论文成果
Interfacial engineering improved internal electric field contributing to direct Z-scheme-dominated mechanism over CdSe/SL-ZnIn2S4/MoSe2 heterojunction for efficient photocatalytic hydrogen evolution
- 发布时间：2024-01-19
- 点击次数：
- 关键字：CONSTRUCTION; COMPOSITES; DESIGN
- 摘要：Purposefully design and steering charge flow in heterostructure remains a crucial challenge for realizing efficient solar-to-fuel conversion. Herein, a newfangled ternary dual direct Z-scheme-dominated heterostructure of CdSe/ lower-coordinated S atoms (S-L)-rich ZnIn2S4/MoSe2 (CdSe/S-L-ZIS/MoSe2) is fabricated, where the lower-coordinated S atoms in ZIS can serve as the highly active sites for anchoring CdSe and MoSe2 & nbsp;on the surface of ZIS through Cd-S and Mo-S bonds. The optimized CdSe/S-L-ZIS/MoSe2 displays the ultrahigh visible-light (lambda > 420 nm) driven H-2 & nbsp;production rate of 70789.2 umol & BULL;g(- 1)& BULL;h(-1) with an apparent quantum efficiency (AQE) of 44.1% at 420 nm. Mechanism analysis and DFT calculations reveal that the interfacial chemical bond contributes to the intense internal electric field (IEF) in CdSe/S-L-ZIS/MoSe2, and finally lead to the direct Z-scheme-dominated and II-scheme-assisted charge transfer mechanism. This work establishes an atomic-scale interfacial engineering design model on directionally modulating charge transfer for efficient solar energy conversion applications.
- 卷号：431
- 期号：子辑1
- 是否译文：否
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