G. Fredi, S. Jeschke, Athmane Boulaoued, J. Wallenstein, M. Rashidi, Fang Liu, R. Harnden, D. Zenkert, J. Hagberg, G. Lindbergh, P. Johansson, L. Stievano, L. Asp
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Here we further advance this understanding by linking CF microstructure to the lithium insertion mechanism and the resulting electrochemical capacity. Different PAN-based CFs ranging from intermediate- to high-modulus types with distinct differences in microstructure are characterised in detail by SEM and HR-TEM and electrochemical methods. Furthermore, the mechanism of Li-ion intercalation during charge/discharge is studied by in situ confocal Raman spectroscopy on individual CFs. Raman G band analysis reveals a Li-ion intercalation mechanism in the high-modulus fibre reminiscent of that in crystalline graphite. Also, the combination of a relatively low capacity of the high-modulus CFs (ca. 150 mAh g−1) is shown to be due to that the formation of a staged structure is frustrated by an obstructive turbostratic disorder. 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引用次数: 73
摘要
碳纤维(CFs)最初用于结构复合材料,也被证明是高容量锂离子电池的负极。因此,碳纤维可以用作结构电极;在多功能结构电池中同时承载机械负荷和储存电能。迄今为止,基于对石墨微观结构与机械性能之间关系的深刻理解,所有CF微结构设计都是为了实现目标机械性能,例如高强度或高刚度。在这里,我们通过将CF微观结构与锂插入机制和由此产生的电化学容量联系起来,进一步推进了这一理解。利用扫描电镜(SEM)、透射电镜(hrtem)和电化学方法对中高模量型pan基碳纤维进行了详细表征。此外,利用原位共聚焦拉曼光谱研究了锂离子在充放电过程中的插层机理。拉曼G带分析揭示了锂离子在高模量纤维中的嵌入机制,与在结晶石墨中的嵌入机制相似。此外,高模量碳纤维的相对低容量(约150 mAh g−1)的组合被证明是由于阶段结构的形成受到阻碍的涡轮层紊乱。相比之下,具有更高容量(约300 mAh g−1)的中模量碳纤维具有拉曼光谱,表明锂离子插入机制更接近于部分无序碳。基于这些发现,可以通过调整石墨的顺序和晶粒尺寸来实现具有改进的多功能性能的碳纤维。
Graphitic microstructure and performance of carbon fibre Li-ion structural battery electrodes
Carbon fibres (CFs), originally made for use in structural composites, have also been demonstrated as high capacity Li-ion battery negative electrodes. Consequently, CFs can be used as structural electrodes; simultaneously carrying mechanical load and storing electrical energy in multifunctional structural batteries. To date, all CF microstructural designs have been generated to realise a targeted mechanical property, e.g. high strength or stiffness, based on a profound understanding of the relationship between the graphitic microstructure and the mechanical performance. Here we further advance this understanding by linking CF microstructure to the lithium insertion mechanism and the resulting electrochemical capacity. Different PAN-based CFs ranging from intermediate- to high-modulus types with distinct differences in microstructure are characterised in detail by SEM and HR-TEM and electrochemical methods. Furthermore, the mechanism of Li-ion intercalation during charge/discharge is studied by in situ confocal Raman spectroscopy on individual CFs. Raman G band analysis reveals a Li-ion intercalation mechanism in the high-modulus fibre reminiscent of that in crystalline graphite. Also, the combination of a relatively low capacity of the high-modulus CFs (ca. 150 mAh g−1) is shown to be due to that the formation of a staged structure is frustrated by an obstructive turbostratic disorder. In contrast, intermediate-modulus CFs, which have significantly higher capacities (ca. 300 mAh g−1), have Raman spectra indicating a Li-ion insertion mechanism closer to that of partly disordered carbons. Based on these findings, CFs with improved multifunctional performance can be realised by tailoring the graphitic order and crystallite sizes.