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重新审视用于选择性催化还原反应的活化铜-硅铝酸盐分子筛-13(Cu-SSZ-13)催化剂中铜位点的性质。

Revisiting the nature of Cu sites in the activated Cu-SSZ-13 catalyst for SCR reaction.

作者信息

Borfecchia E, Lomachenko K A, Giordanino F, Falsig H, Beato P, Soldatov A V, Bordiga S, Lamberti C

机构信息

Department of Chemistry and INSTM Reference Center , University of Turin , via P. Giuria 7 , 10125 Turin , Italy . Email:

NIS Centre of Excellence , University of Turin , Italy.

出版信息

Chem Sci. 2015 Jan 1;6(1):548-563. doi: 10.1039/c4sc02907k. Epub 2014 Oct 13.

DOI:10.1039/c4sc02907k
PMID:28936309
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5588737/
Abstract

Cu-SSZ-13 is a highly active NH-SCR catalyst for the abatement of harmful nitrogen oxides (NO , = 1, 2) from the exhausts of lean-burn engines. The study of Cu-speciation occurring upon thermal dehydration is a key step for the understanding of the enhanced catalytic properties of this material and for identifying the SCR active sites and their redox capability. Herein, we combined FTIR, X-ray absorption (XAS) and emission (XES) spectroscopies with DFT computational analysis to elucidate the nature and location of the most abundant Cu sites in the activated catalyst. Different Cu species have been found to be dominant as a function of the dehydration temperature and conditions. Data analysis revealed that the dehydration process of Cu cations is essentially completed at 250 °C, with the formation of dehydrated [CuOH] species hosted in close proximity to 1-Al sites in both d6r and 8r units of the SSZ-13 matrix. These species persist at higher temperatures only if a certain amount of O is present in the gas feed, while under inert conditions they undergo virtually total "self-reduction" as a consequence of an OH extra-ligand loss, resulting in bi-coordinated bare Cu cations. Synchrotron characterization supported by computational analysis allowed an unprecedented quantitative refinement of the local environment and structural parameters of these Cu(ii) and Cu(i) species.

摘要

Cu-SSZ-13是一种高活性的NH-SCR催化剂,用于消除贫燃发动机尾气中的有害氮氧化物(NO , = 1, 2)。研究热脱水过程中出现的铜物种形态,是理解该材料增强催化性能、确定SCR活性位点及其氧化还原能力的关键步骤。在此,我们将傅里叶变换红外光谱(FTIR)、X射线吸收(XAS)和发射光谱(XES)与密度泛函理论(DFT)计算分析相结合,以阐明活化催化剂中最丰富的铜位点的性质和位置。已发现不同的铜物种随脱水温度和条件而占主导地位。数据分析表明,铜阳离子的脱水过程在250°C时基本完成,在SSZ-13基质的d6r和8r单元中,脱水后的[CuOH]物种形成于紧邻1-Al位点处。只有当气体进料中存在一定量的O时,这些物种才会在较高温度下持续存在,而在惰性条件下,由于OH额外配体的损失,它们实际上会经历完全的“自还原”,从而产生双配位的裸铜阳离子。同步辐射表征与计算分析相结合,实现了对这些Cu(ii)和Cu(i)物种的局部环境和结构参数前所未有的定量细化。

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