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Structure and compatibility of a magnesium electrolyte with a sulphur cathode.


ABSTRACT: Magnesium metal is an ideal rechargeable battery anode material because of its high volumetric energy density, high negative reduction potential and natural abundance. Coupling Mg with high capacity, low-cost cathode materials such as electrophilic sulphur is only possible with a non-nucleophilic electrolyte. Here we show how the crystallization of the electrochemically active species formed from the reaction between hexamethyldisilazide magnesium chloride and aluminum trichloride enables the synthesis of a non-nucleophilic electrolyte. Furthermore, crystallization was essential in the identification of the electroactive species, [Mg(2)(μ-Cl)(3)·6THF](+), and vital to improvements in the voltage stability and coulombic efficiency of the electrolyte. X-ray photoelectron spectroscopy analysis of the sulphur electrode confirmed that the electrochemical conversion between sulphur and magnesium sulfide can be successfully performed using this electrolyte.

SUBMITTER: Kim HS 

PROVIDER: S-EPMC3266610 | biostudies-literature | 2011 Aug

REPOSITORIES: biostudies-literature

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Structure and compatibility of a magnesium electrolyte with a sulphur cathode.

Kim Hee Soo HS   Arthur Timothy S TS   Allred Gary D GD   Zajicek Jaroslav J   Newman John G JG   Rodnyansky Alexander E AE   Oliver Allen G AG   Boggess William C WC   Muldoon John J  

Nature communications 20110809


Magnesium metal is an ideal rechargeable battery anode material because of its high volumetric energy density, high negative reduction potential and natural abundance. Coupling Mg with high capacity, low-cost cathode materials such as electrophilic sulphur is only possible with a non-nucleophilic electrolyte. Here we show how the crystallization of the electrochemically active species formed from the reaction between hexamethyldisilazide magnesium chloride and aluminum trichloride enables the sy  ...[more]

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