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构建用于增强可见光下析氢活性的CoS/Zn Cd S S型异质结

Construction of CoS /Zn Cd S S-Scheme Heterojunction for Enhancing H Evolution Activity Under Visible Light.

作者信息

Ma Lijun, Xu Jing, Zhao Sheng, Li Lingjiao, Liu Ye

机构信息

School of Chemistry and Chemical Engineering, North Minzu University, Yinchuan, 750021, PR China.

Key Laboratory of Chemical Engineering and Technology, North Minzu University), State Ethnic Affairs Commission, Yinchuan, 750021, PR China.

出版信息

Chemistry. 2021 Nov 11;27(63):15795-15805. doi: 10.1002/chem.202102811. Epub 2021 Oct 6.

DOI:10.1002/chem.202102811
PMID:34453357
Abstract

In the field of photocatalysis, building a heterojunction is an effective way to promote electron transfer and enhance the reducibility of electrons. Herein, the S-scheme heterojunction photocatalyst (CoS /Zn Cd S) of CoS nanospheres modified Zn Cd S solid solution was synthesized and studied. The H evolution rate of the composite catalyst reached 25.15 mmol g  h , which was 3.26 times that of single Zn Cd S, whereas pure CoS showed almost no hydrogen production activity. Moreover, CoS /Zn Cd S had excellent stability and the hydrogen production rate after six cycles of experiments only dropped by 6.19 %. In addition, photoluminescence spectroscopy and photoelectrochemical experiments had effectively proved that the photogenerated carrier transfer rate of CoS /Zn Cd S was better than CoS or Zn Cd S single catalyst. In this study, the synthesized CoS and Zn Cd S were both n-type semiconductors. After close contact, they followed an S-scheme heterojunction electron transfer mechanism, which not only promoted the separation of their respective holes and electrons, but also retained a stronger reduction potential, thus promoting the reduction of H protons in photocatalytic experiments. In short, this work provided a new basis for the construction of S-scheme heterojunction in addition to being used for photocatalytic hydrogen production.

摘要

在光催化领域,构建异质结是促进电子转移和增强电子还原性的有效方法。在此,合成并研究了CoS纳米球修饰的ZnCdS固溶体的S型异质结光催化剂(CoS/ZnCdS)。复合催化剂的析氢速率达到25.15 mmol g  h ,是单一ZnCdS的3.26倍,而纯CoS几乎没有产氢活性。此外,CoS/ZnCdS具有优异的稳定性,经过六个循环实验后的产氢速率仅下降了6.19%。另外,光致发光光谱和光电化学实验有效证明了CoS/ZnCdS的光生载流子转移速率优于CoS或ZnCdS单一催化剂。在本研究中,合成的CoS和ZnCdS均为n型半导体。紧密接触后,它们遵循S型异质结电子转移机制,不仅促进了各自空穴和电子的分离,还保留了较强的还原电位,从而在光催化实验中促进了H质子的还原。简而言之,这项工作除了用于光催化产氢外,还为S型异质结的构建提供了新的依据。

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