| Autor: |
Stephanie F. Linnell, Eun Jeong Kim, Le Anh Ma, Aaron B. Naden, John T. S. Irvine, Reza Younesi, Laurent C. Duda, A. Robert Armstrong |
| Přispěvatelé: |
EPSRC, University of St Andrews. Institute of Behavioural and Neural Sciences, University of St Andrews. School of Chemistry, University of St Andrews. Centre for Energy Ethics, University of St Andrews. Centre for Designer Quantum Materials, University of St Andrews. EaSTCHEM |
| Jazyk: |
angličtina |
| Rok vydání: |
2022 |
| Předmět: |
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| Popis: |
Funding: Faraday Institution (Grant Number(s): FIRG018); Engineering and Physical Sciences Research Council (Grant Number(s): EP/T019298/1, EP/L017008/1, EP/R023751/1); Energimyndigheten (Grant Number(s): 2020-005249); Spring 8 (Grant Number(s): 2019B1604). Oxygen anion redox offers an effective strategy to enhance the energy density of layered oxide positive electrodes for sodium- and lithium-ion batteries. However, lattice oxygen loss and irreversible structural transformations over the first cycle may result in large voltage hysteresis, thereby impeding practical application. Herein, ribbon superstructure ordering of Li/transition-metal-ions was applied to suppress the voltage hysteresis combined with Ti-substitution to improve the cycling stability for P3-Na0.67Li0.2Ti0.15Mn0.65O2. When both cation and anion redox reactions are utilized, Na0.67Li0.2Ti0.15Mn0.65O2 delivers a reversible capacity of 172 mA h g−1 after 25 cycles at 10 mA g−1 between 1.6–4.4 V vs. Na+/Na. Ex-situ X-ray diffraction data reveal that the ribbon superstructure is retained with negligible unit cell volume expansion/contraction upon sodiation/desodiation. The performance as a positive electrode for Li-ion batteries was also evaluated and P3-Na0.67Li0.2Ti0.15Mn0.65O2 delivers a reversible capacity of 180 mA h g−1 after 25 cycles at 10 mA g−1 when cycled vs. Li+/Li between 2.0–4.8 V. Publisher PDF |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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