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Catalytic conversion of C1 molecules under mild conditions

催化作用 一氧化碳 甲烷 化学 分子 甲醇 甲烷氧化偶联 纳米技术 化学工程 组合化学 材料科学 有机化学 工程类
作者
Xiaoju Cui,Rui Huang,Dehui Deng
出处
期刊:EnergyChem [Elsevier BV]
卷期号:3 (1): 100050-100050 被引量:64
标识
DOI:10.1016/j.enchem.2020.100050
摘要

C1 catalysis based on the transformation of methane, carbon monoxide, methanol and carbon dioxide offers great potential for the sustainable production of fuels and chemicals in response to the decrease of the energy consumption and plant maintenance. While the relatively inert nature of CH and CO bond (e.g., methane and carbon dioxide) and uncontrollable coupling of CC bond render the selective activation and controllable transformation of C1 molecules to high-value-added products challenging in C1 chemistry. Catalytic conversion of C1 energy molecules under mild conditions enables a better control of the selectivity of the desired products, however, which requires highly active catalysts to lower the reaction energy barriers. Besides designing efficient catalysts to promote C1 molecules conversion, employing electro-catalysis and photo-catalysis to circumvent the thermodynamic limitations is regarded as promising ways for C1 catalysis at low temperatures. Benefiting from the advanced technology for catalyst synthesis, reactor design, mechanism understanding, catalytic conversion of C1 molecules under mild conditions has made significant progress from 2010 to 2020. In this review, we summarized the typical catalytic processes and representative catalysts for transforming methane, carbon monoxide, methanol and carbon dioxide into high value-added chemicals with a reaction temperatures below 200 °C driven by thermo-catalysis, electro-catalysis, and photo-catalysis. Besides, a short perspective is offered to highlight possible future research directions towards C1 molecules conversion under mild conditions. It is expected to provide a useful reference for the readers to design better catalysts and reaction process for mild conversion of C1 molecules efficiently in future.
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