Citation:
Xueqi Yang, Juntao Zhao, Jiawei Ye, Desen Zhou, Tingmin Di, Jun Zhang. Modulating the d-band center of NNU-55(Fe) for enhanced CO2 adsorption and photocatalytic activity[J]. Acta Physico-Chimica Sinica,
;2025, 41(7): 100074.
doi:
10.1016/j.actphy.2025.100074
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Photocatalytic reduction of carbon dioxide (CO2) has emerged as an effective technology to transform CO2 into valuable chemicals. Metal-organic frameworks (MOFs) show great promise due to their adjustable structures, huge specific surface areas, excellent catalytic properties, and remarkable photo responsiveness. Herein, the MOF material NNU-55(Fe) was employed for the photocatalytic transformation of CO2 into carbon monoxide (CO). Through electronic modulation of the active metal center (Fe-N4) via inorganic anionic ligand tuning, the photocatalytic performance of NNU-55(Fe) MOFs can be easily regulated. Notably, NO-3-coordinated NNU-55(Fe) demonstrated superior catalytic performance compared to SO42-- and Cl--coordinated catalysts, achieving a CO production of 124 μmol·g-1 within 3 h. The stronger electron donation capacity of NO-3 leads to an improved electron density of Fe centers, which lowers the Fe d-band center and enhances the bonding orbital occupancy in the adsorption system, thereby increasing the adsorption strength of CO2 and reduction activity. This study highlights a simple strategy for altering the catalytic activity and electrical structure of MOFs by altering the coordinated inorganic ligands of metal sites, offering a novel approach to developing efficient photocatalytic materials.
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Keywords:
- MOFs,
- Coordination structure,
- d-band center,
- CO2 adsorption,
- Photoreduction
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