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Passive Mitigation of Cascading Propagation in Multi-Cell Lithium Ion Batteries

Journal of the Electrochemical Society

Torres-Castro, Loraine T.; Kurzawski, Andrew K.; Hewson, John C.; Lamb, Joshua H.

The heat generated during a single cell failure within a high energy battery system can force adjacent cells into thermal runaway, creating a cascading propagation effect through the entire system. This work examines the response of modules of stacked pouch cells after thermal runaway is induced in a single cell. The prevention of cascading propagation is explored on cells with reduced states of charge and stacks with metal plates between cells. Reduced states of charge and metal plates both reduce the energy stored relative to the heat capacity, and the results show how cascading propagation may be slowed and mitigated as this varies. These propagation limits are correlated with the stored energy density. Results show significant delays between thermal runaway in adjacent cells, which are analyzed to determine intercell contact resistances and to assess how much heat energy is transmitted to cells before they undergo thermal runaway. A propagating failure of even a small pack may stretch over several minutes including delays as each cell is heated to the point of thermal runaway. This delay is described with two new parameters in the form of gap-crossing and cell-crossing time to grade the propensity of propagation from cell to cell.

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Review - Materials Science Predictions of Thermal Runaway in Layered Metal-Oxide Cathodes: A Review of Thermodynamics

Journal of the Electrochemical Society

Shurtz, Randy S.; Hewson, John C.

Accurate models of thermal runaway in lithium-ion batteries require quantitative knowledge of heat release during thermochemical processes. A capability to predict at least some aspects of heat release for a wide variety of candidate materials a priori is desirable. This work establishes a framework for predicting staged heat release from basic thermodynamic properties for layered metal-oxide cathodes. Available enthalpies relevant to thermal decomposition of layered metal-oxide cathodes are reviewed and assembled in this work to predict potential heat release in the presence of alkyl-carbonate electrolytes with varying state of charge. Cathode delithiation leads to a less stable metal oxide subject to phase transformations including oxygen release when heated. We recommend reaction enthalpies and show the thermal consequences of metal-oxide phase changes and solvent oxidation within the battery are of comparable magnitudes. Heats of reaction are related in this work to typical observations reported in the literature for species characterization and calorimetry. The methods and assembled databases of formation and reaction enthalpies in this work lay groundwork a new generation of thermal runaway models based on fundamental material thermodynamics, capable of predicting accurate maximum cell temperatures and hence cascading cell-to-cell propagation rates.

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Results 26–50 of 209
Results 26–50 of 209