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High-Capacity P2-Type NaxLi0.25Mn0.75O2 Cathode Enabled by Anionic Oxygen Redox
Author(s) -
Xiaoli Chen,
Ning Li,
Elyse A. Kedzie,
Bryan D. McCloskey,
Haolin Tang,
Wei Tong
Publication year - 2019
Publication title -
journal of the electrochemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.258
H-Index - 271
eISSN - 1945-7111
pISSN - 0013-4651
DOI - 10.1149/2.0611916jes
Subject(s) - electrochemistry , cathode , oxygen , redox , manganese , oxide , sodium , chemistry , inorganic chemistry , crystal structure , transition metal , oxygen evolution , ion , electrode , crystallography , catalysis , biochemistry , organic chemistry
Sodium-ion battery technology has attracted significant attention due to its substantial cost advantage and similar operating mechanism to Li-ion batteries. P2-type sodium manganese oxide cathode is one of the most promising candidates, demonstrating both high capacity and good cycling stability. Here, we explore the lattice oxygen activity in layered sodium transition metal oxides. We synthesize a series of sodium lithium manganese oxides, Na x Li 0.25 Mn 0.75 O 2 (x = 0.75 – 0.833), to optimize Na content. We further investigate the charge compensation mechanism for the best performing Na 0.75 Li 0.25 Mn 0.75 O 2 over an extensive electrochemical cycling window. The large charge and discharge capacity is enabled by reversible lattice oxygen redox in the high voltage region (≥2.5 V), along with Mn redox at the voltages below 2.5 V. Additionally, we reveal a small amount of oxygen gas evolution, 0.04% of the total oxygen in Na 0.25 Li 0.25 Mn 0.75 O 2 . This initial study will trigger an interest in the lattice oxygen activity in layered sodium metal oxide cathode, therefore, leading to better understanding of its correlation with crystal structure and electrochemical performance.

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