One-pot synthesis of non-noble metal WS2/g-C3N4 photocatalysts with enhanced photocatalytic hydrogen production

被引:57
作者
Zhou, Yunlong [1 ]
Ye, Xiaoyuan [1 ]
Lin, Dongyao [1 ]
机构
[1] Northeast Elect Power Univ, Sch Energy & Power Engn, Jilin, Jilin, Peoples R China
关键词
WS2; g-C3N4; Non-noble metal; Photocatalytic hydrogen production; IN-SITU SYNTHESIS; CARBON NITRIDE; H-2; EVOLUTION; Z-SCHEME; EFFICIENT PHOTOCATALYST; FACILE SYNTHESIS; MODIFIED G-C3N4; HETEROJUNCTION; COCATALYST; WATER;
D O I
10.1016/j.ijhydene.2019.04.091
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
As an increasing number of photocatalysis are developed, non-noble metal photocatalysts that can be synthesized from earth-abundant and low-cost materials have received a great deal of attention. In this study, non-noble metal WS2/g-C3N4 photocatalysts were prepared by a facile one-pot synthesis. Varying masses of tungsten disulfide (WS2) were successfully loaded onto g-C3N4 and characterized by X-ray diffraction (XRD), inductively coupled plasma optical emission spectrometry (ICP-OES), thermogravimetric analysis (TGA), Fourier transform infrared (FT-IR) spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). These results indicated that the WS2 was successfully synthesized and immobilized closely on the surface of g-C3N4 to form a sheet-like nanostructure. The H-2 generation results showed that the optimal photocatalyst was 0.3-WCN because it had the highest photocatalytic H-2 production of 154 mu mol h(-1) g(-1), which is 34 times higher than bare g-C3N4 and even higher than 0.3 wt% platinum-loaded g-C3N4 . Additionally, the possible mechanism of the photocatalyst was studied by photoluminescence (PL), UV-vis diffuse reflectance spectroscopy (UV-vis DRS) and photoelectrochemical tests, which showed that the WS2 played a key role in improving the efficiency of separation and migration of the photogenerated carriers in g-C3N4 . (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:14927 / 14937
页数:11
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