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- Publisher
- Wiley
- Copyright
- © 2020 Wiley‐VCH GmbH
- ISSN
- 1614-6832
- eISSN
- 1614-6840
- DOI
- 10.1002/aenm.202002128
- Publisher site
- See Article on Publisher Site
Abstract
Mg‐ion batteries (MIBs) possess promising advantages over monovalent Li‐ion battery technology. However, one of the myriad obstacles in realizing highly efficient MIBs is a limited selection of cathode materials that can enable reversible, stable Mg2+ intercalation at a high operating voltage. Here, a scalable method is showcased to synthesize a hydrated MgxV5O12 cathode, which shows a high capacity of ≈160 mAh g−1 with a high voltage of 2.1 V, a decent rate capability, and an outstanding cycling life (e.g., 81% capacity retention after 10 000 cycles). The combination of in situ and ex situ characterizations and first‐principles calculations provides evidence of reversible, facile topochemical Mg2+ intercalation into the expanded 2D channels of the hydrated MgxV5O12 cathode, which results from the synergistic effects of Mg2+ pillars and structural H2O. The findings underscore the advantage of the rich but controllable chemistry of vanadium oxide bronzes in achieving practical multivalent cation mobility.
Journal
Advanced Energy Materials – Wiley
Published: Dec 1, 2020
Keywords: ; ;