4.8 Article

Identifying surface structural changes in layered Li-excess nickel manganese oxides in high voltage lithium ion batteries: A joint experimental and theoretical study

Journal

ENERGY & ENVIRONMENTAL SCIENCE
Volume 4, Issue 6, Pages 2223-2233

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c1ee01131f

Keywords

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Funding

  1. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-SC 0001294, UCSD 51055]
  2. Florida Energy System Consortium through University of Florida [80859]
  3. Office of Basic Energy Sciences, U.S. Department of Energy

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High voltage cathode materials Li-excess layered oxide compounds Li[Ni(x)Li(1/3-2x/3)Mn(2/3-x/3)]O(2) (0 < x < 1/2)are investigated in a joint study combining both computational and experimental methods. The bulk and surface structures of pristine and cycled samples of Li[Ni(1/5)Li(1/5)Mn(3/5)]O(2) are characterized by synchrotron X-Ray diffraction together with aberration corrected Scanning Transmission Electron Microscopy (a-S/TEM). Electron Energy Loss Spectroscopy (EELS) is carried out to investigate the surface changes of the samples before/after electrochemical cycling. Combining first principles computational investigation with our experimental observations, a detailed lithium de-intercalation mechanism is proposed for this family of Li-excess layered oxides. The most striking characteristics in these high voltage high energy density cathode materials are 1) formation of tetrahedral lithium ions at voltage less than 4.45 V and 2) the transition metal (TM) ions migration leading to phase transformation on the surface of the materials. We show clear evidence of a new spinel-like solid phase formed on the surface of the electrode materials after high-voltage cycling. It is proposed that such surface phase transformation is one of the factors contributing to the first cycle irreversible capacity and the main reason for the intrinsic poor rate capability of these materials.

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