Surface investigation on CexZr1-xO2 compounds

被引:170
作者
Daturi, M
Binet, C
Lavalley, JC
Galtayries, A
Sporken, R
机构
[1] ISMRA, Catalyse & Spectrochim Lab, UMR 6506, F-14050 Caen, France
[2] Fac Univ Notre Dame Paix, Lab Interdisciplinaire Spect Electron, B-5000 Namur, Belgium
关键词
D O I
10.1039/a905758g
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
The surface of CexZr1-xO2 compounds has been studied by Fourier transform infrared (FTIR) spectroscopy using adsorbed probe species. Methoxy species, from methanol dissociative adsorption, compensate the coordinative unsaturation of surface cations. From the nu(OC) vibration of methoxy species it was shown that mixed compounds are solid solutions with a surface composition equal to the nominal bulk composition. This result was confirmed by X-ray photoelectron spectroscopy (XPS). However, compared to pure compounds, an increase of exposed Ce4+ cationic sites related to capping oxygen lability was observed for mixed compounds. From the adsorption of CO and pyridine probes it was shown that the Lewis acidities of mixed compounds were intermediate between those of pure ceria and zirconia, which are weak, being slightly higher for zirconia. Using CO2 as a probe for basicity investigation of the surface, it was shown that the various carbonate species observed for mixed compounds were already observed for pure ceria or zirconia with no striking variation of the overall carbonatation. However, from a proposed interpretation of the relative importance of various species, such as monodentate or polydentate carbonates, it was inferred that surface oxygen species are more easily relaxed in ceria-rich mixed compounds than in ceria itself, and that the surface framework of cerium cations is stabilised by zirconium, the effect being the opposite in the case of the surface framework of zirconium ions.
引用
收藏
页码:5717 / 5724
页数:8
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