4.8 Article

Revisiting the Corrosion of the Aluminum Current Collector in Lithium-Ion Batteries

Journal

JOURNAL OF PHYSICAL CHEMISTRY LETTERS
Volume 8, Issue 5, Pages 1072-1077

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.6b02933

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Funding

  1. U.S. Department of Energy, Vehicle Technologies Office
  2. U.S. DOE's Office of Vehicle Technologies Program
  3. U.S. Department of Energy by UChicago Argonne, LLC [DEAC02-06CH11357]
  4. Department of Energy's Office of Biological and Environmental Research and located at Pacific Northwest National Laboratory

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The corrosion of aluminum current collectors and the oxidation of solvents at a relatively high potential have been widely investigated with an aim to stabilize the electrochemical performance of lithium-ion batteries using such components. The corrosion behavior of aluminum current collectors was revisited using a home-build high-precision electrochemical measurement system, and the impact of electrolyte components and the surface protection layer on aluminum foil was systematically studied. The electrochemical results showed that the corrosion of aluminum foil was triggered by the electrochem ical oxidation of solvent molecules, like ethylene carbonate, at a relative high potential. The organic radical cations generated from the electrochemical oxidation are energetically unstable and readily undergo a deprotonation reaction that generates protons and promotes the dissolution of AP(3+) from the aluminum foil. This new reaction mechanism can also shed light on the dissolution of transitional metal at high potentials.

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