Biasing Buckling Direction in Shape-Programmable Hydrogel Sheets with Through-Thickness Gradients

Ying Zhou, Carlos M. Duque, Christian D. Santangelo, Ryan C. Hayward

Research output: Contribution to journalArticle

Abstract

A photocrosslinkable poly(N, N′-diethylacrylamide) copolymer allows for the photolithographic fabrication of hydrogel sheets with nonuniform crosslinking density and swelling ratio. Using this material system, different 3D shapes with nonzero Gaussian curvature K are successfully programmed by prescribing a “metric” defined by in-plane variations in swelling. However, this methodology does not control the direction of buckling adopted by each positive K feature, and therefore cannot controllably select between different isometric shapes defined by a single metric. Here, by introducing gradients in swelling through the thickness of the gel sheet by tuning the absorption of the UV-light used for crosslinking, a preferential buckling direction is locally specified for each feature by the direction of UV exposure. By also controlling the strength of coupling between neighboring features, this is shown to be an effective method to program buckling direction of each unit within a canonical corrugated surface shape.

Original languageEnglish (US)
Article number1905273
JournalAdvanced Functional Materials
DOIs
StateAccepted/In press - Jan 1 2019
Externally publishedYes

Fingerprint

Hydrogel
buckling
Hydrogels
Buckling
Swelling
swelling
Crosslinking
gradients
crosslinking
Ultraviolet radiation
Gels
Copolymers
Tuning
Fabrication
copolymers
tuning
curvature
gels
methodology
fabrication

Keywords

  • curvature
  • hydrogels
  • photolithography
  • shape morphing
  • temperature responsiveness

ASJC Scopus subject areas

  • Chemistry(all)
  • Materials Science(all)
  • Condensed Matter Physics

Cite this

Biasing Buckling Direction in Shape-Programmable Hydrogel Sheets with Through-Thickness Gradients. / Zhou, Ying; Duque, Carlos M.; Santangelo, Christian D.; Hayward, Ryan C.

In: Advanced Functional Materials, 01.01.2019.

Research output: Contribution to journalArticle

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