From Carbon Nitrides to COFs: Opportunities and Prospects in Photocatalytic CO ₂ Reduction

Abstract

Abstract The continuing increase in atmospheric carbon dioxide (CO 2 ), a major greenhouse gas and accelerating climate change are driving demand for innovative mitigation strategies. The photocatalytic CO 2 reduction reaction (PCO 2 RR) presents a promising and sustainable route to convert CO 2 into useful hydrocarbons and fuels utilizing sunlight, thereby mitigating CO 2 emissions. This review examines the developmental aspects of light‐driven CO 2 conversion using organic polymeric photocatalysts, focusing on carbon nitrides (CNs), covalent triazine frameworks (CTFs), and covalent organic frameworks (COFs). These materials are verified to possess great potential for PCO 2 RR, because they offer tunable band gaps, large surface areas, efficient light absorption, and remarkable activity and selectivity in photocatalysis. In this review, the comprehensive analysis of photocatalytic materials (e.g., CNs, CTFs, and COFs) are thoroughly discussed, along with their mechanisms, historical advancements, and urgent roles in PCO 2 RR. Strategies for enhancing the CO 2 photoreduction efficiency of CNs, CTFs, and COFs are also highlighted. Each organic material brings distinct advantages. The review also addresses critical challenges, such as improving efficiency and managing charge transport dynamics for PCO 2 RR. Finally, the review underscores the need to develop scalable CO 2 conversion applications, advance organic photocatalyst material science, and support sustainable energy conversion technologies.