Synthesis and Efficient Visible Light Photocatalytic Hydrogen Evolution of Polymeric g-C3N4 Coupled with CdS Quantum Dots

被引:670
作者
Ge, Lei [1 ,2 ]
Zuo, Fan [1 ]
Liu, Jikai [1 ]
Ma, Quan [1 ]
Wang, Chen [1 ]
Sun, Dezheng [1 ]
Bartels, Ludwig [1 ]
Feng, Pingyun [1 ]
机构
[1] Univ Calif Riverside, Dept Chem, Riverside, CA 92521 USA
[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
ELECTRONIC-STRUCTURE; METHYL-ORANGE; PHOTODEGRADATION; DEGRADATION; PERFORMANCE; MORPHOLOGY; OXIDATION; SERIES; FILMS; O-2;
D O I
10.1021/jp3041692
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
Novel CdS quantum dot (QD)-coupled graphitic carbon nitride (g-C3N4) photocatalysts were synthesized via a chemical impregnation method and characterized by X-ray diffraction, transmission electron microscopy, ultraviolet-visible diffuse reflection spectroscopy, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, and photoluminescence spectroscopy. The effect of CdS content on the rate of visible light photocatalytic hydrogen evolution was investigated for different CdS loadings using platinum as a cocatalyst in methanol aqueous solutions. The synergistic effect of g-C3N4 and CdS QDs leads to efficient separation of the photogenerated charge carriers and, consequently, enhances the visible light photocatalytic H-2 production activity of the materials. The optimal CdS QD content is determined to be 30 wt %, and the corresponding H-2 evolution rate was 17.27 mu mol.h(-1) under visible light irradiation, similar to 9 times that of pure g-C3N4. A possible photocatalytic mechanism of the CdS/g-C3N4 composite is proposed and corroborated by photoluminescence spectroscopy and photoelectrochemical curves.
引用
收藏
页码:13708 / 13714
页数:7
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