Organic reactions for the electrochemical and photochemical production of chemical fuels from CO2 - The reduction chemistry of carboxylic acids and derivatives as bent CO2 surrogates

被引:24
|
作者
Luca, Oana R. [1 ]
Fenwick, Aidan Q. [1 ]
机构
[1] CALTECH, Div Chem & Chem Engn, Joint Ctr Artificial Photosynth, Pasadena, CA 91125 USA
关键词
N-HETEROCYCLIC CARBENE; CARBON-DIOXIDE; ELECTROCATALYTIC REDUCTION; AROMATIC-ALDEHYDES; DEOXYGENATION; CONVERSION; HYDROSILYLATION; ELECTROREDUCTION; CATALYSTS; DECARBOXYLATION;
D O I
10.1016/j.jphotobiol.2015.04.015
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The present review covers organic transformations involved in the reduction of CO2 to chemical fuels. In particular, we focus on reactions of CO2 with organic molecules to yield carboxylic acid derivatives as a first step in CO2 reduction reaction sequences. These biomimetic initial steps create opportunities for tandem electrochemical/chemical reductions. We draw parallels between long-standing knowledge of CO2 reactivity from organic chemistry, organocatalysis, surface science and electrocatalysis. We point out some possible non-faradaic chemical reactions that may contribute to product distributions in the production of solar fuels from CO2. These reactions may be accelerated by thermal effects such as resistive heating and illumination. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:26 / 42
页数:17
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