Study on modification of titanium-based metal-organic framework and catalytic performance

被引:0
|
作者
Qu Y. [1 ,2 ]
Zhang B. [1 ,2 ]
Shi J. [1 ,2 ]
Tan X. [1 ,2 ]
Han B. [1 ,2 ]
Yang G. [1 ]
Zhang J. [1 ,2 ]
机构
[1] Institute of Chemistry, Chinese Academy of Sciences, Beijing
[2] School of Chemical Sciences, University of Chinese Academy of Sciences, Beijing
来源
Huagong Xuebao/CIESC Journal | 2020年 / 71卷 / 01期
关键词
Catalyst; Metal-organic framework; NH[!sub]2[!/sub]-MIL-125; Oxidation; Photochemistry;
D O I
10.11949/0438-1157.20191213
中图分类号
学科分类号
摘要
A series of materials were prepared by modifying titanium based metal-organic framework material NH2-MIL-125 with hydrogen peroxide at a certain temperature. The effects of modification methods and conditions on the properties of materials were studied systematically. However, NH2-MIL-125 as a photocatalyst suffers from low catalytic activity and stability, which largely restrict its practical applications. In order to improve the catalytic activity of NH2-MIL-125, a solvothermal route by using H2O2 was used to modify NH2-MIL-125. A series of materials were synthesized by treating NH2-MIL-125 with different volumes of H2O2 at different temperatures. X-ray diffraction, scanning electron microscope, transmission electron microscope, ultraviolet-visible light absorption spectroscopy, Fourier-transform infrared spectroscopy, X-ray photoelectron spectroscopy and N2 adsorption analysis were used to characterize the structures and properties of the obtained product. Furthermore, their photocatalytic performances for the visible-light-driven oxidation of benzyl alcohol were tested. The results show that the product modified by 10 ml H2O2 at 50℃ exhibits excellent catalytic activity and selectivity. The maximum turnover frequency is nearly 6 times as high as that of NH2-MIL-125 at the same experimental conditions. The partial loss of organic ligands and the introduction of peroxide groups could generate more catalytic-active sites, which is responsible for the improved catalytic activity. © All Right Reserved.
引用
收藏
页码:283 / 289
页数:6
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