Regulating Cation Interactions for Zero-Strain and High-Voltage P2-type Na2/3Li1/6Co1/6Mn2/3O2 Layered Oxide Cathodes of Sodium-Ion Batteries

被引:48
|
作者
Zou, Peichao [1 ]
Yao, Libing [1 ]
Wang, Chunyang [1 ]
Lee, Sang Jun [2 ]
Li, Tianyi [3 ]
Xin, Huolin L. [1 ]
机构
[1] Univ Calif Irvine, Dept Phys & Astron, Irvine, CA 92697 USA
[2] Stanford Synchrotron Radiat Lightsource, SLAC Natl Accelerator Lab, Menlo Pk, CA 94025 USA
[3] Argonne Natl Lab, X Ray Sci Div, Lemont, IL 60439 USA
基金
美国国家科学基金会;
关键词
Cation Interaction; Layered Oxide; Sodium-Ion Batteries; Superstructure; Zero Strain; TRANSITION-METAL OXIDES; ELECTRODE; SUBSTITUTION; P3; P2;
D O I
10.1002/anie.202304628
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Deep sodium extraction/insertion of sodium cathodes usually causes undesired Jahn-Teller distortion and phase transition, both of which will reduce structural stability and lead to poor long-cycle reliability. Here we report a zero-strain P2- Na2/3Li1/6Co1/6Mn2/3O2 cathode, in which the lithium/cobalt substitution contributes to reinforcing the host structure by reducing the Mn3+/Mn4+ redox, mitigating the Jahn-Teller distortion, and minimizing the lattice change. 94.5 % of Na+ in the unit structure can be reversibly cycled with a charge cut-off voltage of 4.5 V (vs. Na+/Na). Impressively, a solid-solution reaction without phase transitions is realized upon deep sodium (de)intercalation, which poses a minimal volume deviation of 0.53 %. It attains a high discharge capacity of 178 mAh g(-1), a high energy density of 534 Wh kg(-1), and excellent capacity retention of 95.8 % at 1 C after 250 cycles.
引用
收藏
页数:7
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