Efficient photocatalytic H2 evolution over NiS-PCN Z-scheme composites via dual charge transfer pathways

被引:49
作者
Zhang, Ping [1 ]
Wu, Li-jun [1 ]
Pan, Wei-guo [2 ,3 ]
Bai, Shu-cheng [1 ]
Guo, Rui-tang [2 ,3 ]
机构
[1] Tongji Univ, Sch Mech Engn, Shanghai, Peoples R China
[2] Shanghai Univ Elect Power, Coll Energy & Mech Engn, Shanghai, Peoples R China
[3] Shanghai Engn Res Ctr Power Generat Environm Prot, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
S and O defected PCN; NiS; Dual fast transfer pathways; H-2; production; GRAPHITIC CARBON NITRIDE; LIGHT-DRIVEN PHOTOCATALYST; HYDROGEN EVOLUTION; G-C3N4; NANOSHEETS; PHOTOCHEMICAL-SYNTHESIS; ASSISTED SYNTHESIS; METAL; HETEROJUNCTION; SEPARATION; INTERFACE;
D O I
10.1016/j.apcatb.2021.120040
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
In this study, both narrow band-gap semiconductor NiS and S and O defects modification were introduced into the design of PCN photocatalyst to enhance its photocatalytic performance. The O and S defects, on one hand, provided the higher specific area and more charge separation sites, and constituted the dual fast charge transfer pathways with NiS through the N-C-S-Ni bonds and N-C-O-Ni-S bonds, which greatly increased the carrier transfer kinetics at the interface and restricted the carrier recombination. On the other hand, the midgap level derived from S and O defects also enhanced the absorption of visible light and accommodated more excited electrons. Furthermore, Z-scheme mode could form as Ni2+ species were reduced to metallic Ni-0 to acts as charge transfer mediator under irradiation. As such, a maximum hydrogen evolution rate of 1239.3 mu mol/g/h was achieved over 5%NiS/SO-Melon composite, nearly 31.4 times the rate of pristine PCN.
引用
收藏
页数:12
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