General Strategy To Fabricate Strong and Tough Low-Molecular-Weight Gelator-Based Supramolecular Hydrogels with Double Network Structure

被引:93
作者
Chen, Feng
Chen, Qiang [1 ]
Zhu, Lin [1 ]
Tang, Ziqing [1 ]
Li, Qingfeng [2 ]
Qin, Gang [1 ]
Yang, Jia [1 ]
Zhang, Yanxian [3 ]
Ren, Baiping [3 ]
Zheng, Jie [3 ]
机构
[1] Henan Polytech Univ, Sch Mat Sci & Engn, Jiaozuo 454003, Peoples R China
[2] Zhoukou Normal Univ, Key Lab Rare Earth Funct Mat & Applicat, Zhoukou 466001, Peoples R China
[3] Univ Akron, Dept Chem & Biomol Engn, Akron, OH 44325 USA
基金
美国国家科学基金会;
关键词
HIGH MECHANICAL STRENGTH; HYBRID HYDROGELS; NANOCOMPOSITE HYDROGELS; FATIGUE RESISTANCE; SOFT MATERIALS; SELF-RECOVERY; POLYMER; GEL; ROBUST; ENHANCEMENT;
D O I
10.1021/acs.chemmater.8b00063
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
Low-molecular-weight gelator (LMWG)-based supramolecular hydrogels, self-assembled by small molecules via noncovalent interactions, have recently attracted great attention due to their unique structure-property relationship and potential applications spanning from functional materials to biomedical devices. Unfortunately, many LMWG-based supramolecular hydrogels are mechanically weak and can not even be handled by conventional tensile and tearing tests. Here, we propose several design principles to fabricate new LMWG-based hydrogels with a true double-network structure (G4 center dot K+/PDMAAm DN gels), consisting of the supramolecular self-assembly of guanosine, B(OH)(3) and KOH as the first, physical G4 center dot K+ network and the covalently cross-linked poly(N,N'-dimethyacrylamide) (PDMAAm) as the second, chemical network. Different from those LMWG-based supramolecular hydrogels, G4 center dot K+/PDMAAm DN gels exhibit high tensile properties (elastic modulus = 0.307 MPa, tensile stress = 0.273 MPa, tensile strain = 17.62 mm/mm, and work of extension = 3.23 MJ/m(3)) and high toughness (tearing energies = 1640 J/m(2)). Meanwhile, the dynamic, noncovalent bonds in the G4 center dot K+ network can reorganize and reform after being broken, resulting in rapid self-recovery property and excellent fatigue resistance. The stiffness/toughness of G4 center dot K+/PDMAAm DN gels can be recovered by 65%/58% with 1 min resting at room temperature, and the recovery rates are further improved with the increase of temperatures and resting times. Interestingly, G4 center dot K+/PDMAAm DN gels also exhibit UV-triggered luminescence due to the unique G4-quartet structure in the G4 center dot K+ supramolecular first network. A new toughening mechanism is proposed to interpret the high strength and toughness of G4 center dot K+/PDMAAm DN gels. We believe that our design principles, along with new G4 center dot K+/PDMAAm DN gel system, will provide a new viewpoint for realizing the tough and strong LMWG-based gels.
引用
收藏
页码:1743 / 1754
页数:12
相关论文
共 53 条
[21]   A novel hydrogel with high mechanical strength: A macromolecular microsphere composite hydrogel [J].
Huang, Ting ;
Xu, Hongguang ;
Jiao, Kexin ;
Zhu, Liping ;
Brown, Hugh R. ;
Wang, Huiliang .
ADVANCED MATERIALS, 2007, 19 (12) :1622-+
[22]   Highly Conductive Ionic-Liquid Gels Prepared with Orthogonal Double Networks of a Low-Molecular-Weight Gelator and Cross-Linked Polymer [J].
Kataoka, Toshikazu ;
Ishioka, Yumi ;
Mizuhata, Minoru ;
Minami, Hideto ;
Maruyama, Tatsuo .
ACS APPLIED MATERIALS & INTERFACES, 2015, 7 (41) :23346-23352
[23]   Hydrogels for tissue engineering [J].
Lee, KY ;
Mooney, DJ .
CHEMICAL REVIEWS, 2001, 101 (07) :1869-1879
[24]   Hybrid Hydrogels with Extremely High Stiffness and Toughness [J].
Li, Jianyu ;
Illeperuma, Widusha B. K. ;
Suo, Zhigang ;
Vlassak, Joost J. .
ACS MACRO LETTERS, 2014, 3 (06) :520-523
[25]   Hydrophobically associated hydrogels based on acrylamide and anionic surface active monomer with high mechanical strength [J].
Li, Wenbo ;
An, Huiyong ;
Tan, Ying ;
Lu, Cuige ;
Liu, Chang ;
Li, Pengchong ;
Xu, Kun ;
Wang, Pixin .
SOFT MATTER, 2012, 8 (18) :5078-5086
[26]   Recoverable and Self-Healing Double Network Hydrogel Based on κ-Carrageenan [J].
Liu, Sijun ;
Li, Lin .
ACS APPLIED MATERIALS & INTERFACES, 2016, 8 (43) :29749-29758
[27]   Oppositely Charged Polyelectrolytes Form Tough, Self-Healing, and Rebuildable Hydrogels [J].
Luo, Feng ;
Sun, Tao Lin ;
Nakajima, Tasuku ;
Kurokawa, Takayuki ;
Zhao, Yu ;
Sato, Koshiro ;
Bin Ihsan, Abu ;
Li, Xufeng ;
Guo, Honglei ;
Gong, Jian Ping .
ADVANCED MATERIALS, 2015, 27 (17) :2722-+
[28]   Dual enzymatic formation of hybrid hydrogels with supramolecular-polymeric networks [J].
Mao, Yanjie ;
Su, Teng ;
Wu, Qing ;
Liao, Chuanan ;
Wang, Qigang .
CHEMICAL COMMUNICATIONS, 2014, 50 (92) :14429-14432
[29]   Tunable drug delivery using chemoselective functionalization of hydrogels [J].
Mauri, Emanuele ;
Rossi, Filippo ;
Sacchetti, Alessandro .
MATERIALS SCIENCE AND ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS, 2016, 61 :851-857
[30]   Necking phenomenon of double-network gels [J].
Na, YH ;
Tanaka, Y ;
Kawauchi, Y ;
Furukawa, H ;
Sumiyoshi, T ;
Gong, JP ;
Osada, Y .
MACROMOLECULES, 2006, 39 (14) :4641-4645