Facile solvothermal synthesis of mesoporous manganese ferrite (MnFe 2 O 4 ) microspheres as anode materials for lithium-ion batteries
Journal of Colloid and Interface Science, ISSN: 0021-9797, Vol: 398, Page: 185-192
2013
- 155Citations
- 101Captures
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Metrics Details
- Citations155
- Citation Indexes155
- 155
- CrossRef122
- Captures101
- Readers101
- 101
Article Description
We report the synthesis and characterization of the mesoporous manganese ferrite (MnFe 2 O 4 ) microspheres as anode materials for Li-ion batteries. MnFe 2 O 4 microspheres were synthesized by a facile solvothermal method using Mn(CH 3 COO) 2 and FeCl 3 as metal precursors in the presence of CH 3 COOK, CH 3 COOC 2 H 5, and HOCH 2 CH 2 OH. The samples were characterized by X-ray diffraction, transmission electron microscopy, scanning electron microscopy, nitrogen adsorption, thermal gravimetric, X-ray photoelectron spectroscopy, temperature programmed reduction, and temperature programmed oxidation. The synthesized mesoporous MnFe 2 O 4 microspheres composed of nanoparticles (10–30 nm) were 100–500 nm in diameter and had surface areas between 60.2 and 86.8 m 2 g −1, depending on the CH 3 COOK amounts added in the preparation. After calcined at 600 °C, MnFe 2 O 4 was decomposed to Mn 2 O 3 and Fe 2 O 3 mixture. The mesoporous MnFe 2 O 4 microspheres calcined at 400 °C showed a capacity of 712.2 mA h g −1 at 0.2 C and 552.2 mA h g −1 at 0.8 C after 50 cycles, and an average capacity fading rate of around 0.28%/cycle and 0.48%/cycle, much better than those of the samples without calcination and calcined at 600 °C. The work would be helpful in the fabrication of binary metal oxide anode materials for Li-ion batteries.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0021979713001318; http://dx.doi.org/10.1016/j.jcis.2013.01.067; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84876486883&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/23489612; https://linkinghub.elsevier.com/retrieve/pii/S0021979713001318; https://dx.doi.org/10.1016/j.jcis.2013.01.067
Elsevier BV
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