Electroplated Electrodes for Continuous and Mass‐Efficient Electrochemical Hydrogenation.

Electrocatalytic hydrogenations (ECH) enable the reduction of organic substrates upon usage of electric current and present a sustainable alternative to conventional processes if green electricity is used. Opposed to most current protocols for electrode preparation, this work presents a one‐step binder‐ and additive‐free production of silver‐ and copper‐electroplated electrodes. Controlled adjustment of the preparation parameters allows for the tuning of catalyst morphology and its electrochemical properties. Upon optimization of the deposition protocol and carbon support, high faradaic efficiencies of 93 % for the ECH of the Vitamin A‐ and E‐synthon 2‐methyl‐3‐butyn‐2‐ol (MBY) are achieved that can be maintained at current densities of 240 mA cm−2 and minimal catalyst loadings of 0.2 mg cm−2, corresponding to an unmatched production rate of 1.47 kgMBE gcat−1 h−1. For a continuous hydrogenation process, the protocol can be directly transferred into a single‐pass operation mode giving a production rate of 1.38 kgMBE gcat−1 h−1. Subsequently, the substrate spectrum was extended to a total of 17 different C−C−, C−O− and N−O−unsaturated compounds revealing the general applicability of the reported process. Our results lay an important groundwork for the development of electrochemical reactors and electrodes able to directly compete with the palladium‐based thermocatalytic state of the art. [ABSTRACT FROM AUTHOR]