Electronic Structure and Photocatalytic Activity of Dual Z-Scheme CdS@Bi2S3–MoS2 Heterostructures with a Full Spectrum

异质结 纳米棒 光催化 X射线光电子能谱 材料科学 制氢 电子顺磁共振 热液循环 分解水 水热合成 电子结构 纳米技术 化学工程 化学 光电子学 催化作用 核磁共振 物理 计算化学 有机化学 工程类 生物化学
作者
Dan Han,Wei Mo,Ning Yang,Lei Zuo,Qinghua Sun,Xianghua Zeng
出处
期刊:ACS applied energy materials [American Chemical Society]
卷期号:7 (24): 11879-11889 被引量:7
标识
DOI:10.1021/acsaem.4c02173
摘要

Two-dimensional Bi2S3 is considered a better photocatalyst when combined with CdS. To deeply understand electronic structures between CdS and Bi2S3, CdS@Bi2S3 core–shell nanorods (NRs) were synthesized with a two-step hydrothermal method, and CdS@Bi2S3–MoS2 composites were obtained with MoS2 nanoparticles decorated on the surface of CdS@Bi2S3 NRs. Then, the energy band alignments in CdS@Bi2S3–MoS2 were constructed from XPS and UPS measurements, and dual z-scheme CdS@Bi2S3–MoS2 heterostructures were confirmed from charge transfer with electron spin resonance (ESR) signals of •O2– and •OH. Finally, the photocatalytic hydrogen activities were carried out with the prepared samples. The results showed that the optimized CdS@Bi2S3 core–shell NRs have a hydrogen production rate of 4.29 mmol·h–1·g–1, which is 8.4 times higher than that of the pure CdS nanorods, and the optimized CdS@Bi2S3–MoS2 heterostructure has a hydrogen production rate of 8.72 mmol·h–1·g–1, which is 17 times higher than that of the pure CdS NRs. The enhanced photocatalytic activity can be ascribed to the dual z-scheme heterostructure and full-spectrum absorption; the former is favorable for the efficient separation of the photogenerated electron–hole pairs, and the latter is beneficial to the production of more photogenerated carriers. The studies will be helpful to understand the electronic structures of Bi2S3 and the related heterostructures.
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