Engineering Interface with One-Dimensional Co₃O₄ Nanostructure in Catalytic Membrane Electrode: Toward an Advanced Electrocatalyst for Alcohol Oxidation.

Abstract

Electrochemical oxidation has attracted vast interest as a promising alternative to traditional chemical processes in fine chemical synthesis owing to its fast and sustainable features. An electrocatalytic membrane reactor (ECMR) with a three-dimensional (3D) electrode has been successfully designed for the selective oxidation of alcohols with high current efficiency to the corresponding acids or ketones. The anode electrode was fabricated by the in situ loading of one-dimensional (1D) Co₃O₄ nanowires (NWs) on the conductive porous Ti membrane (Co₃O₄ NWs/Ti) via the combination of a facile hydrothermal synthesis and subsequent thermal treatment. The electrocatalytic oxidation (ECO) results of alcohols exhibited superior catalytic performance with a higher current efficiency on the Co₃O₄ NWs/Ti membrane compared with those of Co₃O₄ nanoparticles on the Ti membrane (Co₃O₄ NPs/Ti). Even under low reaction temperatures such as 0 °C, it still displayed a very high ECO activity for alcohol oxidation in the ECMR. For example, >99% conversion and 92% selectivity toward benzoic acid were obtained for the benzyl alcohol electrooxidation. The electrode is particularly effective for the cyclohexanol oxidation, and a selectivity of >99% to cyclohexanone was achieved at 0 °C, higher than most reported noble-metal catalysts under the aerobic reaction conditions. The extraordinary electrocatalytic performance of the 3D Co₃O₄ NWs/Ti membrane electrode demonstrates the significant influence of morphology effect and engineering interfaces in membrane electrodes on the electrocatalytic activity and charge transfer process of nanocatalysts. Our results propose that similar membrane electrodes serve as versatile platforms for the applications of 1D nanomaterials, porous electrodes, and ECMRs.