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用于固态锂金属电池的从平面锂到具有可流动界面的三维锂的转变。

Transforming from planar to three-dimensional lithium with flowable interphase for solid lithium metal batteries.

作者信息

Liu Yayuan, Lin Dingchang, Jin Yang, Liu Kai, Tao Xinyong, Zhang Qiuhong, Zhang Xiaokun, Cui Yi

机构信息

Department of Materials Science and Engineering, Stanford University, Stanford, CA 94305, USA.

Department of Chemical Engineering, Stanford University, Stanford, CA 94305, USA.

出版信息

Sci Adv. 2017 Oct 20;3(10):eaao0713. doi: 10.1126/sciadv.aao0713. eCollection 2017 Oct.

Abstract

Solid-state lithium (Li) metal batteries are prominent among next-generation energy storage technologies due to their significantly high energy density and reduced safety risks. Previously, solid electrolytes have been intensively studied and several materials with high ionic conductivity have been identified. However, there are still at least three obstacles before making the Li metal foil-based solid-state systems viable, namely, high interfacial resistance at the Li/electrolyte interface, low areal capacity, and poor power output. The problems are addressed by incorporating a flowable interfacial layer and three-dimensional Li into the system. The flowable interfacial layer can accommodate the interfacial fluctuation and guarantee excellent adhesion at all time, whereas the three-dimensional Li significantly reduces the interfacial fluctuation from the whole electrode level (tens of micrometers) to local scale (submicrometer) and also decreases the effective current density for high-capacity and high-power operations. As a consequence, both symmetric and full-cell configurations can achieve greatly improved electrochemical performances in comparison to the conventional Li foil, which are among the best reported values in the literature. Noticeably, solid-state full cells paired with high-mass loading LiFePO exhibited, at 80°C, a satisfactory specific capacity even at a rate of 5 C (110 mA·hour g) and a capacity retention of 93.6% after 300 cycles at a current density of 3 mA cm using a composite solid electrolyte middle layer. In addition, when a ceramic electrolyte middle layer was adopted, stable cycling with greatly improved capacity could even be realized at room temperature.

摘要

固态锂金属电池因其显著的高能量密度和降低的安全风险,在下一代储能技术中备受瞩目。此前,人们对固体电解质进行了深入研究,并确定了几种具有高离子电导率的材料。然而,在使基于锂金属箔的固态系统可行之前,仍至少存在三个障碍,即锂/电解质界面处的高界面电阻、低面容量和低功率输出。通过在系统中引入可流动界面层和三维锂来解决这些问题。可流动界面层能够适应界面波动,并始终保证优异的附着力,而三维锂则显著降低了从整个电极水平(几十微米)到局部尺度(亚微米)的界面波动,同时也降低了高容量和高功率运行时的有效电流密度。因此,与传统锂箔相比,对称和全电池配置都能实现大幅改善的电化学性能,这些性能是文献中报道的最佳值之一。值得注意的是,与高质量负载的磷酸铁锂配对的固态全电池,在80°C下,即使在5 C(110 mA·hour/g)的倍率下也表现出令人满意的比容量,并且使用复合固体电解质中间层在3 mA/cm²的电流密度下循环300次后容量保持率为93.6%。此外,当采用陶瓷电解质中间层时,甚至在室温下也能实现具有大幅提高容量的稳定循环。

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