Three-dimensionally ordered macro-/mesoporous bismuth for efficient electrocatalytic CO2 reduction to formate

Abstract

Bismuth (Bi)-based catalysts with nanoporous structures have great potential for electrocatalytic reduction of CO₂ to formate. However, the direct preparation of nanoporous metallic Bi with specific internal structure by the currently used electrodeposition and in situ electroreduction methods is extremely challenging. In this study, three-dimensionally macro-/mesoporous Bi (3DM/m Bi) catalysts were controllably fabricated by combining a low temperature wet-chemical reduction method with a hard-soft dual-template approach. In particular, ammonia gas, acting as an auxiliary reducing agent, gently facilitates the reduction of Bi³⁺ ions within the template, resulting in a well-defined continuous macro/-mesoporous structure. The hierarchical interconnected macro-/mesoporous architecture offers significant advantages: the mesoporous structure offers rich catalytically active sites for CO₂ adsorption, while the macroporous structure accelerates the diffusion of reactants and products. As a result, the 3DM/m Bi catalyst achieves a desirable formate Faradaic efficiency of 95.6 % at -0.9 V vs. reversible hydrogen electrode (RHE) and maintains over 85 % formate selectivity in a wide potential range from -0.8 V to -1.2 V vs. RHE.