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Article Abstract

The electrochemical conversion of CO into liquid fuels is a promising strategy for achieving carbon neutrality. Tin dioxide (SnO) shows a notable ability to electrocatalytically convert CO into formate, though its efficiency is significantly limited by its low catalytic activity. Herein, we construct facet-oriented SnO nanoflowers all standing on a three-dimensional nickel hollow fiber that exhibits superior CO-to-formate electrocatalytic performance. A formate selectivity of 94% and stability of 300 h with a current density of 1.3 A cm at -1.1 V (vs. reversible hydrogen electrode [RHE]) are attained under ambient conditions. Notably, an extremely high CO single-pass conversion rate of 85% is achieved, outperforming prominent catalysts reported in electrocatalysis. The synergetic combination of the unique nanostructures and their advanced spatial configuration is proposed to be responsible for the facet-oriented SnO with a hierarchical structure, providing fully exposed active sites and facilitating mass and charge transfers. Enhanced mass transfer in the hollow fiber electrode verified by electrochemical measurements and well-retained Sn species confirmed by spectroscopy synergistically boost the high CO conversion activity. spectroscopy and theoretical calculation results demonstrate that the SnO(101) facet favors ∗OCHO intermediate formation and ∗HCOOH desorption, leading to high formate selectivity. This study provides a straightforward approach to the precise fabrication of composite hollow fiber electrodes, enabling highly efficient electrocatalytic reactions with gas molecules.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12169250PMC
http://dx.doi.org/10.1016/j.xinn.2025.100844DOI Listing

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