<i>Operando</i> Spectroscopic Analysis of Axial Oxygen-Coordinated Single-Sn-Atom Sites for Electrochemical CO₂ Reduction

Abstract

Sn-based materials have been demonstrated as promising catalysts for the selective electrochemical CO₂ reduction reaction (CO₂RR). However, the detailed structures of catalytic intermediates and the key surface species remain to be identified. In this work, a series of single-Sn-atom catalysts with well-defined structures is developed as model systems to explore their electrochemical reactivity toward CO₂RR. The selectivity and activity of CO₂ reduction to formic acid on Sn-single-atom sites are shown to be correlated with Sn(IV)-N₄ moieties axially coordinated with oxygen (O-Sn-N₄), reaching an optimal HCOOH Faradaic efficiency of 89.4% with a partial current density (<i>j</i>_HCOOH) of 74.8 mA·cm^-2 at -1.0 V vs reversible hydrogen electrode (RHE). Employing a combination of <i>operando</i> X-ray absorption spectroscopy, attenuated total reflectance surface-enhanced infrared absorption spectroscopy, Raman spectroscopy, and ¹¹⁹Sn Mössbauer spectroscopy, surface-bound bidentate tin carbonate species are captured during CO₂RR. Moreover, the electronic and coordination structures of the single-Sn-atom species under reaction conditions are determined. Density functional theory (DFT) calculations further support the preferred formation of Sn-O-CO₂ species over the O-Sn-N₄ sites, which effectively modulates the adsorption configuration of the reactive intermediates and lowers the energy barrier for the hydrogenation of *OCHO species, as compared to the preferred formation of *COOH species over the Sn-N₄ sites, thereby greatly facilitating CO₂-to-HCOOH conversion.