材料科学
自愈水凝胶
兴奋剂
质子化
阳极
化学工程
复合材料
纳米技术
高分子化学
光电子学
物理化学
有机化学
电极
离子
工程类
化学
作者
Haoyuan Liu,Tianxing Kang,Tianxiang Yang,Shufeng Li,Zhen Ma,Junmin Nan
标识
DOI:10.1021/acsami.5c00037
摘要
Silicon oxide (SiOx) is a promising high-capacity anode material of lithium-ion batteries (LIBs), but the inferior electrical conductivity and apparent bulk effect during cycling still seriously hinder its practical application. In this work, poly(acrylic acid) (PAA) is used as a counterbalance ion in doped protonated polyaniline (PANI), which greatly increases the solubility of PANI in water to successfully design PAA@PANI@SA (N-PPS) hydrogels as the binder of SiOx anode with entangled chain-linked foam structure. The high-density electrostatic interactions between the PAA and PANI chains act as a dynamic link to initiate chain entanglement, providing N-PPS with ultrahigh mechanical strength (maximum peel strength of 0.472 N) and fast self-healing properties. After 300 cycles under different test conditions, the N-PPS electrode capacity remained at 1200 mAh g-1, and the battery works stably. A series of molecular dynamics tests demonstrate that N-PPS has excellent ion transport properties (DLi+ = 7.2 × 10-17) and enhanced conductivity (2.12 × 10-3 S cm-1). Quantitative simulations validate that the sufficient ion channels inside the N-PPS entangled chain foam structure can effectively reduce the energy barrier of lithium-ion diffusion, indicating the inherent advantages of the N-PPS binder and the promising prospects for application in the SiOx anode of LIBs.
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