电合成
机制(生物学)
缩放比例
大规模运输
纳米技术
化学
化学物理
生化工程
材料科学
物理
电化学
工程类
物理化学
电极
几何学
量子力学
数学
作者
Zachary J. Oliver,Dylan J. Abrams,Luana Cardinale,Chih‐Jung Chen,Gregory L. Beutner,Seb Caille,Benjamin Cohen,Lin Deng,Moiz Diwan,Michael O. Frederick,Kaid C. Harper,Joel M. Hawkins,Dan Lehnherr,Christine Lucky,Alex M. Meyer,Seonmyeong Noh,Diego Núñez,Kyle W. Quasdorf,Jaykumar Vishwanath Teli,Shannon S. Stahl
标识
DOI:10.1021/acscentsci.4c01733
摘要
Organic electrosynthesis opens new avenues of reactivity and promises more sustainable practices in the preparation of fine chemicals and pharmaceuticals. The full value of this approach will be realized by taking these processes to the production scale; however, achieving this goal will require a better understanding of the influence of mass transport on reaction behavior and the interactions between reactive species and electrodes inherent to organic electrosynthesis. The limited options for cell geometries used on small scale limit elucidation of these features. Here, we show how advanced cell geometries allow us to control the interplay between reaction mechanism and mass transport, leading to improved performance of three modern organic electrosynthetic reactions. Each reaction shows a unique relationship with mass transport, highlighting the importance of understanding this relationship further to maximize the utility of organic electrosynthesis at scale.
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