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通过在位扫描电子显微镜观察硅阳极在硬币型电池中的反应。

Visualization of Si Anode Reactions in Coin-Type Cells via Operando Scanning Electron Microscopy.

机构信息

Department of Applied Chemistry, Graduate School of Engineering, Osaka University , 2-1 Yamada-oka, Suita, Osaka 565-0871, Japan.

Department of Chemistry and Materials Engineering, Kansai University , 3-3-35 Yamate-cho, Suita, Osaka 564-8680, Japan.

出版信息

ACS Appl Mater Interfaces. 2017 Oct 18;9(41):35511-35515. doi: 10.1021/acsami.7b12340. Epub 2017 Oct 4.

Abstract

Understanding the electrochemical behavior and controlling the morphological variations of electrodes are critical for the design of high-capacity batteries. In this article, we describe a newly established operando scanning electron microscopy (SEM) to visualize the battery reactions in a modified coin cell, which allowed the simultaneous collection of electrochemical data and time-resolved images. The investigated silicon (Si)-polyimide-binder electrode exhibited a high capacity (∼1500 mAh g) and a desirable cyclability. Operando SEM revealed that the morphology of the Si anode drastically changed and cracks formed on the electrode because of the lithiation-induced volume expansion of the Si particles during the first charge process. Interestingly, the thickness variation in the Si composite layer was moderated in subsequent cycles. This strongly suggested that cracking caused by the breakage of the stiff binder alleviated the internal stress experienced by Si. On the basis of this finding by the operando SEM technique, patterned Si electrodes with controlled spacing were successfully fabricated, and their improved performance was confirmed.

摘要

了解电极的电化学行为和控制其形态变化对于设计高容量电池至关重要。本文描述了一种新建立的在位扫描电子显微镜(SEM)技术,用于可视化改进的硬币电池中的电池反应,该技术允许同时收集电化学数据和时间分辨图像。研究的硅(Si)-聚酰亚胺-粘合剂电极表现出高容量(约 1500 mAh g)和良好的循环稳定性。在位 SEM 揭示了 Si 阳极的形态剧烈变化,并且由于 Si 颗粒在首次充电过程中由于锂化诱导的体积膨胀,电极上形成了裂纹。有趣的是,在随后的循环中,Si 复合层的厚度变化得到了缓和。这强烈表明,由硬粘合剂断裂引起的开裂缓解了 Si 所经历的内应力。基于在位 SEM 技术的这一发现,成功制备了具有受控间隔的图案化 Si 电极,并证实了其改进的性能。

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