Conductive phthalocyanine-based metal-organic framework as a highly efficient electrocatalyst for carbon dioxide reduction reaction

Porous crystalline metal-organic frameworks (MOFs) are one class of promising electrode materials for CO2 electroreduction reaction (CO2RR) by virtue of their large CO2 adsorption capacities and abundant tunable active sites, but their insulating nature usually leads to low current density. Herein, a two-dimensional (2D) Ni-phthalocyanine-based MOF (NiPc-Ni(NH)(4)) that constructed by 2,3,9,10,16,17,23,24-octaaminophthalocyaninato nickel(II) (NiPc-(NH2)(8)) and nickel(II) ions attained high electrical conductivity due to the high overlap of d-pi conjugation orbitals between the nickel node and the Ni-phthalocyanine substituted o-phenylenediamine. During CO2RR, the NiPc-Ni(NH)(4) nanosheets achieved a high CO Faradaic efficiency of 96.4% at -0.7 V and a large CO partial current density of 24.8 mA cm(-2) at -1.1 V, which surpass all the reported two-dimensional MOF electrocatalysts evaluated in H-cell. The control experiments and density functional theory (DFT) calculations suggested that the Ni-N-4 units of the phthalocyanine ring are the catalytic active sites. This work provides a new route to the design of highly efficient porous framework materials for the enhanced electrocatalysis via improving electrical conductivity.