.jelechem.2022.116479
ER  - 
@article{
author = "Obradović, Maja D. and Gojković, Snežana Lj.",
year = "2022",
abstract = "Thin films of Ni-oxy-hydroxides of different composition and thickness were electrochemically grown on Ni foil electrode: hydrated α-phase, anhydrous β-phase, and two mixed α- and β-phase electrodeposited by potential cycling. The characterization of bare Ni and the deposited films by cycling voltammetry (CV) and electrochemical impedance spectroscopy (EIS) provided data of the initial electrochemically active surface area (ECSA), an amount of Ni-active oxide species, double-layer capacitance, ionic adsorption capacitance and the adsorption pseudocapacitance in the oxygen evolution reaction (OER) potential range. Ni-oxy-hydroxide films were deposited with loading up to 18 monolayers or 25 nmol cm−2. The specific pseudocapacitance was calculated from a linear correlation of the capacitance and the film thickness. Steady-state polarization curves of OER were presented as specific activity obtained by normalization of the currents by ECSA derived from the maximum adsorption pseudocapacitance. Also, polarization curves were given as turnover frequency calculated from the amount of Ni-active oxide species derived from CV. Both method of evaluation of intrinsic activity of Ni-oxy-hydroxide films towards OER gave consistent results and can be used to compare the activity of similar Ni-oxide catalysts.",
publisher = "Elsevier B.V.",
journal = "Journal of Electroanalytical Chemistry",
title = "Challenges in determining the electrochemically active surface area of Ni-oxides in the oxygen evolution reaction",
pages = "116479",
volume = "918",
doi = "10.1016/j.jelechem.2022.116479"
}
Obradović, M. D.,& Gojković, S. Lj.. (2022). Challenges in determining the electrochemically active surface area of Ni-oxides in the oxygen evolution reaction. in Journal of Electroanalytical Chemistry
Elsevier B.V.., 918, 116479.
https://doi.org/10.1016/j.jelechem.2022.116479
Obradović MD, Gojković SL. Challenges in determining the electrochemically active surface area of Ni-oxides in the oxygen evolution reaction. in Journal of Electroanalytical Chemistry. 2022;918:116479.
doi:10.1016/j.jelechem.2022.116479 .
Obradović, Maja D., Gojković, Snežana Lj., "Challenges in determining the electrochemically active surface area of Ni-oxides in the oxygen evolution reaction" in Journal of Electroanalytical Chemistry, 918 (2022):116479,
https://doi.org/10.1016/j.jelechem.2022.116479 . .
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