High-energy O3-Na1−2xCax[Ni0.5Mn0.5]O2 cathodes for long-life sodium-ion batteries
- Authors
- Yu, Tae-Yeon; Kim, Jongsoon; Hwang, Jang-Yeon; Kim, Hyungsub; Han, Geumjae; Jung, Hun-Gi; Sun, Yang-Kook
- Issue Date
- Jul-2020
- Publisher
- ROYAL SOC CHEMISTRY
- Citation
- JOURNAL OF MATERIALS CHEMISTRY A, v.8, no.27, pp 13776 - 13786
- Pages
- 11
- Indexed
- SCIE
SCOPUS
- Journal Title
- JOURNAL OF MATERIALS CHEMISTRY A
- Volume
- 8
- Number
- 27
- Start Page
- 13776
- End Page
- 13786
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/2040
- DOI
- 10.1039/d0ta04847j
- ISSN
- 2050-7488
2050-7496
- Abstract
- To facilitate the practical realization of sodium-ion batteries, the energy density, determined by the output operating voltage and/or capacity, needs to be improved to the level of commercial Li-ion batteries. Herein, O3-type Na0.98Ca0.01[Ni0.5Mn0.5]O2 is synthesized by incorporating Ca2+ into the NaO6 octahedron of Na[Ni0.5Mn0.5]O2 and its potential use as a cathode material for high energy density SIBs is demonstrated. The ionic radius of calcium (≈1.00 Å) is similar to that of sodium (≈1.02 Å); hence, it is energetically favorable for calcium to occupy sites in the sodium layers. Within a wide operating voltage range of 2.0–4.3 V, O3-type Na0.98Ca0.01[Ni0.5Mn0.5]O2 exhibits a reversible O3–P3–O3 phase transition with small volume changes compared to Ca-free Na[Ni0.5Mn0.5]O2 because of the strong interaction between Ca2+ and O2− and delivers a high reversible capacity of 209 mA h g−1 at 15 mA g−1 with improved cycling stability. Moreover, Ca substitution improves the practically useful aspects such as thermal and air stability. A prototype pouch full cell with a hard carbon anode shows an excellent capacity retention of 67% over 300 cycles. Thus, this study provides an efficient and simple method to boost the performance and applicability of layered oxide cathode materials for practical applications.
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