In Situ Visualization of Lithium Ion Intercalation into MoS2 Single Crystals using Differential Optical Microscopy with Atomic Layer Resolution

化学 插层(化学) 原位 离子 锂(药物) 图层(电子) 分辨率(逻辑) 光学显微镜 显微镜 分析化学(期刊) 无机化学 扫描电子显微镜 光学 色谱法 物理 内分泌学 人工智能 有机化学 医学 计算机科学
作者
Azhagurajan Mukkannan,Tetsuya Kajita,Takashi Itoh,Youn-Geun Kim,Kingo Itaya
出处
期刊:Journal of the American Chemical Society [American Chemical Society]
卷期号:138 (10): 3355-3361 被引量:94
标识
DOI:10.1021/jacs.5b11849
摘要

Atomic-level visualization of the intercalation of layered materials, such as metal chalcogenides, is of paramount importance in the development of high-performance batteries. In situ images of the dynamic intercalation of Li ions into MoS2 single-crystal electrodes were acquired for the first time, under potential control, with the use of a technique combining laser confocal microscopy with differential interference microscopy. Intercalation proceeded via a distinct phase separation of lithiated and delithiated regions. The process started at the atomic steps of the first layer beneath the selvedge and progressed in a layer-by-layer fashion. The intercalated regions consisted of Li-ion channels into which the newly inserted Li ions were pushed atom-by-atom. Interlayer diffusion of Li ions was not observed. Deintercalation was also clearly imaged and was found to transpire in a layer-by-layer mode. The intercalation and deintercalation processes were chemically reversible and can be repeated many times within a few atomic layers. Extensive intercalation of Li ions disrupted the atomically flat surface of MoS2 because of the formation of small lithiated domains that peeled off from the surface of the crystal. The current-potential curves of the intercalation and deintercalation processes were independent of the scan rate, thereby suggesting that the rate-determining step was not governed by Butler-Volmer kinetics.
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