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Table · dataset · 2026

Programmable Shape-Morphing in Homogeneous Hydrogels via Interfacial Confinement

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Programmable shape-morphing in hydrogels typically requires complex chemical gradients or oriented fillers, which strongly limits its scalability.

Description

Here, we design a geometric strategy to induce anisotropic deformation in homogeneous hygroscopic hydrogels through interfacial confinement. By mechanically interlocking the hydrogel with a microporous substrate, we suppress lateral expansion at the base and redirect isotropic volume gain into directional displacement.

Systematic variation of sample thickness reveals a morphological transition: thin films undergo quasi-uniaxial vertical swelling, whereas thick films develop mushroom-like architectures featuring coexisting interfacial anisotropy and distal isotropy. Meanwhile, the ionic osmotic pressure (∼10<sup>7</sup> Pa) overwhelmingly exceeds the elastic penalty imposed by the constraint (∼10<sup>5</sup> Pa), which makes the equilibrium water uptake of the corresponding hydrogels irrespective of boundary geometry.

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Poroelastic simulations quantitatively reproduce the experimentally observed deformation profiles, and cross-sectional electron microscopy confirms a stress-attenuation-driven microstructural gradient consistent with Saint-Venant-type decay. These findings establish interfacial confinement as a scalable paradigm for programming hydrogel actuation without requiring compositional heterogeneity, with implications for soft robotics and adaptive devices.

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Microscopy 75%
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