Modulating the bridging units of carbon nitride for highly efficient charge separation and visible-light-responsive photocatalytic H2 evolution

被引:26
|
作者
Liu, Dong [1 ]
Chen, Shengtao [1 ]
Zhang, Yuexing [2 ]
Li, Renjie [1 ]
Peng, Tianyou [1 ]
机构
[1] Wuhan Univ, Coll Chem & Mol Sci, Engn Res Ctr Organosilicon Cpds & Mat, Wuhan 430072, Peoples R China
[2] Dezhou Univ, Coll Chem & Chem Engn, Dezhou 253023, Peoples R China
基金
中国国家自然科学基金;
关键词
Carbon nitride; Charge separation and transfer; Molecular heterojunction; Modulating bridging units; Photocatalytic H 2 evolution; GRAPHITIC CARBON; HYDROGEN; PERFORMANCE; NANOSHEETS; WATER; NMR;
D O I
10.1016/j.apcatb.2023.122805
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 nitrides have attracted broad attention in the field of photocatalytic H2 evolution. However, the design and preparation of carbon nitrides with highly efficient charge separation and transfer are still challenging. Here, we synthesized a novel heptazine derivative-based photocatalyst, named as M+U-x to overcome the inherent limitations of carbon nitrides (C3N4 and C3N5). Experimental and theoretical calculation results reveal that the resultant M+U-x is composed by electron-withdrawing C3N4 and electron-donating C3N5 moieties, which are integrated into the conjugated framework via N-atoms and azo bridging units to form molecular heterojunctions. Among these, M+U-3 can dramatically facilitate the spatial separation of photoinduced charge carriers, delivering significantly high visible-light-responsive H2 evolution activity of 372 & mu;mol h-1 with an AQY of 21.6% at 400 nm. This work provides a novel strategy for rationally modulating the bridging units of carbon nitrides to acquire enhanced charge-carrier mobility and efficient photocatalytic H2 evolution from the molecular level.
引用
收藏
页数:13
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