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SandPedges

Study of Graphite Cycling in Sulfide Solid Electrolytes

Nowadays, most of the commercial Li-ion batteries employ graphite as the active material in negative electrodes. In the race for the next-generation Li-ion batteries, tremendous research efforts in academia and industry are carried out to replace the current flammable liquid electrolyte with a solid electrolyte, which could improve both, the batteries safety and energy density. Our study investigates two different sulfide-based solid electrolytes, 0.75Li2S-0.25P2S5 (LPS) and 0.3LiI-0.7(0.75Li2S-0.25P2S5), in combination with graphite and discloses the stability of the graphite-solid electrolyte interface. Optimizing the electrode morphology is the key to enhance the rate capability of all-solid-state cells. Using the special tender X-ray range allows chemical characterization of sulfur, phosphor and iodine.

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XPEEM post mortem/operando

Post mortem/operando XPEEM: for studying the surface of single particle in Li-ion battery electrodes

X-ray photoemission electron microscopy (XPEEM) with its excellent spatial resolution is a well-suited technique to elucidate the complex electrode-electrolyte interface reactions in Li-ion batteries. It provides element-specific contrast images and enables the acquisition of local X-ray absorption spectra on single particles. Here we demonstrate the strength of post mortem measurements and we show the first electrochemical cell dedicated for operando experiments in all-solid-state batteries.

 

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half-cell with the LiI-LPS solid electrolyte layer and the working electrode

Excellent cycling stability of graphite in all-solid-state battery using sulfide solid electrolyte

All-solid-state lithium ion batteries represent a promising battery technology for boosting the volumetric energy density and promising a superior safety. In this study excellent cycling stability of graphite anode material have been demonstrated in combination with sulfide-based solid electrolyte. Furthermore we evaluated the stability of the graphite-electrolyte interface by analyzing the normalized cumulative irreversible charge during cycling experiments.

 

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