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Synthesis and characterization of carbon black supported Pt-Ru alloy as a model catalyst for fuel cells

机译:synthesis and characterization of carbon black supported pt-Ru alloy as a model catalyst for fuel cells

摘要

A set of bimetallic Pt-Ru catalysts prepared by co-impregnation of carbon black with ruthenium(III) chloride hydrate and hydrogen hexachloroplatinate(IV) hydrate were investigated by temperature-programmed reduction (TPR), chemisorption of hydrogen, transmission electron microscopy (TEM), microcalorimetry of adsorbed CO and a structure-sensitive reaction (n-hexane conversion). The results showed that the volumetric capacities for CO and H-2 adsorption is influenced in the bimetallic Pt-Ru catalysts by the formation of a Pt-Ru alloy. The n-hexane reaction revealed that the reaction mechanism for the pure Pt catalyst mainly occurs via cyclic isomerization and aromatization due to the presence of bigger Pt surface ensembles, whereas the Pt-Ru catalysts exhibited predominantly bond-shift isomerization by the diluting effect of Ru metal addition. The differential heats of CO chemisorption on Pt-Ru catalysts fell between the two monometallic Pt and Ru catalysts extremes. (C) 2004 Elsevier B.V. All rights reserved.
机译:通过程序升温还原(TPR),氢的化学吸附,透射电子显微镜(TEM)研究了炭黑与氯化钌(III)水合物和六氯铂酸氢盐(IV)水合物的共浸渍制备的一组双金属Pt-Ru催化剂。 ),吸附的CO的量热法和结构敏感的反应(正己烷转化)。结果表明,Pt-Ru合金的形成影响了双金属Pt-Ru催化剂中CO和H-2的吸附容量。正己烷反应表明,纯Pt催化剂的反应机理主要是由于存在较大的Pt表面团簇而通过环状异构化和芳构化而发生,而Pt-Ru催化剂则主要通过Ru的稀释作用表现出键移异构化。金属添加。在Pt-Ru催化剂上CO化学吸附的不同热量介于两个单金属Pt和Ru催化剂极限之间。 (C)2004 Elsevier B.V.保留所有权利。

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