In situ assembly of ultrafine Mn3O4 nanoparticles into MIL-101 for selective aerobic oxidation

被引:23
作者
Fu, Yu
Guo, Yanglong
Guo, Yun
Wang, Yunsong
Wang, Li
Zhan, Wangcheng [1 ]
Lu, Guanzhong [1 ]
机构
[1] East China Univ Sci & Technol, Sch Chem & Mol Engn, Key Lab Adv Mat, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
METAL-ORGANIC FRAMEWORK; SUPPORTED GOLD NANOPARTICLES; MANGANESE OXIDES; OXYGEN REDUCTION; MOLECULAR-OXYGEN; BENZYL ALCOHOL; RAMAN-SPECTRA; CATALYST; NANOCATALYSTS; ENCAPSULATION;
D O I
10.1039/c7cy00912g
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
Nanosize metal oxides generally possess high catalytic activity, but they tend to agglomerate into larger particles during a reaction. Therefore, the preparation of nanosize metal oxides with high stability is a crucial challenge. A novel and facile approach involving impregnation followed by a double solvent method was developed to directly encapsulate ultrafine Mn3O4 nanoparticles (NPs) into the nanocages of metal-organic frameworks (MOFs). A series of MIL-101 encapsulated Mn3O4 NPs were prepared, in which the contents of Mn3O4 ranged from 3.2% to 33%. Ultrafine Mn3O4 NPs with a particle size of about 3 nm have been successfully embedded in the nanocages of MIL-101 with a uniform distribution. The MIL-101 encapsulated Mn3O4 NPs with a Mn3O4 content of 15% exhibits the highest conversion of benzyl alcohol (38.7%) and a >99% selectivity to benzaldehyde. Furthermore, after being repeatedly used 10 times, its catalytic activity is hardly changed. When the content of Mn3O4 NPs was further increased, the catalytic activity of the catalyst decreases, due to aggregated Mn3O4 particles with a large size which formed outside the MIL-101 matrix.
引用
收藏
页码:4136 / 4144
页数:9
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