Nonaqueous rechargeable magnesium
(Mg) batteries suffer from the
complicated and moisture-sensitive electrolyte chemistry. Besides
electrolytes, the practicality of a Mg battery is also confined by
the absence of high-performance electrode materials due to the intrinsically
slow Mg2+ diffusion in the solids. In this work, we demonstrated
a rechargeable aqueous magnesium ion battery (AMIB) concept of high
energy density, fast kinetics, and reversibility. Using a superconcentration
approach we expanded the electrochemical stability window of the aqueous
electrolyte to 2.0 V. More importantly, two new Mg ion host materials,
Li superconcentration approach we expanded the electrochemical stability
window of the aqueous electrolyte to 2.0 V. More importantly, two
new Mg ion host materials, Li3V2(PO4)3 and poly pyromellitic dianhydride, were developed and
employed as cathode and anode electrodes, respectively. Based on comparisons
of the aqueous and nonaqueous systems, the role of water is identified
to be critical in the Mg ion mobility in the intercalation host but
remaining little detrimental to its non-diffusion controlled process.
Compared with the previously reported Mg ion cell delivers an unprecedented
high power density of 6400 W kg ion cell delivers an unprecedented
high power density of 6400 W kg while retaining 92% of the initial
capacity after 6000 cycles, pushing the Mg ion cell to a brand new
stage.