As one of the most amazing aspects of life, all living
organisms
are formed by self-assembly, a fundamental biological design process
in which ordered nanostructures are assembled from small parts. For
example, most of the biological tissues contain structurally soft
and hard parts that are usually hierarchically organized at nano or
micro levels to achieve specific functions. Hydrogels are one of the
most promising soft materials owing to their potential applications
in building of biological tissues and stretchable sensors. In this
work, a series of hydrogels are synthesized through the co-self-assembly
of two types of amphiphiles in their aqueous solution prior to polymerization.
Soft and hard parts with nanostructures of different order parameters
are incorporated into the hydrogels. The hydrophilic segment (as soft
phases) of the polymer network provides water absorption, fluid flow,
and softness, whereas the hydrophobic segment (as hard phases) provides
strength and tearing and fracture resistance. Appropriate soft/hard
nanostructures and their interfaces allow for the tailoring of the
desired morphological and mechanical properties, including a different
wetting ability, toughness, energy dissipation, self-recovery, and
fracture resistance arising from their nanostructures. This work provides
insights into the design of nanostructured anisotropic hydrogels with
controlled morphological and mechanical properties.