Open AccessEnhanced Cycling and Rate Capability by Epitaxially Matched Conductive Cubic TiO Coating on LiCoO2 Cathode Films
Author(s) -
Deepak P. Singh,
Yorick A. Birkhölzer,
Daniel M. Cunha,
Thijs Dubbelink,
Shitian Huang,
T.A. Hendriks,
Caroline Lievens,
Mark Huijben
Publication year - 2021
Publication title -
acs applied energy materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.833
H-Index - 36
ISSN - 2574-0962
DOI - 10.1021/acsaem.1c00603
Subject(s) - materials science , electrolyte , cathode , chemical engineering , dissolution , oxide , lithium cobalt oxide , coating , electrode , nanotechnology , lithium ion battery , metallurgy , chemistry , power (physics) , physics , battery (electricity) , quantum mechanics , engineering
Layered lithium transition-metal oxides, such as LiCoO 2 and its doped and lithium-rich analogues, have become the most attractive cathode material for current lithium-ion batteries due to their excellent power and energy densities. However, parasitic reactions at the cathode-electrolyte interface, such as metal-ion dissolution and electrolyte degradation, instigate major safety and performance issues. Although metal oxide coatings can enhance the chemical and structural stability, their insulating nature and lattice mismatch with the adjacent cathode material can act as a physical barrier for ion transport, which increases the charge-transfer resistance across the interface and impedes cell performance at high rates. Here, epitaxial engineering is applied to stabilize a cubic (100)-oriented TiO layer on top of single (104)-oriented LiCoO 2 thin films to study the effect of a conductive coating on the electrochemical performance. Lattice matching between the (104) LiCoO 2 surface facets and the (100) TiO plane enables the formation of the titanium mono-oxide phase, which dramatically enhances the cycling stability as well as the rate capability of LiCoO 2 . This cubic TiO coating enhances the preservation of the phase and structural stability across the (104) LiCoO 2 surface. The results suggest a more stable Co 3+ oxidation state, which not only limits the cobalt-ion dissolution into the electrolyte but also suppresses the catalytic degradation of the liquid electrolyte. Furthermore, the high c-rate performance combined with high Columbic efficiency indicates that interstitial sites in the cubic TiO lattice offer facile pathways for fast lithium-ion transport.