多硫化物
扫描电子显微镜
电解质
锂(药物)
化学
聚合物
化学工程
溶解
硫黄
阳极
材料科学
分析化学(期刊)
有机化学
电极
物理化学
复合材料
内分泌学
工程类
医学
作者
Hugues Marceau,Chi-Su Kim,Andrea Paolella,Sébastien Ladouceur,Marin Lagacé,Mohamed Chaker,Ashok K. Vijh,Abdelbast Guerfi,C. Julien,A. Mauger,Michel Armand,Pierre Hovington,Karim Zaghib
标识
DOI:10.1016/j.jpowsour.2016.03.093
摘要
Lithium/solid polymer electrolyte (SPE)/sulfur cells were studied in operando by two techniques: Scanning Electron Microscope (SEM) and ultraviolet–visible absorption spectroscopy (UV–vis). During the operation of the cell, extensive polysulfide dissolution in the solid polymer electrolyte (cross-linked polyethylene oxide) leads to the formation of a catholyte. A clear micrograph of the thick passivation layer on the sulfur-rich anode and the decreased SPE thickness by cycling confirmed the failure mechanism; the capacity decays by reducing the amount of active material, and by contributing to a charge inhibiting mechanism called polysulfide shuttle. The formation of elemental sulfur is clearly visible in real time during the charge process beyond 2.3 V. The non-destructive in operando UV–vis study also shows the presence of characteristic absorption peaks evolving with cycling, demonstrating the accumulation of various polysulfide species, and the predominant formation of S42− and of S62− during discharge and charge, respectively. This finding implies that the charge and discharge reactions are not completely reversible and proceed along different pathways.
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