Coulombically-stabilized oxygen hole polarons enable fully reversible oxygen redox

التفاصيل البيبلوغرافية
العنوان: Coulombically-stabilized oxygen hole polarons enable fully reversible oxygen redox
المؤلفون: Abate, Iwnetim I., Pemmaraju, C. Das, Kim, Se Young, Hsu, Kuan H., Sainio, Sami, Moritz, Brian, Vinson, John, Toney, Michael F., Yang, Wanli, Gent, William E., Devereaux, Thomas P., Nazar, Linda F., Chueh, William C.
سنة النشر: 2020
المجموعة: Condensed Matter
مصطلحات موضوعية: Condensed Matter - Materials Science
الوصف: Stabilizing high-valent redox couples and exotic electronic states necessitate 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 show that coulombic interactions between oxidized oxide-anions and the interlayer Na vacancies can disfavor rehybridization and stabilize hole polarons on oxygen 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.
Comment: 19 pages, 4 Figures, Research Article
نوع الوثيقة: Working Paper
DOI: 10.1039/D1EE01037A
URL الوصول: http://arxiv.org/abs/2010.13107
رقم الأكسشن: edsarx.2010.13107
قاعدة البيانات: arXiv