聚苯胺
电致变色
材料科学
储能
纳米技术
自组装
导电聚合物
自愈水凝胶
超分子化学
化学工程
高分子化学
聚合物
有机化学
复合材料
聚合
分子
电极
量子力学
功率(物理)
物理化学
工程类
化学
物理
作者
Suryakamal Sarma,Neha Jain,Love Bansal,Ram A. Vishwakarma,Aditya Prasun,Tarun Kumar Sahu,Rajesh Kumar,Tridib K. Sarma
标识
DOI:10.1021/acsami.5c08151
摘要
Conductive polymer hydrogels combine the electrical conductivity of organic polymers with the high water content, porosity, and tissue-mimicking properties of hydrogels, making them ideal for bioelectronic interfaces. However, traditional polymer matrices often lack biocompatibility, self-healing ability, dynamic reconfigurability, and tunable mechanical properties. To address these challenges, herein we report a dimeric guanosine monophosphate (GMP)-based supramolecular hydrogel that self-assembles into a fibrillar network with intrinsic peroxidase-mimetic activity in a metal-free, microconfined environment. This unique catalytic property enables the in situ oxidative polymerization of aniline into polyaniline nanofibers, forming a hybrid conductive hydrogel with excellent mechanical strength, self-healing capability, stimuli-responsive sol-gel transitions, and high ionic conductivity. The resulting hydrogel was used to fabricate electrochromic energy-storing electrodes and "all-solid-state" supercapacitors with high capacitance (343 mF cm-2) and energy density (93.36 Wh cm-2). This work highlights the potential of small biomolecules as artificial enzyme mimics and structural matrices for transforming biomolecular self-assemblies into functionally conductive hydrogels. The integration of biomolecules for enzyme-mimetic catalysis for generating the conducting polymer hydrogels might provide a versatile platform for advancing bioelectronic technologies.
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