电解质
二聚体
材料科学
电化学
锡
电极
无机化学
化学工程
粒径
粒子(生态学)
钠
离子
相间
体积膨胀
分解
催化作用
溶剂
碳酸丙烯酯
作者
C. Murugesan,Aaron B. Naden,Paul A. Connor,A. Robert Armstrong,John T.S. Irvine
摘要
ABSTRACT The electrochemical performance of tin (Sn) electrodes for sodium ion batteries (NIBs) is investigated, focusing on the challenges of severe volume expansion during cycling and electrolyte incompatibility. Micron‐sized Sn delivers better cycle life than nanoparticles; however, limited research exists on the combined effects of particle size and electrolyte compatibility. In‐house synthesized Sn particles (50 nm–1 µm) and commercial micron‐sized Sn (5–35 µm), using 1 m NaPF 6 in both EC:DEC (carbonate‐based) and in diglyme electrolytes are compared. The diglyme‐based electrolyte demonstrates stable cycling over 150 cycles despite a theoretical volume expansion of up to 430% upon sodiation, which results from the formation of a robust and flexible solid–electrolyte interphase (SEI) that maintains electrode integrity. In contrast, carbonate‐based electrolytes exhibit rapid capacity fading due to catalytic decomposition of the solvent on Sn nanoparticles. The findings highlight the critical influence of electrolyte composition and particle size on the stability and reversibility of Sn‐based negative electrodes for NIBs.
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