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聚丙烯酸粘结剂分子量对锂离子电池硅合金/石墨复合负极性能的影响

Influence of the Molecular Weight of Poly-Acrylic Acid Binder on Performance of Si-Alloy/Graphite Composite Anodes for Lithium-Ion Batteries.

作者信息

Kasinathan Raam, Marinaro Mario, Axmann Peter, Wohlfahrt-Mehrens Margret

机构信息

ZSW-Center for Solar Energy and Hydrogen Research Baden-Württemberg Helmholtzstraße 8 89081 Ulm Germany.

出版信息

Energy Technol (Weinh). 2018 Nov;6(11):2256-2263. doi: 10.1002/ente.201800302. Epub 2018 Oct 10.

Abstract

In this study Si-alloy/graphite composite electrodes are manufactured using water-soluble poly-acrylic acid (PAA) binder of different molecular weights (250, 450 and 1250 kg mol). The study aims to assess the behavior of the different binders across all the steps needed for electrodes preparation and on their influence on the electrodes electrochemical behavior. At first, rheological properties of the water-based slurries containing Si-alloy, graphite, conductive carbon and PAA are studied. After coating, the adhesion strength and electronic conductivity of the manufactured electrodes are evaluated and compared. Finally, the electrochemical behavior of the composite anodes is evaluated. The electrodes show high gravimetric as well as high areal capacity (∼750 mAh/g; ∼3 mAh/cm). The influence of the binder on the first cycle irreversible loss is considered as well as its effectiveness in minimizing the electrode volume variation upon lithiation/de-lithiation. It is finally demonstrated that the use of 8 wt.% of PAA-250k in the electrode formulation leads to the best performance in terms of high rate performance and long term stability.

摘要

在本研究中,使用不同分子量(250、450和1250 kg·mol)的水溶性聚丙烯酸(PAA)粘结剂制备了硅合金/石墨复合电极。该研究旨在评估不同粘结剂在电极制备所需的所有步骤中的行为,以及它们对电极电化学行为的影响。首先,研究了含有硅合金、石墨、导电碳和PAA的水基浆料的流变性能。涂覆后,对制备电极的粘附强度和电子电导率进行评估和比较。最后,评估复合阳极的电化学行为。这些电极显示出高比容量以及高面积容量(约750 mAh/g;约3 mAh/cm)。还考虑了粘结剂对首次循环不可逆损失的影响,以及其在锂化/脱锂时最小化电极体积变化的有效性。最终证明,在电极配方中使用8 wt.% 的PAA-250k在高倍率性能和长期稳定性方面表现出最佳性能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc6d/6358114/ce9d1d75f690/ENTE-6-2256-g001.jpg

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