Hydrophilic hydrogen-bonded organic frameworks/g-C3N4 all-organic Z-scheme heterojunction for efficient visible-light photocatalytic hydrogen production and dye degradation

被引:25
|
作者
Shi, Haixian [1 ]
Feng, Dengchong [1 ]
Li, Hanmei [1 ]
Yu, Dingshan [1 ]
Chen, Xudong [1 ]
机构
[1] Sun Yat Sen Univ, Sch Chem, Key Lab High Performance Polymer based Composites, Key Lab Polymer Composite Funct Mat,Minist Educ, Guangzhou 510275, Peoples R China
基金
中国国家自然科学基金;
关键词
Hydrogen-bonded organic frameworks; Graphitic carbon nitride nanosheets; Photocatalysis stability; Z-scheme heterojunction; CHARGE-CARRIER DYNAMICS; CARBON NITRIDE; WATER; SEPARATION; EVOLUTION; NANOTUBE; G-C3N4; MOF;
D O I
10.1016/j.jphotochem.2022.114292
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
Herein, a novel all-organic Z-scheme hydrogen-bonded organic frameworks (HOFs)/g-C3N4 nanosheets (CNNS) heterojunction photocatalyst is synthesized through an in-situ electrostatic method. Characterization and density functional theory studies together verify that the band structures with staggered alignment between HOFs and CNNS can induce a rapid Z-scheme interfacial charge-transfer pathway. Combing the complementary advantages of HOFs and CNNS, the fabricated Z-scheme HOFs/CNNS heterojunction inhibits photoinduced electron-hole recombination and more charge carriers are accumulated to produce highly reactive substances (center dot O-2(-), center dot OH and h(+)). In addition, the superior hydrophilicity of HOFs can enhance the interaction of HOFs/CNNS heterojunction with water molecules and methyl orange pollutant, which is beneficial to boosting photocatalytic activity. Therefore, in contrast to inactive pure HOFs, the novel Z-scheme HOFs/CNNS heterojunction exhibits a high photocatalytic hydrogen evolution rate of 4450 mu mol h(-1)g(-1) with an apparent quantum efficiency (AQY) of 22 % at 450 nm, which is approximately 11 times higher than that of pure CNNS. Additionally, such heterojunction enables 100 % degradation of methyl orange within 60 min.
引用
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页数:11
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