Parallels between enzyme catalysis, electrocatalysis, and photoelectrosynthesis

被引:6
|
作者
Nishiori, Daiki [1 ,2 ]
Wadsworth, Brian L. [1 ,2 ]
Moore, Gary F. [1 ,2 ]
机构
[1] Arizona State Univ, Sch Mol Sci, Tempe, AZ 85281 USA
[2] Arizona State Univ, Biodesign Inst, Ctr Appl Struct Discovery CASD, Tempe, AZ 85281 USA
来源
CHEM CATALYSIS | 2021年 / 1卷 / 05期
基金
美国国家科学基金会;
关键词
REDOX POLYMER ELECTRODES; DRIVEN OXYGEN EVOLUTION; ENERGY-CONVERSION; ARTIFICIAL PHOTOSYNTHESIS; ELECTROCHEMICAL REACTIONS; PHOTOCURRENT GENERATION; HYDROGEN EVOLUTION; MOLECULAR CATALYSIS; FUMARATE REDUCTASE; CYCLIC VOLTAMMETRY;
D O I
10.1016/j.checat.2021.09.008
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Catalysts are central to accelerating chemistry in biology and technology. In biochemistry, the relationship between the velocity of an enzymatic reaction and the concentration of chemical substrates is described via the Michaelis- Menten model. The modeling and benchmarking of synthetic molecular electrocatalysts are also well developed. However, such efforts have not been as rigorously extended to photoelectrosynthetic reactions, where, in addition to chemical substrates and charge carriers, light is a required reagent. In this perspective, we draw parallels between concepts involving enzyme catalytic efficiency, the benchmarking of molecular electrocatalysts, and the performance of photoelectrosynthetic assemblies, while highlighting key differences, assumptions, and limitations.
引用
收藏
页码:978 / 996
页数:19
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