苯甲醛
光催化
苯甲醇
材料科学
异质结
水溶液
化学工程
过氧化氢
相(物质)
双水相体系
光化学
催化作用
化学
有机化学
光电子学
工程类
作者
Linqian Li,Xiaobing Huo,Shipeng Chen,Qiang Luo,Wei Wang,Yifan Wang,Ning Wang
出处
期刊:Small
[Wiley]
日期:2023-05-17
卷期号:19 (38)
被引量:10
标识
DOI:10.1002/smll.202301865
摘要
Abstract Coupling the photoproduction of solar fuel and value‐added chemicals is highly attractive, as it maximizes the utilization of incident sunlight and the economic value of photocatalytic reactions. Constructing intimate semiconductor heterojunction for these reactions is highly desirable due to accelerated charge separation at the interfacial contact, but is challenged by material synthesis. Here, an active heterostructure bearing intimate interface, consisting of discrete Co 9 S 8 nanoparticles anchored on cobalt doped ZnIn 2 S 4 using a facile in situ one‐step strategy, can drive photocatalytic co‐production of H 2 O 2 and benzaldehyde from a two‐phase water/benzyl alcohol system with spatial product separation is reported. The heterostructure yields a high production amount of 49.5 and 55.8 mmol L −1 for H 2 O 2 and benzaldehyde under visible‐light soaking, respectively. The synchronous elemental Co doping and intimate heterostructure establishment substantially improve the overall reaction kinetics. Mechanism studies reveal that H 2 O 2 generated in the aqueous phase undergoes photodecomposition forming hydroxyl radical, which is subsequently transferred into the organic phase to oxidize benzyl alcohol into benzaldehyde. This study offers fertile guidelines for creating integrated semiconductors and broadens the avenue toward the coupled production of solar fuels and industrially important chemicals.
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