Construction of amphoteric hydrogel electrolytes with charge modification: An investigation of ion migration mechanism and antibacterial property

电解质 机制(生物学) 离子 电荷(物理) 财产(哲学) 化学工程 材料科学 化学物理 化学 物理化学 有机化学 物理 电极 工程类 哲学 量子力学 认识论
作者
Shao-Fei Sun,Xiaoya Zhao,Ce Gao,Ling‐Ping Xiao,Run‐Cang Sun
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:495: 153781-153781 被引量:3
标识
DOI:10.1016/j.cej.2024.153781
摘要

Some challenges still hinder the advancement of hydrogel electrolytes, such as low ionic conductivity and restricted flexibility, which obstacle the effective integration of supercapacitors for flexible wearable devices. We developed an amphoteric hydrogel electrolyte with a highly ionic conductivity of 46.64 mS·cm−1, 927.32 % of tensile strain and compressive strain to 85 % in ambient air. Through lignin sulfomethylation and chitosan quaternization, abundant charge groups were introduced to the structure of hydrogel electrolyte to achieve charge modification. These charged groups not only promoted the dissociation of KOH, but also formed ion transport channels to enhance the migration of K+ and OH–. Note that the hydrogel also had significant antibacterial activity, enhancing its practical applicability. Moreover, the flexible supercapacitor constructed with this hydrogel electrolyte showed excellent capacitive performance, achieving a notable specific capacitance of 192.6F·g−1 and a high energy density of 45.2 Wh·kg−1 under a current density of 0.5 A·g−1. In addition, the flexible supercapacitor also demonstrated remarkable rate performance and cycle stability, which maintained nearly constant coulombic efficiency (99.7 %) and retaining 86.1 % of capacitance retention after 10,000 charge–discharge cycles. Moreover, the flexible supercapacitor maintained stability under bend and load conditions, showing good deformation adaptability.
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