Construction of heterostructured MIL-125/Ag/g-C3N4 nanocomposite as an efficient bifunctional visible light photocatalyst for the organic oxidation and reduction reactions

双功能 纳米复合材料 光催化 可见光谱 吸附 X射线光电子能谱 氧化还原 材料科学 化学工程 表面等离子共振 纳米颗粒 化学 光化学 纳米技术 催化作用 有机化学 光电子学 冶金 工程类
作者
Zhiwang Yang,Xueqing Xu,Xixi Liang,Lei Cheng,Yuhan Cui,Wenhua Wu,Yaoxia Yang,Zhe Zhang,Ziqiang Lei
出处
期刊:Applied Catalysis B-environmental [Elsevier BV]
卷期号:205: 42-54 被引量:253
标识
DOI:10.1016/j.apcatb.2016.12.012
摘要

Photocatalytic synthesis using visible light is a desirable chemical process because of its potential to utilize sunlight. A heterostructured MIL-125/Ag/g-C3N4 nanocomposite was implemented as an efficient bifunctional visible-light response catalyst for the photoreduction of nitrocompounds and the oxidation of alcohols. The photocatalyst was prepared via an accessible method and characterized by XRD, SEM, TEM, XPS, FT-IR, N2 adsorption–desorption isotherm, UV–vis DRS, PL and EIS. The reactive efficiency of the photocatalyst depends on two primary factors, one is the light adsorption of catalysts, Ag nanoparticles (NPs) were photodeposited on the surface of g-C3N4 and MIL-125 to increase visible-light absorption via the surface plasmon resonance. And the other is the separation efficiency of the photogenerated charge carrier. As an electron-conduction bridge in the interface between MIL-125 and g-C3N4, Ag NPs could facilitate the direct migration of photoinduced electrons from g-C3N4 to MIL-125 and retard the recombination of electron-holes. Therefore, the MIL-125/Ag/g-C3N4 sample shows highest photocatalytic activity compared with MIL-125, g-C3N4, MIL-125/Ag and MIL-125/g-C3N4. A corresponding photocatalytic mechanism of these reactions was discussed in detail. Moreover, the photoreduction of nitrocompounds and oxidation of the alcohols with superior conversions and selectivities were obtained, and the catalyst can be recycled four times. It is concluded that MIL-125/Ag/g-C3N4 would be a promising visible light photocatalyst in the field of selective organic transformations.
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