An approach for various
programmable 3D structures based on commercially
available perfluorinated sulfonic-acid ionomers (PFSAs) is presented.
The uniaxial stretching induces the hydrophilic channels of PFSA to
align along the stretching direction, leading to anisotropic swelling
behavior. A bilayer composed of two stretched PFSA membranes with
perpendicular orientation morphs within just a few tens of seconds
into useful shapes including twisted helices, cylindrical helices,
and rings in swollen state depending on the cutting angle and dimensionless
width, similar to prior studies on chiral seedpods. Especially in
the wide width regime, where the stretching energy is dominant to
the bending energy, two different configurations sharing the same
handedness are both stable and provide multiplicity in shape selection
from a single strip through spatial dependent swelling–deswelling
cycles. Using the non-Euclidean geometries from 2D ionomer bilayers,
macroscopic humidity-sensitive actuators, various 3D structures, and
bistable self-folding structures are demonstrated. This facile fabrication
approach for various structures with commercially available ionomers
will provide possible applications for humidity-sensitive, ion-conductive
actuation systems in the future.
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