Constructing an Asymmetric Covalent Triazine Framework to Boost the Efficiency and Selectivity of Visible‐Light‐Driven CO₂ Photoreduction

Abstract

The photocatalytic reduction of CO₂ represents an environmentally friendly and sustainable approach for generating valuable chemicals. In this study, a thiophene-modified highly conjugated asymmetric covalent triazine framework (As-CTF-S) is developed for this purpose. Significantly, single-component intramolecular energy transfer can enhance the photogenerated charge separation, leading to the efficient conversion of CO₂ to CO during photocatalysis. As a result, without the need for additional photosensitizers or organic sacrificial agents, As-CTF-S demonstrates the highest photocatalytic ability of 353.2 µmol g^-1 and achieves a selectivity of ≈99.95% within a 4 h period under visible light irradiation. This study provides molecular insights into the rational control of charge transfer pathways for high-efficiency CO₂ photoreduction using single-component organic semiconductor catalysts.