Synthesis-to-Catalysis Full-Process Cu Assistance in Cu/Fe <sub>5</sub> C <sub>2</sub> @C Catalysts for Photothermocatalytic Fischer–Tropsch Synthesis to Light Olefins
Fischer–Tropsch synthesis (FTS) offers a route for converting syngas from nonpetroleum resources into valuable chemicals, such as light olefins. χ-iron carbide (χ-Fe5C2), the key active phase for olefin production, is plagued by poor stability under practical conditions. Here, we propose a synthesis-to-catalysis full-process Cu-assisted strategy that integrates synthesis, photothermal conversion and reaction regulation into a design framework, thereby enabling a Cu/Fe5C2@C catalyst with improved durability and catalytic performance. The optimized 0.20Cu/Fe5C2@C catalyst achieves 48.7% light olefins selectivity, a 3.1-fold increase in light olefin yield compared to Fe5C2@C, and markedly improved long-term stability under photothermocatalytic FTS. Mechanistic studies reveal that the full-process synergy of Cu enhances catalytic performance by promoting the formation of a highly graphitized carbon shell to stabilize χ-Fe5C2 during synthesis, enhancing photothermal conversion efficiency via localized surface plasmon resonance, and optimizing reactant activation and the CH2* intermediate transformation toward light olefins. This work establishes a full-process regulation paradigm that integrates multistage functions, offering a transformative approach toward high-performance, durable solar-driven FTS for nonpetroleum resource utilization.
Authors
- Shuxin Ouyang (ORCID: https://orcid.org/0000-0002-7650-1245)
- Ruizhe Li
- Jingwen Cheng (ORCID: https://orcid.org/0000-0001-5587-8951)
- Yuan Li (ORCID: https://orcid.org/0000-0002-9785-3856)
- Yunxiang Li (ORCID: https://orcid.org/0000-0001-5440-3014)
- Hong Yuan (ORCID: https://orcid.org/0000-0001-9685-2440)
- P.L. Rui
Institutions
- Central China Normal University (CN)
- Ministry of Education (IR)
- Wuhan Institute of Technology (CN)
Publication Details
- Journal
- ACS Catalysis
- Published
- 2025-12-19
- DOI
- https://doi.org/10.1021/acscatal.5c05986
- Primary Topic
- Catalysts for Methane Reforming
- Type
- article
- Field-Weighted Citation Impact
- 0.00