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Coulombically-stabilized oxygen hole polarons enable fully reversible oxygen redox



Iwnetim I. Abate, Chaitanya D. Pemmaraju, Se-Young Kim, Sami Sainio, Brian Moritz, John Vinson, Michael F. Toney, Wanli Yang, William E. Gent, Thomas P. Devereaux, Linda F. Nazar, William C. Chueh


Stabilizing high-valent redox couples and exotic electronic states necessitates an understanding of the stabilization mechanism. In oxides, whether they are being considered for energy storage or computing, highly oxidized oxide-anion species rehybridize to form short covalent bonds and are related to significant local structural distortions. In intercalation oxide electrodes for batteries, while such reorganization partially stabilizes oxygen redox, it also gives rise to substantial hysteresis. In this work, we investigate oxygen redox in layered Na2−xMn3O7, a positive electrode material with ordered Mn vacancies. We prove that coulombic interactions between oxidized oxide-anions and the interlayer Na vacancies can disfavor rehybridization and stabilize hole polarons on oxygen (O−) at 4.2 V vs. Na/Na+. These coulombic interactions provide thermodynamic energy saving as large as O–O covalent bonding and enable ∼40 mV voltage hysteresis over multiple electrochemical cycles with negligible voltage fade. Our results establish a complete picture of redox energetics by highlighting the role of coulombic interactions across several atomic distances and suggest avenues to stabilize highly oxidized oxygen for applications in energy storage and beyond.
Energy and Environmental Science


Abate, I. , Pemmaraju, C. , Kim, S. , Sainio, S. , Moritz, B. , Vinson, J. , Toney, M. , Yang, W. , Gent, W. , Devereaux, T. , Nazar, L. and Chueh, W. (2021), Coulombically-stabilized oxygen hole polarons enable fully reversible oxygen redox, Energy and Environmental Science, [online],, (Accessed May 25, 2024)


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Created July 1, 2021, Updated October 14, 2021