Polyhedral CeO2 Nanoparticles: Size-Dependent Geometrical and Electronic Structure

被引:109
|
作者
Paun, Cristina [1 ]
Safonova, Olga V. [2 ]
Szlachetko, Jakub [2 ]
Abdala, Paula M. [3 ]
Nachtegaal, Maarten [2 ]
Sa, Jacinto [1 ,2 ]
Kleymenov, Evgeny [2 ]
Cervellino, Antonio [2 ]
Krumeich, Frank [4 ]
van Bokhoven, Jeroen A. [1 ,2 ]
机构
[1] Swiss Fed Inst Technol, Inst Chem & Bioengn, CH-8093 Zurich, Switzerland
[2] Paul Scherrer Inst, CH-5232 Villigen, Switzerland
[3] European Synchrotron Radiat Facil, SNBL, F-38043 Grenoble, France
[4] Swiss Fed Inst Technol, Inorgan Chem Lab, CH-8093 Zurich, Switzerland
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2012年 / 116卷 / 13期
关键词
CERIA NANOPARTICLES; OXIDATION-STATE; OXIDE; REDUCTION; BEHAVIOR;
D O I
10.1021/jp300342b
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
Ceria-based materials have many interesting applications including catalysis, fuel cells, and biology. The size- and shape-dependent changes in the catalytic properties of nanoceria are often attributed to stabilization Ce3+ defects on the nanopartide surface. In this paper, we have performed a systematic analysis of the structure of polyhedral CeO2 nanoparticles of 2-10 nm, under ambient conditions, using a combination of transmission electron microscopy, X-ray diffraction, and X-ray spectroscopy at Ce K- and L-edges. We reveal that under ambient conditions Ce3+ concentration does not depend on the size; however, the unit cell parameter and the pseudo Debye-Waller factors systematically change due to size-dependent surface contribution. The presence of Ce3+ traces relates to the use of Ce3+ precursors during synthesis. Exposure of nanoparticles to an intense beam of X-ray radiation causes reduction of Ce4+ ions, the extent of which is size-dependent.
引用
收藏
页码:7312 / 7317
页数:6
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