TY - JOUR
T1 - High-capacity P2-type NaxLi0.25Mn0.75O2 cathode enabled by anionic oxygen redox
AU - Chen, Xiaoli
AU - Li, Ning
AU - Kedzie, Elyse
AU - McCloskey, Bryan D.
AU - Tang, Haolin
AU - Tong, Wei
N1 - Publisher Copyright:
© The Author(s) 2019. Published by ECS.
PY - 2019
Y1 - 2019
N2 - 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, NaxLi0.25Mn0.75O2 (x = 0.75 - 0.833), to optimize Na content. We further investigate the charge compensation mechanism for the best performing Na0.75Li0.25Mn0.75O2 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 Na0.25Li0.25Mn0.75O2. 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.
AB - 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, NaxLi0.25Mn0.75O2 (x = 0.75 - 0.833), to optimize Na content. We further investigate the charge compensation mechanism for the best performing Na0.75Li0.25Mn0.75O2 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 Na0.25Li0.25Mn0.75O2. 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.
UR - http://www.scopus.com/inward/record.url?scp=85078565767&partnerID=8YFLogxK
U2 - 10.1149/2.0611916jes
DO - 10.1149/2.0611916jes
M3 - Article
AN - SCOPUS:85078565767
SN - 0013-4651
VL - 166
SP - A4136-A4140
JO - Journal of the Electrochemical Society
JF - Journal of the Electrochemical Society
IS - 16
ER -