Water-gas shift reaction over gold nanoparticles dispersed on nanostructured CeOx-TiO2(110) surfaces: Effects of high ceria coverage

被引:12
|
作者
Grinter, D. C. [1 ]
Park, J. B. [1 ]
Agnoli, S. [1 ]
Evans, J. [2 ]
Hrbek, J. [1 ]
Stacchiola, D. J. [1 ]
Senanayake, S. D. [1 ]
Rodriguez, J. A. [1 ]
机构
[1] Brookhaven Natl Lab, Dept Chem, Upton, NY 11973 USA
[2] Cent Univ Venezuela, Fac Ciencias, Caracas 1020A, Venezuela
关键词
STM; TiO2(110); CeO2; Gold; Water-gas shift; MIXED-METAL OXIDE; TITANIA CATALYSTS; AU/CEOX/TIO2(110); INTERFACE; MECHANISM; CLUSTERS; PLATINUM; COPPER; TIO2;
D O I
10.1016/j.susc.2015.10.002
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
Scanning tunnelling microscopy has been used to study the morphology of an overlayer of ceria in contact with a TiO2(110) substrate. Two types of domains were observed after ceria deposition. An ordered ceria film covered half of the surface and high-resolution imaging suggested a near-c(6 x 2) relationship to the underlying TiO2(110)-(1 x 1). The other half of the surface comprised CeOx nanoparticles and reconstructed TiOx supported on TiO2(110)-(1 x 1). Exposure to a small amount of gold resulted in the formation of isolated gold atoms and small clusters on the ordered ceria film and TiO2(110)-(1 x 1) areas, which exhibited significant sintering at 500 K and showed strong interaction between the sintered gold clusters and the domain boundaries of the ceria film. The Au/CeOx/FiO(2)(110) model system proved to be a good catalyst for the water-gas shift (WGS) exhibiting much higher turnover frequencies (TOFs) than Cu(111) and Pt(111) benchmarks, or the individual Au/TiO2(110) and Au/CeO2(111) systems. For Au/CeOx/FiO(2)(110) catalysts, there was a decrease in catalytic activity with increasing ceria coverage that correlates with a reduction in the concentration of Ce3+ formed during WGS reaction conditions. Published by Elsevier B.V.
引用
收藏
页码:34 / 39
页数:6
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