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In Situ Light Microscopy Observation of Sodium Dissolution/Deposition Reaction in Propylene Carbonate-Based Electrolyte

溶解 碳酸丙烯酯 电解质 电化学 碳酸钠 材料科学 电极 化学 无机化学 化学工程 冶金 有机化学 工程类 物理化学
作者
Yuhki Yui,Masahiko Hayashi,Katsuro Hayashi,Jiro Nakamura
出处
期刊:Meeting abstracts 卷期号:MA2015-01 (2): 377-377
标识
DOI:10.1149/ma2015-01/2/377
摘要

Sodium-ion batteries (SIBs) are anticipated as promising alternatives to lithium-ion batteries (LIBs), and many studies have been conducted on electrodes for SIBs using half-cells. In general, sodium metals are used for the counter electrode of half-cells. However, there are few reports [1] on sodium dissolution/deposition, knowledge of which an understanding of which is important for advancing the development of SIBs. In this study, we focused on sodium metal and observed morphologies of sodium dissolution/deposition reactions in propylene carbonate-based electrolyte solution using in situ light microscopy. Morphologies of sodium depositions were observed by using in-situ light microscopy (Lasertec Corp., ECCS B310). The semicircular cell for in-situ light microscopy examination was a stack consisting of a sodium sheet as a counter electrode (0.2 mm thick), an electrolyte solution (1 mol/l NaPF 6 /PC)-soaked polypropylene separator (19 mm in diameter), and a Cu sheet (0.01 mm thick) or sodium sheet (0.2 mm thick) as a working electrode. Electrochemical measurements were performed by using an automatic galvanostatic discharge-charge system (Hokuto HJ1001SD8) at a constant current of 65 mA/cm 2 at room temperature. The sodium deposition reaction on the sodium sheet was observed, and the morphologies were granular and needle-like (not shown here). Figure 1 shows cross-sectional images of sodium deposition on the Cu sheet, separator, and sodium metal. The morphologies of sodium deposition showed no difference from that on sodium sheet. Then, needle-like sodium led to away from the Cu sheet and became “dead sodium”. This suggests that the sodium metal dissolution/deposition efficiency is low. [1] K. Matsumoto et al., J. Power Sources , 265 (2014) 36. Figure 1

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