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Building Elastic Solid Electrolyte Interphases for Stabilizing Microsized Antimony Anodes in Potassium Ion Batteries

机译:构建弹性固体电解质互差,用于稳定钾离子电池中的微链锑阳极

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Alloy anodes composed of microsized particles receive increasing attention recently, which outperform the nanostructured counterparts in both the manufacturing cost and volumetric energy density. However, the pulverization of particles and fracture of solid electrolyte interphase (SEI) during cycling brings about fast capacity degradation. Herein, it is shown how normally considered fragile SEI can become highly elastic through electrolyte chemistry regulation. Compared to the SEI constructed in classic carbonate electrolyte, the atomic force microscopy tests reveal that the one built in ether-based electrolyte doubles the maximum elastic strain to accommodate the repeated swelling-contracting. Such an SEI effectively encapsulates the microsized Sb anodes to prevent the capacity loss from particle isolation. Coupled with an intercalation-assisted alloying reaction mechanism, a sustained capacity of approximate to 573 mAh g(-1) after 180 cycles at 0.1 A g(-1) with outstanding initial Coulombic efficiency is obtained, which is among the highest values achieved in K-ion batteries. This study emphasizes the significance of building robust SEI, which offers the opportunity to enable stable microsized alloy anodes.
机译:由微晶颗粒组成的合金阳极最近接受越来越大,这始终占制造成本和体积能密度的纳米结构对应物。然而,循环期间固体电解质间(SEI)的颗​​粒粉碎和骨折引起快速劣化的劣化。在此,示出了通过电解质化学调节的通常考虑的脆弱SEI可以高度弹性。与在经典碳酸盐电解质中构建的SEI相比,原子力显微镜测试表明,基于乙醚的电解质中的一个是最大弹性应变,以适应重复的溶胀收缩。这种SEI有效地包封了微化的SB阳极​​以防止颗粒隔离的容量损失。与插层辅助的合金化反应机制相结合,获得在0.1Ag(-1)的180次循环后近似为573mahg(-1)的持续容量,获得具有出色的初始库仑效率的初始库仑效率,这是所达到的最高值之​​后K离子电池。本研究强调建立强大的SEI的重要性,这提供了能够实现稳定的微链合金阳极的机会。

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