Computational evaluation of CO₂ conversion into formic acid via a novel adsorption mechanism on metal-free B₄C₁₂

The electrochemical reduction of CO2 (CO2RR) to formic acid (HCOOH) is a promising approach to harness renewable energy for the production of value-added chemicals and contribute to carbon cycling. The search for cost-effective and efficient metal-free electrocatalysts is critical for realizing industrial applications. However, limited literature is available on this topic, primarily because the significant challenge of efficiently activating inert CO2 remains unresolved. In this study, we have designed and applied a novel boron carbide (B4C12) monolayered cage as an electrocatalyst for CO2RR to produce HCOOH. B4C12 exhibits exceptional electronic, dynamic, and thermodynamic stability. Through comprehensive density functional theory computations, we have observed that B4C12 rapidly and stably adsorbs CO2 in a unique eta(3)(O, C, O)-CO2 configuration, resulting in excellent CO2RR activity with a low limiting potential (-0.38 V) and suppressed hydrogen evolution reaction. Our mechanistic investigations reveal that B4C12 donates electrons to facilitate the bending of CO2, anchoring it onto the curved surface effectively. Additionally, the C atom in the eta(3)(O, C, O)-CO2 configuration attracts H+ + e(-) pairs through its active p electron, leading to the observed low limiting potential. This study not only successfully designs a novel class of metal-free electrocatalysts but also provides a promising strategy for advancing CO2RR research in the future.