Bismuth oxide-loaded indium-organic framework catalysts for efficient electrochemical CO2 reduction

J Colloid Interface Sci. 2025 Jun 20;699(Pt 2):138251. doi: 10.1016/j.jcis.2025.138251. Online ahead of print.

Abstract

This study investigated electrocatalytic CO2 reduction using bismuth oxide-loaded indium-organic framework catalysts (MIL-68(In)). Bismuth incorporation increased the density of reactive sites, reduced the energy barrier for intermediate formation, and significantly enhanced formic acid production. In an H-type cell, the Bi1/2@MIL-68(In) catalyst achieved a Faradaic efficiency of 96.9 % for formic acid production at -1.7 V (vs. Ag/AgCl). Experimental results further confirmed that Bi3+ doping enhanced catalyst conductivity and accelerated electron transfer. The integration of Bi2O3 into the MIL-68(In) framework enriched the surface with reactive centers, thereby facilitating CO2 adsorption and activation. Theoretical calculations revealed that Bi1/2@MIL-68(In) stabilized the HCOO* intermediate, thereby reducing the free energy barrier for formic acid formation. This study highlights the potential of metal-organic frameworks (MOFs) as scaffolds for incorporating secondary metals to enhance catalytic performance. The findings provide valuable guidance for the rational design of highly efficient CO2 reduction catalysts.

Keywords: Bismuth doping; Catalytic activity; Electrocatalytic CO(2) reduction; Formic acid; MIL-68(In).