AgWOS Bimetallic Oxysulfides With Synergistic Coupling of Heterovalent States and Vacancy Defects for Boosting Photocatalytic Hydrogen Evolution: An Insightful Case of the W-Doping Plus Hydrazine-Driven Design

Baoqian Yang , Tsz Lok Wan , Xinru Wu , Dong-Hau Kuo , Haoyu Wang , Kening Xiang , Cuizhu Li , Tao Liu , Dongfang Lu , Jinguo Lin , Xiaoyun Chen

Carbon Neutralization ›› 2026, Vol. 5 ›› Issue (1) : e70118

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Carbon Neutralization ›› 2026, Vol. 5 ›› Issue (1) :e70118 DOI: 10.1002/cnl2.70118
RESEARCH ARTICLE
AgWOS Bimetallic Oxysulfides With Synergistic Coupling of Heterovalent States and Vacancy Defects for Boosting Photocatalytic Hydrogen Evolution: An Insightful Case of the W-Doping Plus Hydrazine-Driven Design
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Abstract

Recent studies have indicated that the heterovalent states and vacancy defect structures in bimetallic oxysulfide play a crucial role in pollutant reduction reactions. However, systematic investigations into the synergistic coupling between heterovalent states and vacancy defect structures during the photocatalytic hydrogen evolution reaction (PHER) remain scarce. Herein, a tungsten/oxygen (W/O) co-doped Ag2S bimetallic oxysulfide (AgWOS) with heterovalent W5+/W6+ states and sulfur vacancy (Vs) defects was synthesized via a facile thermohydrolysis method. The combination of W-doping and hydrazine-driven conditions induces abundant Vs defects, which act as active sites for water adsorption and activation, thereby facilitating proton generation in the PHER process. Moreover, the hydrazine-driven condition promotes the formation of heterovalent W5+/W6+ states, which provide efficient electron transfer channels between W5+ and W6+ to boost PHER performance. The optimized AgWOS-2 with a balanced heterovalent n(W5+)/n(W6+) ratio and a high concentration of Vs achieves an impressive PHER rate of 1074.2 µmol·h−1 and an apparent quantum efficiency of 6.21% at 420 nm in pure water. Density functional theory calculations reveal that the synergy between heterovalent states and vacancy defects lowers the water dissociation barrier, accelerates *H generation, and boosts electron transfer between W5+ and W6+. Moreover, S-3p and O-2p orbital hybridization suppresses photocorrosion and improves catalyst stability, enabling AgWOS-2 to retain 91.6% of its initial PHER activity after ten cycles. This study elucidates the synergistic interaction mechanism between heterovalent states and vacancy defects in a bimetallic oxysulfide, offering valuable insights for the rational design of efficient and durable PHER catalysts.

Keywords

bimetal oxysulfide / heterovalent states / hydrazine regulation / photocatalytic hydrogen evolution / sulfur vacancy defects

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Baoqian Yang, Tsz Lok Wan, Xinru Wu, Dong-Hau Kuo, Haoyu Wang, Kening Xiang, Cuizhu Li, Tao Liu, Dongfang Lu, Jinguo Lin, Xiaoyun Chen. AgWOS Bimetallic Oxysulfides With Synergistic Coupling of Heterovalent States and Vacancy Defects for Boosting Photocatalytic Hydrogen Evolution: An Insightful Case of the W-Doping Plus Hydrazine-Driven Design. Carbon Neutralization, 2026, 5(1): e70118 DOI:10.1002/cnl2.70118

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2026 The Author(s). Carbon Neutralization published by Wenzhou University and John Wiley & Sons Australia, Ltd.

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