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Solid-State Lithium-Metal Batteries Based on Antiperovskite Superionic Conductors

机译:基于钙钛矿型超离子导体的固态锂金属电池

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The present study is focused on a relatively new class of solid-state superionic electrolytes with antiperovskite crystal structure. The solid-state electrolyte layers were produced by casting/delamination and deposited on a graphite-based Cu-supported working electrode. The electrolyte charge transfer resistances, electrochemical performance, and chemical stability in a half-cell configuration were evaluated over a broad temperature range from room temperature up to 100°C. The electrochemical cells with lithium metal as a reference electrode demonstrated linear Arrhenius behavior in the temperature range of 23-100°C confirming the absence of phase transformations. Cyclic voltammetry at 50°C and 100°C confirms that the electrochemical cell performance during lithiation/delithiation from 0.05 to 1.0V is reproducible within at least 100 cycles. The solid-state electrolyte electrochemical stability in contact with lithium metal was confirmed by the absence of specific capacity losses during charge/discharge operations (320 cycles at 50°C and 1/5 C-rate) and the observed decrease in charge transfer resistances. Transport of lithium ions between the lithium metal and solid electrolyte in contact with a graphite working electrode provides evidence that antiperovskites can serve as effective and electrochemicalh/ stable electrolytes for a new generation of all-solid-state lithium-ion or lithium metal batteries.
机译:本研究集中于具有抗钙钛矿晶体结构的一类相对较新的固态超离子电解质。固态电解质层通过流延/分层生产并沉积在石墨基Cu负载的工作电极上。在从室温到最高100°C的宽温度范围内,对半电池结构中的电解质电荷转移电阻,电化学性能和化学稳定性进行了评估。以锂金属为参比电极的电化学电池在23-100°C的温度范围内表现出线性Arrhenius行为,证实了不存在相变。在50°C和100°C的循环伏安法证实,在至少100次循环中,可在0.05V至1.0V的锂化/脱锂期间的电化学电池性能可再现。与锂金属接触的固态电解质电化学稳定性通过在充电/放电操作(在50°C和1/5 C速率下320个循环)过程中不存在比容量损失以及所观察到的电荷转移电阻降低而得到证实。锂离子在锂金属和与石墨工作电极接触的固体电解质之间的传输提供了证据,证明钙钛矿可以用作新一代全固态锂离子或锂金属电池的有效且电化学/稳定的电解质。

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