Liquid-phase exfoliated ultrathin Bi nanosheets: Uncovering the origins of enhanced electrocatalytic CO2 reduction on two-dimensional metal nanostructure

Published

Journal Article

© 2018 Elsevier Ltd Electrochemical CO2 reduction has been considered as a promising route for renewable energy storage and carbon-neutral energy cycle. However, the selectivity and stability of electrocatalysts for CO2 reduction need to be improved. Two-dimensional (2D) layered electrocatalysts with high conductivity and abundant active sites have been considered as good candidates for CO2 reduction. Herein, we propose a liquid-exfoliation strategy to prepare ultrathin 2D bismuth (Bi) nanosheets towards efficient electrocatalytic CO2 conversion. Compared with bulk Bi, the increased edge sites on ultrathin Bi nanosheets played a vital role in CO2 adsorption and reaction kinetics, significantly facilitating CO2-to-formate (HCOOH/HCOO-) conversion. Through density functional theory (DFT) calculation, we found that the *OCOH formation step tended to occur on edge sites rather than on facet sites, as confirmed by the lower Gibbs free energies. Benefited from the high conductivity and rich edge sites, Bi nanosheets exhibited a Faradaic efficiency of 86.0% for formate production and a high current density of 16.5 mA cm−2 at − 1.1 V (vs. RHE), much superior to bulk Bi. Moreover, the Bi nanosheets could maintain well-preserved catalytic activity after long-term testing for over consecutive 10 h. We hope this study may provide new insights for the fabrication of novel 2D nanostructured metals for highly-efficient and long-life electrocatalytic CO2 conversion.

Full Text

Duke Authors

Cited Authors

  • Zhang, W; Hu, Y; Ma, L; Zhu, G; Zhao, P; Xue, X; Chen, R; Yang, S; Ma, J; Liu, J; Jin, Z

Published Date

  • November 1, 2018

Published In

Volume / Issue

  • 53 /

Start / End Page

  • 808 - 816

International Standard Serial Number (ISSN)

  • 2211-2855

Digital Object Identifier (DOI)

  • 10.1016/j.nanoen.2018.09.053

Citation Source

  • Scopus