Insight into the Activity and Stability of RhXP Nano-Species Supported on g-C3N4 for Photocatalytic H2 Production

被引:180
作者
Dong, Hongjun [1 ]
Xiao, Mengya [1 ]
Yu, Siyu [1 ]
Wu, Huihui [1 ]
Wang, Yun [1 ]
Sung, Jingxue [2 ]
Chen, Gang [2 ]
Li, Chunmei [1 ]
机构
[1] Jiangsu Univ, Inst Green Chem & Chem Technol, Sch Chem & Chem Engn, Zhenjiang 212013, Jiangsu, Peoples R China
[2] Harbin Inst Technol, MIIT Key Lab Crit Mat Technol New Energy Convers, Sch Chem & Chem Engn, Harbin 150001, Peoples R China
基金
中国国家自然科学基金;
关键词
rhodium phosphide; cocatalyst; carbon nitride; photocatalytic H-2 production; high activity and stability; HYDROGEN EVOLUTION; COCATALYST; HETEROJUNCTION; NANOSHEETS;
D O I
10.1021/acscatal.9b04671
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
Transition-metal phosphides have been demonstrated as cocatalysts with great promise for photocatalytic H-2 production materials, but the insurmountable issue remains maintaining outstanding stability while achieving high photocatalytic efficiency. Herein, the rhodium phosphide (RhPx) nanospecies as cocatalyst is firmly mounted on graphitic carbon nitride (g-C3N4) nanosheets to realize the improved activity and stability for photocatalytic H-2 production. The maximum H-2 production rate over RhPx/g-C3N4 driven by visible light diplays a 5.6-fold improvement compared with Pt/g-C3N4. Meanwhile, the apparent quantum efficiency of 18.4% is achieved at a fixed wavelength of 420 nm that far exceeds the reported g-C3N4 modified with other single-transition-metal phosphides. Particularly, RhPx/g-C3N4 can maintain consistently stable H-2 production when enduring over 25 cyclic reactions with a total of 100 h. The deep insight into the modification effect of RhPx nanospecies reveals that it dramatically facilitates migration and separation of photoinduced electron-hole pairs and heightens interaction at the heterointerfaces between RhPx nanospecies and g-C3N4 nanosheets. This contribution extends the broad potential application of transition-metal phosphides as cocatalysts in the photocatalytic conversion from solar to hydrogen energy.
引用
收藏
页码:458 / 462
页数:9
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