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Bismuth oxide (Bi2O3) emerges as a potent catalyst for converting CO2 to formic acid (HCOOH), leveraging its abundant lattice oxygen and the high activity of its Bi-O bonds. Yet, its durability is usually impeded by the loss of lattice oxygen causing structure alteration and destabilized active bonds. Herein, we report an innovative approach via the interstitial incorporation of indium (In) into the Bi2O3, significantly enhancing bond stability and preserving lattice oxygen. The optimized In-Bi2O3-100 catalyst achieves over 90 % Faradaic efficiency for HCOOH production across a wide potential range, in both H-cells and flow cells, maintaining robust stability after 100 hours of continuous operation. In situ surface-enhanced infrared absorption spectroscopy and theoretical calculations reveal that the interstitial In doping precisely tunes the adsorption of CO2* and OCHO* intermediate, facilitating rapid conversion. Further in situ Raman spectroscopy confirms the role of In bolstering the oxidized structure's stability within Bi2O3, critical for sustaining lattice oxygen during electrochemical CO2 reduction.
Wang et al. (Mon,) studied this question.