On the structure dependence of CO oxidation over CeO2 nanocrystals with well-defined surface planes

被引:565
作者
Wu, Zili [1 ,2 ]
Li, Meijun [1 ]
Overbury, Steven H. [1 ,2 ]
机构
[1] Oak Ridge Natl Lab, Div Chem Sci, Oak Ridge, TN 37831 USA
[2] Oak Ridge Natl Lab, Ctr Nanophase Mat Sci, Oak Ridge, TN 37831 USA
关键词
Ceria nanoshapes; Rods; Cubes; Octahedra; CO oxidation; Structure dependence; In situ spectroscopy; Reaction mechanism; TRANSFORM INFRARED-SPECTROSCOPY; OXYGEN STORAGE; CARBON-MONOXIDE; RAMAN-SPECTROSCOPY; VACANCY FORMATION; AU/SIO2; CATALYST; LOW-TEMPERATURE; DRIFTS-MS; CERIA; ADSORPTION;
D O I
10.1016/j.jcat.2011.09.011
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
CO oxidation is a model reaction for probing the redox property of ceria-based catalysts. In this study. CO oxidation was investigated over ceria nanocrystals with defined surface planes (nanoshapes) including rods ({1 1 0} + {1 0 0}), cubes ({1 0 0}), and octahedra ({1 1 1}). To understand the strong dependence of CO oxidation observed on these different ceria nanoshapes, in situ techniques including infrared and Raman spectroscopy coupled with online mass spectrometer, and temperature-programmed reduction (TPR) were employed to reveal how CO interacts with the different ceria surfaces, while the mobility of ceria lattice oxygen was investigated via oxygen isotopic exchange experiment. CO adsorption at room temperature leads to strongly bonded carbonate species on the more reactive surfaces of rods and cubes but weakly bonded ones on the rather inert octahedra surface. CO-TPR, proceeding via several channels including CO removal of lattice oxygen, surface water-gas shift reaction, and CO disproportionation reaction, reveals that the reducibility of these ceria nanoshapes is in line with their CO oxidation activity, i.e., rods > cubes > octahedra. The mobility of lattice oxygen also shows similar dependence. It is suggested that surface oxygen vacancy formation energy, defect sites, and coordinatively unsaturated sites on ceria play a direct role in facilitating both CO interaction with ceria surface and the reactivity and mobility of lattice oxygen. The oxygen vacancy formation energy, nature and amount of the defect and low coordination sites are intrinsically affected by the surface planes of the ceria nanoshapes. Several reaction pathways for CO oxidation over the ceria nanoshapes are proposed, and certain types of carbonates, especially those associated with reduced ceria surface, are considered among the reaction intermediates to form CO2, while the majority of carbonate species observed under CO oxidation condition are believed to be spectators. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:61 / 73
页数:13
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