Nano-particle assembled porous core-shell ZnMn2O4 microspheres with superb performance for lithium batteries

被引:16
|
作者
Zhang, Tong [1 ]
Yue, Huijuan [2 ]
Qiu, Hailong [1 ]
Wei, Yingjin [1 ]
Wang, Chunzhong [1 ]
Chen, Gang [1 ]
Zhang, Dong [1 ]
机构
[1] Jilin Univ, Key Lab Phys & Technol Adv Batteries, Changchun 130012, Peoples R China
[2] Jilin Univ, State Key Lab Inorgan Synth & Preparat Chem, Changchun 130012, Peoples R China
基金
中国国家自然科学基金;
关键词
nano-particles; microspheres; mechanism; redox; Li-ion battery; ANODE MATERIAL; ELECTROCHEMICAL PERFORMANCE; FACILE SYNTHESIS; CONTROLLABLE SYNTHESIS; TEMPERATURE SYNTHESIS; STORAGE PROPERTIES; FABRICATION; NANOPARTICLES; MN3O4; COMPOSITES;
D O I
10.1088/1361-6528/aa5a49
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Porous ZnMn2O4 microspheres were prepared via a facile co-precipitation method followed by calcination at various temperatures and evaluated as anode materials for lithium ion batteries. The sample prepared at 600 degrees C outperformed the other samples in terms of electrochemical performance with high reversible capacity, high-rate capability, and excellent cycling performance. The capacity of the sample remained as high as 999 mAh g(-1) at a current rate of 100 mA g(-1) after 50 cycles- one of the best ever reported for ZnMn2O4-based materials. A high reversible capacity of 400 mAh g(-1) was retainable at a current density of 2000 mA g(-1) after 2500 cycles. A novel electrochemical reaction mechanism of ZnMn2O4 anodes was established and investigated at length. The Mn3O4 observed during the charge process was largely responsible for the enhanced performance, as confirmed by x- ray photoelectron spectroscopy, scanning electron microscopy, and transmission electron microscopy. The relatively large surface area, abundant porosity, large ion exchange space, and strong mechanical stability of the porous connected 3D framework were responsible for the unique oxidation/ reduction Mn2+-> Mn3+ process we observed.
引用
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页数:11
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