非晶MoS3在全固态钠二次电池中的电极性能

IF 5.4 Q2 CHEMISTRY, PHYSICAL
Gaku Shirota, Akira Nasu, Minako Deguchi, Atsushi Sakuda, Masahiro Tatsumisago, Akitoshi Hayashi
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引用次数: 10

摘要

全固态Na-S二次电池使用大量的钠和硫,是最有吸引力的下一代电池。本研究采用(NH4)2MoS4热分解(TD)和机械化学(MC)工艺制备了两种非晶MoS3 (a-MoS3)作为全固态钠二次电池的电极活性材料,分别为a-MoS3 (TD)和a-MoS3 (MC)。x射线衍射、热重差热分析和x射线光电子能谱(XPS)分析表明,a-MoS3 (TD)和a-MoS3 (MC)具有不同的局部结构。a-MoS3 (TD)和a-MoS3 (MC)电极在全固态钠二次电池中表现出高可逆容量,分别为310 mAh g - 1和260 mAh g - 1。对充放电产物的XPS分析表明,在充放电反应过程中发生了二硫键的解离和形成。结果表明,a- mos3是一种很有前途的全固态钠电池活性电极材料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Electrode performance of amorphous MoS3 in all-solid-state sodium secondary batteries

All-solid-state Na–S secondary batteries that use sodium and sulfur, both available in abundance, are the most attractive next-generation batteries. In this study, two types of amorphous MoS3 (a-MoS3) were prepared as electrode active materials for use in all-solid-state sodium secondary batteries using the thermal decomposition (TD) of (NH4)2MoS4 and mechanochemical (MC) processes, denoted a-MoS3 (TD) and a-MoS3 (MC), respectively. X-ray diffraction, thermogravimetric-differential thermal analysis, and X-ray photoelectron spectroscopy (XPS) analyses revealed that a-MoS3 (TD) and a-MoS3 (MC) had different local structures. The a-MoS3 (TD) and a-MoS3 (MC) electrodes showed high reversible capacities of 310 mAh g−1 and 260 mAh g−1, respectively, for five cycles in all-solid-state sodium secondary batteries. XPS analysis of the discharge–charge products suggested that the dissociation and formation of disulfide bonds occurred during the discharge–charge reaction. The results show that a-MoS3 is a promising active electrode material for all-solid-state sodium batteries.

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来源期刊
CiteScore
9.10
自引率
0.00%
发文量
18
审稿时长
64 days
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