Water‐Based Process to the Preparation of Crack‐Free Thick Films of Li‐Rich‐Layered Oxide Cathode for High‐Performance Pouch Cells

Owning to the low cost and eco‐friendliness, water‐based method for the fabrication of electrode films is attractive for Li‐ion battery industry. Several drawbacks such as sluggish kinetics, crack, and nonuniformity should be overcome before its practical application for anode and cathode electrodes. Herein, a modified water‐based method based on carboxymethyl cellulose/styrene‐butadiene rubber as binder has been established for the successful fabrication of Li‐rich layered oxide (LLO) electrode films without crack. As the additives of aqueous slurry, acetic acid (HAc) can inhibit the corrosion of Al foil, while ethylene carbonate can reduce the surface tension of slurry and alleviate the capillary pressure during drying. Thick LLO electrode films with a high mass loading up to 40 mg cm −2 (area capacity > 9 mAh cm −2 ) can be achieved. Such films have good peeling strength and flexibility that can avoid the removal of active layers from Al foils under the practical operations. Multilayer pouch cells consisted of graphite anode and LLO cathode by the modified water‐based method display excellent electrochemical performances. A 2.4 Ah pouch cell can deliver an energy density of 240 Wh kg −1 and show a high capacity retention of 90.5% after 500 cycles at C/2.

Authors

Institutions

Publication Details

Journal
Energy Technology
Published
2026-04-01
DOI
https://doi.org/10.1002/ente.202502131
Primary Topic
Advancements in Battery Materials
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Water‐Based Process to the Preparation of Crack‐Free Thick Films of Li‐Rich‐Layered Oxide Cathode for High‐Performance Pouch Cells

Weixuan Chen, Bao Qiu, Xufeng Zhou, Zhaoping Liu et al.
Energy Technology
Advancements in Battery Materials
article

Water‐Based Process to the Preparation of Crack‐Free Thick Films of Li‐Rich‐Layered Oxide Cathode for High‐Performance Pouch Cells

Weixuan Chen, Bao Qiu, Xufeng Zhou, Zhaoping Liu, Xiongwu Dong, Liang Chen
article en

Abstract

Owning to the low cost and eco‐friendliness, water‐based method for the fabrication of electrode films is attractive for Li‐ion battery industry. Several drawbacks such as sluggish kinetics, crack, and nonuniformity should be overcome before its practical application for anode and cathode electrodes. Herein, a modified water‐based method based on carboxymethyl cellulose/styrene‐butadiene rubber as binder has been established for the successful fabrication of Li‐rich layered oxide (LLO) electrode films without crack. As the additives of aqueous slurry, acetic acid (HAc) can inhibit the corrosion of Al foil, while ethylene carbonate can reduce the surface tension of slurry and alleviate the capillary pressure during drying. Thick LLO electrode films with a high mass loading up to 40 mg cm −2 (area capacity > 9 mAh cm −2 ) can be achieved. Such films have good peeling strength and flexibility that can avoid the removal of active layers from Al foils under the practical operations. Multilayer pouch cells consisted of graphite anode and LLO cathode by the modified water‐based method display excellent electrochemical performances. A 2.4 Ah pouch cell can deliver an energy density of 240 Wh kg −1 and show a high capacity retention of 90.5% after 500 cycles at C/2.

Energy TechnologyVol. 14(4)
Ningbo University (CN), Ningbo Institute of Industrial Technology (CN)
Openalex Percentile: Top 23%
Advancements in Battery Materials
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.