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Interfacial charge transfer and enhanced photocatalytic mechanisms for Pt nanoparticles loaded onto sulfur-doped g-C3N4 in H2 evolution
被引:20
|作者:
Li, Zizhen
[1
]
Yao, Yuan
[1
]
Gao, Xinyu
[1
]
Bai, Hongcun
[2
]
Meng, Xiangchao
[1
]
机构:
[1] Ocean Univ China, Coll Chem & Chem Engn, Key Lab Marine Chem Theory & Technol, Minist Educ, Qingdao 266100, Peoples R China
[2] Ningxia Univ, State Key Lab High Efficiency Utilizat Coal & Gre, Yinchuan 750021, Ningxia, Peoples R China
基金:
中国博士后科学基金;
关键词:
Photocatalysis;
HER;
Carbon Nitride;
Hydrogen;
Platinum;
HYDROGEN EVOLUTION;
CARBON NITRIDE;
H-2-PRODUCTION ACTIVITY;
TIO2;
PHOTODEGRADATION;
SEMICONDUCTORS;
PERFORMANCE;
COMPOSITES;
GRAPHENE;
WATER;
D O I:
10.1016/j.mtener.2021.100881
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:
C3N4 exhibits great research potential in photocatalytic hydrogen evolution. Herein, sulfur is doped into C3N4 (SCN) by using thiourea as the precursor. The platinum (Pt) nanoparticles (NPs) are photo-deposited onto the surface of S-CN. Photocatalytic activity in H-2 evolution for C3N4 is improved from 0 to 56.58 mmol/h/g(cat) after sulfur doping, and to 742.19 mmol/h/gcat with the modifications of sulfur and Pt NPs. The enhancement in the photocatalytic hydrogen production may be due to the following: (1) the dope of sulfur can optimize the band structure and provide more reactive site for C3N4, (2) the porous morphology of S-CN enhanced the light-harvesting ability of C3N4, (3) Pt NPs with the surface plasmonic resonance effect are capable of absorbing more photons of visible light, and (4) Pt acts as a reservoir of photogenerated charge carriers, inhibiting its recombination. Enhancement mechanism has been deeply explored and comprehensively discussed in this work. (C) 2021 Published by Elsevier Ltd.
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