Systematic variation of the optical bandgap in titanium based isoreticular metal-organic frameworks for photocatalytic reduction of CO2 under blue lightElectronic supplementary information (ESI) available. CCDC 1527303-1527308. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7ta00437k

• Main Authors: Logan, Matthew W, Ayad, Suliman, Adamson, Jeremy D, Dilbeck, Tristan, Hanson, Kenneth, Uribe-Romo, Fernando J
• Format: Journal Article
• Language: English
• Published: 13.06.2017
• ISSN: 2050-7488; 2050-7496
• DOI: 10.1039/c7ta00437k

A series of metal-organic frameworks isoreticular to MIL-125-NH 2 were prepared, where the 2-amino-terephthalate organic links feature N -alkyl groups of increasing chain length (from methyl to heptyl) and varying connectivity (primary and secondary). The prepared materials display reduced optical bandgaps correlated with the inductive donor ability of the alkyl substituent as well as high photocatalytic activity towards the reduction of carbon dioxide under blue illumination operating over 120 h. Secondary N -alkyl substitution (isopropyl, cyclopentyl and cyclohexyl) exhibits larger apparent quantum yields than the primary N -alkyl analogs directly related to their longer lived excited-state lifetime. In particular, MIL-125-NHCyp (Cyp = cyclopentyl) exhibits a small bandgap ( E g = 2.30 eV), a long-lived excited-state ( τ = 68.8 ns) and a larger apparent quantum yield ( Φ app = 1.80%) compared to the parent MIL-125-NH 2 ( E g = 2.56 eV, Φ app = 0.31%, τ = 12.8 ns), making it a promising candidate for the next generation of photocatalysts for solar fuel production based on earth-abundant elements. N -alkyl substitution-from methyl to heptyl-in isoreticular MIL-125-NH 2 MOFs induces a stepwise decrease in the optical bandgap, while increasing CO 2 photoreduction efficiencies.