Subtle Tuning of Catalytic Well Effect in Phthalocyanine Covalent Organic Frameworks for Selective CO₂ Electroreduction into C₂H₄.

Abstract

In the electrocatalytic CO₂ reduction reaction (CO₂RR), the strategic design of a catalytic well capable of regulating the overall confinement effects of catalytic sites holds significant promise for enhancing multiple-electron transfer and C─C coupling efficiency, particularly for the generation of C₂₊ products. Here, a series of Cu-salphen-based covalent organic frameworks (COFs) featuring hydroxyl-induced catalytic well are synthesized, which demonstrate successful application in electrocatalytic CO₂RR to yield multiple-electron transferred products. The meticulously engineered catalytic well, facilitated by multi-hydroxyl groups, manifests robust confinement effects, facilitating selective adsorption, enrichment, and activation of CO₂, intermediate stabilization, and reduction of energy barriers for electrocatalytic CO₂RR. Specifically, product selectivity can be finely tuned from CH₄ to C₂H₄ by modulating the levels of catalytic well, with CuPc-DFP-4OH-Cu exhibiting the most pronounced catalytic well effect, yielding a high 56.86% faradaic efficiency (FE) for C₂H₄ at -0.7 V, while CuPc-DFP-Cu, with the weakest catalytic well effect, achieves a 75.24% FE for CH₄ at -1.0 V. Notably, the attained FE for C₂H₄ (56.86%) surpasses that of all reported COFs to date. Complemented by theoretical calculations and in situ tests, this study delves deeply into the pivotal roles of hydroxyl-induced catalytic well with confinement effects.