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Nishijima, M., Ootani, T., Kamimura, Y., Sueki, T., Murai, S., Fujita, K., Tanaka, K., Ohira, K., Koyama, Y. and Tanaka, I. (2014) Accelerated Discovery of Cathode Materials with Prolonged Cycle Life for Lithium-Ion Battery. Nature Communications, 5, 4553.
https://doi.org/10.1038/ncomms5553

has been cited by the following article:

• TITLE: Structure Refinement of Mn-Substituted LiMnxFe1-xPO4

  AUTHORS: Masakazu Togo, Atsushi Nakahira

  KEYWORDS: Lithium Ion Battery, Olivine Material, Local Structure, Mn Substitution

  JOURNAL NAME: Materials Sciences and Applications, Vol.9 No.6, May 31, 2018

  ABSTRACT: For Mn substituted LiMnxFe1-xPO4 synthesized by hydrothermal process, the structural differences caused by Mn substitution were characterized by SEM, ICP, XRD, XAFS, and FT-IR. In this study, by using XAFS advantageous to the atomic selectivity, the local structure of MeO6 octahedral was investigated. From ICP, Mn composition in the products was similar to Mn addition amount, and the peak shifts of XRD patterns with increasing Mn addition were observed. The lattice constants refined by Rietveld analysis were a = 1.0338 ± 5 nm, b = 0.5995 ± 4 nm and c = 0.4696 ± 1 nm in LiFePO4, and it was expanded linearly with increasing Mn addition. Fe-O bond distance, which was calculated by curve fitting of the radius distribution function of LiMnxFe1-xPO4, was 0.208 nm smaller than 0.214 nm of Mn-O bond. In addition, MeO6 octahedral expansion was affected to PO4 vibrational structure from FT-IR spectra.