Abstract
Magnesium-ion batteries (MIBs) suffer from a low energy density of cathode materials in a conventional nonaqueous electrolyte, contrary to the expectation due to the divalent Mg ion. Here, we report H2V3O8, or V3O7·H2O, as a high-energy cathode material for MIBs. It exhibits reversible magnesiation-demagnesiation behavior with an initial discharge capacity of 231 mAh g-1 at 60 °C, and an average discharge voltage of ∼1.9 V vs Mg/Mg2+ in an electrolyte of 0.5 M Mg(ClO4)2 in acetonitrile, resulting in a high energy density of 440 Wh kg-1. The structural water remains stable during cycling. The crystal structure for Mg0.97H2V3O8 is determined for the first time. Bond valence sum difference mapping shows facile conduction pathways for Mg ions in the structure. The high performance of this material with its distinct crystal structure employing water-metal bonding and hydrogen bonding provides insights to search for new oxide-based stable and high-energy materials for MIBs.
Original language | English |
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Pages (from-to) | 7464-7472 |
Number of pages | 9 |
Journal | Chemistry of Materials |
Volume | 30 |
Issue number | 21 |
DOIs | |
State | Published - 13 Nov 2018 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2018 American Chemical Society.
Funding
This research was supported by the Creative Materials Discovery Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT and Future Planning (2015M3D1A1069707). We are also grateful for the support from LG Chem.
Funders | Funder number |
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Ministry of Science, ICT and Future Planning | 2015M3D1A1069707 |
National Research Foundation of Korea |