Efficient CO reduction to CO + CH at CuCo@NC cathode integrated with CHOH oxidation to methylal at Pt anode in an ionic liquid electrolyte

Electroreduction of CO 2 to energy chemicals in aqueous electrolytes is usually limited by logy OER at the anode and competing HER at the cathode. An N-doped carbon encapsulated Cu-CoO composite (CuCo@NC) fabricated by the facile pyrolysis of Cu and Co salts and melamine mixture was used as a cathode for CO 2 reduction to CO and CH 4 , coupled with the anodic oxidation of CH 3 OH to dimethoxymethane in an ionic liquid-methanol medium to boost the anode reaction. The electrolytic system exhibits efficient redox activity with a higher average FE DMM (58.7%) within 48 h and high instantaneous FE C1 (99.1%) for CO + CH 4 at 24 h. Simultaneous production of the high-value chemicals DMM and CO + CH 4 in an electrolysis cell is achieved. The surface composition and structure of this composite with higher saturation magnetization, specifically the contribution of the Cu, CuO x , and CoO x crystallines to the catalytic performance of CO 2 eRR and magnetic properties, were explored. The catalytic system achieves high activity within 72 h of continuous electrolysis, and the electrode and ionic liquid can remain intact after being used three times, indicating the high operational stability of the CO 2 eRR system. N-doped carbon encapsulated Cu-CoO (CuCo@NC) exhibits high FE (99.1%) for CO 2 eRR to CO + CH 4 , coupled with the anodic oxidation of CH 3 OH to dimethoxymethane in EmimBF 4 -methanol electrolyte, partly substituting for OER and hindering competing HER.