聚丙烯腈
材料科学
电极
阳极
硅
锂离子电池
化学工程
锂(药物)
纳米颗粒
聚合物
原子转移自由基聚合
聚合
纳米技术
高分子化学
电池(电)
复合材料
物理化学
光电子学
化学
量子力学
医学
物理
功率(物理)
内分泌学
工程类
作者
Lei Luo,Yunlong Xu,Huang Zhang,Xiaona Han,Hui Dong,Xing Xu,Chao Chen,Yang Zhang,Jiahao Lin
标识
DOI:10.1021/acsami.6b03046
摘要
Well-defined polyacrylonitriles (PANs) with different molecular weights were synthesized through an activator regenerated by electron-transfer atom-transfer radical polymerization method and employed as binders in silicon negative electrode for lithium-ion batteries. Compared with poly(vinylidene fluoride) and carboxyl methyl cellulose as binders, the electrode performance of PANs is well-improved. Specifically, at 100 mA g–1 from 0.01 to 1.5 V, the initial discharge capacity of PAN100-based electrode is 4147.8 mA h g–1 and still remains about 1639.6 mA h g–1 over 50 cycles. A comprehensive understanding on the improvement mechanism is preliminarily discussed. The results indicate that the superior performance largely depends on the higher lithium ion diffusion efficiency in PAN which results from the weak interaction between lithium ions and PAN polymer chain, and the hydrogen bonds among the nitrile group (C≡N) of PAN, Si nanoparticles, and the current collector, which will lead to an efficient coating of PAN with the Si particles and well-improved adhesion strength, synergistically depressing the structural deterioration of silicon electrodes.
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