Accelerating acidic CO 2 electroreduction: strategies beyond catalysts.

Carbon dioxide electrochemical reduction (CO 2 RR) into high-value-added chemicals offers an alternative pathway toward achieving carbon neutrality. However, in conventional neutral or alkaline electrolyte systems, a significant portion of CO 2 is converted into (bi)carbonate due to the thermodynamically favorable acid-base neutralization reaction between CO 2 and hydroxide ions. This results in the single-pass carbon efficiency (SPCE) being theoretically capped at 50%, presenting challenges for practical applications. Acidic CO 2 RR can completely circumvent the carbonate issue and theoretically achieve 100% SPCE, garnering substantial attention from researchers in recent years. Nevertheless, acidic CO 2 RR currently lags behind traditional neutral/alkaline systems in terms of product selectivity, stability, and energy efficiency, primarily because the abundance of H + ions exacerbates the hydrogen evolution reaction (HER). Encouragingly, significant breakthroughs have been made to address these challenges, with numerous studies indicating that the regulation of the local catalytic environment may be more crucial than the catalyst itself. In this review, we will discuss the main challenges and latest strategies for acidic CO 2 RR, focusing on three key aspects beyond the catalyst: electrolyte regulation, local catalytic environment modification, and novel designs of gas diffusion electrodes (GDEs)/electrolyzers. We will also conclude the current advancement for acidic CO 2 RR and provide an outlook, with the hope that this technology will contribute to achieving carbon neutrality and advance towards practical application.