电泳沉积磷酸铁锂阴极表面的电化学循环诱导电容成分

Crystals Pub Date : 2024-07-18 DOI:10.3390/cryst14070658
Byoung-Nam Park
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引用次数: 0

摘要

在我们的研究中,我们利用交流电压进行电泳沉积(EPD),研究高 C 速率电化学反应如何影响磷酸铁锂(LFP)锂离子电池中的伪电容电荷存储。这种方法大大提高了电池的比容量,在 1 C 速率下可达到约 90 mAh/g,同时具有出色的循环稳定性。虽然我们观察到电池容量在多次循环后有所下降,但电池的电荷存储的伪电容贡献却明显增加。这表现在:CV 期间的峰值位置和电流保持一致,扩散常数稳定在 9.6 × 10-9 cm2∙s-1 的水平。这些发现凸显了电池的耐用性,尤其是在高需求情况下。在经过约 500 次的循环后,与 Fe2+/Fe3+ 氧化还原过程相关的氧化还原峰值在大小和位置上保持不变,这表明电池具有出色的可逆性。
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An Electrochemical-Cycling-Induced Capacitive Component on the Surface of an Electrophoretic-Deposited Lithium Iron Phosphate Cathode
In our research, we apply electrophoretic deposition (EPD) using AC voltage to investigate how high-C-rate electrochemical reactions affect pseudocapacitive charge storage in lithium iron phosphate (LFP) Li-ion batteries. This method significantly raises the battery’s specific capacity, achieving ~90 mAh/g at a 1 C-rate, along with outstanding cycle stability. Although we observe some capacity reduction over numerous cycles, there is a notable increase in the pseudocapacitive contribution to the battery’s charge storage. This is demonstrated by the consistent peak positions and currents during CV and a stable diffusion constant maintained at 9.6 × 10−9 cm2∙s−1. These findings highlight the battery’s durability, especially in high-demand scenarios. After an extended cycling period of ~500 cycles, the redox peaks related to the Fe2+/Fe3+ redox processes remain unchanged in terms of magnitude and position, indicating the battery’s excellent reversibility.
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