Georgina Jahan, Saeme Motevalian, Dambar Hamal, Osama Awadallah, Ana Claus, Natalia Rodrigues de Oliveira, Meer Safa, Bilal El-Zahab
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引用次数: 0
Abstract
In this study, a glass microfibers interlayer (GMI) was used at the interface of the cathode and electrolyte in lithium-sulfur batteries to prevent polysulfides loss from the cathode which contributes to capacity and coulombic efficiency fades during cycling. The interlayer's performance was evaluated using full-cell studies and various visual experiments at commercially relevant sulfur areal loadings. Cells with sulfur loading of 4 mg cm−2 consistently had initial capacities exceeding 1200 mAh g−1 and reached a stable performance at around 900 mAh g−1 after 2 cycles at 2.23 mA cm−2. After 200 cycles the capacity retention remained robust at 95 %, marking an average decay rate of only 0.016 % per cycle. Cathodes with 2.8 mg cm−2 at 1.57 mA cm−2 rate and cathodes with 2 mg cm−2 at 3.3 mA cm−2 high rate exhibit improved rate capability and excellent stability over 400 cycles and 500 cycles respectively with 20 % more capacity retention than non-GMI cells. Post-failure analyses of the cell components revealed the GMI's role in controlling the concentration of soluble polysulfides at the anode and a suitable candidate that can be used alone or in tandem with other approaches to help overcome one of the major problems in lithium-sulfur batteries.
在锂硫电池的阴极和电解液界面上使用了玻璃微纤维夹层(GMI),以防止阴极的多硫化物损失,从而防止循环过程中容量和库仑效率的衰减。使用全电池研究和各种商业相关硫面积负荷的视觉实验来评估中间层的性能。硫负载为4 mg cm−2的电池的初始容量始终超过1200 mAh g−1,在2.23 mA cm−2下循环2次后,其性能稳定在900 mAh g−1左右。在200次循环后,容量保持在95%,这意味着每个循环的平均衰减率仅为0.016%。2.8 mg cm - 2 (1.57 mA cm - 2)和2 mg cm - 2 (3.3 mA cm - 2)的阴极分别在400次和500次循环中表现出更好的倍率能力和优异的稳定性,容量保持率比非gmi电池高20%。电池组件的失效后分析揭示了GMI在控制阳极处可溶性多硫化物浓度方面的作用,以及一个合适的候选材料,可以单独使用或与其他方法串联使用,以帮助克服锂硫电池的一个主要问题。
期刊介绍:
ChemElectroChem is aimed to become a top-ranking electrochemistry journal for primary research papers and critical secondary information from authors across the world. The journal covers the entire scope of pure and applied electrochemistry, the latter encompassing (among others) energy applications, electrochemistry at interfaces (including surfaces), photoelectrochemistry and bioelectrochemistry.