Intercalation-Induced Amorphization Boosts Aqueous Magnesium-Ion Storage

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Abstract
The design of aqueous battery cathode materials that can store divalent ions with high capacity and satisfactory reversibility is of great technical importance and challenge. Here, we report that divalent Mg2+ storage is facilitated by an intercalation-induced amorphization of vanadate electrode materials. Electrokinetic analyses and in situ synchrotron X-ray diffraction and absorption spectroscopy collectively demonstrate that vanadate layered materials (Li–V3O8) undergo a structural transformation to amorphization induced by Mg2+ intercalation, and a reversible restoration of crystalline structure upon Mg2+ deintercalation. Debye scattering simulations suggest that intercalation-induced turbostratic disorder, especially random rotations, translational shifts, oscillatory motions, or varied interlayer spacing of adjacent V–O molecular layers, could be responsible for the observed amorphization. The highly distorted local structure, in turn, facilitates Mg2+ intercalation across the vanadate electrode materials, responsible for nearly 3/7 of the total Mg2+ ions intercalated. The study presented reveals an intriguing relationship between ion transport and the reversible amorphization-to-crystallization dynamics it induces, opening a paradigm for designing advanced aqueous battery electrodes.
Funding Information
  • Division of Chemical, Bioengineering, Environmental and Transport Systems (2514467)

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