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Electrodeposition of High-Surface-Area IrO(2) Films on Ti Felt as an Efficient Catalyst for the Oxygen Evolution Reaction

Under acidic conditions, IrO(2) exhibits high catalytic activity with respect to the oxygen evolution reaction (OER). However, the practical application of Ir-based catalysts is significantly limited owing to their high cost in addition to the scarcity of the metal. Therefore, it is necessary to imp...

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Autores principales: Park, Yu Jin, Lee, Jooyoung, Park, Yoo Sei, Yang, Juchan, Jang, Myeong Je, Jeong, Jaehoon, Choe, Seunghoe, Lee, Jung Woo, Kwon, Jung-Dae, Choi, Sung Mook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7645052/
https://www.ncbi.nlm.nih.gov/pubmed/33195098
http://dx.doi.org/10.3389/fchem.2020.593272
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author Park, Yu Jin
Lee, Jooyoung
Park, Yoo Sei
Yang, Juchan
Jang, Myeong Je
Jeong, Jaehoon
Choe, Seunghoe
Lee, Jung Woo
Kwon, Jung-Dae
Choi, Sung Mook
author_facet Park, Yu Jin
Lee, Jooyoung
Park, Yoo Sei
Yang, Juchan
Jang, Myeong Je
Jeong, Jaehoon
Choe, Seunghoe
Lee, Jung Woo
Kwon, Jung-Dae
Choi, Sung Mook
author_sort Park, Yu Jin
collection PubMed
description Under acidic conditions, IrO(2) exhibits high catalytic activity with respect to the oxygen evolution reaction (OER). However, the practical application of Ir-based catalysts is significantly limited owing to their high cost in addition to the scarcity of the metal. Therefore, it is necessary to improve the efficiency of the utilization of such catalysts. In this study, IrO(2)-coated Ti felt (IrO(2)/Ti) electrodes were prepared as high-efficiency catalysts for the OER under acidic conditions. By controlling the surface roughness of the Ti substrate via wet etching, the optimum Ti substrate surface area for application in the IrO(2)/Ti electrode was determined. Additionally, the IrO(2) film that was electrodeposited on the 30 min etched Ti felt had a large surface area and a uniform morphology. Furthermore, there were no micro-cracks and the electrode obtained (IrO(2)/Ti-30) exhibited superior catalytic performance with respect to the OER, with a mass activity of 362.3 A [Formula: see text] at a potential of 2.0 V (vs. RHE) despite the low Ir loading (0.2 mg cm(−2)). Therefore, this proposed strategy for the development of IrO(2)/Ti electrodes with substrate surface control via wet etching has potential for application in the improvement of the efficiency of catalyst utilization with respect to the OER.
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spelling pubmed-76450522020-11-13 Electrodeposition of High-Surface-Area IrO(2) Films on Ti Felt as an Efficient Catalyst for the Oxygen Evolution Reaction Park, Yu Jin Lee, Jooyoung Park, Yoo Sei Yang, Juchan Jang, Myeong Je Jeong, Jaehoon Choe, Seunghoe Lee, Jung Woo Kwon, Jung-Dae Choi, Sung Mook Front Chem Chemistry Under acidic conditions, IrO(2) exhibits high catalytic activity with respect to the oxygen evolution reaction (OER). However, the practical application of Ir-based catalysts is significantly limited owing to their high cost in addition to the scarcity of the metal. Therefore, it is necessary to improve the efficiency of the utilization of such catalysts. In this study, IrO(2)-coated Ti felt (IrO(2)/Ti) electrodes were prepared as high-efficiency catalysts for the OER under acidic conditions. By controlling the surface roughness of the Ti substrate via wet etching, the optimum Ti substrate surface area for application in the IrO(2)/Ti electrode was determined. Additionally, the IrO(2) film that was electrodeposited on the 30 min etched Ti felt had a large surface area and a uniform morphology. Furthermore, there were no micro-cracks and the electrode obtained (IrO(2)/Ti-30) exhibited superior catalytic performance with respect to the OER, with a mass activity of 362.3 A [Formula: see text] at a potential of 2.0 V (vs. RHE) despite the low Ir loading (0.2 mg cm(−2)). Therefore, this proposed strategy for the development of IrO(2)/Ti electrodes with substrate surface control via wet etching has potential for application in the improvement of the efficiency of catalyst utilization with respect to the OER. Frontiers Media S.A. 2020-10-23 /pmc/articles/PMC7645052/ /pubmed/33195098 http://dx.doi.org/10.3389/fchem.2020.593272 Text en Copyright © 2020 Park, Lee, Park, Yang, Jang, Jeong, Choe, Lee, Kwon and Choi. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Park, Yu Jin
Lee, Jooyoung
Park, Yoo Sei
Yang, Juchan
Jang, Myeong Je
Jeong, Jaehoon
Choe, Seunghoe
Lee, Jung Woo
Kwon, Jung-Dae
Choi, Sung Mook
Electrodeposition of High-Surface-Area IrO(2) Films on Ti Felt as an Efficient Catalyst for the Oxygen Evolution Reaction
title Electrodeposition of High-Surface-Area IrO(2) Films on Ti Felt as an Efficient Catalyst for the Oxygen Evolution Reaction
title_full Electrodeposition of High-Surface-Area IrO(2) Films on Ti Felt as an Efficient Catalyst for the Oxygen Evolution Reaction
title_fullStr Electrodeposition of High-Surface-Area IrO(2) Films on Ti Felt as an Efficient Catalyst for the Oxygen Evolution Reaction
title_full_unstemmed Electrodeposition of High-Surface-Area IrO(2) Films on Ti Felt as an Efficient Catalyst for the Oxygen Evolution Reaction
title_short Electrodeposition of High-Surface-Area IrO(2) Films on Ti Felt as an Efficient Catalyst for the Oxygen Evolution Reaction
title_sort electrodeposition of high-surface-area iro(2) films on ti felt as an efficient catalyst for the oxygen evolution reaction
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7645052/
https://www.ncbi.nlm.nih.gov/pubmed/33195098
http://dx.doi.org/10.3389/fchem.2020.593272
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