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Reductive Treatment of Ga–Pt-Supported Catalytically Active Liquid Metal Solutions (SCALMS) for Propane Dehydrogenation

脱氢 催化作用 X射线光电子能谱 丙烷 化学 氧化物 金属 无机化学 化学工程 分析化学(期刊) 有机化学 工程类
作者
Nnamdi Madubuko,Tzung-En Hsieh,Nora Vorlaufer,Simon Carl,Julien Steffen,Andreas Mölkner,Nicola Taccardi,Johannes Frisch,Regan G. Wilks,Johannes Will,Marco Haumann,Andreas Görling,Erdmann Spiecker,Peter Felfer,Marcus Bär,Peter Wasserscheid
出处
期刊:ACS Catalysis [American Chemical Society]
卷期号:15 (14): 12436-12449
标识
DOI:10.1021/acscatal.5c01463
摘要

A comprehensive investigation of the impact of hydrogen (H2) pretreatments on Ga-Pt supported catalytic active liquid metal solution (SCALMS) for propane dehydrogenation (PDH) is reported. Our approach bridges from model system investigations to real-world catalytic systems, which are tested in continuously operating PDH reactors. The microscopic and spectroscopic findings on model Ga-Pt systems suggest changes in the electronic structure and surface chemistry during SCALMS sample oxidation and H2 pretreatment, indicating potential modifications of the active sites involved in PDH. H2 pretreatments of technical Ga-Pt SCALMS prepared by ultrasonication (US) led to significantly improved activity, i.e., the conversion of propane increased from 10% for the untreated catalyst to 26% for the H2 pretreated (5 h at 823 K) catalyst. We attribute this enhanced activity to the removal of a gallium oxide (GaO x ) shell, as confirmed by synchrotron-based in situ X-ray photoelectron spectroscopy (XPS) as well as in situ transmission electron microscopy (TEM) investigations of Ga-Pt model alloys. These findings are supported by density functional theory (DFT) and machine learned force field (ML-FF) calculations. Increasing the temperature of the H2 treatment to 923 K reduced the deactivation rate of the catalyst to as low as 0.01 h-1, which is 3 times more stable than what was observed for the untreated catalyst. This deactivation is ascribed to bulk restructuring of the alloy, leading to the formation of less active Pt species as confirmed by spectroscopic and microscopic analysis. Our work not only elucidates the fundamental properties, i.e., typology, electronic structure, and reactivity, of isolated Pt atoms in Ga-Pt SCALMS but also proposes underlying mechanisms for the activation and deactivation of PDH catalysts.
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