PANI-Encapsulated Si Nanocomposites with a Chemical Bond Linkage in the Interface Exhibiting Higher Electrochemical Stability as Anode Materials for Lithium-Ion Batteries

材料科学 聚苯胺 共价键 化学键 电化学 聚合 锂(药物) 化学工程 纳米颗粒 表面改性 苯胺 化学稳定性 纳米复合材料 阳极 复合材料 电极 高分子化学 纳米技术 聚合物 有机化学 物理化学 化学 内分泌学 工程类 医学
作者
Renzhong Huang,Yuqiu Xie,Qing Chang,Jian Xiong,Shiqi Guan,Songdong Yuan,Guodong Jiang
出处
期刊:NANO [World Scientific]
卷期号:14 (06): 1950078-1950078 被引量:11
标识
DOI:10.1142/s1793292019500784
摘要

A covalent linkage between polyaniline (PANI) and Si nanoparticles in PANI-encapsulated Si nanocomposites was proposed and achieved by a facile and economical synthetic strategy, in which NH 2 -grafted Si was first obtained via a chemical modification of Si surface and the polymerization of aniline initiated at NH 2 group surface was readily accomplished to get PANI shell. The characterizations suggested that NH 2 groups were successfully introduced onto Si surface and PANI-encapsulated Si nanocomposites with a core/shell structure were fabricated. Electrochemical tests showed that our proposed Si nanocomposites delivered a high initial specific capacity of 2135[Formula: see text]mAh/g and retained 848[Formula: see text]mAh/g after 100 charge/discharge cycles at a current density of 0.1[Formula: see text]A/g, which were superior than that of the normal PANI-encapsulated Si nanocomposites with the absence of chemical bonds in the interface. The enhanced electrochemical performance was ascribed to the surface chemical modification and the introduction of chemical bond in the interface. NH 2 group function of Si could improve the homogeneity of encapsulated PANI shell. Additionally, PANI was tightly anchored to Si nanoparticles via a covalent bond between silicon and PANI, which would greatly inhibit the separation of PANI from Si surface during the expansion/contraction of Si particles. Thus, the structural integrity was maintained. Besides, PANI layer with a unique structure promoted the transport of both electrons and lithium ions.
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