Metal Doping Regulates Electrocatalysts Restructuring During Oxygen Evolution Reaction

Author:

Wang Maoyu12,Muhich Brian A.1,He Zizhou3,Yang Zhenzhen4,Yang Dongqi1,Lucero Marcos1,Nguyen Hoan Kim Khai1,Sterbinsky George E.2ORCID,Árnadóttir Líney1,Zhou Hua2,Fei Ling3,Feng Zhenxing1ORCID

Affiliation:

1. School of Chemical Biological and Environmental Engineering Oregon State University Corvallis OR 97331 United States

2. X-ray Science Division Argonne National Laboratory Lemont IL, 60439 United States

3. Chemical Engineering Department University of Louisiana at Lafayette Lafayette LA 70504 United States

4. Chemical Sciences and Engineering Division Argonne National Laboratory Lemont IL, 60439 United States

Abstract

AbstractHigh‐efficiency and low‐cost catalysts for oxygen evolution reaction (OER) are critical for electrochemical water splitting to generate hydrogen, which is a clean fuel for sustainable energy conversion and storage. Among the emerging OER catalysts, transition metal dichalcogenides have exhibited superior activity compared to commercial standards such as RuO2, but inferior stability due to uncontrolled restructuring with OER. In this study, we create bimetallic sulfide catalysts by adapting the atomic ratio of Ni and Co in CoxNi1‐xSy electrocatalysts to investigate the intricate restructuring processes. Surface‐sensitive X‐ray photoelectron spectroscopy and bulk‐sensitive X‐ray absorption spectroscopy confirmed the favorable restructuring of transition metal sulfide material following OER processes. Our results indicate that a small amount of Ni substitution can reshape the Co local electronic structure, which regulates the restructuring process to optimize the balance between OER activity and stability. This work represents a significant advancement in the development of efficient and noble metal‐free OER electrocatalysts through a doping‐regulated restructuring approach.

Funder

National Science Foundation

Oregon State University

Publisher

Wiley

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