Three-Dimensional Printable, Extremely Soft, Stretchable, and Reversible Elastomers from Molecular Architecture-Directed Assembly

被引:16
|
作者
Nian, Shifeng [1 ]
Zhu, Jinchang [1 ]
Zhang, Haozhe [2 ]
Gong, Zihao [1 ]
Freychet, Guillaume [3 ]
Zhernenkov, Mikhail [3 ]
Xu, Baoxing [2 ]
Cai, Li-Heng [1 ,4 ,5 ]
机构
[1] Univ Virginia, Dept Mat Sci & Engn, Soft Biomatter Lab, Charlottesville, VA 22904 USA
[2] Univ Virginia, Dept Aerosp & Mech Engn, Charlottesville, VA 22904 USA
[3] Brookhaven Natl Lab, Natl Synchrotron Light Source 2, Upton, NY 11973 USA
[4] Univ Virginia, Dept Chem Engn, Charlottesville, VA 22904 USA
[5] Univ Virginia, Dept Biomed Engn, Charlottesville, VA 22904 USA
关键词
SOLVENT-FREE; 3D; RELAXATION; HYDROGELS; DESIGN; MATTER;
D O I
10.1021/acs.chemmater.0c04659
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
3D printing elastomers enables the fabrication of many technologically important structures and devices such as tissue scaffolds, sensors, actuators, and soft robots. However, conventional 3D printable elastomers are intrinsically stiff; moreover, the process of printing often requires external mechanical support and/or post-treatment. Here, we exploit the self-assembly of a responsive linear-bottlebrush-linear triblock copolymer to create stimuli-reversible, extremely soft, and stretchable elastomers and demonstrate their applicability as inks for in situ direct- write printing 3D structures without the aid of external mechanical support or post-treatment. By developing a procedure for controlled synthesis of such architecturally designed block copolymers, we create elastomers with extensibility up to 600% and Young's moduli down to similar to 10(2) Pa, 10(6) times softer than plastics and more than 10(2) times softer than all existing 3D printable elastomers. Moreover, the elastomers are thermostable and remain to be solid up to 180 degrees C, yet they are 100% solvent-reprocessable. Their extreme softness, stretchability, thermostability, and solvent-reprocessability bode well for future applications.
引用
收藏
页码:2436 / 2445
页数:10
相关论文
共 11 条
  • [1] Controlled molecular self-assembly of complex three-dimensional structures in soft materials
    Huang, Changjin
    Quinn, David
    Suresh, Subra
    Hsia, K. Jimmy
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2018, 115 (01) : 70 - 74
  • [2] Self-assembly of guest-induced calix[4]arene nanocapsules into three-dimensional molecular architecture
    Zheng, Guo-li
    Li, Yin-Yan
    Deng, Rui-Ping
    Song, Shu-Yan
    Zhang, Hong-Jie
    [J]. CRYSTENGCOMM, 2008, 10 (06): : 658 - 660
  • [3] Magnetically Directed Self-Assembly of Electrospun Superparamagnetic Fibrous Bundles to Form Three-Dimensional Tissues with a Highly Ordered Architecture
    Lee, Wen-Yu
    Cheng, Wei-Yuan
    Yeh, Yi-Chun
    Lai, Chih-Huang
    Hwang, Shiaw-Min
    Hsiao, Chun-Wen
    Huang, Chia-Wen
    Chen, Mei-Chin
    Sung, Hsing-Wen
    [J]. TISSUE ENGINEERING PART C-METHODS, 2011, 17 (06) : 651 - 661
  • [4] Compacting an assembly of soft balls far beyond the jammed state: Insights from three-dimensional imaging
    Barés, Jonathan
    Cárdenas-Barrantes, Manuel
    Pinzón, Gustavo
    Andò, Edward
    Renouf, Mathieu
    Viggiani, Gioacchino
    Azéma, Emilien
    [J]. Physical Review E, 2023, 108 (04):
  • [5] Ligand-directed molecular architectures: Self-assembly of two-dimensional rectangular metallacycles and three-dimensional trigonal or tetragonal prisms
    Su, CY
    Cai, YP
    Chen, CL
    Smith, MD
    Kaim, W
    zur Loye, HC
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (28) : 8595 - 8613
  • [6] Designing three-dimensional ordered structures from directed self-assembly of block copolymer films in topographical templates
    Cao, Xuguang
    Zhang, Liangshun
    Gu, Jiabin
    Wang, Liquan
    Lin, Jiaping
    [J]. POLYMER, 2015, 72 : 10 - 20
  • [7] Reversible Multielectron Release from Redox-Active Three-Dimensional Molecular Barrels with Ruthenium-Alkenyl Moieties
    Das, Rajorshi
    Linseis, Michael
    Scheerer, Stefan
    Zoller, Katrin
    Senft, Laura
    Ivanovic-Burmazovic, Ivana
    Winter, Rainer F.
    [J]. INORGANIC CHEMISTRY, 2022, 61 (32) : 12662 - 12677
  • [8] Self-assembly of new three-dimensional molecular architectures constructed from silver(I)-hexamethylenetetramine layers with supramolecular interactions
    Zheng, SL
    Tong, ML
    Chen, XM
    Ng, SW
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 2002, (03): : 360 - 364
  • [9] Self-Assembly of Four Coordination Polymers in Three-Dimensional Entangled Architecture Showing Reversible Dynamic Solid-State Structural Transformation and Color-Changing Behavior upon Thermal Dehydration and Rehydration
    Ke, Szu-Yu
    Chang, Ya-Fan
    Wang, Hsin-Yu
    Yang, Ching-Chun
    Ni, Cheng-Wei
    Lin, Gu-Ying
    Chen, Tzu-Ting
    Ho, Mei-Lin
    Lee, Gene-Hsiang
    Chuang, Yu-Chun
    Wang, Chih-Chieh
    [J]. CRYSTAL GROWTH & DESIGN, 2014, 14 (08) : 4011 - 4018
  • [10] 4,4′-Dipyridyl-N,N′-dioxide complexes of metal-thiocyanate/selenocyanate:: π-stacked molecular rods as three-dimensional support for two-dimensional polymeric sheets and intra/interchain S•••S interaction dependent architecture of the R22(8) synthon driven assembly of one-dimensional polymeric chains
    Jana, Atish Dipankar
    Manna, Subal Chandra
    Rosair, Georgina M.
    Drew, Michael G. B.
    Mostafa, Golam
    Chaudhuri, Nirmalendu Ray
    [J]. CRYSTAL GROWTH & DESIGN, 2007, 7 (07) : 1365 - 1372