Toughening Elastomer while Lowering Hysteresis Using Peptide Cross-Linkers
Source abstract
Abstract
Various strategies were proposed to toughen elastomers; however, they usually result in high hysteresis, particularly for those toughened by introducing sacrificial bonds. To overcome the trade-off relationship between toughness and hysteresis, here poly(benzyl acrylate) elastomers were synthesized using poly(γ-benzyl- l -glutamate)-based peptide cross-linkers. The α-helical peptide segments introduced into the polymeric network act like molecule-sized springs. They absorb energy when loaded but return it when unloading. Therefore, the peptide-cross-linked elastomer exhibits enhanced toughness and simultaneously a lowered hysteresis. Besides high toughness and low hysteresis, the elastomer also presents high ductility (break strain: 4700%), flexibility, crack-insensitivity (fracture toughness: 1.25 × 10 4 J m –2 ), and fatigue resistance (fatigue threshold: 9.27 × 10 2 J m –2 ). In addition, the adhesive properties of the elastomer are also improved. The adhesion strength on polypropylene is up to 5.50× 10 2 kPa. Thirty days of immersion in water leads to only a small decrease in adhesion strength, demonstrating excellent long-term underwater adhesion stability. Taking advantage of the high toughness, low hysteresis, and excellent adhesion strength of the elastomer, a composite hydrogel strain sensor was designed. Human motion was successfully monitored both in the air and underwater.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Sensor and Energy Harvesting Materials · Advanced Materials and Mechanics · Supramolecular Self-Assembly in Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Laboratory of Functional Polymer Materials, Institute of Polymer Chemistry, College of Chemistry
Nankai University
School of Chemistry
Tiangong University
Cangzhou Institute of Tiangong University
Funding
Natural Science Foundation of Hebei Province · National Natural Science Foundation of China · Cangzhou City · Cangzhou Institute of Tiangong University
References (61)
Show source-provided references
1. 10.1126/science.aap811410.1126/science.aap8114 ↗
2. 10.1126/sciadv.aat762910.1126/sciadv.aat7629 ↗
3. 10.1021/acsmaterialslett.2c0084710.1021/acsmaterialslett.2c00847 ↗
4. 10.1038/s41467-020-14446-210.1038/s41467-020-14446-2 ↗
5. 10.1126/science.aao035010.1126/science.aao0350 ↗
6. 10.1126/science.124849410.1126/science.1248494 ↗
7. 10.1021/acs.chemmater.9b0087110.1021/acs.chemmater.9b00871 ↗
8. 10.1002/adfm.20211024410.1002/adfm.202110244 ↗
9. 10.1016/j.polymer.2019.12168610.1016/j.polymer.2019.121686 ↗
10. 10.1002/adma.20030490710.1002/adma.200304907 ↗
11. 10.1039/b924290b10.1039/b924290b ↗
12. 10.1002/adma.20210149810.1002/adma.202101498 ↗
13. 10.1002/adma.20200852310.1002/adma.202008523 ↗
14. 10.1002/anie.20211590410.1002/anie.202115904 ↗
15. 10.1021/acs.macromol.0c0050010.1021/acs.macromol.0c00500 ↗
16. 10.1039/C9TA10909A10.1039/C9TA10909A ↗
17. 10.1021/acs.macromol.9b0041910.1021/acs.macromol.9b00419 ↗
18. 10.1002/1521-4095(200012)12:23<1835::AID-ADMA1835>3.0.CO;2-T10.1002/1521-4095(200012)12:23<1835::AID-ADMA1835>3.0.CO;2-T ↗
19. 10.1002/mame.20040003410.1002/mame.200400034 ↗
20. 10.1002/adfm.20221329410.1002/adfm.202213294 ↗
21. 10.1073/pnas.182142011610.1073/pnas.1821420116 ↗
22. 10.1021/acsami.1c2478410.1021/acsami.1c24784 ↗
23. 10.1039/D4MH00174E10.1039/D4MH00174E ↗
24. 10.1016/j.cej.2024.15380410.1016/j.cej.2024.153804 ↗
25. 10.1021/acs.macromol.2c0056310.1021/acs.macromol.2c00563 ↗
26. 10.1016/j.cej.2021.12883910.1016/j.cej.2021.128839 ↗
27. 10.1038/s41467-022-34522-z10.1038/s41467-022-34522-z ↗
28. 10.1021/bm201800v10.1021/bm201800v ↗
29. 10.1002/adfm.20220731710.1002/adfm.202207317 ↗
30. 10.1021/acssuschemeng.7b0069810.1021/acssuschemeng.7b00698 ↗
31. 10.1002/pola.2818710.1002/pola.28187 ↗
32. 10.1021/ma800476x10.1021/ma800476x ↗
33. 10.1071/CH1115610.1071/CH11156 ↗
34. 10.1002/marc.20080070010.1002/marc.200800700 ↗
35. 10.1002/macp.1967.02103012610.1002/macp.1967.021030126 ↗
36. 10.1039/C7PY01725A10.1039/C7PY01725A ↗
37. 10.1002/mabi.20220034410.1002/mabi.202200344 ↗
38. 10.1016/S0009-2614(99)01201-410.1016/S0009-2614(99)01201-4 ↗
39. 10.1093/protein/13.11.76310.1093/protein/13.11.763 ↗
40. 10.1039/C4PY00554F10.1039/C4PY00554F ↗
41. 10.1016/0043-1648(74)90055-610.1016/0043-1648(74)90055-6 ↗
42. 10.1002/anie.20230176210.1002/anie.202301762 ↗
43. 10.1021/ma901951s10.1021/ma901951s ↗
44. 10.1039/C6SM01694D10.1039/C6SM01694D ↗
45. 10.1021/acs.chemrev.0c0108810.1021/acs.chemrev.0c01088 ↗
46. 10.1038/s41467-022-30021-310.1038/s41467-022-30021-3 ↗
47. 10.1002/adma.20250612910.1002/adma.202506129 ↗
48. 10.1021/acsapm.2c0010210.1021/acsapm.2c00102 ↗
49. 10.1021/acsapm.4c0369210.1021/acsapm.4c03692 ↗
50. 10.1126/sciadv.adj041110.1126/sciadv.adj0411 ↗
51. 10.1002/adma.20230112410.1002/adma.202301124 ↗
52. 10.1163/15685610778119233710.1163/156856107781192337 ↗
53. 10.1038/nmat446310.1038/nmat4463 ↗
54. 10.1039/C8PY00868J10.1039/C8PY00868J ↗
55. 10.1002/advs.20240093810.1002/advs.202400938 ↗
56. 10.1021/acsami.1c1268710.1021/acsami.1c12687 ↗
57. 10.1016/j.cej.2020.12643110.1016/j.cej.2020.126431 ↗
58. 10.1039/C9TA14224J10.1039/C9TA14224J ↗
59. 10.1002/adfm.20220978710.1002/adfm.202209787 ↗
60. 10.1002/adfm.20240970310.1002/adfm.202409703 ↗
61. 10.1002/smll.20231007210.1002/smll.202310072 ↗