Electrochemical, Magnetic, and Structural Investigation of the Li x (Mn y Fe1 - y )PO4 Olivine Phases

• Published in: Chemistry of materials Vol. 18; no. 3; pp. 804 - 813
• Main Authors: Yamada, Atsuo, Takei, Yuki, Koizumi, Hiroshi, Sonoyama, Noriyuki, Kanno, Ryoji, Itoh, Keiji, Yonemura, Masao, Kamiyama, Takashi
• Format: Journal Article
• Language: English
• Published: American Chemical Society 07-02-2006
• ISSN: 0897-4756; 1520-5002
• DOI: 10.1021/cm051861f

A series of synthetic heterosite−purpurite, (Mn y Fe1 - y )PO4 (y < 0.8), with negligible disorder and impurities, was obtained by chemical oxidation of the well-crystallized isotypic tryphillite−lithiophilite series, Li(Mn y Fe1 - y )PO4 (ordered olivine structure, space group Pnma). Comparative magnetic and X-ray/neutron powder diffraction investigations of the two solid−solution lines were performed as a function of Mn content to increase understanding of the electrochemical activity loss of Mn3+/Mn2+ in the Li x (Mn y Fe1 - y )PO4 electrode system. Introducing Mn ions into the 4c site did not cause significant change in the local geometry of M2+O6 and PO4 polyhedra, while the M3+O6 octahedra became severely distorted with an increase in the number of Jahn−Teller active Mn3+ ions. The edge-sharing geometry of M3+O6 and PO4 polyhedra fixed the shared O3‘−O3‘ interatomic distance, causing selective strong elongation of the M3+−O3‘ distance with small shrinkage of other M3+−O1, M3+−O2, and M3+−O3 bond lengths. The overall distortion of the MO6 octahedra with M = Mn3+ was much larger than the corresponding change in the unit-cell orthorombicity and significantly increased asymmetry in the M−O−M superexchange interaction. All samples exhibited antiferromagnetism; however, the trivalent series had more than a sevenfold larger decrease in Neel temperature T N (from ca. 130 K at y = 0 to ca. 50 K at y = 0.8) compared to the divalent series (from ca. 52 K at y = 0 to ca. 35 K at y =1) as a function of the Mn content y.