Mimicking π Backdonation in Ce-MOFs for Solar-Driven Ammonia Synthesis

被引:89
作者
Zhang, Congmin [1 ]
Xu, Yanling [1 ]
Lv, Chade [1 ]
Zhou, Xin [1 ]
Wang, Yu [1 ]
Xing, Weinan [2 ]
Meng, Qingqiang [1 ]
Kong, Yi [1 ]
Chen, Gang [1 ]
机构
[1] Harbin Inst Technol, Sch Chem & Chem Engn, Dept Mat Chem, Harbin 150001, Heilongjiang, Peoples R China
[2] Nanjing Forestry Univ, Coll Biol & Environm, Nanjing 210037, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
nitrogen fixation; mimicking; pi backdonation; cerium; MOFs; METAL-ORGANIC FRAMEWORKS; NITROGEN-FIXATION; OXYGEN VACANCIES; REDUCTION; CONVERSION; CERIA;
D O I
10.1021/acsami.9b08682
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
pi Backdonation is the core process to break through the kinetically complex and energetic hurdle for catalyzing effectively the NH3 synthesis but only occurs on certain transition metals with empty and filled d orbitals. Herein, mimicking pi backdonation enables MOF-76(Ce) materials to convert N-2/NH3 effectively. Note that, by virtue of the intrinsic mechanism of ligand-to-metal charge transfer, metal cerium species in MOF-76(Ce) serve as an electron sink for accumulating the photogenerated electrons. Taken together, experimental and theoretical analyses reveal that such metal cerium species with coordination unsaturated state (Ce-CUS) on a MOF-76(Ce) nanorod surface can also provide unoccupied and occupied 4f orbitals to accept from and then donate electrons back to nitrogen molecules. Remarkably, it shows outstanding photocatalytic nitrogen reduction performance with high average NH3 yield (34 mu mol g(-1) h(-1)) under ambient conditions. This work provides fresh insights into rational designing and engineering highly active catalysts with rare earth elements.
引用
收藏
页码:29917 / 29923
页数:7
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