TY - JOUR
T1 - Hierarchical hydrogen bonds directed multi-functional carbon nanotube-based supramolecular hydrogels
AU - Du, Ran
AU - Wu, Juanxia
AU - Chen, Liang
AU - Huang, Huan
AU - Zhang, Xuetong
AU - Zhang, Jin
PY - 2014/4/9
Y1 - 2014/4/9
N2 - Supramolecular hydrogels (SMHs) are three-dimensional networks filled with a large amount of water. The crosslinking force in the 3D network is always constructed by relatively weak and dynamic non-covalent interactions, and thus SMHs usually possess extremely high susceptibility to external environment and can show extraordinary stimuli-responsive, self-healing or other attractive properties. However, the overall crosslinking force in hydrogel networks is difficult to flexibly modulate, and this leads to limited functions of the SMHs. In this regard, hierarchical hydrogen bonds, that is, the mixture of relatively strong and relatively weak hydrogen bonds, are used herein as crosslinking force for the hydrogel preparation. The ratio of strong and weak hydrogen bonds can be finely tuned to tailor the properties of resultant gels. Thus, by delicate manipulation of the overall crosslinking force in the system, a hydrogel with multiple (thermal, pH and NIR light) responsiveness, autonomous self-healing property and interesting temperature dependent, reversible adhesion behavior is obtained. This kind of hierarchical hydrogen bond manipulation is proved to be a general method for multiple-functionality hydrogel preparation, and the resultant material shows potential for a range of applications. Carbon nanotube-based multiple responsive (thermal, pH, NIR light) supramolecular hydrogels with extraordinary self-healing performance and interesting adhesion behavior are prepared via simple mixing aqueous solution of carboxylic carbon nanotubes and polyethylene polyamine, and the ratio of strong hydrogen bonds to weak ones in hydrogel could be finely tuned by controlling the relative content of two precursors.
AB - Supramolecular hydrogels (SMHs) are three-dimensional networks filled with a large amount of water. The crosslinking force in the 3D network is always constructed by relatively weak and dynamic non-covalent interactions, and thus SMHs usually possess extremely high susceptibility to external environment and can show extraordinary stimuli-responsive, self-healing or other attractive properties. However, the overall crosslinking force in hydrogel networks is difficult to flexibly modulate, and this leads to limited functions of the SMHs. In this regard, hierarchical hydrogen bonds, that is, the mixture of relatively strong and relatively weak hydrogen bonds, are used herein as crosslinking force for the hydrogel preparation. The ratio of strong and weak hydrogen bonds can be finely tuned to tailor the properties of resultant gels. Thus, by delicate manipulation of the overall crosslinking force in the system, a hydrogel with multiple (thermal, pH and NIR light) responsiveness, autonomous self-healing property and interesting temperature dependent, reversible adhesion behavior is obtained. This kind of hierarchical hydrogen bond manipulation is proved to be a general method for multiple-functionality hydrogel preparation, and the resultant material shows potential for a range of applications. Carbon nanotube-based multiple responsive (thermal, pH, NIR light) supramolecular hydrogels with extraordinary self-healing performance and interesting adhesion behavior are prepared via simple mixing aqueous solution of carboxylic carbon nanotubes and polyethylene polyamine, and the ratio of strong hydrogen bonds to weak ones in hydrogel could be finely tuned by controlling the relative content of two precursors.
KW - carbon nanotubes
KW - hierarchical hydrogen bonds
KW - self-healing
KW - stimuli-responsive
KW - supramolecular hydrogel
UR - http://www.scopus.com/inward/record.url?scp=84891836203&partnerID=8YFLogxK
U2 - 10.1002/smll.201302649
DO - 10.1002/smll.201302649
M3 - Article
C2 - 24130077
AN - SCOPUS:84891836203
SN - 1613-6810
VL - 10
SP - 1387
EP - 1393
JO - Small
JF - Small
IS - 7
ER -