High-efficiency charge separation of Z-scheme 2D/ 2D C3N4/C3N5 nonmetal VdW heterojunction photocatalyst with enhanced hydrogen evolution activity and stability

被引:30
作者
Su, Nan [1 ]
Cheng, Shasha [1 ]
Zhang, Pingfan [1 ]
Dong, Hongjun [1 ]
Fang, Yuhai [1 ]
Zhou, Xiangtong [2 ]
Wang, Yun [1 ]
Li, Chunmei [1 ]
机构
[1] Jiangsu Univ, Inst Green Chem & Chem Technol, Sch Chem & Chem Engn, Zhenjiang 212013, Peoples R China
[2] Jiangsu Univ, Sch Environm & Safety Engn, Zhenjiang 212013, Peoples R China
基金
中国国家自然科学基金;
关键词
Z-Scheme nonmetal VdW; heterojunction; TC-TC coupling effect; Photocatalytic H2 production; G-C3N4; NANOSHEETS;
D O I
10.1016/j.ijhydene.2022.09.188
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
The interfacial charge transfer control is a key and arduous issue for propelling the migration/separation of photogenerated carriers for heterojunction photocatalysts. Here, a new 2D/2D C3N4/C3N5 nonmetal van der Waals (VdW) heterojunction is fabricated by the simple self-assembly technique in acidic medium, whose charge separation efficiency is promoted dramatically, thus being endowed with the high-efficiency photocatalytic hydrogen evolution (PHE) performance. The PHE rate reaches up to 3.33 mmol h-1 g-1 under the visible light and the apparent quantum efficiency (AQE) of 20.6% is achieved at 420 nm on the optimal 2D/2D C3N4/C3N5-5% sample. Furthermore, the 2D/2D C3N4/C3N5 nonmetal VdW heterojunction also exhibits the desired stability because there was no significant decrease after PHE reaction of 10 cycles with total 40 h. Such outstanding PHE activity and stability originate from the impelled separation of photoinduced charge car-riers and the powerful interfacial interaction through forming Z-Scheme charge transfer path and TC-TC coupling effect between C3N4 and C3N5 nanosheets. This work takes a sig-nificant guiding and demonstration for designing and exploiting other novel nonmetallic polymer-based VdW heterojunctions in the photocatalytic application field.(c) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:41010 / 41020
页数:11
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