Dynamic in situ observation of automotive catalysts for emission control using X-ray absorption fine structure

被引:40
|
作者
Nagai, Yasutaka [1 ]
Dohmae, Kazuhiko [1 ]
Teramura, Kentaro [2 ]
Tanaka, Tsunehiro [2 ]
Guilera, Gemma [3 ]
Kato, Kazuo [4 ]
Nomura, Masaharu [5 ]
Shinjoh, Hirofumi [1 ]
Matsumoto, Shin'ichi [6 ]
机构
[1] Toyota Cent Res & Dev Labs Inc, Aichi 4801192, Japan
[2] Kyoto Univ, Dept Mol Engn, Kyoto 6158510, Japan
[3] European Synchrotron Radiat Facil, F-38043 Grenoble, France
[4] Japan Synchrotron Radiat Res Inst, SPring 8, Sayo, Hyogo 6795198, Japan
[5] High Energy Accelerator Res Org, Inst Mat Struct Sci, Photon Factory, Tsukuba, Ibaraki 3050801, Japan
[6] Toyota Motor Co Ltd, Aichi 4718572, Japan
关键词
Ceria-zirconia; Oxygen storage capacity; Platinum; Sintering; XAFS; Automotive catalyst; CERIA-BASED OXIDE; CE1-XZRXO2; NANOPARTICLES; REDUCTION BEHAVIOR; TURBO-XAS; OXYGEN; XANES; REDISPERSION; OXIDATION; ALUMINA; EXAFS;
D O I
10.1016/j.cattod.2008.10.031
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Two main pivotal Subjects of research in automotive catalysts were studied by modern X-ray absorption analysis techniques. One is oxygen storage/release behaviour, and the other is sintering inhibition of Pt particles. First, three types of CeO2-ZrO2 (Ce:Zr = 1:1 molar ratio) compounds with different oxygen storage/release capacities and different structural properties were prepared, and the valence change of Ce as a function of temperature during oxygen release/storage processes was investigated. The reduction of surface Ce mainly occurred in the range 100-170 degrees C, and the reduction of bulk Ce progressed at high temperatures of 170 degrees C and above. The Ce reduction behaviour depended not only on the homogeneity of the Ce and Zr for bulk reduction at high temperatures but also on the particle size of the CeO2-ZrO2 samples for surface reduction at low temperatures. Secondly, sintering inhibition of Pt in Pt/Al2O3, Pt/MgO and Pt/ceria-based catalysts after 800 degrees C ageing in air was studied. We found that the Pt-O-M (M = Mg, Ce) bond acted as an anchor and inhibited the sintering of Pt particles on MgO or ceria-based oxide. Especially, it was noteworthy that the Pt-O-Ce4+ bond on the ceria-based support breaks easily through the reduction of Ce (Ce4+ -> Ce3+) during the usual stoichiometric and reducing conditions. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:279 / 287
页数:9
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