Published May 2022 | Version v1
Journal article

Surface design with cation and anion dual gradient stabilizes high-voltage LiCoO2

  • 1. School of Advanced Materials, Peking University Shenzhen Graduate School, Shenzhen, 518055 (China)
  • 2. State Key Laboratory of Functional Materials for Informatics, Shanghai Institute of Microsystem and Information Technology, Chinese Academy of Sciences, Shanghai, 200050 (China)
  • 3. Institute of Marine Biomedicine, Shenzhen Polytechnic, Shenzhen, 518055 (China)

Description

LiCoO2 (LCO) is the most successful cathode material for commercial lithium-ion batteries. Cycling LCO to high potentials up to 4.5 V or even 4.6 V can significantly elevate the capacity but cause structural degradation due to the serious surface side reaction between the highly oxidized Co4+ and O species with organic electrolytes. To tackle this concern, a new strategy, constructing cation and anion dual gradients at the surface of LCO (DG-LCO), is proposed. Specifically, the electrochemically inactive cation and anion are selected to substitute Co3+ and O2 at the surface in a gradated manner, thus minimizing the highly oxidized Co4+ and O species at high potentials and suppressing the induced surface side reactions. Unexpectedly, this dual gradient design leads to a spinel-like surface structure coherently with bulk layered structure, which facilitates Li+ diffusion kinetics. Thus, DG-LCO achieves high capacity and excellent cycling stability at 4.6 V (≈216 mA h g1 at 0.1 C, a capacity retention of 88.6% after 100 cycles in 1.8 A h pouch full cell at 1 C), as well as improved rate capability (≈140 mA h g1 at 5 C). These studies provide useful guidelines for future design of cathode materials with long lifespan and high rate capability. (© 2022 Wiley-VCH GmbH)

Availability note (English)

Available from: http://dx.doi.org/10.1002/aenm.202200813

Additional details

Identifiers

Publishing Information

Journal Title
Advanced Energy Materials (Internet)
Journal Volume
12
Journal Issue
20
Journal Page Range
p. 1-10
ISSN
1614-6840
CODEN
ADEMBC

Optional Information

Notes
AID: 2200813