期刊
CHEMISTRY OF MATERIALS
卷 22, 期 3, 页码 1059-1070出版社
AMER CHEMICAL SOC
DOI: 10.1021/cm902023h
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资金
- NSERC
We report new solid state and hydrothermal synthetic routes to (Li,Na)(2)FePO4F that incorporate carbon-containing additives and result in good electrochemical properties of this Li (or Na) ion electrode material. Single crystal X-ray diffraction analysis of Na2FePO4F prepared by flux growth confirms the unusual structural features of this compound that include pairs of face-sharing metal octahedra and [6 + 1] coordination of the sodium ions. Facile Na-Li ion-exchange occurs upon reflux With lithium salts, upon electrochemical cycling in a cell (vs. Li), and also in a cell simply equilibrated at OCV. The material does not exhibit typical two-phase behavior on electrochemical cycling. A combination of a redox process which occurs With little structural strain, and ion scrambling give rise to a solid solution-like sloping voltage profile on charge-discharge, although localization of the Fe2+/3+ in the mixed valence single phase intermediate, Na1.5FePO4F drives a very small structural distortion. Temperature-dependent Mossbauer spectroscopy measurements confirm this localization, at least on short time scales (10(-8) s), which persists to 370 degrees C. Finally, polycrystalline powders of other members of this family of compounds (Na2CoPO4F, Na2NiPO4F) were synthesized for the first time. Na2CoPO4F has a Co2+/Co3+ potential near 4.8 V. Mixed-metal phosphates of the form Na-2(Fe1-xMx)PO4F, where M = Co, Mg, were also synthesized and found to be promising positive electrode materials for Li-ion or Na-ion energy storage devices.
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