Impact of surface coating on electrochemical and thermal behaviors of a Li-rich Li1.2Ni0.16Mn0.56Co0.08O2 cathode

Umair Nisar, Ramesh Petla, Sara Ahmad Jassim Al-Hail, Aisha Abdul Quddus, Haya Monawwar, Abdul Shakoor, Rachid Essehli, Ruhul Amin

Research output: Contribution to journalArticlepeer-review

35 Scopus citations

Abstract

Lithium-rich layered oxide materials are considered as potential cathode materials for future high-performance lithium-ion batteries (LIBs) owing to their high operating voltage and relatively high specific capacity. However, perceptible issues such as poor rate performance, poor capacity retention, and voltage degradation during cycling need to be improved before the successful commercialization of the material. In this report, zirconia coated Li1.2Ni0.16Mn0.56Co0.08O2 (NMC) (where ZrO2 = 1.0, 1.5 and 2.0 wt%) materials are synthesized using a sol-gel assisted ball milling approach. A comparison of structural, morphological and electrochemical properties is examined to elucidate the promising role of ZrO2 coating on the performance of the NMC cathode. A uniform and homogeneous ZrO2 coating is observed on the surface of NMC particles as evident by TEM elemental mapping images. The ZrO2 coated NMCs exhibit significantly improved electrochemical performance at a higher C-rate as compared to pristine material. 1.5% ZrO2 coated NMC demonstrates better cycling stability (95% capacity retention) than pristine NMC (77% capacity retention) after 50 cycles. All ZrO2 coated NMC materials demonstrated improved thermal stability compared to pristine material. The difference in onset temperature of 2 wt% ZrO2 coated and pristine NMC is 20 °C. The improved electrochemical performance of ZrO2 coated NMC can be attributed to the stabilization of its surface structure due to the presence of ZrO2.

Original languageEnglish
Pages (from-to)15274-15281
Number of pages8
JournalRSC Advances
Volume10
Issue number26
DOIs
StatePublished - Apr 17 2020

Funding

This publication was made possible by NPRP Grant 11S-1225-170128 from Qatar National Research Fund (a member of the Qatar Foundation). Statements made herein are solely the responsibility of the authors. Authors would like to acknowledge the technical support from Oak Ridge National Laboratory (ORNL), Oak Ridge, TN, USA, and Central Laboratory Unit (CLU), Qatar University, Doha, Qatar. We also acknowledge Core Labs at Qatar Environment and Energy Research Institute (QEERI), HBKU, Qatar for SEM and TEM analysis.

FundersFunder number
Central Laboratory Unit
HBKU
Oak Ridge National Laboratory
Qatar Foundation
Qatar National Research Fund
Qatar University

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