光催化
材料科学
电子转移
氢
肖特基势垒
量子效率
费米能级
贵金属
分解水
金属
化学物理
电子
催化作用
化学工程
化学
光电子学
光化学
物理
冶金
二极管
工程类
有机化学
量子力学
生物化学
作者
Zhiqiang Li,Wei Zhou,Yuan Tang,Xin Tan,Yizhong Zhang,Zikang Geng,Yu-Chen Guo,Lequan Liu,Tao Yu,Jinhua Ye
出处
期刊:Chemsuschem
[Wiley]
日期:2021-08-19
卷期号:14 (21): 4752-4763
被引量:35
标识
DOI:10.1002/cssc.202101670
摘要
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-WS2 with excellent conductivity can function for this reaction. Herein, 1T-WS2 /Zn0.5 Cd0.5 S is constructed via a simple and feasible grinding approach. The composite containing 7.5 % 1T-WS2 in 1T-WS2 /Zn0.5 Cd0.5 S achieves a hydrogen evolution rate of 61.65 mmol g-1 h-1 and an external quantum efficiency of 8.04 % at 420 nm, which is 37 times that of bare Zn0.5 Cd0.5 S (1.67 mmol g-1 h-1 ). The electrical conductivity of metallic 1T-WS2 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-WS2 and Zn0.5 Cd0.5 S form a Schottky junction, which promotes the transfer of photogenerated electrons from Zn0.5 Cd0.5 S to 1T-WS2 . More importantly, the close interface contact between 1T-WS2 and Zn0.5 Cd0.5 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-WS2 in the photocatalytic hydrogen evolution process.
科研通智能强力驱动
Strongly Powered by AbleSci AI