电解质
海藻糖
化学
柔性电子器件
储能
阳极
法拉第效率
纳米技术
成核
水溶液
胶粘剂
化学工程
材料科学
有机化学
图层(电子)
电极
工程类
功率(物理)
物理化学
物理
量子力学
作者
Song Yang,Qing Wu,Yue Li,Fusheng Luo,Jinlong Zhang,Kui Chen,Yang You,Jun Huang,Haibo Xie,Yiwang Chen
标识
DOI:10.1002/ange.202409160
摘要
Flexible and high‐performance aqueous Zn‐ion batteries (ZIBs), coupled with low cost and safe, are considered as one of the most promising energy storage candidates for wearable electronics. However, most of hydrogel electrolytes suffer from poor mechanical properties and interfacial chemistry, which limits them to suppressed performance levels in flexible ZIBs, especially under harsh mechanical strains. Herein, a bio‐inspired multifunctional hydrogel electrolyte network (polyacrylamide (PAM)/trehalose) with improved mechanical and adhesive properties was developed via a simple trehalose network‐repairing strategy to stabilize the interfacial chemistry for highly reversible flexible ZIBs. As a result, the trehalose‐modified PAM hydrogel exhibits a superior strength and stretchability up to 100 kPa and 5338%, respectively, as well as strong adhesive properties to various substrates. Also, the PAM/trehalose hydrogel electrolyte provides superior anti‐corrosion capability for Zn anode and regulates Zn nucleation/growth, resulting in achieving a high Coulombic efficiency of 98.8%, and long‐term stability over 2400 h. Importantly, the flexible Zn//MnO2 pouch cell exhibits excellent cycling performance under different bending conditions, which offers a great potential in flexible energy‐related applications and beyond.
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