Hydrogel-based devices have attracted
tremendous attention
due
to their potential applications in sensors and soft actuators. However,
it is still a challenge for hydrogel-based devices to be integrated
with high conductivity, sustainability, reusability, extraordinary
mechanical strength, and high stretchability. Herein, a multiple-network
hydrogel has been developed via a simple one-pot method based on poly(vinyl
alcohol) (PVA), Gleditsia sinensis polysaccharide
gum (GSG), and 2,2,6,6-tetramethylpiperidin-1-oxyl (TEMPO)-oxidated
nanocellulose (TOCNF), using borax as a cross-linker. The optimal
hydrogel (PGB-TOCNF) exhibited high mechanical strength (378 kPa),
stretchability (548% breaking elongation), and compressibility (92%
compression strain), as well as considerable conductive behavior.
Importantly, the unique self-healing, reformable, and injectable properties
of the polysaccharide-based hydrogel could be due to dynamic and reversible
borate ester bonds and could also be locked by the formation of PVA
nanocrystals during the freezing–thawing process. This work
broadens the avenue for designing polysaccharide-derived hydrogels
for applications in sensors, wearable electronics, and soft robots.