Phase diagram of Mg insertion into chevrel phases, MgxMo6T8 (T = S, Se).: 2.: The crystal structure of triclinic MgMo6Se8

被引:66
作者
Levi, E. [1 ]
Lancry, E.
Mitelman, A.
Aurbach, D.
Isnard, O.
Djurado, D.
机构
[1] Bar Ilan Univ, Dept Chem, IL-52900 Ramat Gan, Israel
[2] Univ Grenoble 1, CNRS, Lab Cristallog, F-38042 Grenoble 9, France
[3] Inst Max Von Laue Paul Langevin, F-38042 Grenoble 9, France
[4] Univ Grenoble 1, CEA Grenoble, DRFMC, SPrAM,CNRS,UMR5819,Lab Elect Mol Organ & Hybride, F-38054 Grenoble 9, France
关键词
D O I
10.1021/cm060715m
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Chevrel phases (CPs), MxMo6T8 (M = metal, T = S, Se), may be used as unique cathode materials for rechargeable Mg batteries because they ensure the high mobility of multivalent cations. However, the electrochemical behavior is strongly affected by the host composition. For the selenide, the intercalation process is completely reversible, while partial Mg trapping occurs upon its extraction from the sulfide at room temperature. A combination of powder X-ray and high-resolution neutron diffraction was used to study the crystal structure of triclinic MgMo6Se8, especially for determining the precise location of the Mg2+ cations within the host lattice. It was shown that the crystal structure of the selenide is similar to that of triclinic Fe2Mo6S8: The Mg2+ cations are distributed between two sites ( per formula unit) with a square-pyramidal anion coordination. The environment analysis of all the cation sites based on the bond valence sum theory led us to propose the most favorable routes for Mg2+ ion transport, as well as to explain the peculiarities of the electrochemical behavior of the CPs as intercalation materials for Mg batteries.
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页码:3705 / 3714
页数:10
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