Loading…
Surface-enriched Co engineering promoting electronic conductivity for single-crystalline Ni-based layered oxide cathodes
•A surface cobalt-rich single-crystalline cathodes were synthesized without any new phase genaration.•The cobalt-rich surface enhances charge transfer kinetics and curbs the dissolution of Mn from the bulk lattice.•The kinetics processes of cathodes were investigated in all-solid-state batteries.•Th...
Saved in:
Published in: | Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2024-04, Vol.485, p.149575, Article 149575 |
---|---|
Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | •A surface cobalt-rich single-crystalline cathodes were synthesized without any new phase genaration.•The cobalt-rich surface enhances charge transfer kinetics and curbs the dissolution of Mn from the bulk lattice.•The kinetics processes of cathodes were investigated in all-solid-state batteries.•The connection between electronic percolation and rate capability has been clarified.
Single-crystalline layered oxides are at the forefront of the development of high-energy lithium-ion battery (LiB) electrode materials, offering prolonged durability by circumventing the crack-related structural reconstruction and mechanical collapse seen in their polycrystalline counterparts. However, the sluggish carrier transport in large-crystalline particles impedes their rate capability. While most research has prioritized improving ion diffusion, the pivotal role of electron transport in electrochemical kinetics has been relatively overlooked. Herein, we enhance the kinetics of charge transfer and inhibit Mn dissolution from the bulk lattice by modulating the cobalt concentration on the surface of a single-crystalline Ni-based layered oxide cathode, LiNi0.5Co0.2Mn0.3O2. Liquid pouch-type full cells employing surface Co-concentrated cathodes exhibit exceptional high-temperature (55 °C) specific capacity (193.6 mAh g−1 at 0.2C), capacity retention (90.1 % after 2000 cycles at 1 C), and impressive rate performance at 12C. Moreover, by utilizing the varying composition-related kinetics in the composite cathode of sulfide-based all-solid-state batteries (ASSBs), we find that surface-enriched Co modification enhances the electronic percolation within the composite cathode, significantly contributing to the rate performance of ASSBs, beyond the effect of ion diffusion. This research underscores the significance of electronic properties in single-crystalline layered oxides for achieving high-power LiBs and ASSBs. |
---|---|
ISSN: | 1385-8947 |
DOI: | 10.1016/j.cej.2024.149575 |