Redox-active covalent organic nanosheets (CONs) as a metal-free electrocatalyst for selective CO2 electro-reduction to the liquid fuel methanol†
Abstract
In essence, the utilization of renewable energy in the carbon dioxide reduction reaction (CO2RR) holds the potential to transform carbon emissions into valuable chemicals, encompassing a range of hydrocarbons and alcohols. Herein, we have implemented a redox-active triphenylamine (TPA)-based covalent organic nanosheets (CONs) as a metal-free electrocatalyst for CO2 reduction in 0.2 M phosphate buffer (pH-7.2). The reaction produced methanol as the only carbonaceous liquid product reaching a maximum faradaic efficiency (FE) of 51.6% under mild reaction conditions in aqueous medium. Moreover, the corresponding overpotential of the reaction was as low as 210 mV illustrating the superiority of this metal-free electrocatalyst. The mechanistic aspects are supported through experimental in situ RAS-IR (reflection–absorption), in situ Raman study as well as computational study. The superior performance of the electrocatalyst is believed to be due to the presence of redox-active 2-D nanosheets with exposed active sites. This work unlocks a way to produce methanol efficiently by the electrochemical reduction of CO2.
- This article is part of the themed collection: Functional Framework Materials