4.6 Article

Concurrent Reaction and Plasticity during Initial Lithiation of Crystalline Silicon in Lithium-Ion Batteries

Journal

JOURNAL OF THE ELECTROCHEMICAL SOCIETY
Volume 159, Issue 3, Pages A238-A243

Publisher

ELECTROCHEMICAL SOC INC
DOI: 10.1149/2.020203jes

Keywords

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Funding

  1. National Science Foundation [CMMI-1031161]
  2. DoD, Air Force Office of Scientific Research, National Defense Science and Engineering Graduate (NDSEG) [32 CFR 168a]
  3. Div Of Civil, Mechanical, & Manufact Inn
  4. Directorate For Engineering [1031161] Funding Source: National Science Foundation

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In an electrochemical cell, crystalline silicon and lithium react at room temperature, forming an amorphous phase of lithiated silicon. The reaction front-the phase boundary between the crystalline silicon and the lithiated silicon-is atomically sharp. Evidence has accumulated recently that the velocity of the reaction front is limited by the rate of the reaction at the front, rather than by the diffusion of lithium through the amorphous phase. This paper presents a model of concurrent reaction and plasticity. We identify the driving force for the movement of the reaction front, and accommodate the reaction-induced volumetric expansion by plastic deformation of the lithiated silicon. The model is illustrated by an analytical solution of the co-evolving reaction and plasticity in a spherical particle. We derive the conditions under which the lithiation-induced stress stalls the reaction. We show that fracture is averted if the particle is small and the yield strength of lithiated silicon is low. Furthermore, we show that the model accounts for recently observed lithiated silicon of anisotropic morphologies. (C) 2011 The Electrochemical Society. [DOI: 10.1149/2.020203jes] All rights reserved.

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