Petričević, Aleksandar M.

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orcid::0000-0001-5954-3569
  • Petričević, Aleksandar M. (2)
  • Petričević, Aleksandar (1)
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Author's Bibliography

Correct determination of the hydrogen evolution reaction parameters at Ni foam electrode modified by electrodeposited Ni-Sn alloy layer

Gojgić, Jelena D.; Petričević, Aleksandar M.; Krstajić Pajić, Mila N.; Jović, Vladimir D.

(Inženjersko društvo za koroziju, 2024)

TY  - JOUR
AU  - Gojgić, Jelena D.
AU  - Petričević, Aleksandar M.
AU  - Krstajić Pajić, Mila N.
AU  - Jović, Vladimir D.
PY  - 2024
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/7409
AB  - The example of the procedure for the correct determination of the parameters of hydrogen evolution reaction (HER), the exchange current density (jo) and relaxation time (τo) for intermediate (adsorbed hydrogen, Hads) adsorption at modified porous Ni-based electrode are presented in this work. Such a procedure is applicable for the HER at all electrode materials. The value of jo was obtained from the intercept at η = 0 mV from the η vs. log (Rct-1) dependence (η-overpotential), while the value of τo was obtained from the intercept at η = 0 mV from the logτ vs. η dependence. It was shown that for the correct determination of jo and τo, it is necessary to correct applied η for the jRs drop, by recording current density (j) for applied η and correcting it for jRs.
AB  - Na primeru izdvajanja vodonika na Ni-Sn/Ni pena 800 elektrodi u ovom radu je prikazana procedura korektnog određivanja parametara ove reakcije, a to su: gustina struje izmene (jo) i relaksaciono vreme adsorpcije intermedijara () (Hads). Vrednost jo je određena iz odsečka za  = 0 mV zavisnosti  vs. log(Rct-1 ) ( - prenapetost), dok je vrednost o određena iz odsečka za  = 0 mV zavisnosti log vs. . Pokazano je da je za korektno određivanje ovih parametara neophodno korigovati gustinu struje pri svakoj zadatoj prenapetosti za vrednost omskog pada napona jRs.
PB  - Inženjersko društvo za koroziju
T2  - Zaštita materijala
T1  - Correct determination of the hydrogen evolution reaction parameters at Ni foam electrode modified by electrodeposited Ni-Sn alloy layer
T1  - Procedura korektnog određivanja parametara reakcije izdvajanja vodonika na elektrodi od Ni pene modifikovane elektrohemijski istaloženom Ni-Sn legurom
EP  - 10
IS  - 1
SP  - 3
VL  - 65
DO  - 10.62638/zasmat1039
ER  - 
@article{
author = "Gojgić, Jelena D. and Petričević, Aleksandar M. and Krstajić Pajić, Mila N. and Jović, Vladimir D.",
year = "2024",
abstract = "The example of the procedure for the correct determination of the parameters of hydrogen evolution reaction (HER), the exchange current density (jo) and relaxation time (τo) for intermediate (adsorbed hydrogen, Hads) adsorption at modified porous Ni-based electrode are presented in this work. Such a procedure is applicable for the HER at all electrode materials. The value of jo was obtained from the intercept at η = 0 mV from the η vs. log (Rct-1) dependence (η-overpotential), while the value of τo was obtained from the intercept at η = 0 mV from the logτ vs. η dependence. It was shown that for the correct determination of jo and τo, it is necessary to correct applied η for the jRs drop, by recording current density (j) for applied η and correcting it for jRs., Na primeru izdvajanja vodonika na Ni-Sn/Ni pena 800 elektrodi u ovom radu je prikazana procedura korektnog određivanja parametara ove reakcije, a to su: gustina struje izmene (jo) i relaksaciono vreme adsorpcije intermedijara () (Hads). Vrednost jo je određena iz odsečka za  = 0 mV zavisnosti  vs. log(Rct-1 ) ( - prenapetost), dok je vrednost o određena iz odsečka za  = 0 mV zavisnosti log vs. . Pokazano je da je za korektno određivanje ovih parametara neophodno korigovati gustinu struje pri svakoj zadatoj prenapetosti za vrednost omskog pada napona jRs.",
publisher = "Inženjersko društvo za koroziju",
journal = "Zaštita materijala",
title = "Correct determination of the hydrogen evolution reaction parameters at Ni foam electrode modified by electrodeposited Ni-Sn alloy layer, Procedura korektnog određivanja parametara reakcije izdvajanja vodonika na elektrodi od Ni pene modifikovane elektrohemijski istaloženom Ni-Sn legurom",
pages = "10-3",
number = "1",
volume = "65",
doi = "10.62638/zasmat1039"
}
Gojgić, J. D., Petričević, A. M., Krstajić Pajić, M. N.,& Jović, V. D.. (2024). Correct determination of the hydrogen evolution reaction parameters at Ni foam electrode modified by electrodeposited Ni-Sn alloy layer. in Zaštita materijala
Inženjersko društvo za koroziju., 65(1), 3-10.
https://doi.org/10.62638/zasmat1039
Gojgić JD, Petričević AM, Krstajić Pajić MN, Jović VD. Correct determination of the hydrogen evolution reaction parameters at Ni foam electrode modified by electrodeposited Ni-Sn alloy layer. in Zaštita materijala. 2024;65(1):3-10.
doi:10.62638/zasmat1039 .
Gojgić, Jelena D., Petričević, Aleksandar M., Krstajić Pajić, Mila N., Jović, Vladimir D., "Correct determination of the hydrogen evolution reaction parameters at Ni foam electrode modified by electrodeposited Ni-Sn alloy layer" in Zaštita materijala, 65, no. 1 (2024):3-10,
https://doi.org/10.62638/zasmat1039 . .

Hydrogen evolution at Ni foam electrodes and Ni-Sn coated Ni foam electrodes

Gojgić, Jelena D.; Petričević, Aleksandar M.; Rauscher, Thomas; Bernäcker, Christian I.; Weißgärber, Thomas; Pavko, Luka; Vasilić, Rastko; Krstajić Pajić, Mila N.; Jović, Vladimir D.

(Elsevier B.V., 2023)

TY  - JOUR
AU  - Gojgić, Jelena D.
AU  - Petričević, Aleksandar M.
AU  - Rauscher, Thomas
AU  - Bernäcker, Christian I.
AU  - Weißgärber, Thomas
AU  - Pavko, Luka
AU  - Vasilić, Rastko
AU  - Krstajić Pajić, Mila N.
AU  - Jović, Vladimir D.
PY  - 2023
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/6577
AB  - The hydrogen evolution reaction (HER) was investigated in 1.0 M KOH at 25 °C at Ni foams with different pore sizes (450–1200 µm), and at the Ni-Sn/Ni foam electrodes, where Ni-Sn alloys were electrodeposited from the pyrophosphate-glycine bath using controlled potential coulometry (CPC) technique. The cross-section analysis revealed that rough Ni-Sn alloy covers complete available inner and outer foam surface, while investigated coating composition varied from 62 to 80 at% Ni (20–38 at% Sn). Comparing the HER polarization curves, the overpotential at j = −200 mA cm−2 was 427 mV lower for Ni-Sn samples than for bare Ni foams, while Tafel slopes changed from − 120 mV dec−1 at bare Ni foams to − 50 mV dec−1 for Ni-Sn/Ni foam samples. The lowest overpotential at − 100 mA cm−2 achieved is as low as − 77 mV. These cathodes could be promising 3D materials for industrial water electrolysis in zero-gap membrane flow cells.
PB  - Elsevier B.V.
T2  - Applied Catalysis A: General
T1  - Hydrogen evolution at Ni foam electrodes and Ni-Sn coated Ni foam electrodes
SP  - 119312
VL  - 663
DO  - 10.1016/j.apcata.2023.119312
ER  - 
@article{
author = "Gojgić, Jelena D. and Petričević, Aleksandar M. and Rauscher, Thomas and Bernäcker, Christian I. and Weißgärber, Thomas and Pavko, Luka and Vasilić, Rastko and Krstajić Pajić, Mila N. and Jović, Vladimir D.",
year = "2023",
abstract = "The hydrogen evolution reaction (HER) was investigated in 1.0 M KOH at 25 °C at Ni foams with different pore sizes (450–1200 µm), and at the Ni-Sn/Ni foam electrodes, where Ni-Sn alloys were electrodeposited from the pyrophosphate-glycine bath using controlled potential coulometry (CPC) technique. The cross-section analysis revealed that rough Ni-Sn alloy covers complete available inner and outer foam surface, while investigated coating composition varied from 62 to 80 at% Ni (20–38 at% Sn). Comparing the HER polarization curves, the overpotential at j = −200 mA cm−2 was 427 mV lower for Ni-Sn samples than for bare Ni foams, while Tafel slopes changed from − 120 mV dec−1 at bare Ni foams to − 50 mV dec−1 for Ni-Sn/Ni foam samples. The lowest overpotential at − 100 mA cm−2 achieved is as low as − 77 mV. These cathodes could be promising 3D materials for industrial water electrolysis in zero-gap membrane flow cells.",
publisher = "Elsevier B.V.",
journal = "Applied Catalysis A: General",
title = "Hydrogen evolution at Ni foam electrodes and Ni-Sn coated Ni foam electrodes",
pages = "119312",
volume = "663",
doi = "10.1016/j.apcata.2023.119312"
}
Gojgić, J. D., Petričević, A. M., Rauscher, T., Bernäcker, C. I., Weißgärber, T., Pavko, L., Vasilić, R., Krstajić Pajić, M. N.,& Jović, V. D.. (2023). Hydrogen evolution at Ni foam electrodes and Ni-Sn coated Ni foam electrodes. in Applied Catalysis A: General
Elsevier B.V.., 663, 119312.
https://doi.org/10.1016/j.apcata.2023.119312
Gojgić JD, Petričević AM, Rauscher T, Bernäcker CI, Weißgärber T, Pavko L, Vasilić R, Krstajić Pajić MN, Jović VD. Hydrogen evolution at Ni foam electrodes and Ni-Sn coated Ni foam electrodes. in Applied Catalysis A: General. 2023;663:119312.
doi:10.1016/j.apcata.2023.119312 .
Gojgić, Jelena D., Petričević, Aleksandar M., Rauscher, Thomas, Bernäcker, Christian I., Weißgärber, Thomas, Pavko, Luka, Vasilić, Rastko, Krstajić Pajić, Mila N., Jović, Vladimir D., "Hydrogen evolution at Ni foam electrodes and Ni-Sn coated Ni foam electrodes" in Applied Catalysis A: General, 663 (2023):119312,
https://doi.org/10.1016/j.apcata.2023.119312 . .
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5

Oxygen reduction reaction on electrochemically deposited sub-monolayers and ultra-thin layers of Pt on (Nb-Ti)2AlC substrate

Petričević, Aleksandar; Jović, Vladimir D.; Krstajić Pajić, Mila N.; Zabinski, Piotr; Elezović, Nevenka R.

(Engineers Society for Corrosion, 2022)

TY  - JOUR
AU  - Petričević, Aleksandar
AU  - Jović, Vladimir D.
AU  - Krstajić Pajić, Mila N.
AU  - Zabinski, Piotr
AU  - Elezović, Nevenka R.
PY  - 2022
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5353
AB  - Catalytic activity towards the oxygen reduction reaction (ORR) in 0.5 M H2SO4 was investigated at sub-monolayers and ultra-thin layers (corresponding to 10, 30 and 100 monolayers, (MLs)) of Pt electrochemically deposited on (Nb-Ti)2AlC substrate. Electrochemical deposition of Pt layers on (Nb-Ti)2AlC substrate was achieved from the solution containing 3 mM K2PtCl4 + 0.5 M NaCl (pH 4) under the conditions of convective diffusion (RPM = 400) using linear sweep voltammetry (LSV) at a sweep rate of 2 mV s-1, by determining limiting potential for deposition of each Pt sample from the QPt vs. E curves. The Pt samples were characterized X-ray photoelectron spectroscopy (XPS). XPS analysis showed that practically the whole surface of (Nb-Ti)2AlC substrate is covered with homogeneous layer of Pt, while Pt ion reduction was complete to metallic form – Pt(0) valence state. Then oxygen reduction was studied at rotating disc electrode by cyclic voltammetry and linear sweep voltammetry. Two different Tafel slopes were observed, one close to 60 mV dec-1 in low current densities region and second one ~ 120 mV dec-1 in high current densities region. This novel catalyst exhibited higher activity in comparison to carbon supported one, in terms of mass activity – kinetic current density normalized to Pt loading.
AB  - Ispitivana je reakcija redukcije kiseonika na tankim slojevima platine u 0.5 mol dm-3 H2SO4. Tanki
slojevi platine – čija količina naelektrisanja odgovara 10, 30 i 100 teorijskih monoslojeva Pt su
istaloženi na nosaču od (Nb-Ti)2AlC. Za elektrohemijsko taloženje je korišćen rastvor 3 mM
K2PtCl4 + 0.5 M NaCl pH = 4, u uslovima konvektivne difuzije (RPM = 400) primenom metode
linearne skenirajuće voltametrije (LSV) pri brzini promene potencijala od 2 mV s-1
. Elektrohemijski
dobijeni platinski katalizatori na pomenutom nosaču su okarakterisani metodom fotoelektronske
spektroskopija X-zraka (XPS), kao i elektrohemijskim tehnikama.
Za određivanje realne elektrohemijski aktivne površine elektrode je primenjena ciklična
voltametrija, integracijom ispod anodnog dela voltamograma u oblasti adsorpcije vodonika na
potpotencijalima. Za ispitivanje kinetike reakcije redukcije kiseonika je korišćena metoda linearne
skenirajuće voltametrije na rotirajućoj disk elektrodi. Dobijene su dve vrednosti Tafelovog nagiba,
jedna približno 60 mV dek-1
u oblasti malih prenapetosti, a druga ~ 120 mV dek-1
, u oblasti većih
gustina struje. Katalitička aktivnost katalizatora je poređena sa vrednostima iz literature dobijenim
na platini na ugljeničim nosačima na 0.85 V prema reverzibilnoj vodoničnoj elektrodi, izražena kao
kinetička gustina struje po realnoj površini electrode, ili specifična aktivnost – izražena kao
kinetička gustina struje po masi platine. Pokazano je da katalizator sa 10 monoslojeva platine
poseduje veoma dobru katalitičku aktivnost, posebno izraženu po masi istaložene platine.
PB  - Engineers Society for Corrosion
T2  - Zaštita materijala
T1  - Oxygen reduction reaction on electrochemically deposited sub-monolayers and ultra-thin layers of Pt on (Nb-Ti)2AlC substrate
T1  - Reakcija redukcije kiseonika na elektrohemijski istaloženim tankim slojevima platine na (Nb-Ti)2alc nosaču
EP  - 164
IS  - 2
SP  - 153
VL  - 63
DO  - 10.5937/zasmat2202153P
ER  - 
@article{
author = "Petričević, Aleksandar and Jović, Vladimir D. and Krstajić Pajić, Mila N. and Zabinski, Piotr and Elezović, Nevenka R.",
year = "2022",
abstract = "Catalytic activity towards the oxygen reduction reaction (ORR) in 0.5 M H2SO4 was investigated at sub-monolayers and ultra-thin layers (corresponding to 10, 30 and 100 monolayers, (MLs)) of Pt electrochemically deposited on (Nb-Ti)2AlC substrate. Electrochemical deposition of Pt layers on (Nb-Ti)2AlC substrate was achieved from the solution containing 3 mM K2PtCl4 + 0.5 M NaCl (pH 4) under the conditions of convective diffusion (RPM = 400) using linear sweep voltammetry (LSV) at a sweep rate of 2 mV s-1, by determining limiting potential for deposition of each Pt sample from the QPt vs. E curves. The Pt samples were characterized X-ray photoelectron spectroscopy (XPS). XPS analysis showed that practically the whole surface of (Nb-Ti)2AlC substrate is covered with homogeneous layer of Pt, while Pt ion reduction was complete to metallic form – Pt(0) valence state. Then oxygen reduction was studied at rotating disc electrode by cyclic voltammetry and linear sweep voltammetry. Two different Tafel slopes were observed, one close to 60 mV dec-1 in low current densities region and second one ~ 120 mV dec-1 in high current densities region. This novel catalyst exhibited higher activity in comparison to carbon supported one, in terms of mass activity – kinetic current density normalized to Pt loading., Ispitivana je reakcija redukcije kiseonika na tankim slojevima platine u 0.5 mol dm-3 H2SO4. Tanki
slojevi platine – čija količina naelektrisanja odgovara 10, 30 i 100 teorijskih monoslojeva Pt su
istaloženi na nosaču od (Nb-Ti)2AlC. Za elektrohemijsko taloženje je korišćen rastvor 3 mM
K2PtCl4 + 0.5 M NaCl pH = 4, u uslovima konvektivne difuzije (RPM = 400) primenom metode
linearne skenirajuće voltametrije (LSV) pri brzini promene potencijala od 2 mV s-1
. Elektrohemijski
dobijeni platinski katalizatori na pomenutom nosaču su okarakterisani metodom fotoelektronske
spektroskopija X-zraka (XPS), kao i elektrohemijskim tehnikama.
Za određivanje realne elektrohemijski aktivne površine elektrode je primenjena ciklična
voltametrija, integracijom ispod anodnog dela voltamograma u oblasti adsorpcije vodonika na
potpotencijalima. Za ispitivanje kinetike reakcije redukcije kiseonika je korišćena metoda linearne
skenirajuće voltametrije na rotirajućoj disk elektrodi. Dobijene su dve vrednosti Tafelovog nagiba,
jedna približno 60 mV dek-1
u oblasti malih prenapetosti, a druga ~ 120 mV dek-1
, u oblasti većih
gustina struje. Katalitička aktivnost katalizatora je poređena sa vrednostima iz literature dobijenim
na platini na ugljeničim nosačima na 0.85 V prema reverzibilnoj vodoničnoj elektrodi, izražena kao
kinetička gustina struje po realnoj površini electrode, ili specifična aktivnost – izražena kao
kinetička gustina struje po masi platine. Pokazano je da katalizator sa 10 monoslojeva platine
poseduje veoma dobru katalitičku aktivnost, posebno izraženu po masi istaložene platine.",
publisher = "Engineers Society for Corrosion",
journal = "Zaštita materijala",
title = "Oxygen reduction reaction on electrochemically deposited sub-monolayers and ultra-thin layers of Pt on (Nb-Ti)2AlC substrate, Reakcija redukcije kiseonika na elektrohemijski istaloženim tankim slojevima platine na (Nb-Ti)2alc nosaču",
pages = "164-153",
number = "2",
volume = "63",
doi = "10.5937/zasmat2202153P"
}
Petričević, A., Jović, V. D., Krstajić Pajić, M. N., Zabinski, P.,& Elezović, N. R.. (2022). Oxygen reduction reaction on electrochemically deposited sub-monolayers and ultra-thin layers of Pt on (Nb-Ti)2AlC substrate. in Zaštita materijala
Engineers Society for Corrosion., 63(2), 153-164.
https://doi.org/10.5937/zasmat2202153P
Petričević A, Jović VD, Krstajić Pajić MN, Zabinski P, Elezović NR. Oxygen reduction reaction on electrochemically deposited sub-monolayers and ultra-thin layers of Pt on (Nb-Ti)2AlC substrate. in Zaštita materijala. 2022;63(2):153-164.
doi:10.5937/zasmat2202153P .
Petričević, Aleksandar, Jović, Vladimir D., Krstajić Pajić, Mila N., Zabinski, Piotr, Elezović, Nevenka R., "Oxygen reduction reaction on electrochemically deposited sub-monolayers and ultra-thin layers of Pt on (Nb-Ti)2AlC substrate" in Zaštita materijala, 63, no. 2 (2022):153-164,
https://doi.org/10.5937/zasmat2202153P . .
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