Sustainable and Facile Route to Nearly Monodisperse Spherical Aggregates of CeO2 Nanocrystals with Ionic Liquids and Their Catalytic Activities for CO Oxidation

被引:107
作者
Li, Zhen-Xing [1 ,2 ]
Li, Le-Le [1 ,2 ]
Yuan, Quan [1 ,2 ]
Feng, Wei [1 ,2 ]
Xu, Jun [1 ,2 ]
Sun, Ling-Dong [1 ,2 ]
Song, Wei-Guo [3 ]
Yan, Chun-Hua [1 ,2 ]
机构
[1] Peking Univ, Beijing Natl Lab Mol Sci, State Key Lab Rare Earth Mat Chem & Applicat, Beijing 100871, Peoples R China
[2] Peking Univ, PKU HKU Joint Lab Rare Earth Mat & Bioinorgan Che, Beijing 100871, Peoples R China
[3] Chinese Acad Sci, Inst Chem, Beijing 100080, Peoples R China
关键词
D O I
10.1021/jp807348n
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
This article reports a novel preparation of nearly monodisperse spherical aggregates of CeO2 nanocrystals by using ionic liquid (1-hexadecyl-3-methylimidazolium bromide, C(16)MimBr) as both template and solvent. The products were characterized with X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution TEM (HRTEM), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, UV-vis spectroscopy, FT-IR spectroscopy, and N-2 adsorption-desorption methods. The spherical aggregates, with average diameter of 100 - 150 nm, are composed of ca. 3.5 nm CeO2 nanocrystals as building units, giving rise to three-dimensional (313) open porous structures with high Brunauer-Emmett-Teller surface area of 119 m(2).g(-1). Mesoporous CeO2 with surface area up to 227 m(2).g(-1) was prepared by simply tuning the amount of the ionic liquids. Loaded with 5 wt% CuO, both the spherical aggregates and the mesoporous CeO2 exhibit high catalytic activities for CO conversion with 100% conversion rates at low temperature of 150 degrees C, suggesting potential applications in preferential oxidation (PROX) and water-gas shift reaction (WGSR). This sustainable and facile method may be extended to the preparation of other metal oxide nanoarchitectures and provides guidance for structure-controlled synthesis.
引用
收藏
页码:18405 / 18411
页数:7
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