Engineering a NiAl-LDH/CoSx S-Scheme heterojunction for enhanced photocatalytic hydrogen evolution

被引:43
|
作者
Liu, Yanan [1 ]
Ma, Xiaohua [1 ]
Jin, Zhiliang [1 ]
机构
[1] North Minzu Univ, Sch Chem & Chem Engn, Ningxia Key Lab Solar Chem Convers Technol, Key Lab Chem Engn & Technol,State Ethn Affairs Co, Yinchuan 750021, Ningxia, Peoples R China
关键词
Photocatalytic; Hydrogen evolution; S-scheme heterostructure; EFFICIENT DEGRADATION; OXYGEN EVOLUTION; CARBON NITRIDE; H-2; LDH; PEROXYMONOSULFATE; PERFORMANCE; NANOFLOWERS; COCATALYST; REDUCTION;
D O I
10.1016/j.jcis.2021.11.065
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
The use of semiconductors to construct heterojunctions to suppress the rapid recombination of photogenerated charges and holes is considered to be an effective way to improve the efficiency of photocatalytic hydrogen evolution. Herein, cobalt sulfide (CoSx) nanoparticles are cultivated in situ in the folds of three-dimensional flower-like nickel-aluminium layered double hydroxides (NiAl-LDHs) using a facile solvothermal method. The hydrogen production rate of the binary CoSx/NiAl-LDH heterojunction reaches 3678.59 lmol/g/h, which is 83.74 and 22 times the rates of CoSx and NiAl-LDH, respectively. The unique three-dimensional structure of NiAl-LDH facilitates the growth of CoSx and shortens the transfer pathway of photogenerated electrons. More importantly, the built-in electric field formed at the interface and the S-type charge transport mechanism caused by the bending of the energy band enhance not only charge separation but also maintain the strong oxidation ability of the holes. In this study, the newly designed S-scheme heterojunction offers a new strategy for enhancing photocatalytic water splitting. (c) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页码:686 / 697
页数:12
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