多硫化物
材料科学
硫黄
阴极
价(化学)
氧气
兴奋剂
离子
化学工程
化学稳定性
空位缺陷
吸附
电解质
化学物理
电极
物理化学
化学
光电子学
结晶学
冶金
有机化学
工程类
作者
Zhangxiang Hao,Rui Zeng,Lixia Yuan,Qiming Bing,Jing-yao Liu,Jingwei Xiang,Yunhui Huang
出处
期刊:Nano Energy
[Elsevier]
日期:2017-10-01
卷期号:40: 360-368
被引量:71
标识
DOI:10.1016/j.nanoen.2017.08.039
摘要
To tackle the issue of low sulfur utilization and inferior cycle stability of sulfur cathode, we first report a new perovskite-type La0.6Sr0.4CoO3-δ (LSC) immobilizer to anchor the intermediate polysulfides via chemical interaction. The experimental results and theoretical calculations demonstrate that Sr doping results in valence variation in Co along with oxygen vacancy; The Co ions with mixed valence have strong adsorption to the polysulfide ions while the existence of oxygen vacancy enhances the binding strength between Li2S4 and LSC. Based on LSC, a dual coxial LSC/[email protected] nanocable is successfully designed and fabricated. With a sulfur loading of 2.1 mg cm−2, the LSC/[email protected] cathodes demonstrate a high reversible capacity of 996 mA h g−1 at 0.5 C and an outstanding cycle stability with only 0.039% capacity fade per cycle over 400 cycles. Even with a high sulfur loading of 5.4 mg cm−2, the LSC/[email protected] cathode can still deliver similar sulfur utilization and excellent cycling stability. The excellent cycle stability benefits from the chemical interaction between LSC and polysulfides, and the physical entrapment of the carbon shell. Moreover, the highly conductive [email protected] host and the porous interconnected fiber web-like architecture facilitate the mass transfer during charge/discharge process synchronously.
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