journal article·2015-10-28

Bioinspired Smart Actuator Based on Graphene Oxide-Polymer Hybrid Hydrogels

Tao Wang, Jiahe Huang, Yiqing Yang, Enzhong Zhang, Weixiang Sun, Zhen Tong

Publisher page

Abstract

Rapid response and strong mechanical properties are desired for smart materials used in soft actuators. A bioinspired hybrid hydrogel actuator was designed and prepared by series combination of three trunks of tough polymer-clay hydrogels to accomplish the comprehensive actuation of "extension-grasp-retraction" like a fishing rod. The hydrogels with thermo-creep and thermo-shrinking features were successively irradiated by near-infrared (NIR) to execute extension and retraction, respectively. The GO in the hydrogels absorbed the NIR energy and transformed it into thermo-energy rapidly and effectively. The hydrogel with adhesion or magnetic force was adopted as the "hook" of the hybrid hydrogel actuator for grasping object. The hook of the hybrid hydrogel actuator was replaceable according to applications, even with functional materials other than hydrogels. This study provides an innovative concept to explore new soft actuators through combining response hydrogels and programming the same stimulus.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advanced Sensor and Energy Harvesting Materials · Advanced Materials and Mechanics · Micro and Nano Robotics

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Research Institute of Materials Science and State Key Laboratory of Luminescent Materials and Devices, South China University of Technology, Guangzhou 510640, China

Funding

Ministry of Science and Technology of the People's Republic of China · Guangdong Province · National Natural Science Foundation of China · Ministry of Education of the People's Republic of China

References (35)

Show source-provided references
1. Okuzaki H. · 2014
2. 10.1039/c3bm60288e10.1039/c3bm60288e ↗
3. 10.1039/c3cs60031a10.1039/c3cs60031a ↗
4. 10.1071/CH1115610.1071/CH11156 ↗
5. 10.1002/1521-4095(20020816)14:16<1120::AID-ADMA1120>3.0.CO;2-910.1002/1521-4095(20020816)14:16<1120::AID-ADMA1120>3.0.CO;2-9 ↗
6. 10.1016/j.carbon.2013.06.00310.1016/j.carbon.2013.06.003 ↗
7. 10.1039/C4TA02866J10.1039/C4TA02866J ↗
8. 10.1038/nature1140910.1038/nature11409 ↗
9. 10.1038/nmat371310.1038/nmat3713 ↗
10. 10.1038/ncomms612410.1038/ncomms6124 ↗
11. 10.1038/nmat285810.1038/nmat2858 ↗
12. 10.1021/ja201017510.1021/ja2010175 ↗
13. 10.1002/adma.20120322910.1002/adma.201203229 ↗
14. 10.1002/adma.20130281010.1002/adma.201302810 ↗
15. 10.1002/pen.2407610.1002/pen.24076 ↗
16. 10.1021/cm401919c10.1021/cm401919c ↗
17. 10.1021/acs.macromol.5b0014210.1021/acs.macromol.5b00142 ↗
18. 10.1021/am507100m10.1021/am507100m ↗
19. 10.1021/acsami.5b0018410.1021/acsami.5b00184 ↗
20. Yu Y. · J. Mater. Sci. · 2015 · 50 · 345710.1007/s10853-015-8905-4 ↗
21. 10.1016/j.colsurfb.2015.03.00210.1016/j.colsurfb.2015.03.002 ↗
22. 10.1016/j.carbpol.2014.10.01110.1016/j.carbpol.2014.10.011 ↗
23. 10.1002/smll.20140165110.1002/smll.201401651 ↗
24. 10.1021/jp901284d10.1021/jp901284d ↗
25. 10.1016/j.tibtech.2013.03.00210.1016/j.tibtech.2013.03.002 ↗
26. 10.1002/anie.20100646410.1002/anie.201006464 ↗
27. 10.1021/ja01539a01710.1021/ja01539a017 ↗
28. 10.1021/ma300859b10.1021/ma300859b ↗
29. 10.1021/ma034366i10.1021/ma034366i ↗
30. 10.1039/C1SM06484C10.1039/C1SM06484C ↗
31. 10.1016/j.jconrel.2015.05.17210.1016/j.jconrel.2015.05.172 ↗
32. 10.1002/anie.20140077510.1002/anie.201400775 ↗
33. 10.1016/j.polymer.2013.02.00810.1016/j.polymer.2013.02.008 ↗
34. 10.1016/j.polymer.2009.02.02010.1016/j.polymer.2009.02.020 ↗
35. 10.1002/mame.20140011010.1002/mame.201400110 ↗