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关于无贵金属助催化剂1T-WS修饰的ZnCdS用于增强光催化析氢反应运行机制的见解

Insights into the Operation of Noble-Metal-Free Cocatalyst 1T-WS -Decorated Zn Cd S for Enhanced Photocatalytic Hydrogen Evolution.

作者信息

Li Zhiqiang, Zhou Wei, Tang Yuan, Tan Xin, Zhang Yizhong, Geng Zikang, Guo Yuchen, Liu Lequan, Yu Tao, Ye Jinhua

机构信息

School of Environmental Science and Engineering, Tianjin University, No. 135 Yaguan Road, Jinnan District, Tianjin, 300350, P. R. China.

School of Science, Tianjin University, No. 135 Yaguan Road, Jinnan District, Tianjin, 300350, P. R. China.

出版信息

ChemSusChem. 2021 Nov 4;14(21):4752-4763. doi: 10.1002/cssc.202101670. Epub 2021 Sep 29.

DOI:10.1002/cssc.202101670
PMID:34409761
Abstract

Due to inefficient charge separation and low surface catalytic conversion efficiencies, cocatalysts are required for achieving photocatalytic hydrogen evolution. Being a noble-metal-free cocatalyst, metallic 1T-WS with excellent conductivity can function for this reaction. Herein, 1T-WS /Zn Cd S is constructed via a simple and feasible grinding approach. The composite containing 7.5 % 1T-WS in 1T-WS /Zn Cd S achieves a hydrogen evolution rate of 61.65 mmol g  h and an external quantum efficiency of 8.04 % at 420 nm, which is 37 times that of bare Zn Cd S (1.67 mmol g  h ). The electrical conductivity of metallic 1T-WS reduces the transfer impedance at the interface and thus accelerates the non-radiative energy transfer and electron transport rate. The different Fermi levels of 1T-WS and Zn Cd S form a Schottky junction, which promotes the transfer of photogenerated electrons from Zn Cd S to 1T-WS . More importantly, the close interface contact between 1T-WS and Zn Cd S results in strong electron interactions, which is conducive to the spatial separation of photogenerated electrons and holes. This work will further expand the application of 1T-WS in the photocatalytic hydrogen evolution process.

摘要

由于电荷分离效率低下和表面催化转化效率较低,需要助催化剂来实现光催化析氢。作为一种无贵金属的助催化剂,具有优异导电性的金属1T-WS可用于此反应。在此,通过一种简单可行的研磨方法构建了1T-WS/Zn Cd S。在1T-WS/Zn Cd S中含有7.5% 1T-WS的复合材料在420nm处实现了61.65 mmol g  h的析氢速率和8.04%的外量子效率,这是裸Zn Cd S(1.67 mmol g  h)的37倍。金属1T-WS的导电性降低了界面处的转移阻抗,从而加速了非辐射能量转移和电子传输速率。1T-WS和Zn Cd S不同的费米能级形成了肖特基结,促进了光生电子从Zn Cd S向1T-WS的转移。更重要的是,1T-WS和Zn Cd S之间紧密的界面接触导致了强烈的电子相互作用,这有利于光生电子和空穴的空间分离。这项工作将进一步拓展1T-WS在光催化析氢过程中的应用。

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