Tuning Electronic Effects in P-Block Metal-C60 Catalysts for Highly Selective CO2 Reduction to Formate
- PMID: 41805105
- DOI: 10.1002/smll.202514087
Tuning Electronic Effects in P-Block Metal-C60 Catalysts for Highly Selective CO2 Reduction to Formate
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.
© 2026 The Author(s). Small published by Wiley‐VCH GmbH.
References
-
- 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.
-
- 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.
-
- 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.
-
- 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.
-
- 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.
Grants and funding
LinkOut - more resources
Full Text Sources
