The synergistic effect with S-vacancies and built-in electric field on a TiO2/MoS2 photoanode for enhanced photoelectrochemical performance

被引:67
作者
Han, Jianhua [1 ]
Zhang, Shaoce [2 ]
Song, Qinggong [1 ]
Yan, Huiyu [1 ]
Kang, Jianhai [1 ]
Guo, Yanrui [1 ]
Liu, Zhifeng [1 ,2 ]
机构
[1] Civil Aviat Univ China, Coll Sci, Tianjin 300300, Peoples R China
[2] Tianjin Chengjian Univ, Tianjin Key Lab Bldg Green Funct Mat, Sch Mat Sci & Engn, Tianjin 300384, Peoples R China
基金
中国国家自然科学基金;
关键词
MOS2 ULTRATHIN NANOSHEETS; ACTIVE EDGE SITES; P-N-JUNCTION; OXYGEN VACANCIES; HYDROGEN EVOLUTION; NANOROD ARRAYS; WATER; HETEROJUNCTION; DEFECT; OXIDE;
D O I
10.1039/d0se01515f
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
It is significant to design an electrode with high carrier separation and transport efficiency in a photoelectrochemical water splitting system. In this study, we utilized a facile H2O2 etching method for modulating S-vacancies in a TiO2/MoS2 nanostructure to enhance photoelectrochemical performance. The as-prepared TiO2/MoS2 with S-vacancies demonstrates an increased photocurrent density of 1.56 mA cm(-2) at 1.23 V vs. RHE, which is 2.14 times higher than that of pristine TiO2 (0.73 mA cm(-2) at 1.23 V vs. RHE). An appropriate energy level alignment between TiO2 and MoS2 and defect modulation are demonstrated in this study. The photo-generated electrons and holes are effectively separated and transported due to the built-in electric field in TiO2/MoS2. Moreover, the surface oxygen production reaction is enhanced due to its plenty exposed reaction active sites. This study demonstrates the synergistic effects of S-vacancies and built-in electric field in enhancing the carrier separation and transport properties. Furthermore, this study provides a universal strategy in designing high quality photoelectrodes in the photoelectrochemical system.
引用
收藏
页码:509 / 517
页数:9
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