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Lithium-Oxygen Electrochemistry in Non-Aqueous Solutions

Journal

ISRAEL JOURNAL OF CHEMISTRY
Volume 55, Issue 5, Pages 508-520

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ijch.201400135

Keywords

electrochemistry; lithiumoxygen batteries; oxygen reduction; radicals; redox chemistry

Funding

  1. ISF, Israel Science Foundation
  2. Ministry of Science and Technology, Israel
  3. Israel Science Foundation [1469/13]
  4. Ethel and David Resnick Chair in Active Oxygen Chemistry

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Pairing lithium and oxygen in aprotic solvents can theoretically lead to one of the most promising electrochemical cells available. If successful, this system could compete with technologies such as the internal combustion engine and provide an energy density that can accommodate electric vehicle demands. However, there are many problems that have inhibited this technology from becoming realistic. One of the main reasons is capacity fading after only a few cycles, which is caused by the instability of electrolyte solutions in the presence of reduced oxygen species like O-2(.-) and O-2(2-). In recent years, using various analytical tools, researchers have been able to isolate the breakdown products arising from the reactions occurring between the aprotic solvent and the reduced oxygen species. Nevertheless, no solvents have yet been found that are fully stable throughout the reduction and oxidation processes. However, an understanding of these decomposition mechanisms can help us in designing new systems that are more stable toward the aggressive conditions taking place in LiO2 cell operation. This review will include analytical studies on the most widely used solvents in current LiO2 research.

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