Helen M, Reddy M Anji, Diemant Thomas, Golla-Schindler Ute, Behm R Jürgen, Kaiser Ute, Fichtner Maximilian
Helmholtz Institute Ulm (HIU), D-89081 Ulm, Germany.
Institute of Surface Chemistry and Catalysis, Ulm University, D-89081 Ulm, Germany.
Sci Rep. 2015 Jul 15;5:12146. doi: 10.1038/srep12146.
Lithium-sulphur batteries have generated tremendous research interest due to their high theoretical energy density and potential cost-effectiveness. The commercial realization of Li-S batteries is still hampered by reduced cycle life associated with the formation of electrolyte soluble higher-order polysulphide (Li2Sx, x = 4-8) intermediates, leading to capacity fading, self-discharge, and a multistep voltage profile. Herein, we have realized a practical approach towards a direct transformation of sulphur to Li2S2/Li2S in lithium-sulphur batteries by alteration of the reaction pathway. A coconut shell derived ultramicroporous carbon-sulphur composite cathode has been used as reaction directing template for the sulphur. The lithiation/delithiation and capacity fading mechanism of microporous carbon confined sulphur composite was revealed by analyzing the subsurface using X-ray photoelectron spectroscopy. No higher-order polysulphides were detected in the electrolyte, on the surface, and in the subsurface of the cathode composite. The altered reaction pathway is reflected by a single-step profile in the discharge/charge of a lithium-sulphur cell.
锂硫电池因其高理论能量密度和潜在的成本效益而引发了巨大的研究兴趣。锂硫电池的商业实现仍受到与电解质可溶性高阶多硫化物(Li2Sx,x = 4 - 8)中间体形成相关的循环寿命缩短的阻碍,这会导致容量衰减、自放电以及多步电压曲线。在此,我们通过改变反应途径实现了一种在锂硫电池中将硫直接转化为Li2S2/Li2S的实用方法。一种由椰壳衍生的超微孔碳硫复合阴极已被用作硫的反应导向模板。通过使用X射线光电子能谱分析阴极复合材料的次表面,揭示了微孔碳限制硫复合材料的锂化/脱锂和容量衰减机制。在阴极复合材料的电解质、表面和次表面均未检测到高阶多硫化物。锂硫电池充放电过程中的单步曲线反映了改变后的反应途径。