4.8 Article

Kinetic Phase Evolution of Spinel Cobalt Oxide during Lithiation

Journal

ACS NANO
Volume 10, Issue 10, Pages 9577-9585

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.6b04958

Keywords

Co3O4 nanoparticles; lithium-ion battery; in situ TEM

Funding

  1. Center for Functional Nanomaterials, Brookhaven National Laboratory,
  2. U.S. Department Of Energy (DOE), Office of Basic Energy Science [DE- SC0012704]
  3. DOE/BES, Division of Materials Science and Engineering [DE-SC0012704]
  4. U.S. Department of Energy, Office of Science, Basic Energy Sciences [DE-SC0012673]
  5. Minta Martin award at University of Maryland
  6. National Science Foundation [TG-DMR130142]

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Spinel cobalt oxide has been proposed to undergo a multiple-step reaction during the electrochemical lithiation process. Understanding the kinetics of the lithiation process in this compound is crucial to optimize its performance and cyclability. In this work, we have utilized a low-angle annular dark-field scanning transmission electron microscopy method to visualize the dynamic reaction process in real time and study the reaction kinetics at different rates. We show that the particles undergo a two-step reaction at the single-particle level, which includes an initial intercalation reaction followed by a conversion reaction. At low rates, the conversion reaction starts after the intercalation reaction has fully finished, consistent with the prediction of density functional theoretical calculations. At high rates, the intercalation reaction is overwhelmed by the subsequently nucleated conversion reaction, and the reaction speeds of both the intercalation and conversion reactions are increased. Phase-field simulations show the crucial role of surface diffusion rates of lithium ions in controlling this process. This work provides microscopic insights into the reaction dynamics in non-equilibrium conditions and highlights the effect of lithium diffusion rates on the overall reaction homogeneity as well as the performance.

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