异质结
光催化
材料科学
载流子
催化作用
热液循环
瓶颈
析氧
化学工程
纳米技术
光电子学
限制
电场
密度泛函理论
有效核电荷
带隙
氧气
能量转换效率
耗尽区
化学反应工程
电荷(物理)
电子迁移率
电子能带结构
光化学
科技与社会
作者
Shuai Zhang,Tao Sun,Hui Lü,Guanqi Wang,Wei Sun,Xueying Cheng,Xingjing Zhang,Renquan Guan,Chunbo Liu
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2026-06-23
卷期号:19 (9): 94908930-94908930
被引量:3
标识
DOI:10.26599/nr.2026.94908930
摘要
Abstract Sulfide-based photocatalysts hold promise for visible-light-driven H2O2 synthesis; however, the low efficiency of photogenerated charge carrier separation and migration remains a critical bottleneck limiting their overall yield. In response to this challenge, the construction of S-scheme heterojunctions represents a promising strategy to expedite charge carrier migration, enhance charge utilization, and consequently boost photocatalytic H2O2 production. This study successfully prepared an S-scheme ZnIn2S4/Bi2MoO6 heterojunction photocatalyst, bridged by interfacial Mo–S bonds, via a hydrothermal method. This catalyst achieved a high production rate of up to 1387 μmol·g−1·h−1 in the photocatalytic generation of H2O2. Combining in-situ spectroscopic characterization with density functional theory calculations, it was clarified that the formation of Mo–S bonds induces the construction of the S-scheme heterojunction. The synergistic effect of the interfacial built-in electric field and band alignment drives the spatial separation and directional migration of photogenerated charge carriers, as well as the dynamic evolution of the key oxygen intermediate, thereby enabling the efficient generation of H2O2 via the two-electron oxygen reduction reaction pathway. This work provides a novel interfacial engineering strategy and mechanistic insights for designing efficient and stable S-scheme heterojunction catalysts for the green photocatalytic synthesis of H2O2.
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