Insights into size-dependent activity and active sites of Au nanoparticles supported on TS-1 for propene epoxidation with H2 and O2

被引:81
|
作者
Feng, Xiang [1 ]
Duan, Xuezhi [1 ]
Qian, Gang [1 ]
Zhou, Xinggui [1 ]
Chen, De [2 ]
Yuan, Weikang [1 ]
机构
[1] E China Univ Sci & Technol, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
[2] Norwegian Univ Sci & Technol, Dept Chem Engn, N-7491 Trondheim, Norway
关键词
Propene epoxidation; Uncalcined TS-1; Size-dependent activity; Au active sites; Corner sites; GAS-PHASE EPOXIDATION; DIRECT PROPYLENE EPOXIDATION; GOLD NANOPARTICLES; CO OXIDATION; DEPOSITION-PRECIPITATION; SHIFT CATALYSIS; AU/TS-1; PERFORMANCE; TEMPERATURE; CLUSTERS;
D O I
10.1016/j.jcat.2014.05.006
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
Propene epoxidation with H-2/O-2 is a typical structure-sensitive reaction. For a given support containing tetra-coordinated Ti species such as TS-1, the catalytic activity is greatly influenced by supported Au nanoparticle size. The identification of size-dependent activity of Au catalyst was achieved over a series of Au nanoparticles (2.6-5.1 nm) deposited on the exterior surface of TS-1 by employing uncalcined TS-1. Through this approach, we could obtain very stable Au catalysts with distinguishable and uniform-sized Au particles, which are critical for structure-sensitivity analysis. The PO formation rate (mol(po) s(-1) mol(Au)(-1)) over these catalysts was found to vary with average Au diameter (d) as d(-2.7 +/- 0.3). Moreover, typical Au nanoparticles on uncalcined TS-1 appeared as truncated cuboctahedron with top facet of (1 1 1). Model calculations derived from the representative Au particle shape and the above size-dependent activity were then performed to show that corner sites of Au nanoparticles are dominant Au active sites for propene epoxidation. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:99 / 104
页数:6
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