Covalent organic framework films grown on spongy g-C3N4 for efficient photocatalytic hydrogen production

被引:10
|
作者
Ding, Jingya [3 ]
Lou, Yaqin [1 ,2 ]
Dong, Guomeng [1 ,2 ]
Zhang, Yiwei [1 ,2 ]
机构
[1] Southeast Univ, Sch Chem & Chem Engn, Nanjing 211189, Peoples R China
[2] Southeast Univ, Jiangsu Optoelect Funct Mat & Engn Lab, Nanjing 224051, Peoples R China
[3] Yancheng Inst Technol, Sch Chem & Chem Engn, Yancheng 224051, Peoples R China
基金
中国国家自然科学基金;
关键词
g-C3N4; Covalent organic frameworks; S-scheme heterojunction; Photocatalytic hydrogen production; DFT; S-SCHEME HETEROJUNCTION; CARBON NITRIDE; ENERGY; WATER; CRYSTALLINE; DIOXIDE;
D O I
10.1016/j.jphotochem.2023.114590
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
Photocatalytic hydrogen production promisingly mitigates and ameliorates the status quo of energy shortage and decarbonization of the energy supply. Given this, a photocatalyst was prepared by modifying spongy g-C3N4 with covalent organic frameworks (COFs). As an electron acceptor with a large specific surface, COFs can trap more transition electrons, leading to an increase in the photogenerated carriers involved in the surface reaction and increasing the active sites of the photocatalyst. The S-scheme heterojunction structure formed in g-C3N4/COFs composite catalyst triggers a decrease in the recombination rate of photogenerated electron-hole pairs as well as an increase in photogenerated electrons. The photocatalytic hydrogen production rate reached the maximum value of 7788.10 mu mol center dot h(-1)center dot g(-1), almost 7 times that of g-C3N4. The AQE of the catalyst reached 29.6 %. The electron transfer path from g-C3N4 to COFs was verified by density functional theory (DFT) calculation.
引用
收藏
页数:8
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