Single-Atom-Functionalized Covalent Organic Frameworks for Efficient CO2 Conversion: Electronic Structure Insights from First-Principles Simulations

Designing highly efficient catalysts with tunable reactivity and activity for the selective reduction of CO₂ is a challenging task that necessitates a thorough understanding of the catalyst electronic structure. In this work, we aim at systematically understanding the impact of single-atom functionalization on the electronic structure and CO₂ reduction activity of a hydrazine-based covalent organic framework (HCOF) using first-principles simulations. Our results demonstrate that the hydrazine linkages in the covalent organic framework (COF) are adequate for stabilizing a range of single atoms, resulting in a flexible electronic structure for successful activation of the centrosymmetric CO₂ molecule. We show that the single-atom-functionalized HCOF (SA-HCOF) systems bind the CO₂ molecule strongly in a selective manner with very high binding energies of −0.38 to −2.98 eV. In addition, through rigorous electronic structure analysis encompassing the distribution of d-states near the Fermi level and Bader charge analysis, we establish robust correlations between the CO₂ binding energy and the key electronic properties of the catalysts. The computed reaction pathways indicate that the Cr- and Co-based single-atom catalysts (SACs) show remarkable activity for CO₂ reduction to CO and HCOOH with very low limiting potentials of −0.61 and −0.52 V, respectively. Further, the CO₂ reduction activity of the COF-stabilized SACs was successfully correlated to the adsorption free energy of CO and HCOO intermediates which in turn depend on electronic properties such as the net Bader charge accumulated on the CO₂ molecule and the d-band center of the isolated metal atoms. These findings underscore the pivotal role of the electronic structure of isolated metal atoms stabilized on COFs in modulating the CO₂ reactivity and reduction activity, thereby providing crucial insights for the rational design of high-performance catalysts for CO₂ utilization.