通过Li(+) 中介增强Mg/S电池化学的可逆性
Tao Gao, Malachi Noked, Alex J Pearse
1Electrochemistry Branch, Power and Energy Division Sensor and Electron Devices Directorate, U.S. Army Research Laboratory , Adelphi, Maryland 20783, United States.
Journal of the American Chemical Society
|September 12, 2015
概括
研究人员开发了一种可逆/硫电池,使用一种新的策略,通过离子激活聚硫化物. 这一突破为下一代储能提供了高容量和稳定的循环运行.
科学领域:
- 材料科学
- 电化学
- 能量储存
背景情况:
- (Mg) 金属是下一代电池的一个有前途的阳极,因为它具有很高的容量和没有树的沉积.
- 现有的Mg电池面临着阴极材料的限制,阻碍了能量密度.
- /硫 (Mg/S) 电池具有潜力,但由于不活跃的MgSx物种,其可逆性较差.
研究的目的:
- 开发一种高能量密度的可充电Mg电池.
- 为了克服Mg/S电池系统的可逆性问题.
- 让一个真正可逆的Mg/S电池具有增强的性能.
主要方法:
- 研究使用离子 (Li+) 来激活电化学不活跃的MgSx物种.
- 结合了没有的Mg阳极和可逆的多硫化物阴极.
- 使用光谱和显微特征进行机械洞察.
主要成果:
- 实现了真正可逆的Mg/S电池,容量高达1000mAh/g.
- 经过30个周期的稳定循环.
- 确定了+对MgSx的化学反应是可逆性的关键.
结论:
- 使用Li+激活MgSx的新策略可以实现可逆Mg/S电池.
- 这种方法显著提高了Mg电池的能量密度和循环寿命.
- 这为实用,高性能可充电电池铺平了道路.
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