Synthesis and characterization of composite visible light active photocatalysts MoS2-g-C3N4 with enhanced hydrogen evolution activity

被引:385
作者
Ge, Lei [1 ,2 ]
Han, Changcun [2 ]
Xiao, Xinlai [2 ]
Guo, Lele [2 ]
机构
[1] China Univ Petr, Coll Sci, Key Lab Heavy Oil Proc, 18 Fuxue Rd, Beijing 102249, Peoples R China
[2] China Univ Petr, Coll Sci, Dept Mat Sci & Engn, Beijing 102249, Peoples R China
基金
美国国家科学基金会;
关键词
Graphitic carbon nitride; Molybdenum disulfide; Photocatalysis; Hydrogen evolution; Composite photocatalysts; GRAPHITIC CARBON NITRIDE; REDUCED GRAPHENE OXIDE; EFFICIENT PHOTOCATALYSTS; ELECTRONIC-STRUCTURE; H-2; EVOLUTION; MOS2; TIO2; G-C3N4; WATER; SEMICONDUCTOR;
D O I
10.1016/j.ijhydene.2013.04.006
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
Molybdenum disulfide (MoS2) and graphitic carbon nitride (g-C3N4) composite photocatalysts were prepared via a facile impregnation method. The physical and photophysical properties of the MoS2-g-C3N4 composite photocatalysts were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), high-resolution transmission electron microcopy (HRTEM), ultraviolet-visible diffuse reflection spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS) and photoluminescence (PL) spectroscopy. The photoelectrochemical (PEC) measurements were tested via several on-off cycles under visible light irradiation. The photocatalytic hydrogen evolution experiments indicate that the MoS2 co-catalysts can efficiently promote the separation of photogenerated charge carriers in g-C3N4, and consequently enhance the H-2 evolution activity. The 0.5wt% MoS2-g-C3N4 sample shows the highest catalytic activity, and the corresponding H-2 evolution rate is 23.10 mu mol h(-1), which is enhanced by 11.3 times compared to the unmodified g-C3N4. A possible photocatalytic mechanism of MoS2 co-catalysts on the improvement of visible light photocatalytic performance of g-C3N4 is proposed and supported by PL and PEC results. Copyright (c) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:6960 / 6969
页数:10
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