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Facile method to synthesize Na-enriched Na1+xFeFe(CN)6 frameworks as cathode with superior electrochemical performance for sodium-ion batteries

机译:一种简便的合成富钠的Na1 + xFeFe(CN)6骨架作为阴极的方法,具有优异的钠离子电池电化学性能

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摘要

Different Na-enriched Na1+xFeFe(CN)6 samples can be synthesized by a facile one-step method, utilizing Na4Fe(CN)6 as the precursor in a different concentration of NaCl solution. As-prepared samples were characterized by a combination of synchrotron X-ray powder diffraction (S-XRD), Mössbauer spectroscopy, Raman spectroscopy, magnetic measurements, thermogravimetric analysis, X-ray photoelectron spectroscopy, and inductively coupled plasma analysis. The electrochemical results show that the Na1.56Fe[Fe(CN)6]·3.1H2O (PB-5) sample shows a high specific capacity of more than 100 mAh g-1 and excellent capacity retention of 97% over 400 cycles. The details structural evolution during Na-ion insertion/extraction processes were also investigated via in situ synchrotron XRD. Phase transition can be observed during the initial charge and discharge process. The simple synthesis method, superior cycling stability, and cost-effectiveness make the Na-enriched Na1+xFe[Fe(CN)6] a promising cathode for sodium-ion batteries.
机译:可以通过简便的一步法,以Na4Fe(CN)6为前体,在不同浓度的NaCl溶液中,合成不同的富Na1 + xFeFe(CN)6样品。制备的样品通过同步加速器X射线粉末衍射(S-XRD),穆斯堡尔光谱,拉曼光谱,磁测量,热重分析,X射线光电子能谱和电感耦合等离子体分析相结合来表征。电化学结果表明,Na1.56Fe [Fe(CN)6]·3.1H2O(PB-5)样品在400个循环中显示出超过100 mAh g-1的高比容量,出色的容量保持率达97%。还通过原位同步加速器XRD研究了Na离子插入/提取过程中的详细结构演变。在初始充放电过程中可以观察到相变。简单的合成方法,优异的循环稳定性和成本效益使富含Na的Na1 + xFe [Fe(CN)6]成为钠离子电池的有希望的阴极。

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