Controllable Preparation of N-modified Cu-MOFs for Enhanced Steering CO2 Electroreduction Toward CH4 Products
The catalyst materials 0N-Cu-MOF, 1N-Cu-MOF, and 2N-Cu-MOF were successfully synthesized usinga solvothermal method, and using different concentrations of nitrogen-modified Cu organic frameworks (xN-Cu-MOF).Characterizations using X-ray diffraction (XRD), scanning electron microscopy (SEM), fourier transform infrared (FT-IR) spectroscopy, X-ray photoelectron spectroscopy (XPS), and Brunauer-Emmett-Teller (BET) surface area analysis showed that 1N-Cu-MOF had the largest SSA and pore size among the three materials synthesized.1N-Cu-MOF exhibited the largest pore size and specific surface area among the three materials, which had a decisive effect on CO 2 reduction.In addition, stability and CO 2 reduction reaction (CO 2 RR) activity were evaluated by linear sweep voltmeter, cyclic voltmeter, electrochemical impedance spectroscopy, and time flow tests.Faradaic efficiency (FE) was determined by product analysis.Among the three catalyst materials, 1N-Cu-MOF showed the best catalytic performance at 50 mAcm -2 (maximum current density).The charge transfer resistance was 8.23 , the average current density was 19.9 mAcm -2 , and the FE of methane (CH 4 ) production showed a high efficiency of 70.45 % when tested for 12 h at an overpotential of -0.35 V (to-RHE).
Authors
- Yilei Sun
- Kunjie Li (ORCID: https://orcid.org/0000-0002-1742-6433)
- Won-Chun Oh (ORCID: https://orcid.org/0009-0007-7654-5997)
- Haixia Wang (ORCID: https://orcid.org/0000-0002-5782-8242)
- Ze-Da Meng
- Yao Liu (ORCID: https://orcid.org/0009-0000-1843-0517)
Institutions
- Aluminum Corporation of China (China) (CN)
- Hanseo University (KR)
- Suzhou University of Science and Technology (CN)
- Soochow University (CN)
Publication Details
- Journal
- Korean Journal of Materials Research
- Published
- 2025-08-27
- DOI
- https://doi.org/10.3740/mrsk.2025.35.8.352
- Primary Topic
- CO2 Reduction Techniques and Catalysts
- Type
- article
- Field-Weighted Citation Impact
- 0.00