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Elucidating the Phase Transformation of Li4Ti5O12 Lithiation at the Nanoscale

机译:在纳米级阐明Li4Ti5O12锂化的相变

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This work provides insight regarding the fundamental lithiation and delithiation mechanism of the popular lithium ion battery anode material, Li4Ti5O12 (LTO). Our results quantify the extent of reaction between Li4Ti5O12 and Li4Ti5O12 at the nanoscale, during the first cycle. Lithium titanate's discharge (lithiation) and charge (delithiation) reactions are notoriously difficult to characterize due to the zero-strain transition occurring between the end members Li4Ti5O12 and Li7Ti5O12. Interestingly, however, the latter compound is electronically conductive, while the former is an insulator. We take advantage of this critical property difference by using conductive atomic force microscopy (c-AFM) to locally monitor the phase transition between the two structures at various states of charge. To do so, we perform ex situ characterization on electrochemically cycled LTO thin-films that are never exposed to air. We provide direct confirmation of the manner in which the reaction occurs, which proceeds via percolation channels within single grains. We complement scanning probe analyses with an X-ray photoelectron spectroscopy (XPS) study that identifies and explains changes in the LTO surface structure and composition. In addition, we provide a computational analysis to describe the unique electronic differences between LTO and its lithiated form.
机译:这项工作提供了有关流行的锂离子电池负极材料Li4Ti5O12(LTO)的基本锂化和脱锂机理的见解。我们的结果量化了在第一个循环中,纳米级的Li4Ti5O12和Li4Ti5O12之间的反应程度。众所周知,钛酸锂的放电(锂化)和电荷(脱锂)反应难以表征,因为在端基Li4Ti5O12和Li7Ti5O12之间发生了零应变转变。然而,有趣的是,后者是导电的,而前者是绝缘体。我们通过使用导电原子力显微镜(c-AFM)来局部监视两种结构在不同电荷状态下的相变,从而利用了这一关键特性差异。为此,我们对从未暴露于空气的电化学循环LTO薄膜进行了非原位表征。我们提供了反应发生方式的直接确认,该反应是通过单个颗粒内的渗滤通道进行的。我们通过X射线光电子能谱(XPS)研究来补充扫描探针分析,该研究可以识别并解释LTO表面结构和组成的变化。此外,我们提供了计算分析来描述LTO及其锂化形式之间的独特电子差异。

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