Fluorine substitution enabled superior performance of NaxMn2-xO1.5F0.5 (x=1.05-1.3) type Na-rich cathodeopen access
- Authors
- Ganesan, Bala Krishnan; Moorthy, Megala; Thangavel, Ranjith; Nam, Kyung-Wan; Aravindan, Vanchiappan; Lee, Yun-Sung
- Issue Date
- Feb-2023
- Publisher
- Elsevier B.V.
- Keywords
- Fluorine substitution; Sodium-rich cathode; Oxygen loss; Sodium ion battery
- Citation
- Chemical Engineering Journal, v.454, pp 1 - 9
- Pages
- 9
- Indexed
- SCIE
SCOPUS
- Journal Title
- Chemical Engineering Journal
- Volume
- 454
- Start Page
- 1
- End Page
- 9
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/25825
- DOI
- 10.1016/j.cej.2022.139876
- ISSN
- 1385-8947
1873-3212
- Abstract
- Among the various sodium cathodes, the potential of Na-rich layered oxides is yet to be fully utilized. Unlike their Li counterparts, they are least explored and are at least a generation behind in development. Addressing the same, herein, NaxMn2-xO1.5F0.5 (x = 1.05-1.3) type cathodes were synthesized successfully and analyzed as potential electrodes for Na-ion battery applications. Oxygen loss in Na-based transition metal oxides is a common issue, and it is effectively addressed by fluorine substitution. In contrast to exploring a particular stoichiometry as in other Na-deficient layered cathodes, herein, Na-content was gradually increased from 1.05 to 1.3. The cathodes were synthesized using a conventional solid-state approach and quenched to achieve high crystallinity. Compounds with different sodium stoichiometry were electrochemically tested in a half-cell configuration. Among these compounds, the Na1.2Mn0.8O1.5F0.5 electrode exhibited very high capacities of 178 and 122 mAhg(-1) at current densities of 10 and 1000 mA g(-1), respectively. The Na-rich Na1.2Mn0.8O1.5F0.5 cathode was systematically analyzed to understand the mechanism underlying its superior performance using various structural and electrochemical analyses. Furthermore, to demonstrate its practicality, the Na-rich Na1.2Mn0.8O1.5F0.5 cathode was coupled with a hard carbon and Na-In alloy anode in a full-cell assembly.
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Collections - College of Engineering > Department of Energy and Materials Engineering > 1. Journal Articles

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