Interfacial Charge Transfer in MoS2/TiO2 Heterostructured Photocatalysts: The Impact of Crystal Facets and Defects

被引:18
|
作者
Wei, Tingcha [1 ]
Lau, Woon Ming [2 ]
An, Xiaoqiang [3 ]
Yu, Xuelian [4 ]
机构
[1] Beijing Computat Sci Res Ctr, Beijing 100193, Peoples R China
[2] Univ Sci & Technol Beijing, Ctr Green Innovat, Sch Math & Phys, Beijing 100083, Peoples R China
[3] Tsinghua Univ, Ctr Water & Ecol, State Key Joint Lab Environm Simulat & Pollut Con, Sch Environm, Beijing 100084, Peoples R China
[4] China Univ Geosci, Beijing Key Lab Mat Utilizat Nonmetall Minerals &, Natl Lab Mineral Mat, Sch Mat Sci & Technol, Beijing 100083, Peoples R China
来源
MOLECULES | 2019年 / 24卷 / 09期
基金
中国国家自然科学基金;
关键词
crystal facets; oxygen vacancy; molybdenum sulfide; titanium dioxide; photocatalysts; charge transfer; TIO2 NANOTUBE ARRAYS; HYDROGEN-PRODUCTION; MOS2; WATER; PERFORMANCE; SEPARATION; SIZE;
D O I
10.3390/molecules24091769
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
One of the most challenging issues in photocatalytic hydrogen evolution is to efficiently separate photocharge carriers. Although MoS2 loading could effectively improve the photoactivity of TiO2, a fundamental understanding of the charge transfer process between TiO2 and MoS2 is still lacking. Herein, TiO2 photocatalysts with different exposed facets were used to construct MoS2/TiO2 heterostructures. XPS, ESR, together with PL measurements evidenced the Type II electron transfer from MoS2 to {001}-TiO2. Differently, electron-rich characteristic of {101}-faceted TiO2 were beneficial for the direct Z-scheme recombination of electrons in TiO2 with holes in MoS2. This synergetic effect between facet engineering and oxygen vacancies resulted in more than one order of magnitude enhanced hydrogen evolution rate. This finding revealed the elevating mechanism of constructing high-performance MoS2/TiO2 heterojunction based on facet and defect engineering.
引用
收藏
页数:11
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