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通过在高充电速率下控制 SEI 形成来改善硬碳电极性能。

Improvement of Hard Carbon Electrode Performance by Manipulating SEI Formation at High Charging Rates.

机构信息

School of Chemical Engineering , The University of Queensland , St Lucia Campus , Brisbane 4072 , Australia.

出版信息

ACS Appl Mater Interfaces. 2019 Sep 25;11(38):34796-34804. doi: 10.1021/acsami.9b07449. Epub 2019 Sep 10.

Abstract

There is a growing demand for high-rate rechargeable batteries for powering electric vehicles and portable electronics. Here, we demonstrate a strategy for improving electrode performance by controlling the formation of solid electrolyte interphase (SEI). A composite electrode consisting of hard carbon (HC) and carbon nanotubes (CNTs) was used to study the formation of the SEI at different charging rates in an electrolyte consisting of 1 M NaClO in a mixed solvent with ethylene carbonate (EC) and propylene carbonate (PC), as well as fluoroethylene carbonate (FEC) additive. The half-cell method was used to form the SEI at different charging rates (e.g., 1, 10, and 100 A/g). Symmetric capacitor cells were employed to study ion transport properties through the SEI. It was found that the SEI is a primary factor responsible for limiting the capacity of the composite anode material in conventional ester-based electrolytes. The electrode with the SEI formed at 100 A/g exhibited the lowest impedance and delivered nearly twice the capacity of the electrode with the SEI formed at 1 A/g. This significant difference is due to a thin SEI formed at the fast charging rate, as has been observed with ether-based electrolytes. An identical decay rate (0.11 mA h/g per cycle) was observed on the electrodes with SEIs formed at different charging rates in an ester electrolyte. No chemical difference among the three SEI layers was found. However, morphological differences of the SEI layers were observed. This difference is believed to account for the different electrochemical behaviors of the electrodes. This work shows that high charging rates can result in the formation of an optimal SEI layer, contradicting the widely accepted practice of using low charging rates during the SEI formation in alkali-ion batteries.

摘要

人们对可用于电动车辆和便携式电子设备的高倍率可再充电电池的需求日益增长。在这里,我们展示了一种通过控制固体电解质界面(SEI)形成来改善电极性能的策略。使用由硬碳(HC)和碳纳米管(CNT)组成的复合电极,在包含 1 M NaClO 的电解质中研究了在不同充电速率下 SEI 的形成,该电解质的混合溶剂中含有碳酸乙烯酯(EC)和碳酸丙烯酯(PC),以及氟代碳酸乙烯酯(FEC)添加剂。使用半电池方法在不同充电速率(例如 1、10 和 100 A/g)下形成 SEI。采用对称电容器电池研究了离子通过 SEI 的传输特性。结果发现,SEI 是限制复合阳极材料在传统酯基电解质中容量的主要因素。在 100 A/g 下形成 SEI 的电极表现出最低的阻抗,并提供了在 1 A/g 下形成 SEI 的电极容量的近两倍。这种显著差异是由于在快速充电速率下形成的薄 SEI,这在醚基电解质中已经观察到。在酯基电解质中,在不同充电速率下形成 SEI 的电极上观察到相同的衰减率(每循环 0.11 mA h/g)。在三个 SEI 层中未发现化学差异。然而,观察到 SEI 层的形态差异。这种差异被认为是电极的不同电化学行为的原因。这项工作表明,高充电速率可导致形成最佳的 SEI 层,这与在碱离子电池中形成 SEI 期间使用低充电速率的广泛接受的做法相矛盾。

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