Impregnation of semiconductor CdS NPs in MOFs cavities via double solvent method for effective photocatalytic CO2 conversion

被引:62
作者
Ding, Deng [1 ]
Jiang, Zhuo [1 ]
Jin, Jingpeng [1 ]
Li, Junjie [1 ]
Ji, Dong [1 ]
Zhang, Youxiang [1 ]
Zan, Ling [1 ,2 ]
机构
[1] Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China
[2] Wuhan Univ, Suzhou Inst, Suzhou 215000, Peoples R China
关键词
Metal-organic-framework; Double solvent; In situ growth; CdS; CO2; photoreduction; METAL-ORGANIC FRAMEWORKS; GRAPHITIC CARBON NITRIDE; ARTIFICIAL PHOTOSYNTHESIS; HYDROGEN EVOLUTION; 001; FACETS; DEHYDROGENATION; NANOPARTICLES; INTEGRATION; NANOSHEETS; CATALYSTS;
D O I
10.1016/j.jcat.2019.05.015
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
Construction of MOF-based photocatalysts is promising work due to their considerable active sites and flexible structures. Herein, we present a facile double solvent and in-situ-growth strategy to integrate CdS NPs with MIL-101(Cr) to engineer CdS/MIL-101(Cr) composite photocatalyst. As-prepared CdS/ MIL-101(Cr) samples were characterized by TEM, SEM, BET, EPR, XPS, TPC and ESI. CdS/MIL-101(Cr) exhibited remarkable enhanced activity for conversion CO2 to CO under visible light irradiation, and the 36% CdS/MIL-101(Cr) showed the optimal performance in the all samples. The superior activity was attributed to following factors. The strong interaction between CdS and MIL-101(Cr) promoted the separation and transferring of the photogenerated charge carriers. A higher utilization efficiency of photoelectrons could be achieved with the MIL-101(Cr) possessing multiple absorptions and active sites for the photoreduction of CO2. Also, CdS/MIL-101(Cr) provided a special transferring path for photoelectrons, from CdS to MIL-101(Cr), then to photoreduction of CO2 , which could be certified by the calculation of energy-level and the survey of center dot O-2(-) of CdS and MIL-101(Cr). (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:21 / 31
页数:11
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