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Sodiation via Heterogeneous Disproportionation in FeF_2 Electrodes for Sodium-Ion Batteries

机译:FeF_2电极中非均相歧化的钠离子电池成膜

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Sodium-ion batteries utilize various electrode materials derived from lithium batteries. However, the different characteristics inherent in sodium may cause unexpected cell reactions and battery performance. Thus, identifying the reactive discrepancy between sodiation and lithiation is essential for fundamental understanding and practical engineering of battery materials. Here we reveal a heterogeneous sodiation mechanism of iron fluoride (FeF_2) nanoparticle electrodes by combining in situ/ex situ microscopy and spectroscopy techniques. In contrast to direct one-step conversion reaction with lithium, the sodiation of FeF_2 proceeds via a regular conversion on the surface and a disproportionation reaction in the core, generating a composite structure of 1-4 nm ultrafine Fe nanocrystallites (further fused into conductive frameworks) mixed with an unexpected Na_3FeF_6 phase and a NaF phase in the shell. These findings demonstrate a core-shell reaction mode of the sodiation process and shed light on the mechanistic understanding extended to generic electrode materials for both Li- and Na-ion batteries.
机译:钠离子电池利用衍生自锂电池的各种电极材料。但是,钠固有的不同特性可能会导致意外的电池反应和电池性能。因此,识别干化和锂化之间的反应差异对于电池材料的基本理解和实际工程至关重要。在这里,我们通过结合原位/异位显微镜和光谱技术揭示了氟化铁(FeF_2)纳米粒子电极的异质化机理。与直接与锂进行一步式转化反应相反,FeF_2的磺化反应通过在表面进行规则转化和核中的歧化反应进行,从而生成1-4 nm超细Fe纳米微晶的复合结构(进一步融合到导电骨架中) )在外壳中与意外的Na_3FeF_6相和NaF相混合。这些发现证明了增盐过程的核-壳反应模式,并阐明了对锂离子电池和钠离子电池的通用电极材料所具有的机理的理解。

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