Krüger Helge, Cavers Heather, Offermann Jakob, Polonskyi Oleksandr, Adelung Rainer, Hansen Sandra
Institute for Material Science, University of Kiel, Kaiserstraße 2, 24143 Kiel, Germany.
ACS Appl Mater Interfaces. 2023 Feb 22;15(7):10203-10211. doi: 10.1021/acsami.2c05285. Epub 2023 Feb 14.
Lithium-ion batteries are one of the most important energy storage devices of the future and pave the way for a greener society. In this context, the demand for batteries with high energy density is increasing significantly and is reaching the limits of the technology currently in use. Therefore, intensive research is being conducted to utilize a new class of materials for energy storage. The most promising alternatives to today's nickel-based cathode and graphite anode materials are silicon and sulfur. Both silicon and sulfur are abundant and cheap and possess extremely high theoretical specific capacities of 4200 mAh/g and 1675 mAh/g, respectively. One of the biggest challenges with sulfur-based batteries is the polysulfide shuttle effect, which occurs with sulfur cathodes, leading to an insulating passivation layer, especially on the commonly used lithium metal anodes. Therefore, to replace lithium metal anodes with silicon, it is of major importance to understand the reactivity of polysulfides with silicon. To investigate the effect of lithium polysulfides on the performance of the anodes in the critical formation cycles, mesoporous silicon anodes were galvanostatically cycled in electrolytes containing different concentrations of polysulfides. In this process, the anodes were analyzed after one, five and ten cycles by X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy to determine the composition of the SEI. Higher concentrations of polysulfides in the electrolyte result in more inorganic, oxide-containing species in the SEI. Silicon anodes with lower amounts of surface oxide show little or negative effect on the performance in the presence of polysulfides, while anodes with large amounts of surface oxide show higher impedance during cycling, an effect that is enhanced with increasing polysulfide content.
锂离子电池是未来最重要的储能装置之一,为更绿色的社会铺平了道路。在这种背景下,对高能量密度电池的需求正在显著增加,并且正在达到当前使用技术的极限。因此,正在进行深入研究以利用新型材料进行能量存储。当今镍基阴极和石墨阳极材料最有前景的替代品是硅和硫。硅和硫都储量丰富且价格低廉,理论比容量分别极高,达到4200 mAh/g和1675 mAh/g。硫基电池最大的挑战之一是多硫化物穿梭效应,这种效应发生在硫阴极上,会导致形成绝缘钝化层,尤其是在常用的锂金属阳极上。因此,用硅替代锂金属阳极时,了解多硫化物与硅的反应性至关重要。为了研究多硫化锂在关键形成循环中对阳极性能的影响,在含有不同浓度多硫化物的电解质中对介孔硅阳极进行恒电流循环。在此过程中,在1、5和10个循环后通过X射线光电子能谱(XPS)和拉曼光谱对阳极进行分析,以确定SEI的组成。电解质中较高浓度的多硫化物会导致SEI中含有更多的无机含氧化合物。表面氧化物含量较低的硅阳极在存在多硫化物的情况下对性能几乎没有负面影响或有负面影响,而表面氧化物含量高的阳极在循环过程中显示出更高的阻抗,随着多硫化物含量的增加,这种影响会增强。