Redox behavior of palladium at start-up in the Perovskite-type LaFePdOx automotive catalysts showing a self-regenerative function

被引:135
作者
Uenishi, M [1 ]
Taniguchi, M
Tanaka, H
Kimura, M
Nishihata, Y
Mizuki, J
Kobayashi, T
机构
[1] Daihatsu Motor Co Ltd, Mat Res & Dev Div, Gamo, Shiga 5202593, Japan
[2] Daihatsu Motor Co Ltd, Mat Res & Dev Div, Ikeda, Osaka 5638651, Japan
[3] Cataler Corp, Div Res & Dev, Ogasa, Shizuoka 4371492, Japan
[4] Japan Atom Res Inst, Synchrotron Radiat Res Ctr, Sayo, Hyogo 6795148, Japan
[5] Natl Inst Adv Ind Sci & Technol AIST, Res Inst Ubiquitous Energy Devices, Ikeda, Osaka 5638577, Japan
关键词
perovskite; three-way catalyst; self-regenerative function; crystal structure; automotive emission; the intelligent catalyst;
D O I
10.1016/j.apcatb.2004.11.011
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
In order to elucidate the superior start-up activity of LaFePdOx catalysts in practical automotive emission control, the redox property of Pd species in a Perovskite-type LaFe0.95Pd0.053O catalyst was studied at temperatures ranging from 100 to 400 ° C using X-ray spectroscopic techniques. In a reductive atmosphere, and even at temperatures as low as 100 ° C, Pd-0 species is partially segregated out onto the catalyst surface from the B-site of the Perovskite-type matrix of LaFe0.95Pd0.05O3. Passing through successive oxidizing atmospheres, the segregated Pd-0 species is re-oxidized into Pd2+ at 200-300 ° C. The formation of a solid solution between the re-oxidized Pd species and the Perovskite-type matrix begins to be seen at around 400 ° and accelerates at higher temperatures. Thus a quasi-reversible redox reaction between the surface Pd-0 and the cationic Pd in the LaFe0.95Pd0.05O3 matrix takes place. The start-up activity of LaFePdxOx catalysts can be attributed to Pd-0 that segregates under the reductive atmosphere which is a natural part of the redox fluctuation in automotive exhaust gases at 100-200 ° C. © 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:267 / 273
页数:7
相关论文
共 20 条
[1]   XANES-TPR STUDY OF CU-PD BIMETALLIC CATALYSTS - APPLICATION OF FACTOR-ANALYSIS [J].
FERNANDEZGARCIA, M ;
ALVAREZ, CM ;
HALLER, GL .
JOURNAL OF PHYSICAL CHEMISTRY, 1995, 99 (33) :12565-12569
[2]  
HECK RM, 1995, CATALYTIC AIR POLLUT, P94
[3]   NOTE ON THE K EXTENDED X-RAY ABSORPTION FINE-STRUCTURE DEBYE-WALLER FACTOR [J].
ISHII, T .
JOURNAL OF PHYSICS-CONDENSED MATTER, 1992, 4 (40) :8029-8034
[4]   PROMISING CATALYST FOR AUTO EXHAUST [J].
LIBBY, WF .
SCIENCE, 1971, 171 (3970) :499-&
[5]   ACCURATE BOND LENGTH DETERMINATION BY EXAFS METHOD [J].
MAEDA, H .
JOURNAL OF THE PHYSICAL SOCIETY OF JAPAN, 1987, 56 (08) :2777-2787
[6]  
MALLET T, 1997, APPL CATAL B-ENVIRON, V14, P85
[7]   LOW-COST OXYGEN ELECTRODE MATERIAL [J].
MEADOWCROFT, DB .
NATURE, 1970, 226 (5248) :847-+
[8]   STABILITY OF THE PEROVSKITE PHASE LABO3 (B = V, CR, MN, FE, CO, NI) IN REDUCING ATMOSPHERE .1. EXPERIMENTAL RESULTS [J].
NAKAMURA, T ;
PETZOW, G ;
GAUCKLER, LJ .
MATERIALS RESEARCH BULLETIN, 1979, 14 (05) :649-659
[9]   Self-regeneration of a Pd-perovskite catalyst for automotive emissions control [J].
Nishihata, Y ;
Mizuki, J ;
Akao, T ;
Tanaka, H ;
Uenishi, M ;
Kimura, M ;
Okamoto, T ;
Hamada, N .
NATURE, 2002, 418 (6894) :164-167
[10]  
NISHIHATA Y, IN PRESS J PHYS CHEM