在精电解质电池中评估阴极动力学
Zi-Xian Chen1,2, Qian Cheng1,2, Xi-Yao Li3
1School of Materials Science and Engineering, Beijing Institute of Technology, Beijing 100081, China.
Journal of the American Chemical Society
|July 10, 2023
概括
-硫 (Li-S) 电池中的稀疏电解质阻碍了性能. 这项研究确定了硫核化过程中的激活极化为关键极限,为改进Li-S电池设计提供了见解.
科学领域:
- 材料科学
- 电化学
- 能量储存
背景情况:
- -硫 (Li-S) 电池具有超越离子技术的高能量密度潜力.
- 实现高能量密度需要精益电解质条件,这具有悖论性的降低了电池性能,特别是硫阴极运动.
研究的目的:
- 在低电解质条件下,系统地解并确定电池中硫阴极的主要动力限制因子.
- 为开发有效的提高Li-S电池性能策略提供指导.
主要方法:
- 开发了一种结合电化学阻抗光谱 (EIS) 和静电间歇定位技术 (GITT) 的方法.
- 将阴极两极分离为激活,度和欧姆元件.
主要成果:
- 在硫化核化过程中确定了激活偏振作为电解质与硫 (E/S) 比率下降的主要限制性因素.
- 表面电荷转移动力较慢被证实是稀薄电解质性能降低的主要原因.
- 一种新型的二硫胺电解质降低了激活极化,使Li-S电池能够在4μL mg-1 (0.2C) 的低E/S比率下达到985mAhg-1.
结论:
- 在硫化核化过程中的激活极化是薄电解质Li-S电池的关键瓶.
- 这些发现指导了针对性的策略的设计,例如电解质修改,以克服动力限制并推进Li-S电池技术.
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