选择性CO2/CO电还原制C3+化合物的催化剂

EES catalysis Pub Date : 2025-05-15 DOI:10.1039/D5EY00047E
Ngoc Huan Tran, Moritz W. Schreiber and Marc Fontecave
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引用次数: 0

摘要

电还原二氧化碳和一氧化碳为有机化合物被认为是一种很有前途的方法:(1)探索替代化石碳的碳源;(ii)将电能储存为稳定的化学能;(三)为化学工业生产有用的电子化学品和电子燃料。虽然人们普遍认为只有铜基催化剂才能促进多碳化合物的形成,而多碳化合物主要局限于乙烯和乙醇,但最近的研究对这一假设提出了挑战。在这篇综述中,我们提供了详尽的,结构和机理分析的固体材料,已报道作为催化剂的电还原CO2和CO更复杂的分子。这篇综述阐明了除铜外,镍、铁和钼等金属具有促进C-C偶联反应形成化学工业中重要分子的潜力,如丙烷、丙醇和丁醇,同时提供了可观的法拉第效率。因此,本综述为CO2R和COR的研究提供了新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Catalysts for selective CO2/CO electroreduction to C3+ compounds

Catalysts for selective CO2/CO electroreduction to C3+ compounds

Electroreduction of carbon dioxide and carbon monoxide to organic compounds is considered a promising way for (i) exploring a source of carbon alternative to fossil carbon; (ii) storing electrical energy as stable chemical energy; and (iii) producing useful e-chemicals and e-fuels for the chemical industry. While it is generally considered that only Cu-based catalysts facilitate the formation of multicarbon compounds, which are mainly limited to ethylene and ethanol, recent studies have challenged this assumption. In this review, we provide exhaustive, structural and mechanistic analyses of the solid materials that have been reported as catalysts for electroreduction of CO2 and CO to more complex molecules. This review elucidates that besides copper, metals such as nickel, iron and molybdenum have the potential to favor C–C coupling reactions to form important molecules in the chemical industry, such as propane, propanol, and butanol, along with offering substantial faradaic efficiencies. Thus, this review offers fresh perspectives on CO2R and COR.

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