In situ construction of elemental phosphorus nanorod-modified TiO2 photocatalysts for efficient visible-light-driven H2 generation

被引:41
|
作者
Li, Shuang [1 ]
Ng, Yun Hau [2 ]
Zhu, Ruixue [3 ]
Lv, Sijie [1 ]
Wu, Chunxiao [1 ]
Liu, Yuxi [1 ]
Jing, Lin [1 ]
Deng, Jiguang [1 ]
Dai, Hongxing [1 ]
机构
[1] Beijing Univ Technol, Fac Environm & Life,Lab Catalysis Chem & Nanosci, Sch Environm & Chem Engn,Key Lab Beijing Reg Air, Dept Environm Chem Engn,Beijing Key Lab Green Cat, Beijing 100124, Peoples R China
[2] City Univ Hong Kong, Sch Energy & Environm, Kowloon, Tat Chee Ave, Hong Kong, Peoples R China
[3] Shanghai Tech Univ, Sch Phys Sci & Technol, Shanghai 201210, Peoples R China
关键词
Red phosphorus; Hydrogen evolution; Photocatalysis; TiO2; PHOTOCATALYTIC HYDROGEN-PRODUCTION; TRANSIENT ABSORPTION; WATER; ANATASE; NANOPARTICLES; MOS2; EVOLUTION; GRAPHENE; COMPOSITES; SEPARATION;
D O I
10.1016/j.apcatb.2021.120412
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
In this work, we constructed a red phosphorus (RP)/TiO2 composite system via a chemical vapor deposition strategy. The evolution of the fibrous phased RP nanorods on the surface of anatase TiO2 spheres was rationally adjusted by controlling the composition of precursors. The optimal RP/TiO2 composite exhibited a significantly enhanced visible-light-driven photocatalytic H2 generation rate of 681 mu mol h-1 g-1. The tightly interior surface bonding between RP and TiO2 greatly promoted the efficient charge transfer and redistribution by suppressing the charge recombination and self-trapping processes within TiO2, resulting in prolonged lifetimes of the active charges during the photocatalytic process as investigated in detailed using femtosecond time-resolved transient absorption (fs-TA) spectroscopy.
引用
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页数:8
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