Abstract
Mg batteries have potential advantages in terms of safety, cost, and reliability over existing battery technologies, but their practical implementations are hindered by the lack of amenable high-voltage cathode materials. The development of cathode materials is complicated by limited understandings of the unique divalent Mg2+ ion electrochemistry and the interaction/transportation of Mg2+ ions with host materials. Here, it is shown that highly dispersed vanadium oxide (V2O5) nanoclusters supported on porous carbon frameworks are able to react with Mg2+ ions reversibly in electrolytes that are compatible with Mg metal, and exhibit high capacities and good reaction kinetics. They are able to deliver initial capacities exceeding 300 mAh g-1 at 40 mA g-1 in the voltage window of 0.5 to 2.8 V. The combined electron microscope, spectroscopy, and electrochemistry characterizations suggest a surface-controlled pseudocapacitive electrochemical reaction, and may be best described as a molecular energy storage mechanism. This work can provide a new approach of using the molecular mechanism for pseudocapacitive storage of Mg2+ for Mg batteries cathode materials.
Original language | English (US) |
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Pages (from-to) | 3446-3453 |
Number of pages | 8 |
Journal | Advanced Functional Materials |
Volume | 26 |
Issue number | 20 |
DOIs | |
State | Published - May 24 2016 |
All Science Journal Classification (ASJC) codes
- Chemistry(all)
- Materials Science(all)
- Condensed Matter Physics