Active site modulation in UiO-66(Ce) MOFs by Al3+doping for boosting photocatalysis

被引:0
作者
Liu, Cheng [1 ]
Chen, Huiling [1 ]
Chen, Qi [1 ]
Bi, Jinhong [2 ]
Yu, Jimmy C. [3 ]
Wu, Ling [1 ]
机构
[1] Fuzhou Univ, Coll Chem, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350116, Peoples R China
[2] Fuzhou Univ, Dept Environm Sci & Engn, Minhou 350108, Fujian, Peoples R China
[3] Chinese Univ Hong Kong, Dept Chem, Shatin, Hong Kong, Peoples R China
基金
中国国家自然科学基金;
关键词
Photocatalysis; UiO-66(Ce); Metal doping; Active sites; METAL-ORGANIC FRAMEWORKS; VISIBLE-LIGHT; SELECTIVE OXIDATION; NANOPARTICLES; ACTIVATION; EXCITATION; REDUCTION; EFFICIENT; ALCOHOL;
D O I
10.1016/j.jcat.2024.115670
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A series of Al3+-doped UiO-66(Ce) MOFs (U(CexAl1_ x)) was developed to reveal the roles of metal doping on active site formation and substrate activation in photocatalytic selective transformation of amines to imines. Al3+ doping induced crystal structure distortion to form coordinately unsaturated metal (Al, Ce) sites as Lewis acid sites to chemisorb and activate benzylamine (BA). In situ FTIR revealed that the Al site with stronger acid strength facilitated BA activation. The activation degree of N-H bonds in BA was evaluated by changes of calculated force constant. The intermediate products were confirmed through time-dependent in situ FTIR. The Al3+-doped sample U(Ce0.90Al0.10), the optimal catalyst, showed a significantly increased BA conversion (97.6 %) than that (47.5 %) of undoped sample, which was attributed to enough active sites and the optimal charge mobility. Finally, the present study proposes a synergistic photocatalytic mechanism associated with molecular activation to demonstrate selective oxidation pathways at the molecular level.
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页数:11
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