4.7 Article

Ionic coordination strengthening of temperature-driven gradient hydrogel actuators with rapid responsiveness

Journal

COMPOSITES PART B-ENGINEERING
Volume 245, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.compositesb.2022.110210

Keywords

Hydrogel actuators; High strength; Tunicate cellulose nanocrystals; Ionic coordination; Rapid responsiveness

Funding

  1. National Key Research and Development Program of China [2018YFE0123700]
  2. National Natural Science Foundation of China [52073217, 51873164]
  3. Key Research and Development Program of Hubei Province [2020BCA079]
  4. Key Project of Yunnan Tobacco Industry Co. Ltd. [2020XY01]

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This study presents a stimuli-responsive hydrogel actuator composed of a copolymer of NIPAM and SPA monomers, along with TCNCs nanofillers. The TCNCs were gradient arranged across the hydrogel thickness through electrophoresis, resulting in a gradient crosslinking density of networks. The hydrogel actuator exhibited high strength through Zr4+/- SO3- ionic coordination and showed rapid bending velocity, excellent stability, and good cycling performance in response to temperature changes. The hydrogel actuator could also be utilized as a soft robot for object lifting and transportation by adjusting the environment temperature.
Emerging applications of stimuli-responsive hydrogels as soft actuators and robotics have attracted great attention, but they face challenges in practical applications due to their poor mechanical properties, low driving force, and low actuation speed. Herein, we presented tough hydrogel actuators composed of a copolymer of N- isopropylacrylamide (NIPAM) and 3-sulfopropyl methacrylate potassium salt (SPA) monomers, and tunicate cellulose nanocrystals (TCNCs). The negatively charged TCNCs as nanofillers were gradient arranged by a direct current electric field (DC-EF) via electrophoresis. After in situ polymerization, TCNCs gradient distributed across the thickness of hydrogel, resulting in the formation of gradient crosslinking density of networks. Hydrogel actuators with high strength were obtained via Zr4+/- SO3- ionic coordination, whose tensile strength was about 200 times of hydrogel without ionic coordination. These hydrogel actuators exhibited rapid bending velocity, excellent stability, and good cycling performance in response to temperature. Importantly, these hydrogel ac-tuators could be designed as soft robots to lift and transport objects by changing environment temperature. This work provided a facile yet efficient strategy to fabricate soft actuators with high strength and rapid responsiveness.

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