Design of Zeolitic Imidazolate Framework Derived Nitrogen-Doped Nanoporous Carbons Containing Metal Species for Carbon Dioxide Fixation Reactions

被引:58
|
作者
Toyao, Takashi [1 ]
Fujiwaki, Mika [1 ]
Miyahara, Kenta [1 ]
Kim, Tae-Ho [2 ]
Horiuchi, Yu [1 ]
Matsuoka, Masaya [1 ]
机构
[1] Osaka Prefecture Univ, Grad Sch Engn, Dept Appl Chem, Naka Ku, 1-1 Gakuen Cho, Osaka 5998531, Japan
[2] Sun Moon Univ, Div Mech & ICT Convergence Engn, Asan Chung Nam ZA-336708, South Korea
基金
新加坡国家研究基金会; 日本学术振兴会; 日本科学技术振兴机构;
关键词
carbon dioxide fixation; cyclic carbonate synthesis; doping; nanostructures; zeolitic imidazolate framework; ROOM-TEMPERATURE SYNTHESIS; ORGANIC FRAMEWORK; CYCLIC CARBONATES; OXYGEN REDUCTION; POROUS CARBON; POLYCARBONATE PRODUCTION; HETEROGENEOUS CATALYST; DIRECT CARBONIZATION; EFFICIENT FIXATION; DIMETHYL CARBONATE;
D O I
10.1002/cssc.201500780
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Various N-doped nanoporous carbons containing metal species were prepared by direct thermal conversion of zeolitic imidazolate frameworks (ZIFs; ZIF-7, -8, -9, and -67) at different temperatures (600, 800, and 1000 degrees C). These materials were utilized as bifunctional acid-base catalysts to promote the reaction of CO2 with epoxides to form cyclic carbonates under 0.6MPa of CO2 at 80 degrees C. The catalyst generated by thermal conversion of ZIF-9 at 600 degrees C (C600-ZIF-9) was found to exhibit a higher catalytic activity than the other ZIFs, other conventional catalysts, and other metal-organic framework catalysts. The results of various characterization techniques including elemental analysis, X-ray diffraction, X-ray photoelectron spectroscopy, X-ray absorption spectroscopy, and transmission electron microscopy show that C600-ZIF-9 contains partly oxidized Co nanoparticles and N species. Temperature-programmed desorption measurements by using CO2 and NH3 as probe molecules revealed that C600-ZIF-9 has both Lewis acid and Lewis base catalytic sites. Finally, the substrate scope was extended to seven other kinds of epoxides.
引用
收藏
页码:3905 / 3912
页数:8
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