Published February 1, 2015 | Version v1
Journal article

Synthesis of porous LiFe0.2Mn1.8O4 with high performance for lithium-ion battery

  • 1. State Key Laboratory of Metal Matrix Composites, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240 (China)
  • 2. The Faculty of Engineering, University of Wollongong, NSW 2522 (Australia)

Description

Highlights: • Porous LiFe0.2Mn1.8O4 was fabricated with P123 as a template through a nitrate decomposition method • A high rate capacity and cycling stability were demonstrated when used as cathode in LIBs • This strategy is expected to fabricate other multiple metal oxides with porous structures - Abstract: A facile and effective route was developed for the fabrication of LiFe0.2Mn1.8O4 with porous structures by using Pluronic P-123 as a soft template, based on a nitrate decomposition method. The resultant LiFe0.2Mn1.8O4 was characterized by XRD, SEM, as well as N2 adsorption/desorption measurements which showed a porous structure with a pore size centered at 20 nm. When used as cathode materials in lithium battery, the as-synthesized LiFe0.2Mn1.8O4 exhibited a discharge capacity of 122 mAh g−1 at 1 C and 102 mAh g−1 at 5 C. Moreover, after 500 cycles, the capacity retention (108 mAh g−1) reached 88% of the initial capacity at 1 C. As compared with conventional cathode LiMn2O4, the high performance is believed to originate from the combined effects of porous structure, iron doping and highly crystalline nature of the obtained LiFe0.2Mn1.8O4. This strategy is expected to allow the fabrication of other multiple metal oxides with porous structures for high performance cathode materials

Availability note (English)

Available from http://dx.doi.org/10.1016/j.electacta.2014.12.047

Additional details

Identifiers

DOI
10.1016/j.electacta.2014.12.047;
PII
S0013-4686(14)02482-7;

Publishing Information

Journal Title
Electrochimica Acta
Journal Volume
154
Journal Page Range
p. 17-23
ISSN
0013-4686
CODEN
ELCAAV

Optional Information

Copyright
Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.