Skorodumova, Natalia

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Authority KeyName Variants
01ca86c1-5882-4c43-9569-458bd671efd0
  • Skorodumova, Natalia (1)
  • Skorodumova, Natalia V. (1)
Projects
Bilateral cooperation project between the Republic of Serbia and the Federal Republic of Germany (project years 2020–2021, No. 22), as well as the ERC and DFG. Carl Tryggers Foundation for Scientific Research
Strengthening of the MagBioVin Research and Innovation Team for Development of Novel Approaches for Tumour Therapy based on Nanostructured Materials Development, characterization and application nanostructured and composite electrocatalysts and interactive supports for fuel cells and water electrolysis
Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 451-03-68/2020-14/200053 (University of Belgrade, Institute for Multidisciplinary Research) Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 451-03-68/2020-14/200146 (University of Belgrade, Faculty of Physical Chemistry)
Advanced technologies for monitoring and environmental protection from chemical pollutants and radiation burden Lithium-ion batteries and fuel cells - research and development
Fabrication and characterization of nano-photonic functional structrues in biomedicine and informatics NATO Project [EAP.SFPP 984925]
Serbian Academy of Sciences and Arts [F-190] Swedish Research Council [2014-5993]
The computations and data handling were enabled by resources provided by the Swedish National Infrastructure for Computing (SNIC) at National Supercomputer Centre (NSC) at Link¨oping University, partially funded by the Swedish Research Council through grant agreement No. 2018-05973. The networking support from COST action MP1407 is greatly appreciated.

Author's Bibliography

High-performance hydrogen evolution electrocatalysis using proton-intercalated TiO2 nanotube arrays as interactive supports for Ir nanoparticles

Lačnjevac, Uroš; Vasilić, Rastko; Dobrota, Ana S.; Đurđić, Slađana Z.; Tomanec, Ondřej; Zbořil, Radek; Mohajernia, Shiva; Nguyen, Nhat Truong; Skorodumova, Natalia; Manojlović, Dragan D.; Elezović, Nevenka; Pašti, Igor; Schmuki, Patrik

(Royal Society of Chemistry, 2020)

TY  - JOUR
AU  - Lačnjevac, Uroš
AU  - Vasilić, Rastko
AU  - Dobrota, Ana S.
AU  - Đurđić, Slađana Z.
AU  - Tomanec, Ondřej
AU  - Zbořil, Radek
AU  - Mohajernia, Shiva
AU  - Nguyen, Nhat Truong
AU  - Skorodumova, Natalia
AU  - Manojlović, Dragan D.
AU  - Elezović, Nevenka
AU  - Pašti, Igor
AU  - Schmuki, Patrik
PY  - 2020
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/4288
AB  - Developing ultraefficient electrocatalytic materials for the hydrogen evolution reaction (HER) with low content of expensive platinum group metals (PGMs) via low-energy-input procedures is the key to the successful commercialization of green water electrolysis technologies for sustainable production of high-purity hydrogen. In this study, we report a facile room-temperature synthesis of ultrafine metallic Ir nanoparticles on conductive, proton-intercalated TiO2 nanotube (H-TNT) arrays via galvanic displacement. A series of experiments demonstrate that a controlled transformation of the H-TNT surface microstructure from neat open-top tubes to disordered nanostripe bundles (“nanograss”) is highly beneficial for providing an abundance of exposed Ir active sites. Consequently, for nanograss-engineered composites, outstanding HER activity metrics are achieved even at very low Ir(III) precursor concentrations. An optimum Ir@TNT cathode loaded with 5.7 μgIr cm−2 exhibits an overpotential of −63 mV at −100 mA cm−2 and a mass activity of 34 A mgIr−1 at −80 mV under acidic conditions, along with excellent catalytic durability and structural integrity. Density functional theory (DFT) simulations reveal that the hydrogen-rich TiO2 surface not only stabilizes the deposited Ir and weakens its H binding strength to a moderate intensity, but also actively takes part in the HER mechanism by refreshing the Ir catalytic sites near the Ir|H–TiO2 interface, thus substantially promoting H2 generation. The comprehensive characterization combined with theory provides an in-depth understanding of the electrocatalytic behavior of H-TNT supported PGM nanoparticles and demonstrates their high potential as competitive electrocatalyst systems for the HER.
PB  - Royal Society of Chemistry
T2  - Journal of Materials Chemistry A
T1  - High-performance hydrogen evolution electrocatalysis using proton-intercalated TiO2 nanotube arrays as interactive supports for Ir nanoparticles
VL  - 8
IS  - 43
SP  - 22773
EP  - 22790
DO  - 10.1039/D0TA07492F
ER  - 
@article{
author = "Lačnjevac, Uroš and Vasilić, Rastko and Dobrota, Ana S. and Đurđić, Slađana Z. and Tomanec, Ondřej and Zbořil, Radek and Mohajernia, Shiva and Nguyen, Nhat Truong and Skorodumova, Natalia and Manojlović, Dragan D. and Elezović, Nevenka and Pašti, Igor and Schmuki, Patrik",
year = "2020",
abstract = "Developing ultraefficient electrocatalytic materials for the hydrogen evolution reaction (HER) with low content of expensive platinum group metals (PGMs) via low-energy-input procedures is the key to the successful commercialization of green water electrolysis technologies for sustainable production of high-purity hydrogen. In this study, we report a facile room-temperature synthesis of ultrafine metallic Ir nanoparticles on conductive, proton-intercalated TiO2 nanotube (H-TNT) arrays via galvanic displacement. A series of experiments demonstrate that a controlled transformation of the H-TNT surface microstructure from neat open-top tubes to disordered nanostripe bundles (“nanograss”) is highly beneficial for providing an abundance of exposed Ir active sites. Consequently, for nanograss-engineered composites, outstanding HER activity metrics are achieved even at very low Ir(III) precursor concentrations. An optimum Ir@TNT cathode loaded with 5.7 μgIr cm−2 exhibits an overpotential of −63 mV at −100 mA cm−2 and a mass activity of 34 A mgIr−1 at −80 mV under acidic conditions, along with excellent catalytic durability and structural integrity. Density functional theory (DFT) simulations reveal that the hydrogen-rich TiO2 surface not only stabilizes the deposited Ir and weakens its H binding strength to a moderate intensity, but also actively takes part in the HER mechanism by refreshing the Ir catalytic sites near the Ir|H–TiO2 interface, thus substantially promoting H2 generation. The comprehensive characterization combined with theory provides an in-depth understanding of the electrocatalytic behavior of H-TNT supported PGM nanoparticles and demonstrates their high potential as competitive electrocatalyst systems for the HER.",
publisher = "Royal Society of Chemistry",
journal = "Journal of Materials Chemistry A",
title = "High-performance hydrogen evolution electrocatalysis using proton-intercalated TiO2 nanotube arrays as interactive supports for Ir nanoparticles",
volume = "8",
number = "43",
pages = "22773-22790",
doi = "10.1039/D0TA07492F"
}
Lačnjevac, U., Vasilić, R., Dobrota, A. S., Đurđić, S. Z., Tomanec, O., Zbořil, R., Mohajernia, S., Nguyen, N. T., Skorodumova, N., Manojlović, D. D., Elezović, N., Pašti, I.,& Schmuki, P.. (2020). High-performance hydrogen evolution electrocatalysis using proton-intercalated TiO2 nanotube arrays as interactive supports for Ir nanoparticles. in Journal of Materials Chemistry A
Royal Society of Chemistry., 8(43), 22773-22790.
https://doi.org/10.1039/D0TA07492F
Lačnjevac U, Vasilić R, Dobrota AS, Đurđić SZ, Tomanec O, Zbořil R, Mohajernia S, Nguyen NT, Skorodumova N, Manojlović DD, Elezović N, Pašti I, Schmuki P. High-performance hydrogen evolution electrocatalysis using proton-intercalated TiO2 nanotube arrays as interactive supports for Ir nanoparticles. in Journal of Materials Chemistry A. 2020;8(43):22773-22790.
doi:10.1039/D0TA07492F .
Lačnjevac, Uroš, Vasilić, Rastko, Dobrota, Ana S., Đurđić, Slađana Z., Tomanec, Ondřej, Zbořil, Radek, Mohajernia, Shiva, Nguyen, Nhat Truong, Skorodumova, Natalia, Manojlović, Dragan D., Elezović, Nevenka, Pašti, Igor, Schmuki, Patrik, "High-performance hydrogen evolution electrocatalysis using proton-intercalated TiO2 nanotube arrays as interactive supports for Ir nanoparticles" in Journal of Materials Chemistry A, 8, no. 43 (2020):22773-22790,
https://doi.org/10.1039/D0TA07492F . .
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A study of ordered mesoporous carbon doped with Co and Ni as a catalyst of oxygen reduction reaction in both alkaline and acidic media

Gavrilov, Nemanja; Momcilovic, Milan; Dobrota, Ana S.; Stanković, Dalibor; Jokić, Bojan; Babić, Biljana; Skorodumova, Natalia V.; Mentus, Slavko V.; Pasti, Igor A.

(Elsevier Science Sa, Lausanne, 2018)

TY  - JOUR
AU  - Gavrilov, Nemanja
AU  - Momcilovic, Milan
AU  - Dobrota, Ana S.
AU  - Stanković, Dalibor
AU  - Jokić, Bojan
AU  - Babić, Biljana
AU  - Skorodumova, Natalia V.
AU  - Mentus, Slavko V.
AU  - Pasti, Igor A.
PY  - 2018
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2088
AB  - The incorporation of trace amounts ( lt  0.2%) of Co and Ni noticeably enhanced the catalytic activity of nitrogen free ordered mesoporous carbon (OMC) towards oxygen reduction reaction (ORR). (Co,Ni)-doped OMCs were characterized by N-2-adsorption measurements, X-ray powder diffraction, field emission scanning electron microscopy and Raman spectroscopy methods, and their ORR activity was estimated by voltammetry on rotating disk electrode in acidic and alkaline media. (Co,Ni)-doped OMCs show modest activities in acidic media, while the catalytic activity in alkaline media is rather high. The measured activities are compared to the Pt-based and Pt-free ORR catalysts reported in the literature. The number of electrons consumed per O-2 in metal-doped OMCs was found to vary between 2 and 4, which is advantageous in comparison to metal-free OMC. Also, the mass activities of metal-doped OMCs were found to be up to 2.5 times higher compared to that of metal-free OMC. We suggest that the ORR activity is governed by a balance between (i) textural properties, which determine the electrochemically accessible surface of the catalyst and which are influenced by the addition of a metal precursor, and (ii) novel active sites formed upon the introduction of metals into the carbon structure. In particular, our Density Functional Theory calculations suggest that Co and Ni atoms embedded into the single vacancies of graphene can activate the O-2 molecule and contribute to the decomposition of peroxide.
PB  - Elsevier Science Sa, Lausanne
T2  - Surface and Coatings Technology
T1  - A study of ordered mesoporous carbon doped with Co and Ni as a catalyst of oxygen reduction reaction in both alkaline and acidic media
VL  - 349
SP  - 511
EP  - 521
DO  - 10.1016/j.surfcoat.2018.06.008
ER  - 
@article{
author = "Gavrilov, Nemanja and Momcilovic, Milan and Dobrota, Ana S. and Stanković, Dalibor and Jokić, Bojan and Babić, Biljana and Skorodumova, Natalia V. and Mentus, Slavko V. and Pasti, Igor A.",
year = "2018",
abstract = "The incorporation of trace amounts ( lt  0.2%) of Co and Ni noticeably enhanced the catalytic activity of nitrogen free ordered mesoporous carbon (OMC) towards oxygen reduction reaction (ORR). (Co,Ni)-doped OMCs were characterized by N-2-adsorption measurements, X-ray powder diffraction, field emission scanning electron microscopy and Raman spectroscopy methods, and their ORR activity was estimated by voltammetry on rotating disk electrode in acidic and alkaline media. (Co,Ni)-doped OMCs show modest activities in acidic media, while the catalytic activity in alkaline media is rather high. The measured activities are compared to the Pt-based and Pt-free ORR catalysts reported in the literature. The number of electrons consumed per O-2 in metal-doped OMCs was found to vary between 2 and 4, which is advantageous in comparison to metal-free OMC. Also, the mass activities of metal-doped OMCs were found to be up to 2.5 times higher compared to that of metal-free OMC. We suggest that the ORR activity is governed by a balance between (i) textural properties, which determine the electrochemically accessible surface of the catalyst and which are influenced by the addition of a metal precursor, and (ii) novel active sites formed upon the introduction of metals into the carbon structure. In particular, our Density Functional Theory calculations suggest that Co and Ni atoms embedded into the single vacancies of graphene can activate the O-2 molecule and contribute to the decomposition of peroxide.",
publisher = "Elsevier Science Sa, Lausanne",
journal = "Surface and Coatings Technology",
title = "A study of ordered mesoporous carbon doped with Co and Ni as a catalyst of oxygen reduction reaction in both alkaline and acidic media",
volume = "349",
pages = "511-521",
doi = "10.1016/j.surfcoat.2018.06.008"
}
Gavrilov, N., Momcilovic, M., Dobrota, A. S., Stanković, D., Jokić, B., Babić, B., Skorodumova, N. V., Mentus, S. V.,& Pasti, I. A.. (2018). A study of ordered mesoporous carbon doped with Co and Ni as a catalyst of oxygen reduction reaction in both alkaline and acidic media. in Surface and Coatings Technology
Elsevier Science Sa, Lausanne., 349, 511-521.
https://doi.org/10.1016/j.surfcoat.2018.06.008
Gavrilov N, Momcilovic M, Dobrota AS, Stanković D, Jokić B, Babić B, Skorodumova NV, Mentus SV, Pasti IA. A study of ordered mesoporous carbon doped with Co and Ni as a catalyst of oxygen reduction reaction in both alkaline and acidic media. in Surface and Coatings Technology. 2018;349:511-521.
doi:10.1016/j.surfcoat.2018.06.008 .
Gavrilov, Nemanja, Momcilovic, Milan, Dobrota, Ana S., Stanković, Dalibor, Jokić, Bojan, Babić, Biljana, Skorodumova, Natalia V., Mentus, Slavko V., Pasti, Igor A., "A study of ordered mesoporous carbon doped with Co and Ni as a catalyst of oxygen reduction reaction in both alkaline and acidic media" in Surface and Coatings Technology, 349 (2018):511-521,
https://doi.org/10.1016/j.surfcoat.2018.06.008 . .
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