Please use this identifier to cite or link to this item: http://elar.urfu.ru/handle/10995/131556
Title: NiFe Layered Double Hydroxide Electrocatalyst Prepared via an Electrochemical Deposition Method for the Oxygen Evolution Reaction
Authors: Praveen, Kumar, M.
Sasikumar, M.
Arulraj, A.
Rajasudha, V.
Murugadoss, G.
Kumar, M. R.
Gouse, Peera, S.
Mangalaraja, R. V.
Issue Date: 2022
Publisher: MDPI
Citation: Praveen Kumar, M, Sasikumar, M, Arulraj, A, Rajasudha, V, Murugadoss, G, Kumar, MR, Gouse Peera, S & Mangalaraja, RV 2022, 'NiFe Layered Double Hydroxide Electrocatalyst Prepared via an Electrochemical Deposition Method for the Oxygen Evolution Reaction', Catalysts, Том. 12, № 11, 1470. https://doi.org/10.3390/catal12111470
Praveen Kumar, M., Sasikumar, M., Arulraj, A., Rajasudha, V., Murugadoss, G., Kumar, M. R., Gouse Peera, S., & Mangalaraja, R. V. (2022). NiFe Layered Double Hydroxide Electrocatalyst Prepared via an Electrochemical Deposition Method for the Oxygen Evolution Reaction. Catalysts, 12(11), [1470]. https://doi.org/10.3390/catal12111470
Abstract: Herein, we aimed to obtain NiFe layered double hydroxide (LDH) with a controlled phase and surface morphology as a highly active and stable oxygen evolution catalyst via the electrochemical deposition method, which was thermodynamically stable for the oxygen evolution reaction (OER) in an alkaline medium. The NiFe-LDH sample was analyzed by sophisticated instruments and tested as an electrocatalyst on Toray carbon (TC). The NiFe-LDH electrocatalyst showed an excellent performance with lower overpotential of 0.27 V at 35 mA cm−2 and higher density of 125 mA cm−2 for OER in the 1 M KOH electrolyte solution. Moreover, the prepared catalyst exhibited unpredictable long-time stability for 700 h. From our knowledge, NiFe-LDH is a robust highly stable electrocatalyst compared to the recent reports. © 2022 by the authors.
Keywords: (OXY)HYDROXIDES PHASES
ELECTROCHEMICAL DEPOSITION
LONG-TIME STABILITY
NIFE-LDH ELECTROCATALYST
OER
URI: http://elar.urfu.ru/handle/10995/131556
Access: info:eu-repo/semantics/openAccess
cc-by
License text: https://creativecommons.org/licenses/by/4.0/
SCOPUS ID: 85148749917
WOS ID: 000894739800001
PURE ID: 32895095
bb1ab6a9-27fb-402e-b877-a8ce3b36f905
ISSN: 2073-4344
DOI: 10.3390/catal12111470
metadata.dc.description.sponsorship: ANID-FONDECYT, (3200076, 3220475)
Ministry of Education and Science of the Russian Federation, Minobrnauka
Ministry of Science, ICT and Future Planning, MSIP, (2021R1F1A1046648)
National Research Foundation of Korea, NRF
Ural Federal University, UrFU
Agencia Nacional de Investigación y Desarrollo, ANID
M.P.K., A.A., and R.V.M. acknowledge the Chilean national agency for research and development (ANID-FONDECYT Projects No.: 3220475 and 3200076), Chile for the financial support. The author (G.M.) thanks the Chancellor, President and Vice Chancellor, Satyabhama Institute of Science and Technology, Chennai for the support and encouragement. One of the authors (M.R.K.) thanks the contract no. 40/is2. Also M. Rajesh Kumar gratefully acknowledges research funding from the Ministry of Science and Higher Education of the Russian Federation (Ural Federal University project within the Priority 2030 Program). This research is also supported by the National Research Foundation of Korea (NRF) funded by the Korean government, Ministry of Science and ICT (MSIT) (Grant No. 2021R1F1A1046648), Republic of Korea.
Appears in Collections:Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC

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