Ruthenium oxychloride supported by manganese oxide for stable oxygen evolution in acidic media
Despite the recent advances in enhancing the durability and reducing the overpotential of ruthenium (Ru)-based electrocatalysts for acidic oxygen evolution reaction (OER), their stability hardly meets the requirement of practical application. Moreover, a cost-effective strategy to stabilize the high...
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sg-ntu-dr.10356-1686412023-06-16T15:40:03Z Ruthenium oxychloride supported by manganese oxide for stable oxygen evolution in acidic media Zhao, Yunxing Hu, Jun Chiang, Chao-Lung Li, Ying Yang, Weichuang Yang, Zhenhai Hung, Wei-Hsuan Lin, Yan-Gu Chen, Zhong Li, Bin Gao, Pingqi Li, Hong School of Materials Science and Engineering School of Mechanical and Aerospace Engineering School of Electrical and Electronic Engineering Centre for Micro-/Nano-electronics (NOVITAS) CNRS International NTU THALES Research Alliances Engineering::Materials Electrolysis Manganese Oxide Despite the recent advances in enhancing the durability and reducing the overpotential of ruthenium (Ru)-based electrocatalysts for acidic oxygen evolution reaction (OER), their stability hardly meets the requirement of practical application. Moreover, a cost-effective strategy to stabilize the highly active but unstable Ru species is desirable. Herein, we report a stable electrocatalyst for acidic OER by dispersing the Ru oxychloride active species into a manganese oxide support (RuOCl@MnOx) to form highly dispersed Ru-O-Mn without the alteration of vibrational modes and bond parameters of the MnO6 group, as suggested by Raman and synchrotron radiation characterization studies. The catalyst is stable for continuous operation over 280 h with an overpotential of 228 mV at 10 mA cm−2 and over 200 h at 100 mA cm−2, among the most stable low-mass-loading Ru-based OER electrocatalysts in acidic media. Complementary theoretical calculations ascribe the excellent stability to its high oxidation potential and low formation/surface energies, consistent with experimental observations. The enhanced activity is attributed to the four-coordinated Ru site that bears a low overpotential determined by the formation of O* from OH*. Our work thus offers a new strategy for synthesizing robust OER electrocatalysts of PEM electrolyzers with superior activity. Agency for Science, Technology and Research (A*STAR) Nanyang Technological University Published version The work was partially supported by A*STAR Science & Engineering Research Council AME IRG funding (A1983c0029) and Nanyang Technological University via an ACE grant (NTUACE2021-02). H. J. is thankful for financial support from the National Natural Science Foundation of China (Grant No. 21676216). 2023-06-13T02:42:11Z 2023-06-13T02:42:11Z 2022 Journal Article Zhao, Y., Hu, J., Chiang, C., Li, Y., Yang, W., Yang, Z., Hung, W., Lin, Y., Chen, Z., Li, B., Gao, P. & Li, H. (2022). Ruthenium oxychloride supported by manganese oxide for stable oxygen evolution in acidic media. Journal of Materials Chemistry A, 10(39), 20964-20974. https://dx.doi.org/10.1039/d2ta05335g 2050-7488 https://hdl.handle.net/10356/168641 10.1039/d2ta05335g 2-s2.0-85139489608 39 10 20964 20974 en Journal of Materials Chemistry A © 2022 The Royal Society of Chemistry. This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. application/pdf |
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Engineering::Materials Electrolysis Manganese Oxide Zhao, Yunxing Hu, Jun Chiang, Chao-Lung Li, Ying Yang, Weichuang Yang, Zhenhai Hung, Wei-Hsuan Lin, Yan-Gu Chen, Zhong Li, Bin Gao, Pingqi Li, Hong Ruthenium oxychloride supported by manganese oxide for stable oxygen evolution in acidic media |
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Despite the recent advances in enhancing the durability and reducing the overpotential of ruthenium (Ru)-based electrocatalysts for acidic oxygen evolution reaction (OER), their stability hardly meets the requirement of practical application. Moreover, a cost-effective strategy to stabilize the highly active but unstable Ru species is desirable. Herein, we report a stable electrocatalyst for acidic OER by dispersing the Ru oxychloride active species into a manganese oxide support (RuOCl@MnOx) to form highly dispersed Ru-O-Mn without the alteration of vibrational modes and bond parameters of the MnO6 group, as suggested by Raman and synchrotron radiation characterization studies. The catalyst is stable for continuous operation over 280 h with an overpotential of 228 mV at 10 mA cm−2 and over 200 h at 100 mA cm−2, among the most stable low-mass-loading Ru-based OER electrocatalysts in acidic media. Complementary theoretical calculations ascribe the excellent stability to its high oxidation potential and low formation/surface energies, consistent with experimental observations. The enhanced activity is attributed to the four-coordinated Ru site that bears a low overpotential determined by the formation of O* from OH*. Our work thus offers a new strategy for synthesizing robust OER electrocatalysts of PEM electrolyzers with superior activity. |
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School of Materials Science and Engineering |
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School of Materials Science and Engineering Zhao, Yunxing Hu, Jun Chiang, Chao-Lung Li, Ying Yang, Weichuang Yang, Zhenhai Hung, Wei-Hsuan Lin, Yan-Gu Chen, Zhong Li, Bin Gao, Pingqi Li, Hong |
format |
Article |
author |
Zhao, Yunxing Hu, Jun Chiang, Chao-Lung Li, Ying Yang, Weichuang Yang, Zhenhai Hung, Wei-Hsuan Lin, Yan-Gu Chen, Zhong Li, Bin Gao, Pingqi Li, Hong |
author_sort |
Zhao, Yunxing |
title |
Ruthenium oxychloride supported by manganese oxide for stable oxygen evolution in acidic media |
title_short |
Ruthenium oxychloride supported by manganese oxide for stable oxygen evolution in acidic media |
title_full |
Ruthenium oxychloride supported by manganese oxide for stable oxygen evolution in acidic media |
title_fullStr |
Ruthenium oxychloride supported by manganese oxide for stable oxygen evolution in acidic media |
title_full_unstemmed |
Ruthenium oxychloride supported by manganese oxide for stable oxygen evolution in acidic media |
title_sort |
ruthenium oxychloride supported by manganese oxide for stable oxygen evolution in acidic media |
publishDate |
2023 |
url |
https://hdl.handle.net/10356/168641 |
_version_ |
1772827131368177664 |