Highly-efficient visible-light-driven photocatalytic H2 evolution integrated with microplastic degradation over MXene/ZnxCd1-xS photocatalyst

被引:167
作者
Cao, Bingqian [1 ]
Wan, Shipeng [1 ,2 ]
Wang, Yanan [1 ]
Guo, Haiwei [1 ,4 ]
Ou, Man [3 ]
Zhong, Qin [1 ]
机构
[1] Nanjing Univ Sci & Technol, Sch Chem & Chem Engn, Nanjing 210094, Jiangsu, Peoples R China
[2] Yonsei Univ, Dept Chem & Biomol Engn, 50 Yonsei Ro, Seoul 120749, South Korea
[3] Nanjing Tech Univ, Sch Energy Sci & Engn, Nanjing 211816, Peoples R China
[4] Natl Univ Singapore, Dept Chem & Biomol Engn, Singapore 117576, Singapore
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Photocatalysis; MXene/ZnxCd1-xS; H-2; evolution; Microplastic degradation; Mechanism analysis; HYDROGEN-PRODUCTION; PERFORMANCE; NANOSHEETS; WATER; CONSTRUCTION; MXENE; MOS2; CDS; NANOCOMPOSITES; COCATALYST;
D O I
10.1016/j.jcis.2021.07.113
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
The development of highly-efficient photocatalyst for H-2 production integrated with microplastic degradation is significant to meet the demand for clean energy and resolve "white pollution". Herein, a series of MXene/ZnxCd1-xS photocatalysts were successfully fabricated for H-2 evolution integrated with degradation of polyethylene terephthalate (PET). The resultant photocatalysts exhibited excellent photocatalytic performance, and the best photocatalytic H-2 evolution rate can reach 14.17 mmol.g(-1).h(-1) in alkaline PET alkaline solution. What's more, the PET was also converted to the useful organic micromolecule, including glycolate, acetate, ethanol, etc. The highly-efficient photocatalytic performance of MXene/ZnxCd1-xS photocatalysts can be attributed to the enhanced separation ability of photocarriers and optimum band structure with enhanced oxidation capacity of valence band. Finally, the photocatalytic mechanism was investigated in detail. Overall, this work supplied a new useful guidance for solving the energy problem and microplastic pollution issues, simultaneously. (C) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页码:311 / 319
页数:9
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