材料科学
法拉第效率
阳极
氟化锂
化学工程
电化学
锂(药物)
枝晶(数学)
储能
纳米技术
无机化学
电极
工程类
内分泌学
物理化学
功率(物理)
物理
医学
化学
量子力学
数学
几何学
作者
Tianpeng Jiao,Meng Xia,Zirong Chen,Yue Zou,Gaopan Liu,Ang Fu,Libao Chen,Zhengliang Gong,Yong Yang,Jianming Zheng
标识
DOI:10.1021/acsami.2c06700
摘要
All-solid-state batteries (ASSBs), particularly based on sulfide solid-state electrolytes (SSEs), are expected to meet the requirements of high-energy-density energy storage. However, the unstable interface between the ceramic pellets and lithium (Li) metal can induce unconstrained Li-dendrite growth with safety concerns. Herein, we design a carbon fluoride-silver (CFx-Ag) composite to modify the SSEs. As lithium fluoride (LiF) nanocrystals can be in situ formed through electrochemical reactions, this LiF-enriched modification layer with high surface energy can more effectively suppress Li dendrite penetration and interfacial reactions between the SSEs and anode. Remarkably, the all-solid-state symmetric cells using a lithium-boron alloy (LiB) anode can stably work to above 2,500 h under 0.5 mA cm-2 and 2 mAh cm-2 at 60 °C without shorting. A modified LiB||LiNi0.6Mn0.2Co0.2O2 (NMC622) full cell also demonstrates an improved capacity retention and high Coulombic efficiency (99.9%) over 500 cycles. This work provides an advanced solid-state interface architecture to address Li-dendrite issues of ASSBs.
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