TY - JOUR
T1 - Cobalt-free O2-type lithium-rich layered oxides
AU - de Boisse, Benoit Mortemard
AU - Jang, Jeonguk
AU - Okubo, Masashi
AU - Yamada, Atsuo
N1 - Funding Information:
Grant-in-Aid for Specially Promoted Research No. 15H05701. M.O. was financially supported by MEXT, Japan; Grant-in-Aid for challenging Exploratory Research. B.M.B. acknowledges the Japan Society for the Promotion of Science for his JSPS fellowship.
Publisher Copyright:
© 2018 The Electrochemical Society.
PY - 2018
Y1 - 2018
N2 - 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]O2−Li[Ni1/3Mn2/3]O2 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.
AB - 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]O2−Li[Ni1/3Mn2/3]O2 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.
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U2 - 10.1149/2.1331814jes
DO - 10.1149/2.1331814jes
M3 - Article
AN - SCOPUS:85067613538
SN - 0013-4651
VL - 165
SP - A3630-A3633
JO - Journal of the Electrochemical Society
JF - Journal of the Electrochemical Society
IS - 16
ER -