Solid-State Electrochemical Carbon Dioxide Capture by Conductive Metal-Organic Framework Incorporating Nickel Bis(diimine) Units

This paper presents the first implementation of electrically conductive metal-organic framework (MOF) Ni3(2,3,6,7,10,11-hexaiminotriphenylene)2 (Ni3(HITP)2) integrated with nickel bis(diimine) (Ni-BDI) units for efficient solid-state electrochemical carbon dioxide (CO2) capture. The electrochemical cell assembled using Ni3(HITP)2 as working electrodes can reversibly capture and release CO2 through potential control. A high-capacity utilization of 96% and a Faraday efficiency of 98% have been achieved. The material also exhibits excellent electrochemical stability with its capacity maintained during 50 capture-release cycles and resistance to general interferences, including O2, H2O, NO2, and SO2. Capacity utilization of up to 35% is obtained at CO2 concentrations as low as 1%. The capture of CO2 at concentrations ranging from 1% to 100% requires exceptionally low energy consumption of only 30.5-72.4 kJ mol-1. Studies combining spectroscopic experiments and computational approaches reveal that the CO2 capture and release mechanism involves reversible carbamate formation on the N atom of the Ni-BDI unit in the MOF upon its one-electron redox reaction.