Transforming non-adhesive hydrogels to reversible tough adhesives via mixed-solvent-induced phase separation

被引:69
作者
Cui, Wei [1 ,6 ]
Zhu, Ruijie [2 ]
Zheng, Yong [3 ]
Mu, Qifeng [3 ]
Pi, Menghan [1 ]
Chen, Qiang [4 ,5 ]
Ran, Rong [1 ]
机构
[1] Sichuan Univ, State Key Lab Polymer Mat Engn, Coll Polymer Sci & Engn, Chengdu 610065, Peoples R China
[2] Hokkaido Univ, Grad Sch Chem Sci & Engn, Sapporo, Hokkaido 0608628, Japan
[3] Hokkaido Univ, Grad Sch Life Sci, Sapporo, Hokkaido 0010021, Japan
[4] Univ Chinese Acad Sci, Wenzhou Inst, Wenzhou 352001, Peoples R China
[5] Henan Polytech Univ, Sch Mat Sci & Engn, Jiaozuo 454003, Henan, Peoples R China
[6] Hokkaido Univ, Global Inst Collaborat Res & Educ GI CoRE, Sapporo, Hokkaido 0010021, Japan
基金
中国国家自然科学基金;
关键词
DOUBLE-NETWORK HYDROGELS; FRACTURE; STIFFNESS;
D O I
10.1039/d1ta00433f
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Realizing tough adhesion between hydrogels and solid surfaces is crucial for developing emerging soft-rigid hybrid devices with a high level of complexity. However, this is extremely challenging for numerous non-adhesive hydrogels due to their weak interfacial interaction with solid surfaces and negligible mechanical dissipation. Here, we report a phase-separation strategy to transform traditionally non-adhesive hydrogels to tough glues for diverse solid surfaces, without the need for chemical treatment. Equilibrating a hydrogel in a mixture of both good and poor solvents induces phase separation, resulting in a significant increment of polymer volume fraction at the surface and in the bulk of the gel. The high-density polymer chains at the gel surface facilitate the formation of dense arrays of noncovalent bonds with the solid surfaces, improving the intrinsic work of adhesion and favoring the force transmission from the crack front to the bulk gel. Meanwhile, the phase-separated structure in the bulk gel allows significant mechanical dissipation upon interfacial separation. Such a synergy contributes to a high interfacial toughness. The tough adhesion, reaching over 1000 J m(-2), is instant and repeatable, with inappreciable loss in the interfacial toughness after over 100 attach/detach cycles. This facile, repeatable phase-separation approach is also universal, and can be induced by various mixed solvents and applies to multiple types of common non-adhesive hydrogels for tough yet detachable gel-solid adhesion.
引用
收藏
页码:9706 / 9718
页数:13
相关论文
共 48 条
[41]  
Vogel A.I., 1989, VOGELS TXB PRACTICAL
[42]   A Superior δ-MnO2 Cathode and a Self-Healing Zn-δ-MnO2 Battery [J].
Wang, Donghong ;
Wang, Lufeng ;
Liang, Guojin ;
Li, Hongfei ;
Liu, Zhuoxin ;
Tang, Zijie ;
Liang, Jianbo ;
Zhi, Chunyi .
ACS NANO, 2019, 13 (09) :10643-10652
[43]   Strength and toughness of adhesion of soft materials measured in lap shear [J].
Wang, Yecheng ;
Yang, Xuxu ;
Nian, Guodong ;
Suo, Zhigang .
JOURNAL OF THE MECHANICS AND PHYSICS OF SOLIDS, 2020, 143
[44]   Instant tough bonding of hydrogels for soft machines and electronics [J].
Wirthl, Daniela ;
Pichler, Robert ;
Drack, Michael ;
Kettlguber, Gerald ;
Moser, Richard ;
Gerstmayr, Robert ;
Hartmann, Florian ;
Bradt, Elke ;
Kaltseis, Rainer ;
Siket, Christian M. ;
Schausberger, Stefan E. ;
Hild, Sabine ;
Bauer, Siegfried ;
Kaltenbrunner, Martin .
SCIENCE ADVANCES, 2017, 3 (06)
[45]   Polyacrylamide hydrogels. I. Network imperfection [J].
Yang, Canhui ;
Yin, Tenghao ;
Suo, Zhigang .
JOURNAL OF THE MECHANICS AND PHYSICS OF SOLIDS, 2019, 131 :43-55
[46]   Hydrogel Adhesion: A Supramolecular Synergy of Chemistry, Topology, and Mechanics [J].
Yang, Jiawei ;
Bai, Ruobing ;
Chen, Baohong ;
Suo, Zhigang .
ADVANCED FUNCTIONAL MATERIALS, 2020, 30 (02)
[47]   Design Molecular Topology for Wet-Dry Adhesion [J].
Yang, Jiawei ;
Bai, Ruobing ;
Li, Jianyu ;
Yang, Canhui ;
Yao, Xi ;
Liu, Qihan ;
Vlassak, Joost J. ;
Mooney, David J. ;
Suo, Zhigang .
ACS APPLIED MATERIALS & INTERFACES, 2019, 11 (27) :24802-24811
[48]  
Yuk H, 2016, NAT MATER, V15, P190, DOI [10.1038/nmat4463, 10.1038/NMAT4463]