聚丙烯腈
材料科学
纳米复合材料
阳极
纳米纤维
化学工程
锂(药物)
碳化
静电纺丝
碳纳米纤维
碳纤维
锂离子电池
复合数
硅
电池(电)
纳米技术
复合材料
碳纳米管
电极
聚合物
冶金
扫描电子显微镜
化学
内分泌学
医学
功率(物理)
物理
物理化学
量子力学
工程类
作者
Ali Ansari Hamedani,Cleva W. Ow‐Yang,Serap Hayat Soytaş
标识
DOI:10.1016/j.jallcom.2022.164734
摘要
The high capacity of silicon (Si) for lithium incorporation makes it a promising anode material for lithium-ion batteries; however, pulverization of Si due to huge volume changes during lithiation/delithiation leads to significant capacity loss during cycling. To address challenges in low cyclability, nanostructured Si in carbon nanocomposites offers an attractive solution. In this study, we report an efficient method for the synthesis of a nanocomposite containing Si nanoparticles homogeneously embedded in an electrically conductive carbon nanofiber (CNF) network. Electrospinning of polyacrylonitrile (PAN) solution containing hydrolyzed tetraethyoxysilane (TEOS), as a Si precursor, and subsequent carbonization of hybrid nanofibers yielded a composite of SiO 2 ultrafine nano-domains in the carbon network (C-SiO 2 ). Low temperature molten salt-assisted aluminothermic reduction of C-SiO 2 nanofibers allowed us to produce a C-Si/SiO x nanocomposite without forming detrimental SiC, which is thermodynamically favorable at high temperatures in a system with a high interfacial surface area between the carbon and SiO 2 phases. The nanocomposite C-Si/SiO x anodes showed a reversible capacity of 860 mAh g −1 at a current rate of 200 mA g −1 , retaining a capacity of 680 mAh g −1 after 100 cycles. In addition, the nanocomposite anodes delivered a reversible capacity of 569 mAh g −1 at a current rate of 400 mA g −1 while maintaining 95% of maximum capacity after subsequent 100 cycles. This study demonstrates the capability of designing nanocomposite anodes from reaction precursors combined with low-temperature aluminothermic reduction to produce a capacity-retaining anode composite of Si nanocrystals uniformly dispersed in the carbon matrix. • Electrospinning of a hybrid solution yielded SiO x domains homogeneously distributed throughout the nanofibers. • SiO 2 was reduced to Si by a low-temperature aluminothermic reduction with Al/AlCl 3 . • The nanocomposite electrodes of C-Si/SiO x showed excellent capacity retention and stability.
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