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

被引:57
|
作者
He, Guang [1 ]
Huq, Ashfia [2 ]
Kan, Wang Hay [1 ]
Manthiram, Arumugam [1 ]
机构
[1] Univ Texas Austin, Mat Sci & Engn Program, Austin, TX 78712 USA
[2] Univ Texas Austin, Texas Mat Inst, Austin, TX 78712 USA
关键词
POSITIVE-ELECTRODE MATERIALS; CARBON-COATED NA3V2(PO4)(3); CRYSTAL-STRUCTURE; LITHIUM INSERTION; ELECTROCHEMICAL PERFORMANCE; SOLVOTHERMAL SYNTHESIS; PHOSPHATES; LIVOPO4; SYSTEM; MATRIX;
D O I
10.1021/acs.chemmater.5b04992
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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.
引用
收藏
页码:1503 / 1512
页数:10
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