An Inorganic/Organic S-Scheme Heterojunction H2-Production Photocatalyst and its Charge Transfer Mechanism

被引:771
作者
Cheng, Chang [1 ]
He, Bowen [1 ]
Fan, Jiajie [2 ]
Cheng, Bei [1 ]
Cao, Shaowen [1 ]
Yu, Jiaguo [1 ,3 ]
机构
[1] Wuhan Univ Technol, State Key Lab Adv Technol Mat Synth & Proc, Wuhan 430070, Peoples R China
[2] Zhengzhou Univ, Sch Mat Sci & Engn, Zhengzhou 450001, Peoples R China
[3] King Abdulaziz Univ, Fac Sci, Dept Phys, Jeddah 21589, Saudi Arabia
基金
中国国家自然科学基金;
关键词
photocatalysis; S‐ scheme heterojunctions; hydrogen evolution; conjugated polymers; CdS;
D O I
10.1002/adma.202100317
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Inspired by natural photosynthesis, constructing inorganic/organic heterojunctions is regarded as an effective strategy to design high-efficiency photocatalysts. Herein, a step (S)-scheme heterojunction photocatalyst is prepared by in situ growth of an inorganic semiconductor firmly on an organic semiconductor. A new pyrene-based conjugated polymer, pyrene-alt-triphenylamine (PT), is synthesized via the typical Suzuki-Miyaura reactions, and then employed as a substrate to anchor CdS nanocrystals. The optimized CdS/PT composite, coupling 2 wt% PT with CdS, exhibits a robust H-2 evolution rate of 9.28 mmol h(-1) g(-1) with continuous release of H-2 bubbles, as well as a high apparent quantum efficiency of 24.3%, which is approximate to 8 times that of pure CdS. The S-scheme charge transfer mechanism between PT and CdS, is systematically demonstrated by photoirradiated Kelvin probe measurement and in situ irradiated X-ray photoelectron spectroscopy analyses. This work provides a protocol for preparing specific S-scheme heterojunction photocatalysts on the basis of inorganic/organic coupling.
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页数:8
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