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通过干磨制备的双金属PtPd/CeO甲烷氧化催化剂的结构演变

Structural Evolution of Bimetallic PtPd/CeO Methane Oxidation Catalysts Prepared by Dry Milling.

作者信息

Mussio Andrea, Danielis Maila, Divins Núria J, Llorca Jordi, Colussi Sara, Trovarelli Alessandro

机构信息

Dipartimento Politecnico, Università degli Studi di Udine and INSTM, via del Cotonificio 108, 33100 Udine, Italy.

Institute of Energy Technologies, Department of Chemical Engineering and Barcelona Research Center in Multiscale Science and Engineering, Universitat Politècnica de Catalunya, EEBE, Eduard Maristany 10-14, 08019 Barcelona, Spain.

出版信息

ACS Appl Mater Interfaces. 2021 Jul 14;13(27):31614-31623. doi: 10.1021/acsami.1c05050. Epub 2021 Jun 2.

DOI:10.1021/acsami.1c05050
PMID:34077185
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8283761/
Abstract

Bimetallic Pt-Pd catalysts supported on ceria have been prepared by mechanochemical synthesis and tested for lean methane oxidation in dry and wet atmosphere. Results show that the addition of platinum has a negative effect on transient light-off activity, but for Pd/Pt molar ratios between 1:1 and 8:1 an improvement during time-on-stream experiments in wet conditions is observed. The bimetallic samples undergo a complex restructuring during operation, starting from the alloying of Pt and Pd and resulting in the formation of unprecedented "mushroom-like" structures consisting of PdO bases with Pt heads as revealed by high-resolution transmission electron microscopy (HRTEM) analysis. On milled samples, these structures are well-defined and observed at the interface between palladium and ceria, whereas those on the impregnated catalyst appear less ordered and are located randomly on the surface of ceria and of large PdPt clusters. The milled catalyst prepared by first milling Pd metal and ceria followed by the addition of Pt shows better performances compared to a conventional impregnated sample and also to a sample obtained by inverting the Pd-Pt milling order. This has been ascribed to the intimate contact between Pd and CeO generated at the nanoscale during the milling process.

摘要

通过机械化学合成法制备了负载在二氧化铈上的双金属Pt-Pd催化剂,并对其在干燥和潮湿气氛中的贫甲烷氧化性能进行了测试。结果表明,铂的添加对瞬态起燃活性有负面影响,但当Pd/Pt摩尔比在1:1至8:1之间时,在潮湿条件下的连续实验中观察到活性有所提高。双金属样品在运行过程中经历了复杂的结构重组,从Pt和Pd的合金化开始,最终形成了前所未有的“蘑菇状”结构,高分辨率透射电子显微镜(HRTEM)分析表明,该结构由带有Pt头部的PdO基部组成。在研磨后的样品上,这些结构清晰明了,在钯和二氧化铈的界面处观察到,而浸渍催化剂上的结构则显得不太规整,随机分布在二氧化铈表面和大的PdPt簇上。与传统浸渍样品以及通过颠倒Pd-Pt研磨顺序获得的样品相比,先研磨Pd金属和二氧化铈然后添加Pt制备的研磨催化剂表现出更好的性能。这归因于研磨过程中在纳米尺度上Pd与CeO之间形成的紧密接触。

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