Published November 1, 2017 | Version v1
Journal article

The mediated synthesis of FeF3 nanocrystals through (NH4)3FeF6 precursors as the cathode material for high power lithium ion batteries

  • 1. Tianjin Key Laboratory of Composite and Functional Materials, Tianjin 300072 (China)
  • 2. Key Laboratory of Advanced Ceramics and Machining Technology, Ministry of Education, Tianjin 300072 (China)
  • 3. School of Materials Science and Engineering, Tianjin University, Tianjin 300072 (China)
  • 4. Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin 300072 (China)

Description

The exploration of cathode materials with high electrochemical performances is critical to improve the energy and power densities of lithium ion batteries (LIBs). Iron fluoride (FeF3) has been proposed as an ideal candidate of LIBs cathode material because of the high discharge plateau and theoretical capacity. In this study, a precursor-mediated method was proposed to synthesize FeF3 nanocrystals (NCs) with different microstructures. These FeF3 NCs were obtained through the thermal decomposition of the precipitated ammonium hexafluoroferrate [(NH4)3FeF6] precursor, and the morphology and crystallinity could be adjusted by varying the ethanol/water volume ratio in the procursor precipitation process. Electrochemical studies demonstrated that FeF3 NC, derived from (NH4)3FeF6 precipitated from the solution with the ethanol/water volume ratio of 20, delivered the initial specific capacity of 217.6 mAh g−1 at 0.2C, associated with excellent rate capability up to 20C (93.8 mAh g−1), and showed the capacity retention of 80.6% after 500 cycles at 20C. These results indicate a tunable and convenient strategy towards nanostructured metals fluorides for high power LIBs.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.electacta.2017.09.081

Additional details

Identifiers

DOI
10.1016/j.electacta.2017.09.081;
PII
S0013-4686(17)31952-7;

Publishing Information

Journal Title
Electrochimica Acta
Journal Volume
253
Journal Issue
Complete
Journal Page Range
p. 545-553
ISSN
0013-4686
CODEN
ELCAAV

Optional Information

Copyright
Copyright (c) 2017 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.