Synthesis and reactivity of gold nanoparticles supported on transition metal doped mesoporous silica

被引:36
作者
Bore, Mangesh T.
Mokhonoana, M. Peter
Ward, Timothy L.
Coville, Neil J.
Datye, Abhaya K. [1 ]
机构
[1] Univ New Mexico, Dept Chem & Nucl Engn, Albuquerque, NM 87131 USA
[2] Univ Witwatersrand, Sch Chem, Inst Mol Sci, ZA-2050 Johannesburg, South Africa
基金
美国国家科学基金会;
关键词
gold nanoparticles; mesoporous silica; aerosol silica; sintering; CO oxidation; cobalt-modified silica;
D O I
10.1016/j.micromeso.2006.05.007
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Mixed mesoporous silica samples with Co, Al and Fe as heteroelements were synthesized. Two classes of mesoporous silica were studied: MCM-41 prepared under basic conditions to yield one dimensional (1-D) pores; and aerosol-derived silica prepared under acidic conditions to yield 1-D pores arranged within spherical particles. The silica surface was subsequently functionalized with amine groups to allow deposition-precipitation of gold nanoparticles. These gold catalysts supported on amine functionalized mixed mesoporous silica were tested for CO oxidation and were found to become active at T > 250 degrees C. The Au particles grew in size after reactivity measurements to sizes larger than the pore diameter; however, the majority of An particles remained within the pores. Our results indicate that the silica walls (1 nm thick) are not able to restrain the growth of Au particle size. The addition of the heteroelement did not lead to a significant improvement in the thermal stability of these catalysts; the major effect was an increase in CO oxidation activity compared to the pure silica. The highest reactivity was seen in cobalt-silica mixed mesoporous oxide prepared by the aerosol method, with a reactivity of 2.3 x 10(-5) mol CO2/s/gcat at 250 degrees C and activation energy of 40 kJ/mol. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:118 / 125
页数:8
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