posted on 2017-07-11, 00:00authored byYan-Jun Liu, Wen-Tao Cao, Ming-Guo Ma, Pengbo Wan
Robust,
stretchable, and strain-sensitive hydrogels have recently attracted
immense research interest because of their potential application in
wearable strain sensors. The integration of the synergistic characteristics
of decent mechanical properties, reliable self-healing capability,
and high sensing sensitivity for fabricating conductive, elastic,
self-healing, and strain-sensitive hydrogels is still a great challenge.
Inspired by the mechanically excellent and self-healing biological
soft tissues with hierarchical network structures, herein, functional
network hydrogels are fabricated by the interconnection between a “soft”
homogeneous polymer network and a “hard” dynamic ferric
(Fe3+) cross-linked cellulose nanocrystals (CNCs–Fe3+) network. Under stress, the dynamic CNCs–Fe3+ coordination bonds act as sacrificial bonds to efficiently dissipate
energy, while the homogeneous polymer network leads to a smooth stress-transfer,
which enables the hydrogels to achieve unusual mechanical properties,
such as excellent mechanical strength, robust toughness, and stretchability,
as well as good self-recovery property. The hydrogels demonstrate
autonomously self-healing capability in only 5 min without the need
of any stimuli or healing agents, ascribing to the reorganization
of CNCs and Fe3+ via ionic coordination. Furthermore, the
resulted hydrogels display tunable electromechanical behavior with
sensitive, stable, and repeatable variations in resistance upon mechanical
deformations. Based on the tunable electromechanical behavior, the
hydrogels can act as a wearable strain sensor to monitor finger joint
motions, breathing, and even the slight blood pulse. This strategy
of building synergistic “soft and hard” structures is
successful to integrate the decent mechanical properties, reliable
self-healing capability, and high sensing sensitivity together for
assembling a high-performance, flexible, and wearable strain sensor.