Si3N4 作为硅的替代品在全固态锂离子电池中的阳极应用

Energy Storage Pub Date : 2024-08-05 DOI:10.1002/est2.70010
Anil Kumar Sharma, Khushbu Sharma, Mukesh Kumar Gupta, Fangqin Guo, Takayuki Ichikawa, Ankur Jain, Shivani Agarwal
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引用次数: 0

摘要

将可再生能源发电与电化学储能相结合,可以解决可再生能源发电的间歇性问题,还能有效缩小供需差距。最近的研究表明,基于 Si3N4 的负电极具有理论容量大、工作电位合适、极化极低的特点,是锂离子电池的理想选择。在本研究中,Si3N4 被用作全固态锂离子电池的负极材料,以硼氢化锂为固态电解质,锂箔为反电极。利用电静态充放电分析研究了其电化学特性,并利用 X 射线衍射(XRD)详细研究了锂化脱锂的机理。在 0.05 C 电流速率下,复合材料在第一个循环中获得的最高容量为 1700 mAhg-1,5 个循环后降至 370 mAhg-1。然而,在随后的循环中观察到了容量的稳定性,在 150 个循环中可达到近 88% 的容量保持率。电化学循环前后的界面电阻分别为 326 Ω 和 13 kΩ,这也得到了微观结构研究的支持,在微观结构研究中,由于热化学反应观察到了裂纹。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Si3N4 as an Alternative of Silicon for the Anode Application in All-Solid-State Li-Ion Batteries

The intermittent nature of renewable energy generation can be tackled by integrating them with electrochemical energy storage, which can also close the gap between supply and demand effectively. It has recently been demonstrated that Si3N4-based negative electrodes are a promising option for lithium-ion batteries due to their large theoretical capacity and appropriate working potential with extremely low polarization. In the present work, Si3N4 was utilized as anode material in all-solid-state lithium-ion battery with lithium borohydride as a solid electrolyte and Li foil placed as a counter electrode. The electrochemical properties were investigated using galvanostatic charge/discharge profiling whereas the mechanism of lithiation delithiation was investigated in detail using x-ray diffraction (XRD). The highest capacity of the composite materials was obtained as 1700 mAhg−1 at 0.05 C current rate in the first cycle, which is reduced to 370 in 5 cycles. However, a stability in the capacity was observed in subsequent cycles and a retention of almost 88% could be achieved in 150 cycles. The interfacial resistance before and after the electrochemical cycling was observed as 326 Ω and 13 kΩ, respectively which is also supported by the microstructural investigations where the cracks are observed because of thermochemical reactions.

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