Graphitic carbon nitride (g-C3N4) synthesis and heterostructures, principles, mechanisms, and recent advances: A critical review

被引:35
|
作者
Molaei, Mohammad Jafar [1 ]
机构
[1] Shahrood Univ Technol, Fac Chem & Mat Engn, Shahrood 3619995161, Iran
关键词
Photocatalyst; Type II heterostructures; Z-Scheme; S-Scheme; Hydrogen production; Z-SCHEME; QUANTUM DOTS; HETEROJUNCTION PHOTOCATALYSTS; II HETEROJUNCTIONS; SINGLE-ATOM; WATER; FABRICATION; EFFICIENT; COCATALYST; NANOSHEETS;
D O I
10.1016/j.ijhydene.2023.05.066
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
Graphitic carbon nitride (g-C3N4) is a semiconductor polymeric photocatalyst with an attractive electronic band structure, a moderate band gap energy, facile synthesis, and functionalization which can be applied as a photocatalyst in the visible light of the spectrum. The main problem of the g-C3N4 photocatalyst is the recombination of the photo -generated electron-hole pairs. The photogenerated electrons in the conduction band (CB) tend to return to the valence band (VB) with subsequent recombination which is unfavored for photocatalysis. It is difficult for a single-component photocatalyst to harvest a large portion of the sunlight spectrum, and simultaneously, possess a suitable spatial charge separation and efficient redox ability. Constructing a heterojunction aims to satisfy the above three factors in a photocatalyst heterojunction system. Constructing g-C3N4-based heterostructures can promote electron-hole pair separation through the charge transfer across the interface of the g-C3N4/semiconductor. In this review, the photocatalysis mechanism is discussed and several types of g-C3N4/semiconductor heterostructuresincluding type II, Z-scheme, and S-scheme heterostructures are explained. Recent advances in different types of g-C3N4-based heterostructures have been addressed. The synthesis methods for mesoporous, 0D, 1D, and 3D g-C3N4 and different modifications on this photocatalyst are reviewed.(c) 2023 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:32708 / 32728
页数:21
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