Tunable Upper Critical Solution Temperature of Poly(N-isopropylacrylamide) in Ionic Liquids for Sequential and Reversible Self-Folding
Source abstract
Abstract
We demonstrate sequential folding of micropatterned polymer actuators by tuning the upper critical solution temperature (UCST) of poly(N-isopropylacrylamide) (PNIPAM) copolymers in the ionic liquid (IL) 1-ethyl-3-methylimidazolium bis(trifluoro-methylsulfonyl) imide. Incorporation of comonomers having different hydrogen-bonding capacities, acrylic acid and methyl acrylate, is shown to shift the UCST of PNIPAM to higher and lower temperatures, respectively. Relying on the ability to tune the transition temperature through copolymerization along with the wide thermal range afforded by the IL as a solvent, we fabricated a photopatterned self-folding device which shows reversible and sequential bending of three sets of hinges. Such sequential and reversible bending of microactuators offers potential for the design of complex self-folding origami and soft robots.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Materials and Mechanics · Advanced Sensor and Energy Harvesting Materials · Liquid Crystal Research Advancements
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Polymer Science and Engineering, University of Massachusetts Amherst, Amherst, Massachusetts 01003, United States
Center for Membranes, Korea Research Institute of Chemical Technology, Daejeon 34114, South Korea
Funding
Division of Materials Research
References (44)
Show source-provided references
1. 10.1002/cind.796_7.x10.1002/cind.796_7.x ↗
2. 10.1177/027836490809023510.1177/0278364908090235 ↗
3. 10.1126/science.125261010.1126/science.1252610 ↗
4. 10.1039/c3sm51003d10.1039/c3sm51003d ↗
5. 10.1038/srep1361610.1038/srep13616 ↗
6. 10.1063/1.475460710.1063/1.4754607 ↗
7. 10.1038/srep1654410.1038/srep16544 ↗
8. 10.1021/am405287p10.1021/am405287p ↗
9. 10.1038/srep3111010.1038/srep31110 ↗
10. 10.1039/C6MH00295A10.1039/C6MH00295A ↗
11. 10.1126/sciadv.160241710.1126/sciadv.1602417 ↗
12. 10.1088/0964-1726/25/10/10LT0210.1088/0964-1726/25/10/10LT02 ↗
13. 10.3390/ijms1101005210.3390/ijms11010052 ↗
14. 10.1016/j.coche.2012.10.00310.1016/j.coche.2012.10.003 ↗
15. 10.1021/la503407z10.1021/la503407z ↗
16. 10.1021/acs.accounts.6b0057010.1021/acs.accounts.6b00570 ↗
17. 10.1016/j.mattod.2014.07.00210.1016/j.mattod.2014.07.002 ↗
18. 10.1126/science.109031310.1126/science.1090313 ↗
19. 10.1016/j.apcata.2009.10.00810.1016/j.apcata.2009.10.008 ↗
20. 10.1126/science.115965210.1126/science.1159652 ↗
21. 10.1021/acs.accounts.6b0030810.1021/acs.accounts.6b00308 ↗
22. 10.1021/acs.jpcb.5b0842510.1021/acs.jpcb.5b08425 ↗
23. 10.1021/jz100617t10.1021/jz100617t ↗
24. 10.1021/jp110605810.1021/jp1106058 ↗
25. 10.1021/la062986h10.1021/la062986h ↗
26. 10.1246/cl.2006.96410.1246/cl.2006.964 ↗
27. 10.1002/adfm.20160156910.1002/adfm.201601569 ↗
28. 10.1002/anie.20141216010.1002/anie.201412160 ↗
29. 10.1021/ma801115210.1021/ma8011152 ↗
30. 10.1016/j.cplett.2013.07.01710.1016/j.cplett.2013.07.017 ↗
31. 10.1039/C5PY00998G10.1039/C5PY00998G ↗
32. 10.1039/C5PY01126D10.1039/C5PY01126D ↗
33. 10.1007/s00396-006-1605-510.1007/s00396-006-1605-5 ↗
34. 10.3390/polym304157510.3390/polym3041575 ↗
35. 10.1021/am507339r10.1021/am507339r ↗
36. 10.1246/bcsj.2011022510.1246/bcsj.20110225 ↗
37. 10.1021/ja045155b10.1021/ja045155b ↗
38. 10.1021/ma300374y10.1021/ma300374y ↗
39. 10.1021/ma034737v10.1021/ma034737v ↗
40. 10.1038/pj.2014.3710.1038/pj.2014.37 ↗
41. 10.1002/adma.20140351010.1002/adma.201403510 ↗
42. 10.1039/C6SM00714G10.1039/C6SM00714G ↗
43. Christensen, S. K.Photo-Reaction of Copolymers with Pendent Benzophenone. Ph.D. Thesis,University of Massachusetts,Amherst, MA, May 2013.
44. 10.1021/jp047480r10.1021/jp047480r ↗