1D/2D CeO2/ZnIn2S4 Z-scheme heterojunction photocatalysts for efficient H2 evolution under visible light

异质结 纳米棒 X射线光电子能谱 光催化 材料科学 可见光谱 光谱学 电子顺磁共振 载流子 分解水 光化学 化学工程 光电子学 纳米技术 化学 催化作用 核磁共振 物理 有机化学 量子力学 工程类
作者
Renqian Jiang,Liang Mao,Yulong Zhao,Junying Zhang,Eugene B. Chubenko,Vitaly P. Bondarenko,Yanwei Sui,Xiuquan Gu,Xiaoyan Cai
出处
期刊:Science China. Materials [Springer Science+Business Media]
卷期号:66 (1): 139-149 被引量:54
标识
DOI:10.1007/s40843-022-2132-8
摘要

The development of a high-efficiency photocatalyst having favorable charge transfer has become an important scientific approach for solar-to-fuel conversion. In this study, the one-dimensional (1D)/2D CeO2/ZnIn2S4 (ZIS) photocatalyst having a Z-scheme heterojunction has been successfully fabricated using the in situ growth of ZIS nanosheets on the CeO2 nanorod surfaces. The optimal H2 production rate of 3.29 mmol g−1 h−1 was achieved with the 15% CeO2/ZIS sample under visible light without any cocatalyst; furthermore, this value was 2.7 and 92.6 times higher than those of pristine ZIS and CeO2, respectively. The remarkable photocatalytic activity can be attributed to the efficient separation of photogenerated carriers as well as the formation of the Z-scheme heterojunction, which maintained the strong reduction of electrons in ZIS for H2 production. The presence of an internal electric field between CeO2 and ZIS has been demonstrated by both density functional theory calculations and Kelvin probe force microscopy. The Z-scheme transfer of photogenerated carriers in the CeO2/ZIS heterojunction has been confirmed by electron paramagnetic resonance spectroscopy and in situ irradiated X-ray photoelectron spectroscopy. This study presents certain insights into the development of efficient Z-scheme photocatalysts for H2 evolution from solar water splitting.
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