Photocatalytic hydrogen evolution and antibiotic degradation by S-scheme ZnCo2S4/TiO2

被引:1
|
作者
Dai, Xiaojun [1 ]
Feng, Sheng [1 ]
Wu, Wei [1 ]
Zhou, Yun [1 ]
Ye, Zhiwei [1 ]
Cao, Xun [1 ]
Wang, Yang [1 ]
Yang, Chengdeng [1 ]
机构
[1] Changzhou Univ, Sch Environm & Safety Engn, Changzhou 213164, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
TiO2; S-scheme heterojunction; Photocatalysis; Hydrogen evolution; TC degradation; BIMETALLIC SULFIDE; H-2; PRODUCTION; HETEROJUNCTION; SOLAR; TIO2; HETEROSTRUCTURE; COMPOSITES; G-C3N4; WATER;
D O I
10.1016/j.ijhydene.2022.05.269
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this study, ZnCo2S4 (ZCS) nanoparticles were coupled on the surface of TiO2 by simple solvothermal method to form S-scheme heterojunction. Compared with ZCS and TiO2, the photocatalytic performance of ZCS/TiO2 under simulated sunlight is significantly improved, and its hydrogen evolution efficiency reaches 5580 mu mol.g(-1).h(-1) with the apparent quantum efficiency (AQY) up to 11.5% at 420 nm, which is 88.3 times and 54.3 times that of TiO2 and ZCS, respectively. Moreover, ZCS/TiO2 also has excellent perfor-mance in the photocatalytic degradation of tetracycline (TC). The enhancement of pho-tocatalytic performance of ZCS/TiO2 is mainly due to S-scheme heterojunction. On the one hand, the S-scheme electron transfer path not only improves the electron-hole separation efficiency, but also improves the charge transfer efficiency. On the other hand, ZCS significantly enhances the visible light absorption of ZCS/TiO2. The photocatalytic mech-anism and S-scheme heterojunction structure is confirmed by XPS, EPR, ultraviolet photoelectron spectroscopy (UPS) and energy band structure. This work provides a new idea for designing and constructing S-scheme heterojunction to improve the performance of photocatalytic hydrogen evolution and TC degradation.(c) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:25104 / 25116
页数:13
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