Photocatalytic Anaerobic Dehydrogenation of Alcohols over Metal Halide Perovskites: A New Acid-Free Scheme for H2 Production

被引:17
作者
Chen, Taoran [1 ]
Weng, Bo [2 ]
Lu, Suwei [1 ]
Zhu, Haixia [3 ]
Chen, Zhihui [3 ]
Shen, Lijuan [1 ]
Roeffaers, Maarten B. J. [2 ]
Yang, Min-Quan [1 ]
机构
[1] Fujian Normal Univ, Coll Environm Sci & Engn, Fujian Key Lab Pollut Control & Resource Reuse, Fuzhou 350007, Peoples R China
[2] Katholieke Univ Leuven, Dept Microbial & Mol Syst, cMACS, 3001 Leuven, Belgium
[3] Cent South Univ, Sch Phys & Elect, Hunan Key Lab Nanophonon & Devices, Changsha 410083, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
CO2; REDUCTION; HYDROGEN-PRODUCTION; FUNNEL STRUCTURE; QUANTUM DOTS; EVOLUTION; GRAPHENE; NANOCRYSTALS; NANOSHEETS; COMPOSITE; EFFICIENT;
D O I
10.1021/acs.jpclett.2c01501
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
Photocatalytic H-2 evolution from haloid acid (HX) solution by metal halide perovskites (MHPs) has been intensively investigated; however, the corrosive acid solution severely restricts its practical operability. Therefore, developing acid-free schemes for H-2 evolution using MHPs is highly desired. Here, we investigate the photocatalytic anaerobic dehydrogenation of alcohols over a series of MHPs (APbX(3), A = Cs+, CH3NH3+ (MA), CH(NH2)(2)(+) (FA); X = Cl-, Br-, I-) to simultaneously produce H-2 and aldehydes. Via the coassembly of Pt and rGO nanosheets on MAPbBr(3) microcrystals, the optimal MAPbBr(3)/rGO-Pt reaches a H-2 evolution rate of 3150 mu mol g(-1) h(-1) under visible light irradiation (780 nm >= lambda >= 400 nm), which is more than 105-fold higher than pure MAPbBr(3) (30 mu mol g(-1) h(-1)). The present work not only brings new ample opportunities toward photocatalytic H-2 evolution but also opens up new avenues for more effective utilization of MHPs in photocatalysis.
引用
收藏
页码:6559 / 6565
页数:7
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