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Updated: Apr 30, 2026

Integrating a Triplet-triplet Annihilation Up-conversion System to Enhance Dye-sensitized Solar Cell Response to Sub-bandgap Light
Published on: September 12, 2014
Recent advances and developments in solar-driven photothermal catalytic CO2 reduction into multicarbon (C2+) products
Xiuting Wu1,2, Senlin Zhang1, Shangbo Ning1
1Research Center for Solar Driven Carbon Neutrality, The College of Physics Science and Technology, Hebei University Baoding 071002 China ningshangbo@hbu.edu.cn jinhua.ye@hbu.edu.cn.
Abstract:
Solar-driven catalytic conversion of carbon dioxide (CO2) into value-added C2+ chemicals and fuels has attracted significant attention over the past decades, propelled by urgent environmental and energy demands. However, the catalytic reduction of CO2 continues to face significant challenges due to inherently slow reduction kinetics. This review traces the historical development and current state of photothermal CO2 reduction, detailing the mechanisms by which CO2 is transformed into C2+ products. A key focus is on catalyst design, emphasizing surface defect engineering, bifunctional active site and co-catalyst coupling to enhance the efficiency and selectivity of solar-driven C2+ synthesis. Key reaction pathways to both C1 and C2+ products are discussed, ranging from CO, CH4 and methanol (CH3OH) synthesis to the production of C2-4 products such as C2-4 hydrocarbons, ethanol, acetic acid, and various carbonates. Notably, the advanced synthesis of C5+ hydrocarbons exemplifies the remarkable potential of photothermal technologies to effectively upgrade CO2-derived products, thereby delivering sustainable liquid fuels. This review provides a comprehensive overview of fundamental mechanisms, recent breakthroughs, and pathway optimizations, culminating in valuable insights for future research and industrial-scale prospect of photothermal CO2 reduction.
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