材料科学
电解质
复合数
锂(药物)
纳米技术
化学物理
化学工程
电极
复合材料
化学
物理化学
医学
工程类
内分泌学
作者
Linshan Luo,Zhefei Sun,Yiwei You,Xiang Han,Chaofei Lan,Shanpeng Pei,Pengfei Su,Zhiyong Zhang,Y. Li,Shaowen Xu,Shengshi Guo,Dingqu Lin,Guangyang Lin,Cheng Li,Weimin Huang,Shunqing Wu,Ming‐Sheng Wang,Songyan Chen
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-01-15
卷期号:18 (4): 2917-2927
被引量:9
标识
DOI:10.1021/acsnano.3c07306
摘要
A commonly used strategy to tackle the unstable interfacial problem between Li1.3Al0.3Ti1.7(PO4)3 (LATP) and lithium (Li) is to introduce an interlayer. However, this strategy has a limited effect on stabilizing LATP during long-term cycling or under high current density, which is due in part to the negative impact of its internal defects (e.g., gaps between grains (GBs)) that are usually neglected. Here, control experiments and theoretical calculations show clearly that the GBs of LATP have higher electronic conductivity, which significantly accelerates its side reactions with Li. Thus, a simple LiCl solution immersion method is demonstrated to modify the GBs and their electronic states, thereby stabilizing LATP. In addition to LiCl filling, composite solid polymer electrolyte (CSPE) interlayering is concurrently introduced at the Li/LATP interface to realize the internal–external dual modifications for LATP. As a result, electron leakage in LATP can be strictly inhibited from its interior (by LiCl) and exterior (by CSPE), and such dual modifications can well protect the Li/LATP interface from side reactions and Li dendrite penetration. Notably, thus-modified Li symmetrical cells can achieve ultrastable cycling for more than 3500 h at 0.4 mA cm–2 and 1500 h at 0.6 mA cm–2, among the best cycling performance to date.
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