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Equilibrium Lithium-Ion Transport Between Nanocrystalline Lithium-Inserted Anatase TiO2 and the Electrolyte

机译:纳米晶插入锂的锐钛矿TiO 2 与电解质之间的平衡锂离子迁移

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摘要

The power density of lithium-ion batteries requires the fast transfer of ions between the electrode and electrolyte. The achievable power density is directly related to the spontaneous equilibrium exchange of charged lithium ions across the electrolyte/electrode interface. Direct and unique characterization of this charge-transfer process is very difficult if not impossible, and consequently little is known about the solid/liquid ion transfer in lithium-ion-battery materials. Herein we report the direct observation by solid-state NMR spectroscopy of continuous lithium-ion exchange between the promising nanosized anatase TiO2 electrode material and the electrolyte. Our results reveal that the energy barrier to charge transfer across the electrode/electrolyte interface is equal to or greater than the barrier to lithium-ion diffusion through the solid anatase matrix. The composition of the electrolyte and in turn the solid/electrolyte interface (SEI) has a significant effect on the electrolyte/electrode lithium-ion exchange; this suggests potential improvements in the power of batteries by optimizing the electrolyte composition.
机译:锂离子电池的功率密度要求离子在电极和电解质之间快速转移。可达到的功率密度直接与带电的锂离子在电解质/电极界面上的自发平衡交换有关。如果不是不可能的话,这种电荷转移过程的直接和独特的表征将非常困难,因此,人们对锂离子电池材料中的固/液离子转移知之甚少。在这里,我们报告通过固态NMR光谱直接观察到有希望的纳米锐钛矿型TiO 2 电极材料与电解质之间的连续锂离子交换。我们的结果表明,跨电极/电解质界面进行电荷转移的能垒等于或大于对通过固体锐钛矿基质扩散的锂离子的势垒。电解质的组成以及固体/电解质界面(SEI)都对电解质/电极锂离子交换产生重大影响;这表明通过优化电解质成分可以潜在地改善电池功率。

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