材料科学
锂(药物)
离子电导率
电极
电解质
离子
电化学
离子键合
纳米技术
枝晶(数学)
复合数
离子运输机
快离子导体
焊剂(冶金)
化学工程
热传导
沉积(地质)
限制电流
电导率
电阻率和电导率
聚合物
离子液体
导电体
电场
聚焦离子束
作者
Sha Peng,Jia Chen,Yu Li,Ying Tao,L Zhang,K. Liu,Zhihong Liu,Xueqing Liu
摘要
ABSTRACT The random distribution of one‐dimensional nanofillers in composite polymer electrolytes (CPEs) typically results in tortuous ion transport pathways, severely limiting ionic conductivity and Li⁺ flux uniformity. Herein, an innovative electric field‐assisted strategy is proposed to construct vertically aligned ion channels in CPEs using lithiated halloysite nanotubes (HNTs–SO₃Li) embedded within a polyurethane acrylate/polyethylene glycol diacrylate (PUA/PEGDA) matrix. Under an alternating electric field, the nanotubes orient perpendicularly, forming continuous, low‐tortuosity pathways that significantly enhance room‐temperature ionic conductivity. The aligned structure not only shortens Li⁺ transport distances but also homogenizes ion flux at the electrode interface, effectively suppressing lithium dendrite growth. Electrochemical characterization reveals exceptional stability. Three‐dimensional structural reconstruction and ion transport simulations further demonstrate that the ordered channels promote uniform Li⁺ distribution and faster ion kinetics compared to disordered systems. This study provides a scalable and efficient approach to designing high‐performance CPEs for next‐generation solid‐state batteries, addressing critical challenges in ionic conductivity, interfacial stability, and dendrite suppression.
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