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负载于固体和液体上的Ga-Pt催化剂上丙烷脱氢反应的原位漫反射红外傅里叶变换光谱和密度泛函理论研究

Operando DRIFTS and DFT Study of Propane Dehydrogenation over Solid- and Liquid-Supported Ga Pt Catalysts.

作者信息

Bauer Tanja, Maisel Sven, Blaumeiser Dominik, Vecchietti Julia, Taccardi Nicola, Wasserscheid Peter, Bonivardi Adrian, Görling Andreas, Libuda Jörg

机构信息

Lehrstuhl für Physikalische Chemie II, Friedrich-Alexander-Universität Erlangen-Nürnberg, Egerlandstraße 3, D-91058 Erlangen, Germany.

Lehrstuhl für Theoretische Chemie, Friedrich-Alexander-Universität Erlangen-Nürnberg, Egerlandstraße 3, D-91058 Erlangen, Germany.

出版信息

ACS Catal. 2019 Apr 5;9(4):2842-2853. doi: 10.1021/acscatal.8b04578. Epub 2019 Feb 15.

DOI:10.1021/acscatal.8b04578
PMID:32477699
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7252903/
Abstract

Supported catalytically active liquid metal solutions (SCALMS) represent a class of catalytic materials that have only recently been developed, but have already proven to be highly active, e.g., for dehydrogenation reactions. Previous studies attributed the catalytic activity to isolated noble metal atoms at the surface of a liquid and inert Ga matrix. In this study, we apply diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) with CO as a probe molecule to Ga/AlO, Pt/AlO, and GaPt/AlO catalysts, to investigate in detail the nature of the active Pt species. Comparison of CO adsorption on Pt/AlO and GaPt/AlO shows that isolated Pt atoms are, indeed, present at the surface of the liquid SCALMS. Combining DRIFTS with online gas chromatography (GC), we investigated the Ga/AlO, Pt/AlO, and GaPt/AlO systems under operando conditions during propane dehydrogenation in CO/propane and in Ar/propane. We find that the Pt/AlO sample is rapidly poisoned by CO adsorption and coke, whereas propane dehydrogenation over GaPt/AlO SCALMS leads to higher conversion with no indication of poisoning effects. We show under operando conditions that isolated Pt atoms are present at the surface of SCALMS during the dehydrogenation reaction. IR spectra and density-functional theory (DFT) suggest that both the Ga matrix and the presence of coadsorbates alter the electronic properties of the surface Pt species.

摘要

负载型催化活性液态金属溶液(SCALMS)代表了一类催化材料,这类材料直到最近才被开发出来,但已被证明具有高活性,例如用于脱氢反应。先前的研究将催化活性归因于液态惰性镓基体表面孤立的贵金属原子。在本研究中,我们将以一氧化碳作为探针分子的漫反射红外傅里叶变换光谱(DRIFTS)应用于Ga/AlO、Pt/AlO和GaPt/AlO催化剂,以详细研究活性铂物种的性质。对Pt/AlO和GaPt/AlO上一氧化碳吸附的比较表明,液态SCALMS表面确实存在孤立的铂原子。将DRIFTS与在线气相色谱(GC)相结合,我们在CO/丙烷和Ar/丙烷中丙烷脱氢的操作条件下研究了Ga/AlO、Pt/AlO和GaPt/AlO体系。我们发现,Pt/AlO样品会因一氧化碳吸附和积炭而迅速中毒,而在GaPt/AlO SCALMS上进行丙烷脱氢可实现更高的转化率,且没有中毒效应的迹象。我们在操作条件下表明,在脱氢反应过程中,SCALMS表面存在孤立的铂原子。红外光谱和密度泛函理论(DFT)表明镓基体和共吸附物的存在都会改变表面铂物种的电子性质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a999/7252903/2f3b576cac1b/cs8b04578_0009.jpg
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