材料科学
阳极
电解质
钼酸盐
化学工程
电导率
电化学
微晶
铋
相(物质)
离子
纳米颗粒
合金
电极
纳米技术
冶金
物理化学
有机化学
化学
工程类
物理
量子力学
作者
Anders Brennhagen,Carmen Cavallo,David S. Wragg,Ponniah Vajeeston,Anja Olafsen Sjåstad,Alexey Y. Koposov,Helmer Fjellvåg
出处
期刊:Nanotechnology
[IOP Publishing]
日期:2022-01-25
卷期号:33 (18): 185402-185402
被引量:11
标识
DOI:10.1088/1361-6528/ac4eb5
摘要
Based on the same rocking-chair principle as rechargeable Li-ion batteries, Na-ion batteries are promising solutions for energy storage benefiting from low-cost materials comprised of abundant elements. However, despite the mechanistic similarities, Na-ion batteries require a different set of active materials than Li-ion batteries. Bismuth molybdate (Bi2MoO6) is a promising NIB anode material operating through a combined conversion/alloying mechanism. We report anoperandox-ray diffraction (XRD) investigation of Bi2MoO6-based anodes over 34 (de)sodiation cycles revealing both basic operating mechanisms and potential pathways for capacity degradation. Irreversible conversion of Bi2MoO6to Bi nanoparticles occurs through the first sodiation, allowing Bi to reversibly alloy with Na forming the cubic Na3Bi phase. Preliminary electrochemical evaluation in half-cellsversusNa metal demonstrated specific capacities for Bi2MoO6to be close to 300 mAh g-1during the initial 10 cycles, followed by a rapid capacity decay.OperandoXRD characterisation revealed that the increased irreversibility of the sodiation reactions and the formation of hexagonal Na3Bi are the main causes of the capacity loss. This is initiated by an increase in crystallite sizes of the Bi particles accompanied by structural changes in the electronically insulating Na-Mo-O matrix leading to poor conductivity in the electrode. The poor electronic conductivity of the matrix deactivates the NaxBi particles and prevents the formation of the solid electrolyte interface layer as shown by post-mortem scanning electron microscopy studies.
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