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超薄锂金属电极在软包电池中的电化学示意图。

Electrochemical Diagram of an Ultrathin Lithium Metal Anode in Pouch Cells.

机构信息

Beijing Key Laboratory of Green Chemical Reaction Engineering and Technology, Department of Chemical Engineering, Tsinghua University, Beijing, 100084, China.

Advanced Research Institute of Multidisciplinary Science, Beijing Institute of Technology, Beijing, 100081, China.

出版信息

Adv Mater. 2019 Sep;31(37):e1902785. doi: 10.1002/adma.201902785. Epub 2019 Aug 5.

Abstract

Lithium (Li) metal is regarded as a "Holy Grail" electrode for next-generation high-energy-density batteries. However, the electrochemical behavior of the Li anode under a practical working state is poorly understood, leading to a gap in the design strategy and the aim of efficient Li anodes. The electrochemical diagram to reveal failure mechanisms of ultrathin Li in pouch cells is demonstrated. The working mode of the Li metal anode ranging from 1.0 mA cm /1.0 mAh cm (28.0 mA/28.0 mAh) to 10.0 mA cm /10.0 mAh cm (280.0 mA/280.0 mAh) is investigated and divided into three categories: polarization, transition, and short-circuit zones. Powdering and the induced polarization are the main reasons for the failure of the Li electrode at small current density and capacity, while short-circuit occurs with the damage of the separator leading to safety concerns being dominant at large current and capacity. The electrochemical diagram is attributed from the distinctive plating/stripping behaviors of Li metal, accompanied by dendrites thickening and/or lengthening, and heterogeneous distribution of dendrites. A clear understanding in the electrochemical diagram of ultrathin Li is the primary step to rationally design an effective Li electrode and render a Li metal battery with high energy density, long lifespan, and enhanced safety.

摘要

金属锂被视为下一代高能量密度电池的“圣杯”电极。然而,人们对实用工作状态下锂阳极的电化学行为了解甚少,这导致在设计策略和高效锂阳极的目标之间存在差距。展示了揭示超薄锂在袋式电池中失效机制的电化学图。研究了工作模式在 1.0 mA cm/1.0 mAh cm(28.0 mA/28.0 mAh)到 10.0 mA cm/10.0 mAh cm(280.0 mA/280.0 mAh)范围内的锂金属阳极,分为三个区域:极化区、过渡区和短路区。在小电流密度和容量下,粉末化和诱导极化是锂电极失效的主要原因,而在大电流和容量下,短路是由于隔离器损坏导致安全问题成为主导。电化学图归因于锂金属独特的电镀/剥离行为,伴随着枝晶变粗和/或变长,以及枝晶的不均匀分布。对超薄锂的电化学图有清晰的认识是合理设计有效锂电极的首要步骤,并使具有高能量密度、长寿命和增强安全性的锂金属电池成为可能。

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