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. 2026 Mar 10:e14087.
doi: 10.1002/smll.202514087. Online ahead of print.

Tuning Electronic Effects in P-Block Metal-C60 Catalysts for Highly Selective CO2 Reduction to Formate

Affiliations

Tuning Electronic Effects in P-Block Metal-C60 Catalysts for Highly Selective CO2 Reduction to Formate

Yukun Xiao et al. Small. .

Abstract

Electrochemical CO2 reduction (CO2R) to formate offers a promising pathway toward sustainable chemical production. Although P-block metals display excellent selectivity, a universal approach for electronically tuning their active sites to simultaneously enhance activity and selectivity has remained challenging. In this work, we employ C60 nanosheets as electron-buffering supports to modulate interfacial charge, and hence to improve the performance of P-block metals in CO2R. Compared with pure indium (Pure In) catalyst, the C60 nanosheets supported In nanoclusters catalyst (In-C60) featuring high oxidation state achieves formate-dominated products across wide current densities, with high faradaic efficiency for formate reaching about 93% at 900 mA cm-2 under alkaline conditions and 97% at 700 mA cm-2 in acid, as well as higher stability exceeding 210 h in alkaline media. Operando infrared spectroscopy reveals that In-C60 promotes *OCHO formation, and fixed-potential density functional theory (DFT) calculations indicate that C60 tunes the In─O antibonding states near the Fermi level, weakening intermediate binding and facilitating the following protonation to formate. The strategy extends to other P-block metals (Bi, Sn, Pb), with the same electronic-tuning effect. This work introduces a generalizable strategy for P-block metal electrocatalysts and a practical route toward efficient, sustainable chemical production.

Keywords: P block metal‐C60; electrochemical CO2 reduction; formate; high current density.

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References

    1. K. P. Kuhl, T. Hatsukade, E. R. Cave, D. N. Abram, J. Kibsgaard, and T. F. Jaramillo, “Electrocatalytic Conversion of Carbon Dioxide to Methane and Methanol on Transition Metal Surfaces,” Journal of the American Chemical Society 136, no. 40 (2014): 14107–14113, https://doi.org/10.1021/ja505791r.
    1. L. Wang, D. C. Higgins, Y. Ji, et al., “Selective Reduction of CO to Acetaldehyde with CuAg electrocatalysts,” Proceedings of the National Academy of Sciences U S A 117, no. 23 (2020): 12572–12575, https://doi.org/10.1073/pnas.1821683117.
    1. P. Li, F. Yang, J. Li, et al., “Nanoscale Engineering of P‐Block Metal‐Based Catalysts Toward Industrial‐Scale Electrochemical Reduction of CO2,” Advanced Energy Materials 13, no. 34 (2023): 2301597.
    1. W. Ma, X. He, W. Wang, S. Xie, Q. Zhang, and Y. Wang, “Electrocatalytic Reduction of CO2 and CO to Multi‐Carbon Compounds Over Cu‐Based Catalysts,” Chemical Society Reviews 50, no. 23 (2021): 12897–12914, https://doi.org/10.1039/D1CS00535A.
    1. K. Peramaiah, M. Yi, I. Dutta, et al., “Catalyst Design and Engineering for CO2 ‐to‐Formic Acid Electrosynthesis for a Low‐Carbon Economy,” Advanced Materials 36, no. 51 (2024): 2404980, https://doi.org/10.1002/adma.202404980.

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