MIL-125(Ti)-derived double vacancy-induced enhanced visible-light-driven TiO2 p-n homojunction for photocatalytic elimination of OFL and Cr(VI)

被引:8
|
作者
Yang, Jie [1 ]
Chen, Le [2 ]
Tan, Wenyi [3 ]
Han, Bing
Xu, Yihan [1 ]
Wang, Wenjing [1 ]
Xu, Jiahui [1 ]
Wang, Yuping [1 ,4 ]
机构
[1] Nanjing Normal Univ, Sch Chem & Mat Sci, Jiangsu Prov Key Lab Mat Cycling & Pollut Control, Nanjing 210023, Peoples R China
[2] Jiangsu Soc Environm Sci, Nanjing 210019, Peoples R China
[3] Nanjing Inst Technol, Adv Ind Technol Res Inst, Jiangsu 211167, Peoples R China
[4] Nanjing Univ Sci & Technol, Jiangsu Key Lab Chem Pollut Control & Resources Re, Nanjing 210094, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Double defect; TiO 2 p-n junction; Photodegradation of ofloxacin; MOFs derivatives; HYDROGEN EVOLUTION; BAND ALIGNMENT; HETEROJUNCTIONS;
D O I
10.1016/j.jece.2023.109721
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The efficient removal of quinolone antibiotics and heavy metal ions Cr(VI) using photocatalysis has attracted increasing attention in the field of environmental remediation. Here, we create a porous TiO2 p-n junction featuring titanium vacancies and oxygen vacancies. The double-deficient TiO2 p-n junction has the same catalytic ability as P25 under UV light. Still, it also can produce copious radicals under visible light excitation to achieve oxidative degradation of ofloxacin and reduced Cr (VI). This is helped by the two reaction centers generated by oxygen and titanium vacancies, the effective light-trapping capacity, and the close interfacial contacts. By adjusting the calcination temperature, oxygen vacancy, and titanium vacancy concentrations, TiO2 p-n junctions with the best photocatalytic activity were produced. In the pH range of 3.63-9.65, TiO2 p-n junctions maintained outstanding activity. The degradation pathway of ofloxacin was examined using theoretical calculations and LCMS. This study provides a technically guided experimental basis for preparing photocatalytic materials with double-defective p-n junctions.
引用
收藏
页数:10
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