Boron-doped rutile TiO2/anatase TiO2/ZrTiO4 ternary heterojunction photocatalyst with optimized phase interface and band structure

被引:24
|
作者
Liu, Changqing [1 ]
Li, Xu [1 ]
Xu, Chenggang [1 ]
Wu, Yuanting [1 ]
Hu, Xuefeng [2 ]
Hou, Xianghui [3 ]
机构
[1] Shaanxi Univ Sci & Technol, Sch Mat Sci & Engn, Shaanxi Key Lab Green Preparat & Functionalizat I, Xian 710021, Peoples R China
[2] Shaanxi Univ Sci & Technol, Sch Environm Sci & Engn, Xian 710021, Peoples R China
[3] Univ Nottingham, Adv Mat Res Grp, Nottingham NG7 2RD, England
基金
中国国家自然科学基金;
关键词
Interface; Surface; Rutile TiO2 / Anatase TiO2 / ZrTiO4; Functional application; HIGHLY EFFICIENT; ANATASE TIO2; GRAPHENE OXIDE; NANOCOMPOSITE; FABRICATION; REDUCTION; CO2; HETEROSTRUCTURE; MICROSPHERES; DEGRADATION;
D O I
10.1016/j.ceramint.2020.05.152
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
To improve the photocatalytic performance of TiO2-based heterostructures, Z-scheme/II-type rutile TiO2(R)/anatase TiO2 (A)/ZrTiO4 ternary heterojunction photocatalyst was designed and prepared via a facile one-step calcining strategy. Phase interface and band structure of the materials were controlled and optimized by regulating R-TiO2/A-TiO2 mass ratio in the TiO2 (A, R)/ZrTiO4 structures using boron doping. The highest photocatalytic performance and excellent catalytic stability of Rhodamine B removal was observed from the heterojunction with a low R-TiO2 /A-TiO2 mass ratio of 0.066, even after five testing cycles, accompanying with low photoluminescence intensity and electrochemical impedance, high photocurrent and charge carrier density (5.12 x 10(22) cm(-3)), and a positive shift of valence band position (from +2.06 to + 2.16 eV). The increased photodegradation behaviour was due to the remarkably enhanced separation efficiency and improved redox ability of the photo-induced charge carriers as a result of the high content of oxygen vacancies and the formed anatase TiO2/rutile TiO(2)Z-scheme heterojunction.
引用
收藏
页码:20943 / 20953
页数:11
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