Conductive Phthalocyanine‐Based Covalent Organic Framework for Highly Efficient Electroreduction of Carbon Dioxide

Abstract

The electroreduction of CO₂ to value-added chemicals such as CO is a promising approach to realize carbon-neutral energy cycle, but still remains big challenge including low current density. Covalent organic frameworks (COFs) with abundant accessible active single-sites can offer a bridge between homogeneous and heterogeneous electrocatalysis, but the low electrical conductivity limits their application for CO₂ electroreduction reaction (CO₂ RR). Here, a 2D conductive Ni-phthalocyanine-based COF, named NiPc-COF, is synthesized by condensation of 2,3,9,10,16,17,23,24-octa-aminophthalocyaninato Ni(II) and tert-butylpyrene-tetraone for highly efficient CO₂ RR. Due to its highly intrinsic conductivity and accessible active sites, the robust conductive 2D NiPc-COF nanosheets exhibit very high CO selectivity (>93%) in a wide range of the applied potentials of -0.6 to -1.1 V versus the reversible hydrogen electrode (RHE) and large partial current density of 35 mA cm^-2 at -1.1 V versus RHE in aqueous solution that surpasses all the conventional COF electrocatalysts. The robust NiPc-COF that is bridged by covalent pyrazine linkage can maintain its CO₂ RR activity for 10 h. This work presents the implementation of the conductive COF nanosheets for CO₂ RR and provides a strategy to enhance energy conversion efficiency in electrocatalysis.