Journal
ADVANCED MATERIALS
Volume 33, Issue 20, Pages -Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.202008235
Keywords
3D printing; diffusion; hierarchical structures; hydrogels; stimuli‐ responsive materials
Categories
Funding
- ONR [N00014-17-1-2117, N00014-18-1-2314]
- AFOSR [FA9550-17-1-0311, FA9550-18-1-0449, FA9550-20-1-0344]
- NSF CAREER award [1724526]
- Hellman Fellows Funds
- University of California, Los Angeles
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A universal approach called cononsolvency photopolymerization has been developed to overcome the trade-off between swelling and mechanical properties in hydrogels. By using this method, hydrogels with unique open porous networks and continuous microchannels are created, resulting in record-high volumetric (de)swelling speeds.
Crosslinked polymers and gels are important in soft robotics, solar vapor generation, energy storage, drug delivery, catalysis, and biosensing. However, their attractive mass transport and volume-changing abilities are diffusion-limited, requiring miniaturization to avoid slow response. Typical approaches to improving diffusion in hydrogels sacrifice mechanical properties by increasing porosity or limit the total volumetric flux by directionally confining the pores. Despite tremendous efforts, simultaneous enhancement of diffusion and mechanical properties remains a long-standing challenge hindering broader practical applications of hydrogels. In this work, cononsolvency photopolymerization is developed as a universal approach to overcome this swelling-mechanical property trade-off. The as-synthesized poly(N-isopropylacrylamide) hydrogel, as an exemplary system, presents a unique open porous network with continuous microchannels, leading to record-high volumetric (de)swelling speeds, almost an order of magnitude higher than reported previously. This swelling enhancement comes with a simultaneous improvement in Young's modulus and toughness over conventional hydrogels fabricated in pure solvents. The resulting fast mass transport enables in-air operation of the hydrogel via rapid water replenishment and ultrafast actuation. The method is compatible with 3D printing. The generalizability is demonstrated by extending the technique to poly(N-tertbutylacrylamide-co-polyacrylamide) and polyacrylamide hydrogels, non-temperature-responsive polymer systems, validating the present hypothesis that cononsolvency is a generic phenomenon driven by competitive adsorption.
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