催化作用
电化学
化学
基质(水族馆)
氧化还原
双水相体系
水溶液
反应机理
无机化学
物理化学
有机化学
电极
海洋学
地质学
作者
Jaeyune Ryu,Daniel T. Bregante,William C. Howland,Ryan P. Bisbey,Corey J. Kaminsky,Yogesh Surendranath
出处
期刊:Nature Catalysis
[Springer Nature]
日期:2021-09-06
卷期号:4 (9): 742-752
被引量:56
标识
DOI:10.1038/s41929-021-00666-2
摘要
Heterogeneous aqueous-phase aerobic oxidations are important catalytic transformations; however, their mechanisms and the role of O2 remain unclear. Here we show that thermochemical aerobic oxidations of organic small molecules can be analysed as two coupled electrochemical half-reactions for O2 reduction and substrate oxidation. We find that the polarization curves of the two half-reactions closely predict the mixed potential of the catalyst measured during thermochemical catalysis across diverse reaction conditions, catalysts and reactant identity. Additionally, we find that driving the substrate oxidation electrochemically without O2 at the mixed potential leads to similar rates and selectivities as for the corresponding thermochemical reactions. These findings indicate that O2 acts as an electron scavenger to supply the electrochemical driving force for substrate oxidation. These studies provide a quantitative and predictive link between thermochemical and electrochemical catalysis, thereby enabling the design of new aerobic oxidation schemes by applying the principles of electrochemistry.
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