Preparation of ultra-stable Li[Ni0.6Co0.2Mn0.2]O2 cathode material with a continuous hydroxide co-precipitation method
Spherical-like Li[Ni0.6Co0.2Mn0.2]O2 (LiNCM622) cathode material is successfully prepared with the precursor of Ni0.6Co0.2Mn0.2(OH)2 (NCM622OH) synthesized via an improved continuous hydroxide co-precipitation method (CHCP). The morphology, particle size distribution and electrochemical performance...
Gespeichert in:
Veröffentlicht in: | Journal of alloys and compounds 2019-07, Vol.793, p.77-85 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Spherical-like Li[Ni0.6Co0.2Mn0.2]O2 (LiNCM622) cathode material is successfully prepared with the precursor of Ni0.6Co0.2Mn0.2(OH)2 (NCM622OH) synthesized via an improved continuous hydroxide co-precipitation method (CHCP). The morphology, particle size distribution and electrochemical performance of the as-prepared cathode materials could not change over time. The CHCP system designed in this work could extremely improve the production efficiency of the LiNCM622 cathode material. The as-prepared LiNCM622 powder presents a type of spherical structure composed of secondary particles with a typical α-NaFeO2 lamellar structure. It delivers an initial discharge capacity of 208.5 mAh/g at 0.1C (18 mA/g) with a capacity retention of 92.9% after 214 cycles in the voltage window of 2.8–4.3 V. Most impressively, the specific capacity could also maintain 101.1 mAh/g even at 10 C, with a capacity loss of only 10.5% after 1200 cycles.
•Spherical Ni0.6Co0.2Mn(OH)2 prepared by continuous hydroxide co-precipitation method.•Electrochemical performance of obtained cathode materials could not change over time.•This CHCP system can enhance the production efficiency of Li[Ni0.6Co0.2Mn0.2]O2.•Even after 1200 cycles at 10C, the discharge capacity can still retain 101.1 mAh/g. |
---|---|
ISSN: | 0925-8388 1873-4669 |
DOI: | 10.1016/j.jallcom.2019.04.123 |