Multi‐Step Screening‐Guided Core‐Shell RuO<sub>2</sub>@TaO<sub>x</sub> Nanorods Electrocatalyst for Acidic Oxygen Evolution Reaction

J Jiayi Li X Xiaohua Yu W Wei‐Hsiang Huang (National Synchrotron Radiation Research Center (NSRRC) Hsinchu 300092 Taiwan) Q Qian Zhang K Kai Wei (State Key Laboratory of Precision and Intelligent Chemistry) X Xiaoyan Zhou Y Yiming Zhu (Shanghai Key Laboratory for R&D and Application of Metallic Functional Materials, Institute of New Energy for Vehicles, School of Materials Science and Engineering) X Xuepeng Zhong (Department of Chemistry Technical University Berlin 10623 Berlin Germany) M Min‐Hsin Yeh (Sustainable Electrochemical Energy Development (SEED) Center National Taiwan University of Science and Technology Taipei 106 Taiwan) N Nicolas Alonso‐Vante (College of Smart Energy Shanghai Jiao Tong University Shanghai 200241 China) J Jiwei Ma (Shanghai Key Laboratory for R&D and Application of Metallic Functional Materials, Institute of New Energy for Vehicles, School of Materials Science and Engineering)

Abstract

AbstractIn the acidic oxygen evolution reaction (OER), the exploration of highly efficient and stable electrocatalysts is essential for the environmentally friendly production of hydrogen. Although RuO2 exhibits high catalytic activity, its solubility and corrosion in acidic environments are of concern. In this study, high‐melting‐point metal oxides were multi‐step rationally screened as protective layers for RuO2 to identify their roles in the acidic OER process. Among them, Ta‐related oxide was selected as the best candidate. To demonstrate the theoretical predictions, RuO2@TaOx with a core‐shell structure was deployed, which exhibited low overpotentials of 163 and 232 mV at 10  and 100 mA cm−2, respectively. In fact, the dense amorphous TaOx layer effectively prevented the dissolution of RuO2 and optimized the charge transfer through interfacial synergy, significantly improving both the activity and durability of OER. Meanwhile, the operando quick X‐ray absorption spectroscopy (Quick‐XAS) confirmed that Ru served as the active site during OER, while Ta inhibited the over‐oxidation of Ru, correlating with theoretical considerations. This study provides a new paradigm using targeted computational screening to guide the design of advanced catalysts, and serves as a proof‐of‐concept for the deployment of high‐melting‐point metal oxides as a protective layer for RuO2 in the acidic OER.

Article Details

Volume / Issue Vol. 64, Issue 41
Published October 06, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (11)

J

Jiayi Li

X

Xiaohua Yu

W

Wei‐Hsiang Huang

National Synchrotron Radiation Research Center (NSRRC) Hsinchu 300092 Taiwan

Q

Qian Zhang

K

Kai Wei

State Key Laboratory of Precision and Intelligent Chemistry

X

Xiaoyan Zhou

Y

Yiming Zhu

Shanghai Key Laboratory for R&D and Application of Metallic Functional Materials, Institute of New Energy for Vehicles, School of Materials Science and Engineering

X

Xuepeng Zhong

Department of Chemistry Technical University Berlin 10623 Berlin Germany

M

Min‐Hsin Yeh

Sustainable Electrochemical Energy Development (SEED) Center National Taiwan University of Science and Technology Taipei 106 Taiwan

N

Nicolas Alonso‐Vante

College of Smart Energy Shanghai Jiao Tong University Shanghai 200241 China

J

Jiwei Ma

Shanghai Key Laboratory for R&D and Application of Metallic Functional Materials, Institute of New Energy for Vehicles, School of Materials Science and Engineering