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Enhancement of the rate capabilities for all-solid-state batteries through the surface oxidation of sulfide solid electrolytes

机译:通过硫化物固体电解质的表面氧化来提高全固态电池的速率能力

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摘要

Lithium-ion conducting sulfide solid electrolytes are promising candidates for all-solid-state lithium ion batteries, which are being developed to meet the increasing demand for high-capacity rechargeable batteries. In this study, a new type of solid electrolyte with a core-shell structure consisting of oxidized-shell surrounding sulfide solid electrolyte (O-SSE) was developed. The influence of the surface oxidation of 80Li(2)S center dot 20P(2)S(5) glass-ceramic electrolyte on a battery using 4 V class cathode material was investigated. The results of X-ray photoelectron spectroscopy depth profiling confirmed that > 80% of the surface of the O-SSE was oxidized from P-S bonds to P-O bonds, and the oxygen remained localized at the surface. The interfacial resistance between the sulfide solid electrolyte and LiNi0.8CO0.15Al0.05O2 (NCA) was significantly decreased by this surface oxidation. The ASSB cell using O-SSE as a cathode solid electrolyte exhibited better discharge performance than 80Li(2)S center dot 20P(2)S(5) glass-ceramic electrolyte and could discharge at a high current density of 2.0 mA.cm(-2). These results demonstrate that surface oxidation of a sulfide solid electrolyte is a new and effective method for reducing the interfacial resistance between the cathode material and solid electrolyte and improving the charge-discharge performance.
机译:锂离子传导硫化物固体电解质是全固态锂离子电池的承诺候选者,正在开发出满足对高容量可充电电池的不断增加的需求。在该研究中,开发了一种具有核 - 壳结构的新型固体电解质,其由周围硫化物固体电解质(O-SSE)组成的氧化壳结构。研究了80LI(2)S中心点20p(2)S(5)玻璃 - 陶瓷电解质在使用4V类阴极材料的电池上的影响的影响。 X射线光电子能谱深度分析的结果证实,O-SSE的表面的80%从P-S键氧化到P-O键,并且氧气保持在表面上。通过该表面氧化显着降低了硫化物固体电解质和LINI0.8CO0.15A10.05O2(NCA)之间的界面抗性。使用O-SSE作为阴极固体电解质的ASSB电池表现出比80LI(2)S中心点20p(2)S(5)玻璃陶瓷电解质更好的放电性能,并且可以以2.0 mA.cm的高电流密度放电( -2)。这些结果表明,硫化物固体电解质的表面氧化是一种新的且有效的方法,用于降低阴极材料和固体电解质之间的界面抗性并改善充放电性能。

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