journal article·2020-08Open access

Supramolecular–covalent hybrid polymers for light-activated mechanical actuation

Chuang Li, Aysenur Iscen, Hiroaki Sai, Kohei Sato, Nicholas A. Sather, Stacey M. Chin, Zaida Álvarez, Liam C. Palmer, George C. Schatz, Samuel I. Stupp

Nature Materials· Volume 19· Issue 8

Abstract

The development of synthetic structures that mimic mechanical actuation in living matter such as autonomous translation and shape changes remains a grand challenge for materials science. In living systems the integration of supramolecular structures and covalent polymers contributes to the responsive behaviour of membranes, muscles and tendons, among others. Here we describe hybrid light-responsive soft materials composed of peptide amphiphile supramolecular polymers chemically bonded to spiropyran-based networks that expel water in response to visible light. The supramolecular polymers form a reversibly deformable and water-draining skeleton that mechanically reinforces the hybrid and can also be aligned by printing methods. The noncovalent skeleton embedded in the network thus enables faster bending and flattening actuation of objects, as well as longer steps during the light-driven crawling motion of macroscopic films. Our work suggests that hybrid bonding polymers, which integrate supramolecular assemblies and covalent networks, offer strategies for the bottom-up design of soft matter that mimics living organisms.
Source: europepmc · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Supramolecular Self-Assembly in Materials · Photochromic and Fluorescence Chemistry · Photoreceptor and optogenetics research

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

References (33)

Show source-provided references
1. Roy, D., Brooks, W. L. A. & Sumerlin, B. S. New directions in thermoresponsive polymers. Chem. Soc. Rev. 42, 7214–7243 (2013).10.1039/c3cs35499g ↗
2. Kocak, G., Tuncer, C. & Butun, V. pH-responsive polymers. Polym. Chem. 8, 144–176 (2017).10.1039/C6PY01872F ↗
3. Zarzar, L. D. & Aizenberg, J. Stimuli-responsive chemomechanical actuation: a hybrid materials approach. Acc. Chem. Res. 47, 530–539 (2014).10.1021/ar4001923 ↗
4. Fukino, T., Yamagishi, H. & Aida, T. Redox-responsive molecular systems and materials. Adv. Mater. 29, 1603888 (2017).10.1002/adma.201603888 ↗
5. Russew, M. M. & Hecht, S. Photoswitches: from molecules to materials. Adv. Mater. 22, 3348–3360 (2010).10.1002/adma.200904102 ↗
6. Szymanski, W., Beierle, J. M., Kistemaker, H. A. V., Velema, W. A. & Feringa, B. L. Reversible photocontrol of biological systems by the incorporation of molecular photoswitches. Chem. Rev. 113, 6114–6178 (2013).10.1021/cr300179f ↗
7. Gelebart, A. H. et al. Making waves in a photoactive polymer film. Nature 546, 632–636 (2017).10.1038/nature22987 ↗
8. Wani, O. M., Zeng, H. & Priimagi, A. A light-driven artificial flytrap. Nat. Commun. 8, 15546 (2017).10.1038/ncomms15546 ↗
9. Lancia, F., Ryabchun, A. & Katsonis, N. Life-like motion driven by artificial molecular machines. Nat. Rev. Chem. 3, 536–551 (2019).10.1038/s41570-019-0122-2 ↗
10. Iwaso, K., Takashima, Y. & Harada, A. Fast response dry-type artificial molecular muscles with [c2]daisy chains. Nat. Chem. 8, 625–632 (2016).10.1038/nchem.2513 ↗
11. Chen, J. W. et al. Artificial muscle-like function from hierarchical supramolecular assembly of photoresponsive molecular motors. Nat. Chem. 10, 132–138 (2018).10.1038/nchem.2887 ↗
12. Yu, Z. L. et al. Simultaneous covalent and noncovalent hybrid polymerizations. Science 351, 497–502 (2016).10.1126/science.aad4091 ↗
13. Chin, S. M. et al. Covalent-supramolecular hybrid polymers as muscle-inspired anisotropic actuators. Nat. Commun. 9, 2395 (2018).10.1038/s41467-018-04800-w ↗
14. Ionov, L. Hydrogel-based actuators: possibilities and limitations. Mater. Today 17, 494–503 (2014).10.1016/j.mattod.2014.07.002 ↗
15. Klajn, R. Spiropyran-based dynamic materials. Chem. Soc. Rev. 43, 148–184 (2014).10.1039/C3CS60181A ↗
16. Satoh, T., Sumaru, K., Takagi, T. & Kanamori, T. Fast-reversible light-driven hydrogels consisting of spirobenzopyran-functionalized poly(N-isopropylacrylamide). Soft Matter 7, 8030–8034 (2011).10.1039/c1sm05797a ↗
17. Marrink, S. J., Risselada, H. J., Yefimov, S., Tieleman, D. P. & de Vries, A. H. The MARTINI force field: Coarse grained model for biomolecular simulations. J. Phys. Chem. B 111, 7812–7824 (2007).10.1021/jp071097f ↗
18. Ziolkowski, B., Florea, L., Theobald, J., Benito-Lopez, F. & Diamond, D. Self-protonating spiropyran-co-NIPAM-co-acrylic acid hydrogel photoactuators. Soft Matter 9, 8754–8760 (2013).10.1039/c3sm51386f ↗
19. Le, X. X., Lu, W., Zhang, J. W. & Chen, T. Recent progress in biomimetic anisotropic hydrogel actuators. Adv. Sci. 6, 1801584 (2019).10.1002/advs.201801584 ↗
20. Satoh, T., Sumaru, K., Takagi, T., Takai, K. & Kanamori, T. Isomerization of spirobenzopyrans bearing electron-donating and electron-withdrawing groups in acidic aqueous solutions. Phys. Chem. Chem. Phys. 13, 7322–7329 (2011).10.1039/c0cp01989e ↗
21. Kuksenok, O. & Balazs, A. C. Stimuli-responsive behavior of composites integrating thermo-responsive gels with photo-responsive fibers. Mater. Horiz. 3, 53–62 (2016).10.1039/C5MH00212E ↗
22. Kuksenok, O. & Balazs, A. C. Designing polymer gels and composites that undergo bio-inspired phototactic reconfiguration and motion. Bioinspir. Biomim. 13, 035004 (2018).10.1088/1748-3190/aaad1c ↗
23. Maeda, S., Hara, Y., Sakai, T., Yoshida, R. & Hashimoto, S. Self-walking gel. Adv. Mater. 19, 3480–3484 (2007).10.1002/adma.200700625 ↗
24. Francis, W., Dunne, A., Delaney, C., Florea, L. & Diamond, D. Spiropyran based hydrogels actuators—walking in the light. Sens. Actuat. B Chem. 250, 608–616 (2017).10.1016/j.snb.2017.05.005 ↗
25. Ortony, J. H. et al. Water dynamics from the surface to the interior of a supramolecular nanostructure. J. Am. Chem. Soc. 139, 8915–8921 (2017).10.1021/jacs.7b02969 ↗
26. Toby, B. H. & von Dreele, R. B. GSAS-II: the genesis of a modern open-source all purpose crystallography software package. J. Appl. Crystallogr. 46, 544–549 (2013).10.1107/S0021889813003531 ↗
27. Ilavsky, J. & Jemian, P. R. Irena: tool suite for modeling and analysis of small-angle scattering. J. Appl. Crystallogr. 42, 347–353 (2009).10.1107/S0021889809002222 ↗
28. Wang, J. M., Wolf, R. M., Caldwell, J. W., Kollman, P. A. & Case, D. A. Development and testing of a general amber force field. J. Comput. Chem. 25, 1157–1174 (2004).10.1002/jcc.20035 ↗
29. Schmidt, M. W. et al. General atomic and molecular electronic-structure system. J. Comput. Chem. 14, 1347–1363 (1993).10.1002/jcc.540141112 ↗
30. Bayly, C. I., Cieplak, P., Cornell, W. D. & Kollman, P. A. A well-behaved electrostatic potential based method using charge restraints for deriving atomic charges: the RESP model. J. Phys. Chem. 97, 10269–10280 (1993).10.1021/j100142a004 ↗
31. Case, D. A. et al. AMBER 2016 (University of California, San Francisco, 2016).
32. Lee, O. S., Cho, V. & Schatz, G. C. Modeling the self-assembly of peptide amphiphiles into fibers using coarse-grained molecular dynamics. Nano Lett. 12, 4907–4913 (2012).10.1021/nl302487m ↗
33. van Gunsteren, W. F. & Berendsen, H. J. C. Thermodynamic cycle integration by computer simulation as a tool for obtaining free energy differences in molecular chemistry. J. Comput. Aided Mol. Des. 1, 171–176 (1987).10.1007/BF01676960 ↗