X射线光电子能谱
材料科学
钛酸锂
阳极
纳米尺度
锂(药物)
相变
表征(材料科学)
纳米技术
相(物质)
化学物理
化学工程
电池(电)
锂离子电池
电极
物理化学
化学
凝聚态物理
量子力学
有机化学
物理
功率(物理)
医学
内分泌学
工程类
作者
Michael G. Verde,Loïc Baggetto,Nina Balke,Gabriel M. Veith,Joon Kyo Seo,Ziying Wang,Ying Shirley Meng
出处
期刊:ACS Nano
[American Chemical Society]
日期:2016-03-15
卷期号:10 (4): 4312-4321
被引量:149
标识
DOI:10.1021/acsnano.5b07875
摘要
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 Li7Ti5O12 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.
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