z-logo
open-access-imgOpen Access
Outside‐In Nanostructure Fabricated on LiCoO 2 Surface for High‐Voltage Lithium‐Ion Batteries
Author(s) -
Mao Shulan,
Shen Zeyu,
Zhang Weidong,
Wu Qian,
Wang Zhuoya,
Lu Yingying
Publication year - 2022
Publication title -
advanced science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.388
H-Index - 100
ISSN - 2198-3844
DOI - 10.1002/advs.202104841
Subject(s) - materials science , lithium cobalt oxide , electrolyte , nanostructure , cathode , chemical engineering , lithium (medication) , spinel , graphite , electrochemistry , cobalt oxide , nanotechnology , ion , cobalt , battery (electricity) , lithium ion battery , electrode , composite material , chemistry , metallurgy , medicine , power (physics) , physics , quantum mechanics , endocrinology , engineering , organic chemistry
Abstract The energy density of batteries with lithium cobalt oxide (LCO) can be maximized by increasing the cut‐off voltage to approach the theoretical capacity limit. However, it is not realized in the practical applications due to the restricted cycle life caused by vulnerable cathode surface in deep delithiation state, where severe side reactions, oxygen/cobalt loss and structure degradation often happen. Here, an outside‐in oriented nanostructure on LiCoO 2 crystals is fabricated. The outer electrochemically stable LiF and Li 2 CoTi 3 O 8 particles perform as physical barrier to prevent damage of both cathodes and electrolytes, while the inner F doping promote Li ions diffusivity and stabilize the lattice oxygen. With the spinel‐like transition layer between them, a solid and complete lithium‐ion transport channel generation along the lithium concentration gradient. Under the protection from this structure, the LiCoO 2 withstand the high voltage of 4.6 V and the LCO/graphite pouch full cell with high loading density exhibits 81.52% energy density retention after 135 cycles at 4.5 V.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here