Phytate Coordination-Enhanced Electrocatalytic Activity of Copper for Nitroarene Hydrogenation through Concerted Proton-Coupled Electron Transfer

Coupling acid–electrolyte proton exchange membrane fuel cells for electricity generation and cathodic hydrogenation for valuable chemical production shows great potential in energy and chemical industry. The key for this promising approach is the identification of cathode electrocatalysts with acid resistance, high activity, and low fabrication cost for practical applications. Among various promising cathodic candidates for this integrative approach, the easily available and cheap Cu suffers from low acidic hydrogenation activity due to kinetically arduous proton adsorption/activation. Inspired by the kinetic advantages of the concerted proton-coupled electron transfer (CPET) over the sequential proton–electron transfer process, herein, we use phytate coordination on Cu surface to overcome the kinetic bottleneck for proton adsorption/activation through the CPET pathway in an acidic half-cell setup; this leads to 1 order of magnitude activity enhancement (36.94-fold) for nitrobenzene hydrogenation. Mechanistic analysis confirms that phytate, as proton acceptor, induces the CPET process and overcomes the above kinetic limitations by tuning the d-band center and concentrating protons on the Cu surface. Consequently, the CPET process facilitates the formation of active hydrogen intermediates for efficient cathodic hydrogenation. This work provides a promising approach to integrate electricity generation and chemical production.