Highly Coupled Dynamically Modulated Electrocatalysts on Wafer‐Scale InGaN/GaN Nanowires on Silicon for Successive Acidic Photoelectrochemical Water Oxidation

W Wengang Gu W Wei Chen W Weiyi Wang (Division of Energy Conversion & Storage, Hefei National Research Center for Physical Sciences at the Microscale, School of Chemistry and Materials Science, CAS Key Laboratory of Mechanical Behavior and Design of Materials (LMBD), School of Engineering Science) X Xin Liu Z Zhixiang Gao Y Yang Kang Y Yuanmin Luo Y Yang Li W Wei Hu R Ran Long (Hefei National Research Center for Physical Sciences at the Microscale, Key Laboratory of Precision and Intelligent Chemistry, School of Chemistry and Materials Science, National Synchrotron Radiation Laboratory, School of Nuclear Science and Technology) H Haiding Sun

Abstract

Abstract Photoelectrochemical water splitting is considered one of the most promising paths for sustainable hydrogen production. However, the sluggish kinetics of the water oxidation reaction and poor stability of the photoanode significantly limit the overall performance of the photoelectrochemical device, particularly under acidic conditions, which poses great challenges for practical applications. Herein, the coupling of unique CoRuO x nanoclusters with dynamic electronic modulation effects to wafer‐scale InGaN nanowires is proposed, demonstrating superior photoelectrochemical activity and stability for acidic water oxidation. Compared with InGaN nanowires loaded with typical RuO₂ cocatalysts, CoRuO x /InGaN photoanodes achieve a remarkable improvement in applied bias photon‐to‐current efficiency from 0.77% to 2.25%, with stable operation for over 500 min under strongly acidic conditions. Such boosted performance is attributed mainly to Co induced dynamic electronic modulation, which enhances oxygen evolution while maintaining the stable operation of CoRuO x /InGaN photoanodes. Initially, the Co sites increased the oxidation state of Ru, enhancing the activity of oxygen evolution. Moreover, during PEC operation, the Co sites stabilized the Ru sites, preventing dissolution of cocatalyst. This unique self‐adaptive process significantly enhances the stability and activity of the photoanode, opening an effective avenue to achieve efficient and durable photoanodes for PEC applications.

Article Details

Volume / Issue Vol. 37, Issue 28
Published July 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (11)

W

Wengang Gu

W

Wei Chen

W

Weiyi Wang

Division of Energy Conversion & Storage, Hefei National Research Center for Physical Sciences at the Microscale, School of Chemistry and Materials Science, CAS Key Laboratory of Mechanical Behavior and Design of Materials (LMBD), School of Engineering Science

X

Xin Liu

Z

Zhixiang Gao

Y

Yang Kang

Y

Yuanmin Luo

Y

Yang Li

W

Wei Hu

R

Ran Long

Hefei National Research Center for Physical Sciences at the Microscale, Key Laboratory of Precision and Intelligent Chemistry, School of Chemistry and Materials Science, National Synchrotron Radiation Laboratory, School of Nuclear Science and Technology

H

Haiding Sun