Redox behavior of palladium at start-up in the Perovskite-type LaFePdOx automotive catalysts showing a self-regenerative function
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 LaFe0.95Pd0.05O3 catalyst was studied at temperatures ranging from 100 to 400°C using X-ray spectroscopic techniques. In a reduct...
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Veröffentlicht in: | Applied catalysis. B, Environmental Environmental, 2005-05, Vol.57 (4), p.267-273 |
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creator | Uenishi, Mari Taniguchi, Masashi Tanaka, Hirohisa Kimura, Mareo Nishihata, Yasuo Mizuki, Junichiro Kobayashi, Tetsuhiko |
description | 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 LaFe0.95Pd0.05O3 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, Pd0 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 Pd0 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°C and accelerates at higher temperatures. Thus a quasi-reversible redox reaction between the surface Pd0 and the cationic Pd in the LaFe0.95Pd0.05O3 matrix takes place. The start-up activity of LaFePdxOx catalysts can be attributed to Pd0 that segregates under the reductive atmosphere which is a natural part of the redox fluctuation in automotive exhaust gases at 100–200°C. |
doi_str_mv | 10.1016/j.apcatb.2004.11.011 |
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In a reductive atmosphere, and even at temperatures as low as 100°C, Pd0 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 Pd0 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°C and accelerates at higher temperatures. Thus a quasi-reversible redox reaction between the surface Pd0 and the cationic Pd in the LaFe0.95Pd0.05O3 matrix takes place. The start-up activity of LaFePdxOx catalysts can be attributed to Pd0 that segregates under the reductive atmosphere which is a natural part of the redox fluctuation in automotive exhaust gases at 100–200°C.</description><identifier>ISSN: 0926-3373</identifier><identifier>EISSN: 1873-3883</identifier><identifier>DOI: 10.1016/j.apcatb.2004.11.011</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>Automotive emission ; Crystal structure ; Perovskite ; Self-regenerative function ; The intelligent catalyst ; Three-way catalyst</subject><ispartof>Applied catalysis. 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B, Environmental</title><description>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 LaFe0.95Pd0.05O3 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, Pd0 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 Pd0 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°C and accelerates at higher temperatures. Thus a quasi-reversible redox reaction between the surface Pd0 and the cationic Pd in the LaFe0.95Pd0.05O3 matrix takes place. The start-up activity of LaFePdxOx catalysts can be attributed to Pd0 that segregates under the reductive atmosphere which is a natural part of the redox fluctuation in automotive exhaust gases at 100–200°C.</description><subject>Automotive emission</subject><subject>Crystal structure</subject><subject>Perovskite</subject><subject>Self-regenerative function</subject><subject>The intelligent catalyst</subject><subject>Three-way catalyst</subject><issn>0926-3373</issn><issn>1873-3883</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNotkD1PwzAYhC0EEqXwDxg8sSX4tfPVBQlVFJAqtUIwW679unVJ4xA7hY78cwLllltOp7uHkGtgKTAobreparWKq5QzlqUAKQM4ISOoSpGIqhKnZMQmvEiEKMU5uQhhyxjjglcj8v2Cxn_RFW7U3vmOektbVdfKuH5HVaQhqi4mfUtdQ-MG6RI7vw_vLmISDy3SuZrh0iy-qOqj3_no9kiHKao-hBho2PhP16ypogFrm3S4xgY79ZeyfaOj880lObOqDnj172PyNnt4nT4l88Xj8_R-niCUEBOjkFmEDHJlbZUVKrMWOWgLwuqJMbY0dlXwDDJtS85NjoAC86zUzFqWgxiTm2Nv2_mPHkOUOxc0Dl8b9H2QfJJnhRg0JnfHIA5r9g47GbTDRqNxHeoojXcSmPwlL7fySF7-kpcAciAvfgCb533s</recordid><startdate>20050526</startdate><enddate>20050526</enddate><creator>Uenishi, Mari</creator><creator>Taniguchi, Masashi</creator><creator>Tanaka, Hirohisa</creator><creator>Kimura, Mareo</creator><creator>Nishihata, Yasuo</creator><creator>Mizuki, Junichiro</creator><creator>Kobayashi, Tetsuhiko</creator><general>Elsevier B.V</general><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>FR3</scope><scope>JG9</scope><scope>KR7</scope><scope>L7M</scope></search><sort><creationdate>20050526</creationdate><title>Redox behavior of palladium at start-up in the Perovskite-type LaFePdOx automotive catalysts showing a self-regenerative function</title><author>Uenishi, Mari ; Taniguchi, Masashi ; Tanaka, Hirohisa ; Kimura, Mareo ; Nishihata, Yasuo ; Mizuki, Junichiro ; Kobayashi, Tetsuhiko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-e171t-dae0fe1415aff846a4ffe21cf13fc9ddf7dfb62414cf722d5e1e3e547c0ff0513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Automotive emission</topic><topic>Crystal structure</topic><topic>Perovskite</topic><topic>Self-regenerative function</topic><topic>The intelligent catalyst</topic><topic>Three-way catalyst</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Uenishi, Mari</creatorcontrib><creatorcontrib>Taniguchi, Masashi</creatorcontrib><creatorcontrib>Tanaka, Hirohisa</creatorcontrib><creatorcontrib>Kimura, Mareo</creatorcontrib><creatorcontrib>Nishihata, Yasuo</creatorcontrib><creatorcontrib>Mizuki, Junichiro</creatorcontrib><creatorcontrib>Kobayashi, Tetsuhiko</creatorcontrib><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Materials Research Database</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Applied catalysis. B, Environmental</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Uenishi, Mari</au><au>Taniguchi, Masashi</au><au>Tanaka, Hirohisa</au><au>Kimura, Mareo</au><au>Nishihata, Yasuo</au><au>Mizuki, Junichiro</au><au>Kobayashi, Tetsuhiko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Redox behavior of palladium at start-up in the Perovskite-type LaFePdOx automotive catalysts showing a self-regenerative function</atitle><jtitle>Applied catalysis. B, Environmental</jtitle><date>2005-05-26</date><risdate>2005</risdate><volume>57</volume><issue>4</issue><spage>267</spage><epage>273</epage><pages>267-273</pages><issn>0926-3373</issn><eissn>1873-3883</eissn><abstract>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 LaFe0.95Pd0.05O3 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, Pd0 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 Pd0 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°C and accelerates at higher temperatures. Thus a quasi-reversible redox reaction between the surface Pd0 and the cationic Pd in the LaFe0.95Pd0.05O3 matrix takes place. The start-up activity of LaFePdxOx catalysts can be attributed to Pd0 that segregates under the reductive atmosphere which is a natural part of the redox fluctuation in automotive exhaust gases at 100–200°C.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.apcatb.2004.11.011</doi><tpages>7</tpages></addata></record> |
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subjects | Automotive emission Crystal structure Perovskite Self-regenerative function The intelligent catalyst Three-way catalyst |
title | Redox behavior of palladium at start-up in the Perovskite-type LaFePdOx automotive catalysts showing a self-regenerative function |
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