Chinese Journal of Catalysis

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Efficient and selective photocatalytic CO2 conversion enabled by FePc nanosheets in a dye-sensitized system

Hua Gaoa, Yong Zhua, Zhibing Wena, Ran Zhaoa, Zhi Chena, Siyao Wanga, Shuanglin Hea, Kuang Penga, Yiwen Tanga, Licheng Suna,b, Fei Lia,*   

  1. aState Key Laboratory of Fine Chemicals, Frontier Science Center for Smart Material, Dalian University of Technology, Dalian 116024, Liaoning, China;
    bCenter of Artificial Photosynthesis for Solar Fuels, School of Science, Westlake University, Hangzhou 310024, Zhejiang, China
  • Received:2025-11-06 Accepted:2025-12-25
  • Supported by:
    National Natural Science Foundation of China (22172018, 22572015, 22302028), the National Key R&D Program of China (2022YFA0911904), the Fundamental Research Funds for the Central Universities (DUT23LAB611, DUT24BS047), and the Liaoning Provincial Natural Science Foundation Joint Fund (Doctoral Research Start-up Project) (2023-BSBA-067).

Abstract: Solar-driven photocatalytic CO2 conversion offers a sustainable solution for greenhouse gas mitigation and renewable energy storage. While metal phthalocyanines (MPc) exhibit excellent CO2 reduction capabilities, their practical application in dispersed photocatalytic systems faces limitations of the stacking of MPc molecules that reduces active site accessibility, and inefficient electron transfer limited by diffusive mass transport. To address these challenges, we developed a bioinspired dye-sensitized RuP-TiO2-FePc nanosheets (NSs) hybrid system, where ultrathin FePc NSs obtained by liquid-phase ultrasonic exfoliation enhance active site exposure and mass transfer, while TiO2 serves as a mediator to facilitate electron transfer between the photosensitizer and FePc NSs. Time-resolved spectroscopic studies demonstrate that TiO2 plays a dual role: it spatially organizes functional components to enable surface electron transfer by shortening intermolecular distances, while also functioning as a semiconductor bridge to facilitate charge transport. This synergistic design achieves a remarkable CO production rate of 27.3 mmol g‒1 h‒1 (> 98% selectivity) and exceptional stability (TONCO = 1363 over 100 h), outperforming many noble-metal-based systems. Our work demonstrates a robust strategy for optimizing bulk catalysts through 2D exfoliation and controlled heterogenization, offering a versatile platform for efficient and durable artificial photosynthesis.

Key words: CO2 reduction, FePc nanosheets, Dye-sensitized photocatalysis, Electron transfer, Artificial photosynthesis