Photocatalytically recovering hydrogen energy from wastewater treatment using MoS2 @TiO2 with sulfur/oxygen dual-defect

被引:112
|
作者
Wu, Yaoyao [1 ]
Chen, Xiaotao [1 ]
Cao, Jiachun [2 ]
Zhu, Yuqing [1 ]
Yuan, Wenjing [1 ]
Hu, Zhuofeng [1 ]
Ao, Zhimin [2 ]
Brudvig, Gary W. [3 ,4 ]
Tian, Fenghui [5 ,6 ,7 ]
Yu, Jimmy C. [8 ]
Li, Chuanhao [1 ]
机构
[1] Sun Yat Sen Univ, Sch Environm Sci & Engn, Guangdong Prov Key Lab Environm Pollut Control &, Guangzhou 510006, Peoples R China
[2] Guangdong Univ Technol, Guangdong Key Lab Environm Catalysis & Hlth Risk, Guangzhou Key Lab Environm Catalysis & Pollut Con, Sch Environm Sci & Engn,Inst Environm Hlth & Poll, Guangzhou 510006, Peoples R China
[3] Yale Univ, Yale Energy Sci Inst, New Haven, CT 06520 USA
[4] Yale Univ, Dept Chem, New Haven, CT 06520 USA
[5] Qingdao Univ, State Key Lab Biofibers & Ecotext, Inst Computat Sci & Engn, Qingdao 266071, Peoples R China
[6] Qingdao Univ, Coll Chem & Chem Engn, Qingdao 266071, Peoples R China
[7] Qingdao Univ, Coll Environm Sci & Engn, Qingdao 266071, Peoples R China
[8] Chinese Univ Hong Kong, Dept Chem, Shatin, Hong Kong, Peoples R China
基金
中国国家自然科学基金;
关键词
Dual-functional photocatalysis; Dual defects; Oxygen vacancy; Resource-recovering wastewater treatment; ACTIVE EDGE SITES; ULTRATHIN NANOSHEETS; ORGANIC POLLUTANTS; VACANCY DEFECT; TIO2; OXIDATION; EVOLUTION; DEGRADATION; GENERATION; SURFACE;
D O I
10.1016/j.apcatb.2021.120878
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
Photocatalysis is a promising technology for energy and environment applications. Herein, a dual-defect heterojunction system of TiO2 hierarchical microspheres with oxygen vacancies modified with ultrathin MoS2-x nanosheets (MoS2-x @TiO2-OV) is designed for simultaneously degrading pollutants and evolving hydrogen. MoS2- x @TiO2-OV exhibits a dramatically enhanced photocatalytic activity with a H2 evolution rate of 2985.16 mu mol g- 1h- 1. In treating the simulated pharmaceutical wastewater, MoS2- x @TiO2-OV is capable of purifying various refractory contaminants, with the highest H2 evolution rate of 41.59 mu mol g- 1h- 1 during enrofloxacin degradation. While treating the simulated coking wastewater, the catalyst achieves a H2 evolution rate of 102.72 mu mol g- 1h- 1 and a mineralization rate of 50%. Computational studies suggest that the dual-defect is superior for the adsorption of H* and producing.OH ('dual-defect boosted dual-function'). Also, the dual-defect sites significantly boosted the charge-carrier separation and transfer efficiencies. This work highlights the crucial role of defect engineering to develop the energy-recovering wastewater treatment approaches.
引用
收藏
页数:11
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