Liyang Lin, Mengjun Li, Ying Yan, Yuanhao Tian, Juan Qing and Susu Chen
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引用次数: 0
摘要
硅作为锂离子电池的负极,其体积膨胀和导电性差的特点极大地限制了其应用。虽然硅的纳米结晶及其表面碳涂层可以在一定程度上得到改善,但颗粒聚集和结构不稳定等严重问题仍未得到有效解决。本文通过液相法、冷冻干燥技术和热处理,成功制备了明胶和海藻酸钠(GE+SA)衍生的碳/硅复合材料。硅纳米颗粒(NPs)被均匀地包裹在掺杂 N 的碳的三维网络中,该网络具有丰富的孔隙结构。在电流密度为 1 A g-1 的条件下循环 300 次后,特定 Si@C 复合电极的可逆容量保持在 580 mAh g-1,显示出良好的循环稳定性。同时,该阳极还具有优异的速率性能,在电流密度为 0.1、0.5、1 和 2 A g-1 时的可逆容量分别为 2230、1458、1101 和 686.6 mAh g-1。GE+SA 衍生的碳/硅复合材料有效地解决了颗粒聚集和碳/硅界面结构不稳定的问题,可以成为锂离子电池负极材料的候选材料之一。
Gelatin and sodium alginate derived carbon/silicon composites as high-performance anode materials for lithium-ion batteries†
The volume expansion and poor conductivity greatly limit the application of silicon as an anode for lithium-ion batteries. Although nanocrystallization of silicon and its surface carbon coating can be improved to some extent, the serious problems of particle aggregation and structural instability have not been effectively solved. In this paper, gelatin and sodium alginate (GE + SA) derived carbon/silicon composites are successfully prepared by a liquid-phase method, the freeze-drying technique, and heat treatment. Si nanoparticles (NPs) are uniformly encapsulated in a three-dimensional network of N-doped carbon that is enriched with a rich pore structure. The reversible capacity of the particular Si@C composite electrode was maintained at 580 mA h g−1 after 300 cycles at a current density of 1 A g−1, showing good cycling stability. Meanwhile, the anode also has excellent rate performance with reversible capacities of 2230, 1458, 1101, and 686.6 mA h g−1 at current densities of 0.1, 0.5, 1, and 2 A g−1, respectively. The GE + SA derived carbon/silicon composites effectively solve the problems of particle aggregation and an unstable carbon/silicon interface structure and can become candidates for anode materials in lithium-ion batteries.