4.6 Article

Distinct Oxygen Redox Activities in Li2MO3 (M = Mn, Ru, Ir)

Journal

ACS ENERGY LETTERS
Volume 6, Issue 10, Pages 3417-3424

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsenergylett.1c01101

Keywords

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Funding

  1. U.S. DOE [DE-AC02-05CH11231]
  2. Department of Energy, Office of Science, Basic Energy Sciences, and Materials Sciences and Engineering Division [DE-AC02-76SF00515]
  3. Vehicle Technologies Office of the U.S. Department of Energy
  4. ALS

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This study re-evaluated the redox reactions in Li2RuO3 and found both Ru and O redox to be highly reversible, contrasting with other Li2MO3 systems. The critical role of transition metals and their coupling to oxygen in maintaining reversible oxygen redox activities for high-energy batteries was highlighted through this research.
Li2MO3 (M = transition metal) systems are parent compounds of Li-rich materials and widely considered to offer oxygen redox for high-energy batteries. However, recent clarifications have revealed that, among the three representative Li2MO3 (M = Mn, Ru, Ir) compounds, no reversible oxygen redox takes place in the Mn and Ir systems. Here, we reevaluate the redox reactions in Li2RuO3 through advanced spectroscopy, which shows both Ru redox and highly reversible O redox (96% initial-cycle reversibility, 80% retained after 10 cycles, and 77% after 50 cycles). This is in sharp contrast with the Li2MnO3 and Li2IrO3 systems and concludes the three distinct oxygen behaviors in the Li2MO3 systems during charging: (i) only irreversible oxygen oxidation in Li2MO3; (ii) reversible Ru and O redox in Li2RuO3; (iii) only cationic redox in Li2IrO3. This work suggests the critical role of transition metals and their coupling to oxygen for maintaining reversible oxygen redox activities for high-energy batteries.

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