4.8 Article

Identifying the Structure of the Intermediate, Li2/3CoPO4, Formed during Electrochemical Cycling of LiCoPO4

Journal

CHEMISTRY OF MATERIALS
Volume 26, Issue 21, Pages 6193-6205

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/cm502680w

Keywords

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Funding

  1. EPSRC for a Doctoral Training Partnership Award
  2. Department of Energy (DOE)
  3. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-SC0001294]
  4. EU
  5. Marie Curie intra-European fellowship
  6. U.S. Department of Energy [DE-AC02-06CH11357]
  7. U.S. DOE, Office of Basic Energy Sciences [DE-AC02-98CH10886]

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In situ synchrotron diffraction measurements and subsequent Rietveld refinements are used to show that the high energy density cathode material LiCoPO4 (space group Pnma) undergoes two distinct two-phase reactions upon charge and discharge, both occurring via an intermediate Li-2/3(Co2+)(2/3)(Co3+)(1/3)PO4 phase. Two resonances are observed for Li2/3CoPO4 with intensity ratios of 2:1 and 1:1 in the P-31 and 7Li NMR spectra, respectively. An ordering of Co2+/Co3+ oxidation states is proposed within a (a X 3b X c) supercell, and Li+/vacancy ordering is investigated using experimental NMR data in combination with first-principles solid-state DFT calculations. In the lowest energy configuration, both the Co3+ ions and Li vacancies are found to order along the b-axis. Two other low energy Li+/vacancy ordering schemes are found only 5 meV per formula unit higher in energy. All three configurations lie below the LiCoPO4CoPO4 convex hull and they may be readily interconverted by Li+ hops along the b-direction.

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