Although elevating CO 2 pressure facilitates electrochemical CO 2 reduction reaction (CO 2 RR), the paired anodic oxygen evolution reaction (OER) can hardly gain the benefit due to its sluggish kinetics at near-neutral pH. Here, we replaced the OER with sulfite electrooxidation reaction (SOR) at near-neutral pH to realize a CO 2 /sulfite concurrent system, which can serve as a promising strategy for the dual treatments of CO 2 and SO 2 in flue gas. The anodic SOR reaction catalyzed by the non-noble nanoporous NiO supported on the nickel foam electrode exhibited a voltage saving by ∼1 V in contrast to the OER at 50 mA cm −2 . On the other hand, BiOI-catalyzed cathodic CO 2 -to-formate conversion at 20 bar CO 2 offered a remarkably broadened potential range and enhanced current density in contrast to the results tested at 1 bar CO 2 . An overall electricity-to-formate energy conversion efficiency of 65% for the CO 2 RR + SOR system was successfully obtained at a cell voltage of 1.8 V, which is 20% higher than that of the CO 2 RR + OER system. Based on these, an efficient and energy-saving full electrolysis system for concurrent electrolysis of CO 2 RR and SOR at 20 bar CO 2 has been successfully constructed.