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Facilitating sustainable oxygen-redox chemistry for P3-type cathode materials for sodium-ion batteries

Authors
Jo, Jae HyeonKim, Hee JaeChoi, Ji UngVoronina, NataliaLee, Kug-SeungIhm, KyuwookLee, Han-KooLim, Hee-DaeKim, HyungseokJung, Hun-GiChung, Kyung YoonYashiro, HitoshiMyung, 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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