Flexible Conductive Composites with Programmed Electrical Anisotropy Using Acoustophoresis
Source abstract
Abstract
Abstract Developing mechanically flexible composite materials with high electrical conductivity is currently hindered by the need to use high loading of conductive filler, which severely limits flexibility. Here, acoustic focusing is used to control arrangement of conductive particles in photopolymer matrices to create composites with both tunable conductivity and flexibility. Acoustophoresis patterns filler particles into highly efficient percolated networks which utilize up to 97% of the particles in the composite, whereas the inefficient stochastic networks of conventional dispersed‐fiber composites utilize <5%. These patterned materials have conductivity an order of magnitude higher than conventional composites made with the same ink, reaching 48% the conductivity of bulk silver within the assembled silver‐particle networks (at 2.6 vol% loading). They also have low particle loading so that they are flexible, withstanding >500 bending cycles without losses in conductivity and changing conductivity only 5% within cycles on average. In contrast, conventional unpatterned composites with the same conductivity require such high loading that they are prohibitively brittle. Finally, modulating the applied acoustic field controls the anisotropy of the conductive networks and produces materials which are either 2D conductive, 1D conductive, or insulating, using the same nozzle and ink, paving the way for versatile multifunctional 3D printing.
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Research context
OpenAlex topics: Electrowetting and Microfluidic Technologies · Chemical and Physical Properties of Materials · Plant and Biological Electrophysiology Studies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Materials Department University of California Santa Barbara Engineering II Building 1355 Santa Barbara CA 93106 USA
MST‐7 Engineered Materials Division of Materials Science and Technology Los Alamos National Laboratory Los Alamos NM 87545 USA
Department of Mechanical Engineering University of Hawai'i at Manoa 2540 Dole Street ‐ Holmes Hall Rm 302 Honolulu HI 96822 USA
Funding
Institute for Collaborative Biotechnologies · Army Research Office · National Science Foundation
References (56)
Show source-provided references
1. 10.1002/adma.20090405410.1002/adma.200904054 ↗
2. 10.1126/science.118238310.1126/science.1182383 ↗
3. 10.1021/acs.chemrev.8b0057310.1021/acs.chemrev.8b00573 ↗
4. 10.1016/j.progpolymsci.2014.06.00210.1016/j.progpolymsci.2014.06.002 ↗
5. 10.1038/nmat245910.1038/nmat2459 ↗
6. 10.1002/adma.20060251510.1002/adma.200602515 ↗
7. 10.1038/nature0771910.1038/nature07719 ↗
8. 10.1016/j.microrel.2010.06.01110.1016/j.microrel.2010.06.011 ↗
9. 10.1021/acsaem.8b0024010.1021/acsaem.8b00240 ↗
10. 10.1016/j.compositesa.2015.05.01410.1016/j.compositesa.2015.05.014 ↗
11. 10.1126/science.116837510.1126/science.1168375 ↗
12. 10.1039/c0jm00264j10.1039/c0jm00264j ↗
13. 10.1002/adma.20050242210.1002/adma.200502422 ↗
14. 10.1038/nature2100310.1038/nature21003 ↗
15. 10.1002/adma.20160642510.1002/adma.201606425 ↗
16. 10.1080/17452759.2016.125318110.1080/17452759.2016.1253181 ↗
17. 10.1126/science.aaf209310.1126/science.aaf2093 ↗
18. 10.1038/nature1454310.1038/nature14543 ↗
19. 10.1002/adma.20170381710.1002/adma.201703817 ↗
20. 10.1038/ncomms964310.1038/ncomms9643 ↗
21. 10.1038/ncomms964110.1038/ncomms9641 ↗
22. 10.1126/science.121413110.1126/science.1214131 ↗
23. 10.1002/adma.20140180410.1002/adma.201401804 ↗
24. 10.1016/j.compscitech.2014.10.00910.1016/j.compscitech.2014.10.009 ↗
25. 10.1038/srep4340110.1038/srep43401 ↗
26. 10.1063/1.308024310.1063/1.3080243 ↗
27. 10.1016/j.carbon.2008.01.01910.1016/j.carbon.2008.01.019 ↗
28. 10.1002/pc.2303110.1002/pc.23031 ↗
29. 10.1103/PhysRevB.79.02430110.1103/PhysRevB.79.024301 ↗
30. 10.1002/admt.20170012210.1002/admt.201700122 ↗
31. 10.1063/1.494363410.1063/1.4943634 ↗
32. 10.1038/nature1975510.1038/nature19755 ↗
33. 10.1002/adma.20150551610.1002/adma.201505516 ↗
34. 10.1080/21663831.2018.143131710.1080/21663831.2018.1431317 ↗
35. 10.1063/1.489801210.1063/1.4898012 ↗
36. 10.1002/ppsc.20170047010.1002/ppsc.201700470 ↗
37. 10.1039/b704864e10.1039/b704864e ↗
38. 10.1016/j.eml.2015.09.00310.1016/j.eml.2015.09.003 ↗
39. 10.1016/j.eml.2016.04.00310.1016/j.eml.2016.04.003 ↗
40. 10.1088/1361-6439/aa62b710.1088/1361-6439/aa62b7 ↗
41. 10.1016/j.sna.2017.06.01610.1016/j.sna.2017.06.016 ↗
42. 10.1146/annurev-matsci-070909-10450210.1146/annurev-matsci-070909-104502 ↗
43. 10.1002/app.1249610.1002/app.12496 ↗
44. 10.1016/j.compositesb.2015.06.01310.1016/j.compositesb.2015.06.013 ↗
45. 10.1098/rspa.1934.021510.1098/rspa.1934.0215 ↗
46. Gor'kov L. P. · Sov. Phys. Dokl. · 1962 · 6 · 773
47. 10.1039/c2lc21068a10.1039/c2lc21068a ↗
48. 10.1103/PhysRevB.71.10420110.1103/PhysRevB.71.104201 ↗
49. 10.1143/JJAP.39.368310.1143/JJAP.39.3683 ↗
50. 10.1016/j.compscitech.2008.06.01810.1016/j.compscitech.2008.06.018 ↗
51. 10.1088/0964-1726/21/1/01200110.1088/0964-1726/21/1/012001 ↗
52. Cortés M. T. · e‐Polym. · 2003 · 3
53. 10.1088/0960-1317/23/10/10500210.1088/0960-1317/23/10/105002 ↗
54. 10.1039/c2lc40612h10.1039/c2lc40612h ↗
55. 10.1039/C7SM00182G10.1039/C7SM00182G ↗
56. 10.1039/b920376a10.1039/b920376a ↗