钯
催化作用
化学
氢
膜
电化学
无机化学
金属
化学工程
光化学
有机化学
电极
物理化学
生物化学
工程类
作者
Aiko Kurimoto,Ryan P. Jansonius,Aoxue Huang,Antonio M. Marelli,David Dvořák,Camden Hunt,Curtis P. Berlinguette
标识
DOI:10.1002/anie.202017082
摘要
Abstract An electrocatalytic palladium membrane reactor (ePMR) uses electricity and water to drive hydrogenation without H 2 gas. The device contains a palladium membrane to physically separate the formation of reactive hydrogen atoms from hydrogenation of the unsaturated organic substrate. This separation provides an opportunity to independently measure the hydrogenation reaction at a surface without any competing H 2 activation or proton reduction chemistry. We took advantage of this feature to test how different metal catalysts coated on the palladium membrane affect the rates of hydrogenation of C=O and C=C bonds. Hydrogenation occurs at the secondary metal catalyst and not the underlying palladium membrane. These secondary catalysts also serve to accelerate the reaction and draw a higher flux of hydrogen through the membrane. These results reveal insights into hydrogenation chemistry that would be challenging using thermal or electrochemical hydrogenation experiments.
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