多硫化物
电解质
硫黄
电极
X射线光电子能谱
化学
傅里叶变换红外光谱
电化学
金属
无机化学
电池(电)
化学工程
材料科学
物理化学
有机化学
功率(物理)
工程类
物理
量子力学
作者
Doron Aurbach,Elad Pollak,Ran Elazari,Gregory Salitra,C. Scordilis Kelley,John Affinito
出处
期刊:Journal of The Electrochemical Society
[The Electrochemical Society]
日期:2009-08-01
卷期号:156 (8): A694-A694
被引量:1158
摘要
Li(metal)–sulfur (Li–S) systems are among the rechargeable batteries of the highest possible energy density due to the high capacity of both electrodes. The surface chemistry developed on Li electrodes in electrolyte solutions for Li–S batteries was rigorously studied using Fourier transform infrared and X-ray photoelectron spectroscopies. A special methodology was developed for handling the highly reactive Li samples. It was possible to analyze the contribution of solvents such as 1-3 dioxolane, the electrolyte , polysulfide , and additives to protective surface films that are formed on the Li electrodes. The role of as a critical component whose presence in solutions prevents a shuttle mechanism that limits the capacity of the sulfur electrodes is discussed and explained herein.
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