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用于将CO还原以生成合成气的金属-氮-碳电催化剂。

Metal-Nitrogen-Carbon Electrocatalysts for CO Reduction towards Syngas Generation.

作者信息

Delafontaine Laurent, Asset Tristan, Atanassov Plamen

机构信息

Chemical & Biomolecular Engineering and National Fuel Cell Research Center, University of California, Irvine, CA, 92697-2580, USA.

出版信息

ChemSusChem. 2020 Apr 7;13(7):1688-1698. doi: 10.1002/cssc.201903281. Epub 2020 Mar 18.

Abstract

Shifting syngas (an H /CO mixture) production away from fossil-fuel-dependent processes (e.g., steam methane reforming and coal gasification) is mandatory, as syngas is of interest as both a fuel and as a value-added chemical precursor. With appropriate electrocatalysts, such as silver-based and metal-nitrogen-carbon (M-N-C) materials, the electrochemical CO reduction reaction (CO RR) allows for the production of CO alongside H (from the hydrogen evolution reaction), and thus leads to syngas generation. In this Minireview, the application of M-N-C electrocatalysts for syngas generation is discussed. The mechanisms leading to different faradaic selectivities for CO are reviewed as a function of the nature of the metal, by using both computational and experimental approaches. The role played by the metal-free moieties in the M-N-C electrocatalysts is underlined. Since M-N-C electrocatalysts only recently entered the CO RR field (as opposed to Cu-, Ag-, or Au-based nanostructures), they have been mainly characterized in static liquid environments, in which the reaction rate is significantly hampered by CO -dissolution/diffusion limitations. Therefore, the design of CO RR electrolyzers for M-N-C electrocatalysts is addressed, and designs such as zero-gap electrolyzers with anionic membranes and humidified CO gas feed at the cathode are highlighted.

摘要

将合成气(一种H₂/CO混合物)的生产从依赖化石燃料的工艺(如蒸汽甲烷重整和煤气化)中转移出来是必不可少的,因为合成气作为燃料和增值化学前体都备受关注。借助合适的电催化剂,如银基和金属-氮-碳(M-N-C)材料,电化学CO还原反应(CO RR)能够在产生H₂(来自析氢反应)的同时生成CO,从而实现合成气的制备。在这篇综述中,我们讨论了M-N-C电催化剂在合成气制备中的应用。通过计算和实验方法,我们综述了根据金属性质导致对CO具有不同法拉第选择性的反应机理。强调了M-N-C电催化剂中无金属部分所起的作用。由于M-N-C电催化剂最近才进入CO RR领域(与基于Cu、Ag或Au的纳米结构不同),它们主要在静态液体环境中进行表征,在这种环境中,反应速率会受到CO溶解/扩散限制的显著阻碍。因此,我们探讨了用于M-N-C电催化剂的CO RR电解槽的设计,并重点介绍了如带有阴离子膜的零间隙电解槽以及在阴极通入加湿CO气体的设计。

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