Fast Li+ Transfer Scaffold Enables Stable High-Rate All-Solid-State Li Metal Batteries

被引:0
|
作者
Song, Libo [1 ,2 ]
He, Yuanyue [1 ,2 ]
Li, Zhendong [2 ]
Peng, Zhe [2 ,3 ]
Yao, Xiayin [2 ,3 ]
机构
[1] Ningbo Univ, Sch Mat Sci & Chem Engn, Ningbo 315211, Peoples R China
[2] Chinese Acad Sci, Ningbo Inst Mat Technol & Engn, Ningbo 315201, Peoples R China
[3] Univ Chinese Acad Sci, Ctr Mat Sci & Optoelect Engn, Beijing 100049, Peoples R China
来源
BATTERIES-BASEL | 2024年 / 10卷 / 06期
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
all-solid-state Li metal battery; Li metal anode; solid electrolyte; dendrite; Li+ transfer kinetics; LITHIUM; ELECTROLYTES; ALPHA-MNO2;
D O I
10.3390/batteries10060189
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Sluggish transfer kinetics caused by solid-solid contact at the lithium (Li)/solid-state electrolyte (SE) interface is an inherent drawback of all-solid-state Li metal batteries (ASSLMBs) that not only limits the cell power density but also induces uneven Li deposition as well as high levels of interfacial stress that deteriorates the internal structure and cycling stability of ASSLMBs. Herein, a fast Li+ transfer scaffold is proposed to overcome the sluggish kinetics at the Li/SE interface in ASSLMBs using an alpha-MnO2-decorated carbon paper (CP) structure (alpha-MnO2@CP). At an atomic scale, the tunnel structure of alpha-MnO2 exhibits a great ability to facilitate Li+ adsorption and transportation across the inter-structure of alpha-MnO2@CP, leading to a high critical current density of 3.95 mA cm(-2) at the Li/SE interface. Meanwhile, uniform Li deposition can be guided along the skeletons of alpha-MnO2@CP with minimized volume expansion, significantly improving the structural stability of the Li/SE interface. Based on these advantages, the ASSLMBs using alpha-MnO2@CP protected the Li anode and can stably cycle up to very high charge/discharge rates of 10C/10C, paving the way for developing high-power ASSLMBs.
引用
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页数:11
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