薄膜
材料科学
X射线光电子能谱
循环伏安法
电化学
电解质
电导率
化学工程
硫化物
金属
快离子导体
玻璃碳
分析化学(期刊)
电极
纳米技术
化学
冶金
有机化学
物理化学
工程类
作者
Madison Olson,Jacob Wheaton,Mary Okkema,Nicholas Oldham,Steve W. Martin
标识
DOI:10.1021/acsaem.3c00294
摘要
Na4P2S7–6xO4.62xN0.92x (NaPSON) glassy solid electrolytes (GSEs) were prepared and tested for their electrochemical properties and processability into thin films. The x = 0.2 composition (NaPSON-2) was found to be highly conducting, non-crystallizable, largely stable against Na-metal, and supports symmetric cell cycling up to >100 μA cm–2 without shorting. For these reasons, it was processed into thin films drawn to 50 μm and tested in symmetric and asymmetric cells. Measurements of the sodium ion conductivity using symmetric cells demonstrated that the conductivity of NaPSON-2 was unchanged by film forming. Galvanostatic cycling at 5 μA cm–2 of a 1.3 mm thick disc of NaPSON-2 showed stability over 450 h, while cycling a 50 μm thin film of NaPSON-2 showed a very slow growth in the resistance. Cyclic voltammetry and X-ray photoelectron spectroscopy of the NaPSON-2 thin film GSE revealed that it did not react with Na-metal at its surface, but rather in the bulk of the film, showing S, Na2S, and Na3P reaction products. The source of the surface stability was determined to be the preferential segregation of trigonally coordinated nitrogen. These low-cost and easily processed NaPSON GSEs provide a system of materials that could provide for significantly lower cost higher energy density grid-scale batteries.
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