Enabling High‐Performance Artificial Muscles via a High Strength Fiber Reinforcement Strategy
Source abstract
Abstract
Abstract Coiled‐polymer‐fiber‐based artificial muscles can provide large contractile actuation stroke. However, it is a challenge to achieve high actuation load and high actuation stroke for artificial muscle simultaneously. Herein, a powerful coiled‐polymer‐fiber‐based artificial muscle with a “rigid‐and‐flexible” structure is fabricated by cotwisting rigid heterocyclic aramid (HA) fibers with flexible silver‐plated nylon (SPN) fibers. The artificial muscle based on coiled HA@SPN fibers can lift a load over 108 MPa with a fast response time of 0.6 s, which is 309 times heavier than the load that human muscle can lift, and generate a work density per temperature of 41.3 J (kg °C)−1. The coiled HA@SPN fiber muscle exhibits high actuation stability of over 30 000 cycles. The coiled HA@SPN fiber muscle can provide a contractile actuation stroke of up to 8.2% and generate an average gravimetric mechanical energy density of 702 J kg−1, which is 18.1 times that of human skeletal muscle (≈38.8 J kg−1). An average contractile power density of 1168 W kg−1 is obtained for coiled HA@SPN fiber muscle, which is 23.4 times that of human skeletal muscle (≈50 W kg−1).
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Advanced Materials and Mechanics · Advanced Sensor and Energy Harvesting Materials · Dielectric materials and actuators
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
College of Polymer Science and Engineering State Key Laboratory of Polymer Materials Engineering Sichuan University Chengdu 610065 China
Funding
National Natural Science Foundation of China · State Key Laboratory of Polymer Materials Engineering
References (42)
Show source-provided references
1. 10.1126/science.110604210.1126/science.1106042 ↗
2. 10.1038/nature1229510.1038/nature12295 ↗
3. 10.1002/adma.20190004210.1002/adma.201900042 ↗
4. 10.1002/adma.20130570810.1002/adma.201305708 ↗
5. 10.1002/adma.20160062810.1002/adma.201600628 ↗
6. 10.1002/admt.20170035910.1002/admt.201700359 ↗
7. 10.1039/D1MH00234A10.1039/D1MH00234A ↗
8. 10.1002/admt.20200089410.1002/admt.202000894 ↗
9. 10.1021/acsnano.1c0501910.1021/acsnano.1c05019 ↗
10. 10.1038/s41586-019-1737-710.1038/s41586-019-1737-7 ↗
11. 10.1021/acsami.1c0642210.1021/acsami.1c06422 ↗
12. 10.1002/adfm.20190016110.1002/adfm.201900161 ↗
13. 10.1002/adma.20150173110.1002/adma.201501731 ↗
14. 10.1002/adma.20190267010.1002/adma.201902670 ↗
15. 10.1002/adma.20170087010.1002/adma.201700870 ↗
16. 10.1126/science.aaa795210.1126/science.aaa7952 ↗
17. 10.1002/adma.20170440710.1002/adma.201704407 ↗
18. 10.1002/adma.20210675710.1002/adma.202106757 ↗
19. 10.1002/adfm.20201064310.1002/adfm.202010643 ↗
20. 10.1126/science.124690610.1126/science.1246906 ↗
21. 10.1039/D1MH00457C10.1039/D1MH00457C ↗
22. 10.1021/acsnano.9b0953310.1021/acsnano.9b09533 ↗
23. 10.1002/adma.20160040510.1002/adma.201600405 ↗
24. 10.1039/D0MH01003K10.1039/D0MH01003K ↗
25. 10.1002/adfm.20220059110.1002/adfm.202200591 ↗
26. 10.1002/admt.20200032910.1002/admt.202000329 ↗
27. 10.1021/acsami.0c2045610.1021/acsami.0c20456 ↗
28. 10.1021/acsami.8b1214410.1021/acsami.8b12144 ↗
29. 10.1021/acsbiomaterials.0c0151010.1021/acsbiomaterials.0c01510 ↗
30. 10.1002/adfm.20180824110.1002/adfm.201808241 ↗
31. 10.1016/j.matt.2022.02.01810.1016/j.matt.2022.02.018 ↗
32. 10.1021/acsami.0c0117910.1021/acsami.0c01179 ↗
33. 10.1016/j.compositesb.2019.10749910.1016/j.compositesb.2019.107499 ↗
34. Yang C. · Compos., Part B: Eng. · 2020 · 21610.1016/j.compositesb.2021.108855 ↗
35. 10.1016/j.compscitech.2019.10783710.1016/j.compscitech.2019.107837 ↗
36. 10.1126/science.122676210.1126/science.1226762 ↗
37. 10.1039/C7NR08595H10.1039/C7NR08595H ↗
38. 10.1039/D1MH00743B10.1039/D1MH00743B ↗
39. 10.1039/C8NA00204E10.1039/C8NA00204E ↗
40. 10.1038/s41467-022-29088-910.1038/s41467-022-29088-9 ↗
41. 10.1021/acsami.0c1422210.1021/acsami.0c14222 ↗
42. 10.1039/C9NR00611G10.1039/C9NR00611G ↗