Enhanced CO oxidation on CeO2/Co3O4 nanojunctions derived from annealing of metal organic frameworks

被引:55
作者
Wang, Changlai [1 ,2 ]
Wang, Dongdong [1 ,2 ]
Yang, Yang [1 ,2 ]
Li, Ren [1 ,2 ]
Chen, Changle [3 ]
Chen, Qianwang [1 ,2 ,4 ]
机构
[1] Univ Sci & Technol China, Dept Mat Sci & Engn, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Peoples R China
[2] Univ Sci & Technol China, Collaborat Innovat Ctr Suzhou Nano Sci & Technol, Hefei 230026, Peoples R China
[3] Univ Sci & Technol China, Dept Polymer Sci & Engn, Hefei 230031, Peoples R China
[4] Chinese Acad Sci, Hefei Inst Phys Sci, High Magnet Field Lab, Hefei 230031, Peoples R China
关键词
HIGH-PERFORMANCE ANODES; LITHIUM-ION BATTERIES; CATALYTIC-OXIDATION; LOW-TEMPERATURE; CARBON; NANOPARTICLES; CO3O4; SURFACE; DFT; NANOCRYSTALS;
D O I
10.1039/c6nr07725k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The interface of nanojunctions plays an important role in the performance of heterogeneous catalysts. However, it is highly challenging to construct nanojunctions which are usually prepared by complex multi-step processes. Metal-organic frameworks (MOFs), with designable metal centers and tunable organic ligands, are promising precursors for the one-step synthesis of nanojunctions. Herein, we prepared porous CeO2/Co3O4 nanojunctions by direct annealing of MOFs in air. These unique nanojunctions exhibit remarkable catalytic activity for CO oxidation, which can achieve complete oxidization of CO to CO2 at 110 degrees C. In contrast, the temperature required for 100% CO oxidation is 190 degrees C for pure Co3O4. Moreover, the nanojunctions can maintain complete CO conversion after 16 h at 110 degrees C. Density functional theory calculations revealed that the enhancement in the catalytic activity of CeO2/Co3O4 nanojunctions can be attributed to the charge transfer through the interfaces of the nanojunctions.
引用
收藏
页码:19761 / 19768
页数:8
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