TY - JOUR
T1 - Highly Stiff and Stretchable DNA Liquid Crystalline Organogels with Super Plasticity, Ultrafast Self-Healing, and Magnetic Response Behaviors
AU - Meng, Zhuojun
AU - Liu, Qing
AU - Zhang, Yi
AU - Sun, Jing
AU - Yang, Chenjing
AU - Li, Hongyan
AU - Loznik, Mark
AU - Göstl, Robert
AU - Chen, Dong
AU - Wang, Fan
AU - Clark, Noel A.
AU - Zhang, Hongjie
AU - Herrmann, Andreas
AU - Liu, Kai
N1 - Publisher Copyright:
© 2021 Wiley-VCH GmbH
PY - 2022/1/20
Y1 - 2022/1/20
N2 - DNA-based gels are attractive materials as they allow intuitive rational design, respond to external physicochemical stimuli, and show great potential for biomedical applications. However, their relatively poor mechanical properties currently limit their technological application considerably as the latter requires mechanical integrity and tunability. With this work, a DNA organogel is reported that gels through supramolecular interactions, which induce mesophase ordering, and that exhibits exceptional stretchability, deformability, plasticity, and biocompatibility. Moreover, the nature of the supramolecular bond enables complete self-healing within 3 s. Most importantly, the DNA-based liquid crystalline organogels exhibit impressive ultimate tensile strengths above 1 MPa, stiffness higher than 20 MPa, and toughness up to 18 MJ m−3, rendering these materials the strongest among reported DNA networks. In addition, the facile access is demonstrated to composite DNA materials by blending magnetic nanoparticles with the organogel matrix giving access to magnetic field induced actuation. It is believed that these findings contribute significantly to the advancement of DNA gels for their use in smart materials and biomedical applications.
AB - DNA-based gels are attractive materials as they allow intuitive rational design, respond to external physicochemical stimuli, and show great potential for biomedical applications. However, their relatively poor mechanical properties currently limit their technological application considerably as the latter requires mechanical integrity and tunability. With this work, a DNA organogel is reported that gels through supramolecular interactions, which induce mesophase ordering, and that exhibits exceptional stretchability, deformability, plasticity, and biocompatibility. Moreover, the nature of the supramolecular bond enables complete self-healing within 3 s. Most importantly, the DNA-based liquid crystalline organogels exhibit impressive ultimate tensile strengths above 1 MPa, stiffness higher than 20 MPa, and toughness up to 18 MJ m−3, rendering these materials the strongest among reported DNA networks. In addition, the facile access is demonstrated to composite DNA materials by blending magnetic nanoparticles with the organogel matrix giving access to magnetic field induced actuation. It is believed that these findings contribute significantly to the advancement of DNA gels for their use in smart materials and biomedical applications.
UR - https://www.scopus.com/pages/publications/85119290186
U2 - 10.1002/adma.202106208
DO - 10.1002/adma.202106208
M3 - 文章
C2 - 34734442
AN - SCOPUS:85119290186
SN - 0935-9648
VL - 34
JO - Advanced Materials
JF - Advanced Materials
IS - 3
M1 - 2106208
ER -