材料科学
电解质
导电体
电容
共晶体系
离子电导率
电导率
纳米技术
储能
延展性(地球科学)
超级电容器
电池(电)
弹性(材料科学)
阳极
工作(物理)
材料设计
电容感应
快离子导体
电极
自愈水凝胶
电化学
电容器
化学工程
压力(语言学)
离子键合
限制
瞬态(计算机编程)
作者
Yixue Chen,Haotian Xie,Qihang Fan,Xuemin Cui
标识
DOI:10.1021/acsami.5c19296
摘要
Conventional eutectic quasi-solid electrolytes (EQSEs), despite their intrinsic safety and sustainability, are fundamentally limited by the mechanical-conductivity trade-off, severely restricting practical deployment. Here, a lignin-engineered double-cross-linked EQSE is reported that overcomes these challenges through synergistic dual-dynamic networks: (1) an organic polyacrylamide/poly(acrylic acid) (PAM/PAA) framework establishing continuous ion-transport channels and (2) Fe 3+ -coordinated cross-links coupled with hydrogen bonding resolving the mechanical-conductivity trade-off. The resultant DES–LN–Fe 3+ electrolyte simultaneously achieves a high ionic conductivity of 0.031 S cm –1 at 25 °C and exceptional ductility (851% strain). When deployed in flexible supercapacitors, it delivers a high specific capacitance of 310.6 F g –1 (0.1 A g –1 ) with exceptional low-temperature resilience (45.8% capacity retention at −40 °C) and cycling stability (95.7% after 10,000 cycles). Notably, the electrolyte doubles as a high-sensitivity strain sensor (gauge factor = 3.183), enabling real-time monitoring of biomechanical motions. This work establishes a dynamic dual-cross-linking paradigm to design multifunctional quasi-solid electrolytes for integrated energy storage and sensing platforms in extreme environments.
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