γ‐MnO2 as an Electron Reservoir for RuO2 Oxygen Evolution Catalyst in Acidic Media

Author:

Jia Wenqi1,Cao Xuejie1,Chen Xiaojie1,Qin Hongye1,Miao Licheng1,Wang Qinglun1,Jiao Lifang1ORCID

Affiliation:

1. Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education) Collaborative Innovation Center of Chemical Science and Engineering (Tianjin) College of Chemistry Nankai University Tianjin 300071 China

Abstract

AbstractDeveloping highly active and durable catalysts in acid conditions remains an urgent issue due to the sluggish kinetics of oxygen evolution reaction (OER). Although RuO2 has been a state‐of‐the‐art commercial catalyst for OER, it encounters poor stability and high cost. In this study, the electronic reservoir regulation strategy is proposed to promote the performance of acidic water oxidation via constructing a RuO2/MnO2 heterostructure supported on carbon cloth (CC) (abbreviated as RuO2/MnO2/CC). Theoretical and experimental results reveal that MnO2 acts as an electron reservoir for RuO2. It facilitates electron transfer from RuO2, enhancing its activity prior to OER, and donates electrons to RuO2, improving its stability after OER. Consequently, RuO2/MnO2/CC exhibits better performance compared to commercial RuO2, with an ultrasmall overpotential of 189 mV at 10 mA cm−2 and no signs of deactivation even after 800 h of electrolysis in 0.5 m H2SO4 at 10 mA cm−2. When applied as the anode in a proton exchange membrane water electrolyzer, the cost‐efficient RuO2/MnO2/CC catalyst only requires a cell voltage of 1.661 V to achieve the water‐splitting current of 1 A cm−2, and the noble metal cost is as low as US$ 0.00962 cm−2, indicating potential for practical applications.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Publisher

Wiley

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