RuO2 with Short‐Range Ordered Tantalum Single Atoms for Enhanced Acidic Oxygen Evolution Reaction

Author:

Wang Xuefeng1,Li Zijian2,Jang Haeseong3,Chen Changsheng4,Liu Shangguo1,Wang Liu1,Kim Min Gyu5,Cho Jaephil6,Qin Qing1,Liu Xien1ORCID

Affiliation:

1. College of Chemical Engineering Qingdao University of Science and Technology Qingdao 266042 China

2. Department of Chemistry City University of Hong Kong Hong Kong SAR 999077 China

3. Department of Advanced Materials Engineering Chung‐Ang University Anseong‐si Gyeonggi‐do 17546 South Korea

4. Department of Applied Physics Research Institute for Smart Energy The Hong Kong Polytechnic University Kowloon Hong Kong SAR 999077 China

5. Beamline Research Division Pohang Accelerator Laboratory (PAL) Pohang 37673 South Korea

6. Department of Energy Engineering School of Energy and Chemical Engineering Ulsan National Institute of Science and Technology (UNIST) Ulsan 689‐798 South Korea

Abstract

AbstractRuthenium Dioxide (RuO2), as one of the most promising alternatives to IrO2, suffers from the severe dissolution and overoxidation of Ru active sites during the acidic oxygen evolution reaction (OER), which hinders its practical application. Herein, the study constructs a short‐range ordered tantalum single atoms‐doped RuO2 catalyst (Ta‐RuO2) with asymmetric Ru‐O‐Ta(‐O‐Ta) active units for the enhanced acidic OER. The Ta‐RuO2 catalyst exhibits superior catalytic activity with an overpotential of 201 mV at 10 mA cm−2 and a long‐lasting stability of 280 h. Physical characterizations combined with electrochemical tests reveal that the incorporation of atomically arranged Ta atoms induces significant tensile strain, effectively optimizing the adsorption strength of oxygen‐containing intermediates by regulating the Ru d‐band center and weakening the Ru‐O covalency, thus boosting the catalytic activity. Furthermore, the formed Ru‐O‐Ta(‐O‐Ta) active local structure is well maintained during the OER process owing to the synergy of strong corrosion resistance of Ta‐O bonds and the electron transfers from Ta to Ru via oxygen bridge stabilizing the Ru sites, contributing to the enhanced stability. This study provides a novel method via incorporation of corrosion‐resistant and short‐range ordered single atoms to significantly enhance the acidic OER stability and activity of cost‐effective catalysts.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Shandong Province

Taishan Scholar Foundation of Shandong Province

Publisher

Wiley

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