Physical Separation of H<sub>2</sub> Activation from Hydrogenation Chemistry Reveals the Specific Role of Secondary Metal Catalysts
Aiko Kurimoto, Ryan P. Jansonius, Aoxue Huang, Antonio M. Marelli, David Dvořák, Camden Hunt, Curtis P. Berlinguette
Abstract
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.