4.8 Article

Oxide-Supported Carbonates Reveal a Unique Descriptor for Catalytic Performance in the Oxidative Coupling of Methane (OCM)

期刊

ACS CATALYSIS
卷 12, 期 15, 页码 9325-9338

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.1c05177

关键词

oxidative coupling of methane (OCM); IR spectroscopy; thermal analysis; TGA; property-descriptor; carbonate decomposition; carbonate stability

资金

  1. Berlin Graduate School of Natural Sciences and Engineering (BIG-NSE) [EXC 314]
  2. DFG Cluster of Excellence UNICAT

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The selection of catalysts for the oxidative coupling of methane (OCM) is summarized in this study. It is found that catalysts with thermodynamically stable carbonate and thermally stable oxide support exhibit good catalytic performance. Experimental correlations between carbonate decomposition temperature and C-2 yield suggest the importance of CO2 adsorption and surface carbonates in selective methane conversion.
The oxidative coupling of methane (OCM) is a promising reaction for the direct conversion of methane to higher hydrocarbons. The reaction can be performed over oxide-based catalysts with very diverse elemental compositions. Yet, despite decades of research, no general common structure-activity relationship has been deduced. Our recent statistical meta-analysis across a wide range of catalyst compositions reported in the literature suggested that only the catalysts combining thermodynamically stable (under reaction conditions) carbonate and thermally stable oxide support exhibit good catalytic performance. Guided by these findings, we now explore experimental correlations between descriptors for structure, stability, and decomposition behavior of supported metal carbonates vs the materials' respective performance in OCM catalysis. In this study, carbonates of Rb, Cs, and Mg were supported on oxides of Sm, Y, Gd, Ce, Sr, and Ba, tested in OCM, and studied by IR spectroscopy and thermal analysis. From the evaluation of six proposed property descriptors, we derive a statistically robust volcano-type correlation between the onset temperature of carbonate decomposition and the C-2 yield, indicating the importance of CO2 adsorption and surface carbonates in selective methane conversion. Moreover, we discuss mechanisms that can account for the observed property-performance correlation across a wide range of OCM catalysts. Carbonate species are suggested to block highly reactive sites during OCM catalysis, which reduces overoxidation and enables the formation of C-2 products.

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