Article ID Journal Published Year Pages File Type
1292005 Journal of Power Sources 2016 8 Pages PDF
Abstract

•Confirmation of the polysulfide dissolution in a polymer electrolyte.•Confirmation of sulfur reappearance near the end of charge.•Anode passivation and reappearance of elemental sulfur are visualized using a SEM.•A difference between the charge and discharge mechanisms is demonstrated.•A high performance UV–Vis spectroscopy methodology has been developed.

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.

Related Topics
Physical Sciences and Engineering Chemistry Electrochemistry
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