Edge electron-rich carbon nitride via π-acceptor frame with high-efficient charge separation for photocatalytic hydrogen evolution and environmental remediation

被引:9
|
作者
Jiao, Yingying [1 ]
Li, Yike [1 ]
Wang, Jianshe [1 ]
He, Zhanhang [1 ]
Li, Zhongjun [1 ]
机构
[1] Zhengzhou Univ, Coll Chem, Zhengzhou 450001, Peoples R China
基金
中国国家自然科学基金;
关键词
Photocatalysis; g-C3N4; Hydroxyls; pi-acceptor; Charge transfer mechanism; TOTAL-ENERGY CALCULATIONS; INTRAMOLECULAR DONOR; G-C3N4; ENHANCEMENT; CONSTRUCTION;
D O I
10.1016/j.jcis.2022.07.001
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
Carbon nitride (g-C3N4) has broad application prospects in photocatalytic hydrogen production, but its photocatalytic efficiency is not ideal because of the rapid recombination of photogenerated electrons and holes. Herein, we developed a green strategy to fabricate hydroxyls and carbon-bridging co-modified g-C3N4 (CCN-OH) through a one-pot copolymerization and hydrothermal treatment. Experiments and density functional theory (DFT) calculations illustrated that carbon substitution of partial bridge nitrogen can improve the degree of electron delocalization to enhance the electron supply capacity of g-C3N4, and the exsitence of the electron-withdrawing -OH group induces electron migration from carbon nitride to hydroxyl group, which further improves the efficiency of photogenerated charge separation. In addition, CCN-OH possess narrower band structure, resulting in an increased visible light utilization efficiency. The as-synthesized CCN-OH9 samples displayed an excellent photocatalytic activity for degradation of tetracycline with apparent reaction rate constant (k) of 0.018 min-1 and photocatalytic hydrogen evolution of 1880.3 mu mol g(-1)h (1), which was respectively 2.2 and 9.8 times higher than that of CN. (c) 2022 Published by Elsevier Inc.
引用
收藏
页码:889 / 898
页数:10
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