Answers are grounded in this paper and cite their sources.
Experimental study demonstrates additive-free electrocatalytic hydrogenation of nitroarenes and ketones, indicating a viable platform for green electrosynthesis.
Electrocatalytic hydrogenation offers a sustainable alternative to conventional thermocatalytic methods, which typically requires high temperature and pressure, and toxic additives. Herein, we report a proton-conductive graphene oxide (GO) membrane reactor that enables selective and additive-free electrocatalytic hydrogenation of nitroarenes and ketones under ambient conditions. The GO membrane, dual functionalized with imidazole and cerium ions, exhibits enhanced proton conductivity (0.160 mS cm−1) and near ideal proton selectivity (t = 0.956) along with improved structural stability in aqueous and mixed solvent environments. Integrated into a two-compartment electrochemical system utilizing molecular hydrogen as the sole reductant, the membrane reactor achieves up to 93% yield with excellent chemoselectivity. Mechanistic investigations indicate an azobenzene-mediated pathway during nitroarene reduction. Compared to conventional proton exchange membrane systems, the developed membrane eliminates the need for supporting electrolytes while maintaining efficient proton transport. This work demonstrates a robust and scalable platform for green electrosynthesis and highlights the potential of functionalized GO membranes in advanced catalytic applications.
No takes yet. Share an insight, caveat, or question.
Moonnee et al. (2026) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: