电解质
离子
材料科学
化学物理
离子键合
空间电荷
阴极
锂(药物)
电荷(物理)
电极
分析化学(期刊)
化学
物理
物理化学
电子
量子力学
有机化学
医学
色谱法
内分泌学
作者
Zhu Cheng,Ming Liu,Swapna Ganapathy,Chao Li,Zhaolong Li,Xiaoyu Zhang,Ping He,Haoshen Zhou,Marnix Wagemaker
出处
期刊:Joule
[Elsevier]
日期:2020-05-07
卷期号:4 (6): 1311-1323
被引量:136
标识
DOI:10.1016/j.joule.2020.04.002
摘要
The influence of space-charge layers on the ionic charge transport over cathode-solid electrolyte interfaces in all-solid-state batteries remains unclear because of the difficulty to unravel it from other contributions to the ion transport over the interfaces. Here, we reveal the effect of the space-charge layers by systematically tuning the space-charge layer on and off between LixV2O5 and Li1.5Al0.5Ge1.5(PO3)4 (LAGP), by changing the LixV2O5 potential and selectively measuring the ion transport over the interface by two-dimensional (2D) NMR exchange. The activation energy is demonstrated to be 0.315 eV for lithium-ion exchange over the space-charge-free interface, which increases dramatically to 0.515 eV for the interface with a space-charge layer. Comparison with a space-charge model indicates that the charge distribution due to the space-charge layer is responsible for the increased interface resistance. Thereby, the present work provides selective and quantitative insight into the effect of space-charge layers over electrode-electrolyte interfaces on ionic transport.
科研通智能强力驱动
Strongly Powered by AbleSci AI