Cobalt-Free O2-Type Lithium-Rich Layered Oxides

被引:44
作者
de Boisse, Benoit Mortemard [1 ]
Jang, Jeonguk [1 ]
Okubo, Masashi [1 ,2 ]
Yamada, Atsuo [1 ,2 ]
机构
[1] Univ Tokyo, Sch Engn, Dept Chem Syst Engn, Bunkyo Ku, Tokyo 1138656, Japan
[2] Kyoto Univ, ESICB, Nishikyo Ku, Kyoto 6148245, Japan
基金
日本学术振兴会;
关键词
ANIONIC REDOX ACTIVITY; CATHODE MATERIAL; O2; STRUCTURE; CHARGE-COMPENSATION; LI; CAPACITY; BATTERIES; ORIGIN; MN; PARTICIPATION;
D O I
10.1149/2.1331814jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
O3-type lithium-rich transition-metal oxides have been attracting interest because of their large specific capacity achieved by additional oxygen-redox reactions. However, their practical application is precluded in part by continuous capacity and voltage fading upon cycling, which mainly originates from layer-to-spinel phase transformation in an O3-type oxide-ion array. In this work, as an attempt to suppress these degradations, we report O2-type cobalt-free lithium-rich layered oxides (Li[Li1/4Mn3/4]O-2-Li[Ni1/3Mn2/3]O-2 solid solution) which deliver large capacities of 220-250 mAh/g without substantial capacity or voltage fading upon cycling. Our study demonstrates that controlling the O2/O3 polymorphism is a promising approach toward designing large capacity positive electrode materials. (C) 2018 The Electrochemical Society.
引用
收藏
页码:A3630 / A3633
页数:4
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