Electrochemical CO2reduction on Pd-modified Cu foil

Bimetallic catalysts can improve CO(2)reduction efficiency via the combined properties of two metals. CuPd shows enhanced CO(2)reduction activity compared to copper alone. Using differential electrochemical mass spectrometry (DEMS) and electrochemical infrared (IR) spectroscopy, volatile products and adsorbed intermediates were measured during CO(2)and CO reduction on Cu and CuPd. The IR band corresponding to adsorbed CO appears 300 mV more positive on CuPd than that on Cu, indicating acceleration of CO(2)reduction to CO. Electrochemical IR spectroscopy measurements in CO-saturated solutions reveal similar potentials for CO adsorption and CO(3)(2-)desorption on CuPd and Cu, indicating that CO adsorption is controlled by desorption of CO32-. DEMS measurements carried out during CO reduction at both electrodes showed that the onset potential for reduction of CO to CH(4)and CH3OH on CuPd is about 200 mV more positive than that on Cu. We attribute these improvements to interaction of Cu and Pd, which shifts the d-band center of the Cu sites.