氧烷
材料科学
电解质
电化学
复合数
化学工程
锂(药物)
离子
金属
快离子导体
同步加速器
复合材料
电极
冶金
光谱学
物理化学
物理
工程类
内分泌学
医学
核物理学
化学
量子力学
作者
Lun Zhang,Junrun Feng,Guanghan Zhu,Jay Hon Cheung Yan,Stuart A. Bartlett,Zhipeng Wang,Zhangxiang Hao,Zhonghui Gao,Feng Ryan Wang
标识
DOI:10.1021/acsami.3c19519
摘要
PEO-LiX solid polymer electrolyte (SPE) with the addition of Li6.4La3Zr1.4Ta0.6O12 (LLZTO) fillers is considered as a promising solid-state electrolyte for solid-state Li-ion batteries. However, the developments of the SPE have caused additional challenges, such as poor contact interface and SPE/Li interface stability during cycling, which always lead to potentially catastrophic battery failure. The main problem is that the real impact of LLZTO fillers on the interfacial properties between SPE and Li metal is still unclear. Herein, we combined the electrochemical measurement and in situ synchrotron-based X-ray absorption near-edge structure (XANES) imaging technology to study the role of LLZTO fillers in directing SPE/Li interface electrochemical performance. In situ XRF-XANES mapping during cycling showed that addition of an appropriate amount of LLZTO fillers (50 wt %) can improve the interfacial contact and stability between SPE and Li metal without reacting with the PEO and Li salts. Additionally, it also demonstrated the beneficial effect of LLZTO particles for suppressing the interface reactions between the Li metal and PEO-LiTFSI SPE and further inhibiting Li-metal dendrite growth. The Li|LiFePO4 batteries deliver long cycling for over 700 cycles with a low-capacity fade rate of 0.08% per cycle at a rate of 0.3C, revealing tremendous potential in promoting the large-scale application of future solid-state Li-ion batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI