S-scheme heterojunction of ZnCdS nanospheres and dibenzothiophene modified graphite carbon nitride for enhanced H2 production

被引:100
作者
Li, Han [1 ]
Tao, Shanren [1 ]
Wan, Sijie [1 ]
Qiu, Guogen [1 ]
Long, Qing [1 ]
Yu, Jiaguo [1 ,2 ]
Cao, Shaowen [1 ]
机构
[1] Wuhan Univ Technol, State Key Lab Adv Technol Mat Synth & Proc, Wuhan 430070, Hubei, Peoples R China
[2] China Univ Geosci, Fac Mat Sci & Chem, Lab Solar Fuel, Wuhan 430074, Hubei, Peoples R China
来源
CHINESE JOURNAL OF CATALYSIS | 2023年 / 46卷
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Photocatalysis; Carbon nitride; ZnCdS; S-scheme heterojunction; Charge transfer; PHOTOCATALYST; REDUCTION; WATER;
D O I
10.1016/S1872-2067(22)64201-3
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
g-C3N4-based photocatalysts with an intramolecular donor-acceptor structure still suffer from in-adequate visible-light absorption and severe charge recombination. Constructing S-scheme hetero-junction is a promising approach to address these issues. Herein, ZCS (ZnCdS nano-spheres)@DBTCN (g-C3N4 modified by dibenzothiophene groups) S-scheme heterojunction photo -catalyst was synthesized through a self-assembly approach. The ZCS@DBTCN material showed a superior photocatalytic H2 production activity of 8.87 mmol g-1 h-1, which is 3.46 and 2.55 times that of pure DBTCN and ZCS, respectively. This enhanced photocatalytic performance could be ascribed to the synergistic effect of intramolecular internal electric field and S-scheme heterojunction, which boosts the separation and transport of photogenerated carriers within the molecular framework and at the interface, and preserves the maximum redox capacity of the spatially separated electrons and holes. Moreover, the S-scheme charge migrate mechanism of ZCS@DBTCN was strongly evi-denced by the in -situ irradiated Kelvin probe force microscopy and in -situ irradiated X-ray photoe-lectron spectroscopy. This study provides a protocol for designing g-C3N4-based hybrid photocata-lysts with high charge separation efficiency and excellent photocatalytic activity.(c) 2023, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:167 / 176
页数:10
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