Consciously Constructing the Robust NiS/g-C3N4 Hybrids for Enhanced Photocatalytic Hydrogen Evolution

被引:122
|
作者
Lin, Xiao [1 ]
Du, Shiwen [1 ]
Li, Chunhe [1 ]
Li, Guojun [1 ]
Li, Youji [2 ]
Chen, Feitai [2 ]
Fang, Pengfei [1 ]
机构
[1] Wuhan Univ, Sch Phys & Technol, Key Lab Nucl Solid State Phys Hubei Prov, Wuhan 430072, Peoples R China
[2] Jishou Univ, Coll Chem & Chem Engn, Jishou 416000, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
Photochemical deposition; NiS/g-C3N4; Hydrogen evolution; Thermal oxidation etching; GRAPHITIC CARBON NITRIDE; G-C3N4; NANOSHEETS; HIGHLY-EFFICIENT; SURFACE-AREA; SPHERES; HETEROJUNCTION; FABRICATION; C3N4;
D O I
10.1007/s10562-020-03118-x
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
Selective growth of cocatalyst on the surface of photocatalyst has been attracted considerable attention due to their efficient charges transfer property. In this study, the robust NiS modified graphitic carbon nitride (g-C3N4) hybrids were successfully synthesized by a facile surface photochemical deposition process. The structure and composition characterization results revealed that the NiS is highly dispersed loading on the surface of g-C3N4 nanosheets, and the NiS/g-C3N4 hybrids possess large surface areas and excellent optical properties. Under the visible light illumination, the NiS/g-C3N4 hybrids with 1.0% weight content of NiS cocatalyst exhibits the highest hydrogen evolution rate of 1346.1 mu mol h(-1) g(-1) with an apparent quantum efficiency (AQE) of 7.67%. On the basis of photoluminescence (PL) spectra and photoelectrochemical methodology, the photocatalytic hydrogen evolution mechanism was proposed. The results demonstrated that the excellent activity arises from the strong electronic coupling, highly efficient charges separation and migration. This work demonstrates a facile photochemical deposition method to consciously construct the robust two-dimensional (2D) hybrids, so as to realize accurate deposition of cocatalyst and efficient migration of photo-generated carriers. [GRAPHICS] .
引用
收藏
页码:1898 / 1908
页数:11
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