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Restructuring highly electron-deficient metal-metal oxides for boosting stability in acidic oxygen evolution reaction

Xinghui Liu, Shibo Xi, Hyunwoo Kim, Ashwani Kumar, Jinsun Lee, Jian Wang, Ngoc Quang Tran, Taehun Yang, Xiaodong Shao, Mengfang Liang, Min Gyu Kim and Hyoyoung Lee ()
Additional contact information
Xinghui Liu: Institute of Basic Science (IBS)
Shibo Xi: Institute of Chemical and Engineering Sciences, A*STAR
Hyunwoo Kim: Sungkyunkwan University (SKKU)
Ashwani Kumar: Institute of Basic Science (IBS)
Jinsun Lee: Institute of Basic Science (IBS)
Jian Wang: Seoul National University
Ngoc Quang Tran: Institute of Basic Science (IBS)
Taehun Yang: Institute of Basic Science (IBS)
Xiaodong Shao: Institute of Basic Science (IBS)
Mengfang Liang: Institute of Basic Science (IBS)
Min Gyu Kim: Pohang University of Science and Technology
Hyoyoung Lee: Institute of Basic Science (IBS)

Nature Communications, 2021, vol. 12, issue 1, 1-11

Abstract: Abstract The poor catalyst stability in acidic oxidation evolution reaction (OER) has been a long-time issue. Herein, we introduce electron-deficient metal on semiconducting metal oxides-consisting of Ir (Rh, Au, Ru)-MoO3 embedded by graphitic carbon layers (IMO) using an electrospinning method. We systematically investigate IMO’s structure, electron transfer behaviors, and OER catalytic performance by combining experimental and theoretical studies. Remarkably, IMO with an electron-deficient metal surface (Irx+; x > 4) exhibit a low overpotential of only ~156 mV at 10 mA cm−2 and excellent durability in acidic media due to the high oxidation state of metal on MoO3. Furthermore, the proton dissociation pathway is suggested via surface oxygen serving as proton acceptors. This study suggests high stability with high catalytic performance in these materials by creating electron-deficient surfaces and provides a general, unique strategy for guiding the design of other metal-semiconductor nanocatalysts.

Date: 2021
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-26025-0

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DOI: 10.1038/s41467-021-26025-0

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