Facilitating sustainable oxygen-redox chemistry for P3-type cathode materials for sodium-ion batteries
- Authors
- Jo, Jae Hyeon; Kim, Hee Jae; Choi, Ji Ung; Voronina, Natalia; Lee, Kug-Seung; Ihm, Kyuwook; Lee, Han-Koo; Lim, Hee-Dae; Kim, Hyungseok; Jung, Hun-Gi; Chung, Kyung Yoon; Yashiro, Hitoshi; Myung, Seung-Taek
- Issue Date
- Apr-2022
- Publisher
- ELSEVIER
- Keywords
- < p> P3-Na- 0.6[Mn Co-0.6( 0.2) Mg- 0.2 ]O- 2< /p> ; < p> NaPO (3)< /p> ; Oxygen redox; Cathode; Sodium; Battery
- Citation
- ENERGY STORAGE MATERIALS, v.46, pp.329 - 343
- Indexed
- SCIE
SCOPUS
- Journal Title
- ENERGY STORAGE MATERIALS
- Volume
- 46
- Start Page
- 329
- End Page
- 343
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/186243
- DOI
- 10.1016/j.ensm.2022.01.028
- ISSN
- 2405-8297
- Abstract
- Herein, the surface of the P3-Na-0.6[Mn0.6Co0.2Mg0.2]O-2 cathode material is fortified by introducing an ionic-conducting sodium-phosphate nanolayer (NaPO3, asymptotic to 10-nm thickness). This layer facilitates Na+-ion diffusion owing to its sufficiently high ionic conductivity ( asymptotic to 10(-6) S cm(-1)). Moreover, the NaPO3 coating layer prevents the precipitation of surface byproducts generated from reaction with the electrolyte. The NaPO3-coated P3-Na-0.6 [Mn0.6Co0.2Mg0.2]O-2 electrode can thus retain over 80% of the first capacity after 200 cycles not only at 0.1C but also at a high rate (5C), with a capacity retention of 88% after 300 cycles. Reversible transition-metal and oxygen redox are evidenced by X-ray absorption near-edge spectroscopy, X-ray photoelectron spectroscopy, time-of-flight secondary-ion mass spectroscopy, and operando differential electrochemical mass spectroscopy, which reveal mitigated surface-byproduct formation. These findings demonstrate the possibility of the use of oxygen redox for high-energy SIBs, ensuring long term cyclability.
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