阳极
锂(药物)
复合数
硅
材料科学
石墨
离子
喷雾干燥
化学工程
纳米颗粒
电极
复合材料
分析化学(期刊)
纳米技术
光电子学
化学
有机化学
内分泌学
物理化学
工程类
医学
作者
Jeng-Ywan Shih,Ying-Ru Chen,Ying-Jeng James Li,Tai‐Feng Hung,Li-Fan Hsu,Yi-De Tsai,Sayee Kannan Ramaraj,Rajan Jose,Chelladurai Karuppiah,Chun‐Chen Yang
标识
DOI:10.1021/acssuschemeng.2c03506
摘要
Morphology plays a vital role in controlling the volume variation in Si-based anode materials and enhances lithium-ion battery performances. Here, we demonstrated advanced techniques that combine electrostatic self-assembly and spray-drying methods to form 3D spherical-like silicon/graphite (denoted "Si/G") composite anode materials. This spherical morphology alleviates issues relating to silicon volume changes that occur in high-rate lithium-ion batteries. Commercial graphite (G) flakes were initially mixed with silicon nanoparticles (ca. 50 nm) to form a bare-Si/G composite through electrostatic interaction; spherical-like composite particles were then obtained through single and double spray-drying processes, giving samples SD1-Si/G and SD2-Si/G, respectively. We examined the charge/discharge characteristics of the fabricated electrodes (CR2032-type coin cells) in the voltage range 0.02–1.5 V (vs Li/Li+). The as-fabricated bare-Si/G, SD1-Si/G, and SD2-Si/G half-cells provided initial discharge specific capacities of 897, 866, and 1020 mA h g–1, respectively. The SD2-Si/G half-cell shows better cycling stability at a high current rate of 400 mA g–1 than the SD1-Si/G and bare-Si/G half-cells due to effective inhibition of the volume change in the more stable spherical structure of the SD2-Si/G composite, as evidenced through in situ dilatometry. Thus, the spherical Si/G composite material produced through this simple spray-drying process had structural characteristics that could effectively resist silicon's high expansion rate, lower the production rate of broken silicon particles, and improve the electrochemical performance of the anode.
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