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Investigation of Reaction Kinetics in Carbon Anode with Nano-Fillers through Impedance Spectroscopy

机译:纳米填料通过阻抗光谱研究碳阳极反应动力学研究

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Lithium-ion batteries have been very successful in consumer electronics as viable and efficient power sources for many small and portable devices such as mobiles, laptop, watches, camcorders, PDAs, cameras and other communication devices. However, poor electronic conduction in electrodes due to an unstable and fragile conducting network of traditional conducting additives is still the limitation for large scale commercialization of this energy storage technology in automotives (such as EVs, HEVs, PHEVs, etc.) where high power density is desired frequently. In addition, poor contact due to large size of active material and sluggish kinetics makes it difficult to achieve their full theoretical capacities at a practical level. The conducting network in an electrode influences the performance of charge transfer kinetics at the electrode-electrolyte interface and ion migration through the solid electrolyte interface (SEI) layer as suggested by an earlier study. In graphitic anode, when an ion of lithium is inserted into the material, the crystal structure of the active material changes with the state of charge (SOC), and the resulting changes affect the intercalation/deintercalation reactions.
机译:锂离子电池在消费电子产品中是非常成功的,因为许多小型和便携式设备,如移动设备,笔记本电脑,手表,摄像机,PDA,摄像机和其他通信设备等许多小型和便携式设备。然而,由于传统导电性添加剂的不稳定和脆弱的网络导致电极的电子传导差仍然是汽车在汽车(例如EVS,HEV,PHEV等)中大规模商业化的限制,其中高功率密度经常需要。此外,由于大尺寸的活性材料和缓慢的动力学,接触不良,使其难以在实际水平下实现完全理论能力。电极中的导电网络影响电极 - 电解质界面处的电荷转移动力学的性能和通过先前研究所提出的通过固体电解质界面(SEI)层的离子迁移。在石墨阳极中,当将锂的离子插入材料中时,活性物质的晶体结构随着电荷状态(SOC)而变化,并且所得的变化影响插入/脱嵌反应。

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