光催化
异质结
过氧化氢
材料科学
制氢
分解水
载流子
光化学
半导体
太阳能
析氧
可持续能源
吸收(声学)
氧气
化学
太阳能转换
催化作用
氢
纳米技术
光电子学
太阳能燃料
氢燃料
化学工程
氧化还原
能量转换
无机化学
带隙
单线态氧
人工光合作用
电化学
工作(物理)
光催化分解水
可持续生产
吸收光谱法
宽禁带半导体
超快激光光谱学
过渡金属
作者
Mengyu Lin,Yunhui He,Xiaolin Guo,Guangcan Xiao,Fang‐Xing Xiao
出处
期刊:Chemsuschem
[Wiley]
日期:2025-10-09
卷期号:18 (23): e202501827-e202501827
被引量:4
标识
DOI:10.1002/cssc.202501827
摘要
Photocatalytic hydrogen peroxide (H2O2) production offers a sustainable alternative to the energy-intensive anthraquinone process. However, developing efficient semiconductor systems for oxygen reduction to H2O2 remains challenging. Herein, we construct an In2S3/Ag2S heterostructure via a cation-exchange strategy, achieving atomic-level interfacial modulation that enhances charge separation and boosts H2O2 production. Spectroscopic and radical trapping experiments identify the dominant active species and confirm a favorable two-electron oxygen reduction pathway. The tailored energy band alignment between In2S3 and Ag2S promotes visible-light absorption and facilitates efficient carrier migration, leading to significantly improved photocatalytic performance. This work provides a feasible approach to designing transition metal chalcogenides (TMCs)-based heterostructures for sustainable H2O2 synthesis and advances solar-to-chemical energy conversion.
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