一氧化碳
二氧化碳电化学还原
醋酸
碳纤维
纳米技术
二氧化碳
电化学
工艺工程
催化作用
化学
材料科学
电极
工程类
有机化学
复合数
复合材料
物理化学
作者
Matthew Jouny,Gregory S. Hutchings,Feng Jiao
出处
期刊:Nature Catalysis
[Nature Portfolio]
日期:2019-12-09
卷期号:2 (12): 1062-1070
被引量:351
标识
DOI:10.1038/s41929-019-0388-2
摘要
The electrochemical conversion of carbon dioxide to value-added chemical products has been heavily explored as a promising strategy for carbon utilization. However, the direct synthesis of multi-carbon (C2+) products suffers from undesired side reactions and relatively low selectivity. Electrochemically converting CO2 to single-carbon products is much more effective and being commercially deployed. Recent studies have shown that CO can be electrochemically transformed further to C2+ at high reaction rates, high C2+ selectivity and inherently improved electrolyte stability, raising the prospect of a two-step pathway to transform CO2. In this Perspective, the progress towards high-rate CO conversion is shown alongside mechanistic insights and device designs that can improve performance even further. A techno-economic analysis of the two-step conversion process and cradle-to-gate lifecycle assessment shows the economic feasibility and improved environmental impact of a high-volume commercial process generating acetic acid and ethylene compared to the current state of the art. Carbon monoxide can be electrochemically transformed to multi-carbon products selectively at high rates, raising the prospect of a two-step pathway to transform CO2 into value-added chemical products. This Perspective highlights recent progress complemented by a techno-economic analysis of the two-step conversion process and cradle-to-gate lifecycle assessment.
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