Constructing crystalline homophase carbon nitride S-scheme heterojunctions for efficient photocatalytic hydrogen evolution

被引:21
|
作者
Luo, Mimi [1 ]
Jiang, Guanjie [1 ]
Yu, Min [1 ]
Yan, Yupeng [1 ]
Qin, Zhangjie [1 ]
Li, Yang [1 ]
Zhang, Qin [1 ]
机构
[1] Jiangxi Agr Univ, Coll Land Resource & Environm, Key Lab Agr Resources & Ecol Poyang Lake Watershed, Minist Agr & Rural Affairs China, Nanchang 330045, Peoples R China
关键词
Photocatalytic hydrogen evolution; Graphitic carbon nitride; S-scheme heterojunction; Au nanoparticles; Crystalline; H-2-EVOLUTION PERFORMANCE; G-C3N4; NANOSHEETS; AU NANOPARTICLES; ACTIVE-SITES; CO2; METAL; FABRICATION; COCATALYST; REDUCTION; DESIGN;
D O I
10.1016/j.jmst.2023.03.038
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The number of photogenerated carriers involved in the photocatalytic reaction is one of the main factors influencing the photocatalytic activity, and constructing S-scheme heterojunctions can significantly enhance the migration of photogenerated carriers, which is regarded as an effective method. In this study, Au nanoparticles (NPs)-supported crystallized heptazine/triazine-based carbon nitride (AHTCN) S-scheme heterojunction photocatalysts are successfully prepared by photoreduction methods. Except for the Au NPs function as an electron mediator, the experiment results and DFT calculations demonstrate that the Fermi energy level of crystallized heptazine/triazine-based heterojunction (HTCN) is pulled down after anchoring Au NPs, and thus the electron transfer path of HTCN changed from Type II-scheme to S-scheme. Owing to S-scheme heterojunction, the optimal AHTCN-2 (2 wt.% Au loaded) exhibits the best photocatalytic hydrogen evolution with a production rate of 715.2 mu mol h -1 g -1 , which significantly outperforms that of the HTCN. This work delivers a new strategy for the construction of S-scheme heterojunctions. (c) 2023 Published by Elsevier Ltd on behalf of The editorial office of Journal of Materials Science & Technology.
引用
收藏
页码:220 / 232
页数:13
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