C2 Product Selectivity by 2D-nanosheet of Layered Zn-doped Cu2(OH)3(NO3)-A Pre-catalyst for Electrochemical CO2 Reduction

The natural carbon cycle cannot mitigate and recycle the excess CO<inf>2</inf> in the atmosphere, leading to a continuous rise in the global temperature. Electrochemical conversion of CO<inf>2</inf> is one of the useful methods to utilise this anthropogenic CO<inf>2</inf> and convert it into value-added chemicals. However, this process suffers the challenges of product selectivity and good Faradaic efficiency. In our current work, we report the role of Zn-doping in the 2D-Nanosheet of Cu<inf>2</inf>(OH)<inf>3</inf>(NO<inf>3</inf>)-a pre-catalyst that undergoes the in-situ transformation into a metallic state along with surface reconstruction. Our studies show, in the aqueous medium, the optimum amount of Zn plays a crucial role in the production of ethanol with the Faradaic efficiency of ∼45.2 % though C−C coupling. Temperature-programmed desorption studies conclude that Zn increases the product selectivity for CO adsorption on Cu<inf>2</inf>(OH)<inf>3</inf>(NO<inf>3</inf>) nanosheets, further facilitating the C−C coupling at higher negative potential. The detailed XPS studies also reveal that the in-situ conversion of Cu²⁺ to Cu⁰ and Cu⁺ at negative potential contributes to the production of C<inf>2</inf> products. The post-catalytic microstructural and spectroscopic studies converge to this point that the cumulative effect of oxidation state, surface reconstruction, as well as the presence of Zn modulate the overall Faradaic efficiency for ethanol formation.