Design Strategies and Perspectives on the Toughening of Hydrogels via Fully Physical Cross-Linking
Source abstract
Abstract
Conventional hydrogels are inherently brittle and mechanically weak, limiting their application in load-bearing or dynamic environments. Although extensive development has been made in hydrogel toughening, the most dominant techniques rely upon chemical cross-linking, which restrains their adaptability and functionality because of the permanence of covalent bonds. While dynamic covalent bonds have been introduced to enhance reversibility in covalently cross-linked systems, they often require harsher conditions, display delayed responsiveness, and involve more complex chemistry. Given these challenges, physical cross-linking methods─such as metal–ligand coordination cross-links, crystalline region formation, electrostatic interactions, hydrophobic association, polymer chain entanglement, host–guest interaction, and hydrogen bonding─have been considered promising strategies to enhance both toughness and dynamic features. These characteristics provide high versatility and practicality, enabling advanced applications in areas such as soft robotics and tissue engineering. This review presents a comprehensive analysis of strategies and perspectives for toughening hydrogels via fully physical cross-linking and highlights emerging applications that exploit the unique advantages of reversible physical networks.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Hydrogels: synthesis, properties, applications · Advanced Materials and Mechanics · biodegradable polymer synthesis and properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute of Materials Research and Engineering (IMRE), Agency for Science, Technology, and Research (A*STAR), 2 Fusionopolis Way, Innovis #08-03, Singapore 138634, Republic of Singapore
Funding
Agency for Science, Technology and Research
References (100+)
Show source-provided references
1. 10.1002/adem.20240094410.1002/adem.202400944 ↗
2. 10.1002/btm2.1068010.1002/btm2.10680 ↗
3. 10.1080/14686996.2025.246949010.1080/14686996.2025.2469490 ↗
4. 10.3390/antibiotics1003024810.3390/antibiotics10030248 ↗
5. 10.1039/D3BM01766D10.1039/D3BM01766D ↗
6. 10.1007/s10853-015-9382-510.1007/s10853-015-9382-5 ↗
7. 10.1515/revce-2020-003910.1515/revce-2020-0039 ↗
8. 10.1002/app.5431210.1002/app.54312 ↗
9. 10.1016/j.eurpolymj.2022.11180710.1016/j.eurpolymj.2022.111807 ↗
10. 10.1016/j.cis.2023.10299910.1016/j.cis.2023.102999 ↗
11. 10.1016/j.carbpol.2024.12191210.1016/j.carbpol.2024.121912 ↗
12. 10.1002/btm2.1031510.1002/btm2.10315 ↗
13. 10.1016/j.aiepr.2023.06.00210.1016/j.aiepr.2023.06.002 ↗
14. 10.1038/s43246-023-00402-210.1038/s43246-023-00402-2 ↗
15. 10.1002/anie.20231083210.1002/anie.202310832 ↗
16. 10.1002/asia.20220067710.1002/asia.202200677 ↗
17. 10.1080/15583724.2022.213752510.1080/15583724.2022.2137525 ↗
18. 10.33448/rsd-v12i8.4307310.33448/rsd-v12i8.43073 ↗
19. 10.1002/pol.2022015410.1002/pol.20220154 ↗
20. 10.3390/gels202001610.3390/gels2020016 ↗
21. 10.1002/adma.20150123410.1002/adma.201501234 ↗
22. 10.1039/D5LP00038F10.1039/D5LP00038F ↗
23. 10.1016/j.eurpolymj.2017.05.02010.1016/j.eurpolymj.2017.05.020 ↗
24. 10.1038/s41578-021-00412-x10.1038/s41578-021-00412-x ↗
25. 10.3390/gels806033910.3390/gels8060339 ↗
26. 10.1021/acs.macromol.3c0096710.1021/acs.macromol.3c00967 ↗
27. 10.3390/biomimetics303001510.3390/biomimetics3030015 ↗
28. 10.1002/adhm.20210001210.1002/adhm.202100012 ↗
29. 10.1016/j.mtcomm.2021.10275710.1016/j.mtcomm.2021.102757 ↗
30. 10.1016/j.eurpolymj.2018.01.02010.1016/j.eurpolymj.2018.01.020 ↗
31. 10.1002/adfm.20160164510.1002/adfm.201601645 ↗
32. 10.1039/D4TA04767B10.1039/D4TA04767B ↗
33. 10.3390/ijms24171304210.3390/ijms241713042 ↗
34. 10.1039/D0TB00424C10.1039/D0TB00424C ↗
35. 10.1002/polb.2472910.1002/polb.24729 ↗
36. 10.1016/j.cej.2024.15614410.1016/j.cej.2024.156144 ↗
37. 10.1016/j.cej.2018.05.08110.1016/j.cej.2018.05.081 ↗
38. 10.1016/j.fochx.2023.10072810.1016/j.fochx.2023.100728 ↗
39. 10.1039/C8BM01246F10.1039/C8BM01246F ↗
40. 10.1007/s43939-025-00178-x10.1007/s43939-025-00178-x ↗
41. 10.3390/gels704018210.3390/gels7040182 ↗
42. 10.1002/adma.20150155810.1002/adma.201501558 ↗
43. 10.1002/marc.20180083710.1002/marc.201800837 ↗
44. 10.1039/D3CS00705G10.1039/D3CS00705G ↗
45. 10.1088/2053-1591/acb98e10.1088/2053-1591/acb98e ↗
46. 10.1016/j.eurpolymj.2021.11097410.1016/j.eurpolymj.2021.110974 ↗
47. 10.1002/adtp.20240016510.1002/adtp.202400165 ↗
48. 10.1021/acs.langmuir.3c0225510.1021/acs.langmuir.3c02255 ↗
49. 10.1007/s13233-025-00380-z10.1007/s13233-025-00380-z ↗
50. 10.1021/ja002845g10.1021/ja002845g ↗
51. 10.1021/ar030284310.1021/ar0302843 ↗
52. Maréchal, Y. 1─the Hydrogen Bond: Formation, Thermodynamic Properties, Classification. In The Hydrogen Bond and the Water Molecule, Maréchal, Y., Ed. Elsevier: Amsterdam, 2007; pp 3-24.10.1016/B978-044451957-3.50002-0 ↗
53. 10.1021/ct600271910.1021/ct6002719 ↗
54. Hassan, C. M.; Peppas, N. A. Structure and Applications of Poly(Vinyl Alcohol) Hydrogels Produced by Conventional Crosslinking or by Freezing/Thawing Methods. In Biopolymers · PVA Hydrogels, Anionic Polymerisation Nanocomposites, Springer Berlin Heidelberg: Berlin, Heidelberg, 2000; pp 37–65.10.1007/3-540-46414-X_2 ↗
55. 10.1016/j.aca.2019.06.02910.1016/j.aca.2019.06.029 ↗
56. 10.1002/smll.20240187010.1002/smll.202401870 ↗
57. 10.1038/s41528-024-00327-x10.1038/s41528-024-00327-x ↗
58. 10.1016/j.eurpolymj.2018.10.03110.1016/j.eurpolymj.2018.10.031 ↗
59. 10.1038/s41586-023-06037-010.1038/s41586-023-06037-0 ↗
60. 10.1002/mabi.20180028110.1002/mabi.201800281 ↗
61. 10.1021/acs.macromol.1c0111510.1021/acs.macromol.1c01115 ↗
62. 10.1038/nchem.89310.1038/nchem.893 ↗
63. 10.1016/j.ijbiomac.2024.13139410.1016/j.ijbiomac.2024.131394 ↗
64. 10.1002/adma.20240008410.1002/adma.202400084 ↗
65. 10.1002/adfm.20240261310.1002/adfm.202402613 ↗
66. 10.1038/s41586-021-03212-z10.1038/s41586-021-03212-z ↗
67. 10.1021/acsnano.3c1106310.1021/acsnano.3c11063 ↗
68. 10.1038/nmat371310.1038/nmat3713 ↗
69. 10.1039/C5SM01423A10.1039/C5SM01423A ↗
70. 10.1021/acs.biomac.9b0122310.1021/acs.biomac.9b01223 ↗
71. 10.1039/C6TB01606E10.1039/C6TB01606E ↗
72. 10.3390/polym1102035210.3390/polym11020352 ↗
73. 10.1021/acsapm.0c0046410.1021/acsapm.0c00464 ↗
74. 10.1039/c2jm32541a10.1039/c2jm32541a ↗
75. 10.1126/sciadv.adj685610.1126/sciadv.adj6856 ↗
76. 10.1039/C5TA08166A10.1039/C5TA08166A ↗
77. 10.1016/j.molliq.2023.12185710.1016/j.molliq.2023.121857 ↗
78. 10.1016/j.colsurfb.2024.11421810.1016/j.colsurfb.2024.114218 ↗
79. 10.1039/D4TB00510D10.1039/D4TB00510D ↗
80. 10.1016/0168-3659(91)90007-Z10.1016/0168-3659(91)90007-Z ↗
81. 10.1002/adfm.20221230210.1002/adfm.202212302 ↗
82. 10.3390/polym1505106510.3390/polym15051065 ↗
83. 10.3390/gels1007044410.3390/gels10070444 ↗
84. 10.1002/smtd.20220159210.1002/smtd.202201592 ↗
85. 10.1002/adma.20240667110.1002/adma.202406671 ↗
86. 10.1021/acs.chemmater.2c0300410.1021/acs.chemmater.2c03004 ↗
87. 10.1016/j.ijbiomac.2022.11.28410.1016/j.ijbiomac.2022.11.284 ↗
88. 10.1038/s41563-022-01195-410.1038/s41563-022-01195-4 ↗
89. 10.1038/s41563-023-01648-410.1038/s41563-023-01648-4 ↗
90. 10.1021/acsmacrolett.5c0018810.1021/acsmacrolett.5c00188 ↗
91. 10.1016/j.cej.2024.15440910.1016/j.cej.2024.154409 ↗
92. 10.1002/smll.20230120410.1002/smll.202301204 ↗
93. 10.1039/D3TA03811D10.1039/D3TA03811D ↗
94. 10.1016/j.eml.2019.10057210.1016/j.eml.2019.100572 ↗
95. 10.1016/j.jmbbm.2025.10702710.1016/j.jmbbm.2025.107027 ↗
96. 10.3390/bioengineering1105041510.3390/bioengineering11050415 ↗
97. 10.1016/j.polymer.2020.12303910.1016/j.polymer.2020.123039 ↗
98. 10.1016/j.carbpol.2019.11559610.1016/j.carbpol.2019.115596 ↗
99. 10.1038/s41467-025-59875-z10.1038/s41467-025-59875-z ↗
100. 10.1039/D0PY00294A10.1039/D0PY00294A ↗