Fast Magnesium Ion Transport in the Bi/Mg3Bi2 Two-Phase Electrode

Abstract

Bi has recently attracted much interest as a promising Mg battery anode to replace the Mg metal, which is ideal but impractical because of instability issues associated with the electrolyte. Our first -principles molecular dynamics study addresses why the alloying reaction of Bi with Mg creates only two crystals of Bi andMg(3)Bi(2) and how Mg ions move in the two crystals. The formation of crystalline Mg3Bi2 is energetically much more favorable than that of amorphous MgxBi (0.0 <= x <= 2.5). This high thermodynamic stability of the Mg3Bi2 crystal serves as a driving force for the complete crystalline Bi/crystalline Mg3Bi2 two-phase reaction, without allowing the formation of amorphous phases typically observed in alloy type anode materials. The Mg ions diffuse preferentially along the [001] direction in both Bi and Mg3Bi2 and diffuse about 6000 times faster in Mg3Bi2 than in Bi. Despite the relatively slow Mg transport in Bi, the absolute kinetics of Mg ions in Bi is reasonable in terms of fast battery operation. Interestingly, the calculated Mg ion diffusivity in Bi is comparable to that for a Li ion in Bi, contrary to the general perspective that multivalent ions are very sluggish compared with monovalent ions. Our study suggests that fast multivalent -ion transport can be achieved when the multivalent ion has weak bonds with the nearest host elements and exhibits small fluctuations in its coordination number and bond length during ion transport.