Amino-functionalized MIL-125(Ti) for photodenitrification of pyridine in fuels via coordination activation by unsaturated Ti 4+ centers.
Shihui WangZhoujun HeLing WuDeling WangRuiru SiXiyao LiuRuo-Wen LiangPublished in: Dalton transactions (Cambridge, England : 2003) (2023)
Due to their explicit structure, metal-organic frameworks (MOFs) have been supposed to be credible platforms to research the micro-mechanism of heterogeneous photocatalysis. In this study, amino-functionalized MOFs (MIL-125(Ti)-NH 2 (denoted as MTi), UiO-66(Zr)-NH 2 (denoted as UZr) and MIL-68(In)-NH 2 (denoted as MIn)) with three different metal centers were synthesized and applied for the denitrification of simulated fuels under visible light irradiation, during which pyridine was used as a typical nitrogen-containing compound. The results showed that MTi had the best activity among the above three MOFs, and the denitrogenation rate increased to 80% after 4 h of visible light irradiation. On the grounds of the theoretical calculation of pyridine adsorption and actual activity experiments, it can be presumed that the unsaturated Ti 4+ metal centers should be the key active sites. Meanwhile, the XPS and in situ infrared results verified that the coordinatively unsaturated Ti 4+ sites facilitate the activation of pyridine molecules through the surface -N⋯Ti- coordination species. The coordination-photocatalysis synergism promotes the efficiency of photocatalytic performance and the corresponding mechanism is proposed.