High carbon utilization in CO2 reduction to multi-carbon products in acidic media

Renewable electricity-powered CO 2 reduction to multi-carbon (C 2+ ) products offers a promising route to realization of low-carbon-footprint fuels and chemicals. However, a major fraction of input CO 2 (>85%) is consumed by the electrolyte through reactions with hydroxide to form carbonate/bicarbonate in both alkaline and neutral reactors. Acidic conditions offer a solution to overcoming this limitation, but also promote the hydrogen evolution reaction. Here we report a design strategy that suppresses hydrogen evolution reaction activity by maximizing the co-adsorption of CO and CO 2 on Cu-based catalysts to weaken H* binding. Using density functional theory studies, we found Pd–Cu promising for selective C 2+ production over C 1 , with the lowest ∆ G OCCOH* and ∆ G OCCOH* - ∆ G CHO* . We synthesized Pd–Cu catalysts and report a crossover-free system (liquid product crossover