详细信息
Nanocasted synthesis of mesoporous LaCoO3 perovskite with extremely high surface area and excellent activity in methane combustion ( EI收录)
文献类型:期刊文献
英文题名:Nanocasted synthesis of mesoporous LaCoO3 perovskite with extremely high surface area and excellent activity in methane combustion
作者:Wang, Yangang[1]; Ren, Jiawen[1]; Wang, Yanqin[1]; Zhang, Fengyuan[1]; Liu, Xiaohui[1]; Guo, Yun[1]; Lu, Guanzhong[1]
机构:[1] Laboratory for Advanced Materials, Research Institute of Industrial Catalysis, East China University of Science and Technology, Shanghai 200237, China
年份:2008
卷号:112
期号:39
起止页码:15293
外文期刊名:Journal of Physical Chemistry C
收录:EI(收录号:20084411665118)
语种:英文
外文关键词:Mesoporous materials - Methane - Binary alloys - Silica - Lanthanum compounds - Nitrogen removal - Nitrogen - Cobalt compounds - Catalytic oxidation - Catalyst activity
摘要:Ordered mesoporous LaCoO3 perovskite with high surface area was synthesized via nanocasting strategy by using ordered mesoporous cubic (Ic3d) vinyl silica as the template. The sample, prepared by filling mesopores in silica template with a La-Co citrate complex precursor followed by calcination and silica removal, was characterized by XRD, TEM, and nitrogen sorption techniques, and its catalytic activity was tested for complete methane oxidation. The wide-angle XRD pattern showed LaCoO3 perovskite was formed and no La-oxide/Co-oxide phases were detected in the obtained material. This LaCoO3 perovskite displayed a high BET surface area of 96.7 m2 g-1 from nitrogen sorption analysis and a three-dimensional ordered mesostructure from TEM images, as well as a small-angle XRD pattern. Moreover, this material showed much higher activity in the complete methane oxidation than the conventional bulk LaCoO3 perovskite. The light-off temperature (T10) and the half-conversion temperature (T50) were at 335 and 470 °C, respectively. Further analysis by means of H2-TPR and XPS techniques showed that the existence of high valent cobalt ions and high content of O22-/O- species contributed to the high activity. ? 2008 American Chemical Society.
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