Natural Polymer-Based Mechanically Strong Hydrogel with Fast Self-Healing for Heavy Metal Ions Removal and Supercapacitor Applications

Hydrogels have attracted significant interest in multifunctional applications. Among them, self-healing hydrogel stands out for its ability to autonomously repair damage through reversible interactions, yet achieving both rapid self-healing and superior mechanical strength remains challenging. In this study, we report the fabrication of a dual cross-linked hydrogel (PAA-Alg-B) prepared via free radical polymerization of acrylic acid and alginic acid, employing N,N′-methylenebisacrylamide, or vinyl-modified nanocellulose as primary cross-linker, with Fe3+ or borax serving as an additional dynamic cross-linker. The resulting borax based hydrogel (PAA-Alg-B) exhibits remarkable fast self-healing efficiency enabled by reversible borate ester bonds and hydrogen bonding. It demonstrates tunable mechanical strength with toughness of 137 kJ/m3 and elongation at break up to 1117%, alongside exceptional swelling capacity (448 g/g). The adsorption studies reveal high removal efficiencies for heavy metals, with maximum capacities of 87.57 mg/g (Cr3+), 114.02 mg/g (Ni2+), and 99.42 mg/g (Cu2+), governed by chemisorption kinetics. The PAA-Alg-B can also be used as a promising solid-state electrolyte and separator for flexible supercapacitors. Protonic modulation via H2SO4 soaking significantly enhances ionic conductivity, electrochemical performance, and cycling stability. These findings highlight the potential of natural polymer-based, mechanically robust, self-healing hydrogels for sustainable wastewater treatment and advanced energy storage applications.