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Surface reconstruction layer boosting interfacial stability of LiCoO2/Li6PS5Cl in bulk all-solid-state Li batteries.

Authors :
Zheng, Shiliang
Li, Zengzhu
He, Zhiwe
Zhao, Wenguang
Liu, Chenyu
Lin, Zhan
Zhuo, Zengqing
Zhang, Bingkai
Source :
Journal of Materials Chemistry A; 4/7/2024, Vol. 12 Issue 13, p7916-7922, 7p
Publication Year :
2024

Abstract

The interfacial compatibility between cathode materials and sulfide solid-electrolytes (SEs) is a critical factor affecting the electrochemical performance of all-solid-state lithium-ion batteries (ASSLBs). This work presents a gas–solid interface reduction reaction (GSIRR) to reduce surface oxygen reactivity by inducing a surface reconstruction layer through in situ generated CoO/Li<subscript>2</subscript>CO<subscript>3</subscript> on the LiCoO<subscript>2</subscript> cathode surface. Experimental results demonstrate that the surface reconstruction layer effectively suppresses interfacial side reactions with Li<subscript>6</subscript>PS<subscript>5</subscript>Cl SE and reduces interface resistance. The LiCoO<subscript>2</subscript> with CoO/Li<subscript>2</subscript>CO<subscript>3</subscript> exhibits high capacity (143 mA h g<superscript>−1</superscript>), excellent cyclability (150 cycles with 89.79% capacity retention at 0.2C), and exceptional rate capability (83.4% capacity retention after 300 cycles at 0.5C in the voltage range of 2.6–4.3 V) in ASSLBs. Furthermore, at a high voltage of 4.6 V and a rate of 0.5C, the specific capacity reaches 168.6 mA h g<superscript>−1</superscript>, and it still maintains a capacity of 139.9 mA h g<superscript>−1</superscript> after 150 cycles. This study highlights the significant impact of the surface chemistry of the oxide cathode on interfacial compatibility and proposes a surface reconstruction strategy based on the GSIRR process for the design of ASSLBs. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20507488
Volume :
12
Issue :
13
Database :
Complementary Index
Journal :
Journal of Materials Chemistry A
Publication Type :
Academic Journal
Accession number :
176248821
Full Text :
https://doi.org/10.1039/d3ta07630j