4.8 Article

β-NaVOPO4 Obtained by a Low-Temperature Synthesis Process: A New 3.3 V Cathode for Sodium-Ion Batteries

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CHEMISTRY OF MATERIALS
卷 28, 期 5, 页码 1503-1512

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AMER CHEMICAL SOC
DOI: 10.1021/acs.chemmater.5b04992

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  1. Office of Vehicle Technologies of the U.S. Department of Energy under the Battery Materials Research (BMR) Program [DE-AC02-05CH11231, 7000389]
  2. Scientific User Facilities Division, Office of Basic Energy Sciences, U.S. Department of Energy
  3. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-AC02-06CH11357]

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Vanadyl phosphates (VOPO4) represent a class of attractive cathodes in lithium-ion batteries. However, the exploration of this type of materials in sodium-ion batteries is rare. Here, we report for the first time the synthesis of orthorhombic beta-NaVOPO4 by first chemically extracting lithium from beta-LiVOPO4 and then inserting sodium into the obtained beta-VOPO4 by a microwave-assisted solvothermal process with NaI, which serves both as a reducing agent and sodium source. Intermediate NaxVOPO4 compositions with x = 0.3, 0.5, and 0.8 have also been obtained by controlling the amount of NaI in the reaction mixture. Joint Rietveld refinement of synchrotron X-ray diffraction (XRD) and neutron diffraction confirms that the fully sodiated beta-NaVOPO4 is isostructural with the lithium counterpart beta-LiVOPO4. Bond valence sum maps suggest that sodium ions possibly diffuse along the [010] direction in the lattice, similar to the ionic conduction pathway in beta-LiVOPO4. Although the initial discharge capacity is low due to the protons in the structure, it steadily increases with cycling with a long plateau at 3.3 V. Ex situ XRD data of cycled beta-VOPO4 and beta-NaVOPO4 electrodes confirm the reversible reaction in sodium cells involving the V4+/V5+ redox couple.

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