Polymer-Halogen Pockets Steering ^*CO Adsorption Configurations for Highly Selective CO₂ Electroreduction.

Abstract

The selective CO₂ electroreduction (CO₂R) toward specific C₂ products represents a critical challenge for practical applicability, requiring precise control over ^*CO intermediates. Herein, a "polymer-halogen" pocketed Cu catalyst is proposed, wherein the adjustable concentration of Iodide ion (I^-) within the pocket enables continuous modulation of ^*CO adsorption configurations on the Cu, thereby enabling tailored CO₂R toward ethylene or ethanol production. A perfluorosulfonic acid (PFSA)-modified CuI catalyst is constructed, where I^- is in situ leaching from CuI and subsequently confined by PFSA as an anion shielding layer to form polymer-halogen pockets. By tuning the thickness of PFSA shell, the amount of I^- in the pocket can be controlled. The surface-enhanced in situ Raman spectroscopy demonstrates that the coverage of ^*CO intermediates on Cu surface increases and tends to adsorb at low coordination Cu sites in catalyst granule for dimerization reaction as the I^- concentration in the pocket increases. Furthermore, the coordination environment exhibits distinct product selectivity. ^*CO at medium-coordinated sites favor ethanol production, while those at low-coordinated sites are conducive to ethylene formation. This strategy enables wide modulation of ethylene-to-ethanol ratios from 0.65 to 3.96, achieving peak Faradaic efficiencies (FE) of 60.3 ± 2.1% for ethylene and 48.3 ± 1.3% for ethanol.