TY - JOUR
T1 - Microfluidic-Directed Hydrogel Fabrics Based on Interfibrillar Self-Healing Effects
AU - Li, Qing
AU - Xu, Zhi
AU - Du, Xiafang
AU - Du, Xiangyun
AU - Cheng, Hengyang
AU - Wu, Guan
AU - Wang, Cai Feng
AU - Cui, Zhanfeng
AU - Chen, Su
N1 - Publisher Copyright:
© Copyright 2018 American Chemical Society.
PY - 2018/12/26
Y1 - 2018/12/26
N2 - Multistructural and versatile fibers have attracted enormous interests in various potential applications ranging from tissue engineering and cells to sensors. However, the controllable fabrication and nonwoven assembly of fibers remain a challenge. Here, we developed a novel strategy to in situ fabricate supramolecular hydrogel fibers via microfluidic spinning technology where self-healing fibers can be nonwoven assembled into fabrics through noncovalent interactions (host-guest interactions). We utilized β-cyclodextrin as the host molecule and N-vinylimidazole as the guest molecule to achieve self-healing supramolecular hydrogel fibers. Through design of different microreactors, the beaded, cylindrical, and knotted structure in fibers were achieved. Additionally, we constructed multidimensional (2D plane, 3D bulk, and 3D spiral textile) materials by using self-healing fibers as building blocks. In virtue of the host-guest assembly, the as-fabricated fabric exhibits high flexibility with high strength and long-term stretching behavior. From a practical standpoint, we employed the hydrogel fibers to construct a self-healing conductive composite wire and a plane-shaped supercapacitor, which could power light-emitting diodes. Our main aim is to clarify the paramount role of designing various fabrics through noncovalent interactions based on the interfibrillar self-healing feature, which gives a new insight into the facile fabrication of fabrics as well as the next-generation wearable textiles.
AB - Multistructural and versatile fibers have attracted enormous interests in various potential applications ranging from tissue engineering and cells to sensors. However, the controllable fabrication and nonwoven assembly of fibers remain a challenge. Here, we developed a novel strategy to in situ fabricate supramolecular hydrogel fibers via microfluidic spinning technology where self-healing fibers can be nonwoven assembled into fabrics through noncovalent interactions (host-guest interactions). We utilized β-cyclodextrin as the host molecule and N-vinylimidazole as the guest molecule to achieve self-healing supramolecular hydrogel fibers. Through design of different microreactors, the beaded, cylindrical, and knotted structure in fibers were achieved. Additionally, we constructed multidimensional (2D plane, 3D bulk, and 3D spiral textile) materials by using self-healing fibers as building blocks. In virtue of the host-guest assembly, the as-fabricated fabric exhibits high flexibility with high strength and long-term stretching behavior. From a practical standpoint, we employed the hydrogel fibers to construct a self-healing conductive composite wire and a plane-shaped supercapacitor, which could power light-emitting diodes. Our main aim is to clarify the paramount role of designing various fabrics through noncovalent interactions based on the interfibrillar self-healing feature, which gives a new insight into the facile fabrication of fabrics as well as the next-generation wearable textiles.
UR - http://www.scopus.com/inward/record.url?scp=85058556527&partnerID=8YFLogxK
U2 - 10.1021/acs.chemmater.8b03579
DO - 10.1021/acs.chemmater.8b03579
M3 - 文章
AN - SCOPUS:85058556527
SN - 0897-4756
VL - 30
SP - 8822
EP - 8828
JO - Chemistry of Materials
JF - Chemistry of Materials
IS - 24
ER -