Self-Healable and Tough Polymer Electrolyte Composites Based on Associative Nanostructural Networks

被引:4
作者
Lee, Yeonbae [1 ]
Kim, Minjun [1 ]
Kim, Heein [1 ]
Lee, Keun Hyung [2 ]
Kim, Sangwon [1 ]
机构
[1] Inha Univ, Dept Environm & Polymer Engn, Incheon 22212, South Korea
[2] Inha Univ, Dept Chem & Chem Engn, Incheon 22212, South Korea
关键词
self-healing; polymer electrolyte composite; ionic liquid; nanostructural association; ionogel; strain sensor; IONIC-LIQUID; TRIBLOCK COPOLYMER; SIDE-CHAIN; HYDROGELS; GELS; BEHAVIOR; CRYSTALLIZATION; IMPEDANCE; TRANSPORT;
D O I
10.1021/acsapm.2c00725
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The development of reversible nanostructural associations in graft copolymer architecture has enabled the fabrication of tough polymer electrolyte composites that exhibit autonomous self-healing properties at room temperature. Random copolymers comprising docosyl acrylates (A22) were employed to form network structures in ionic liquids. The behavior of the resulting composites was found to be dictated by associative domain formation and subsequent changes in the intermolecular interactions. Remarkable mechanical properties were achieved without undermining the self-healing capability via adjustments in the chemical structure. This feature is recognizably different considering the conventional trade-off relationship between selfhealing and mechanical properties. Thermal and scattering experiments were conducted to elucidate the structural evolution of the composites. The relative changes in the electrical properties upon mechanical deformation were utilized to realize self-healable strain sensors.
引用
收藏
页码:5821 / 5830
页数:10
相关论文
共 61 条
[1]   Design of high-toughness polyacrylamide hydrogels by hydrophobic modification [J].
Abdurrahmanoglu, Suzan ;
Can, Volkan ;
Okay, Oguz .
POLYMER, 2009, 50 (23) :5449-5455
[2]   THE RHEOLOGY OF SOLUTIONS OF ASSOCIATING POLYMERS - COMPARISON OF EXPERIMENTAL BEHAVIOR WITH TRANSIENT NETWORK THEORY [J].
ANNABLE, T ;
BUSCALL, R ;
ETTELAIE, R ;
WHITTLESTONE, D .
JOURNAL OF RHEOLOGY, 1993, 37 (04) :695-726
[3]  
Armand M, 2009, NAT MATER, V8, P621, DOI [10.1038/NMAT2448, 10.1038/nmat2448]
[4]   Nanophase separation and hindered glass transition in side-chain polymers [J].
Beiner, M ;
Huth, H .
NATURE MATERIALS, 2003, 2 (09) :595-599
[5]   A Healable Supramolecular Polymer Blend Based on Aromatic π-π Stacking and Hydrogen-Bonding Interactions [J].
Burattini, Stefano ;
Greenland, Barnaby W. ;
Merino, Daniel Hermida ;
Weng, Wengui ;
Seppala, Jonathan ;
Colquhoun, Howard M. ;
Hayes, Wayne ;
Mackay, Michael E. ;
Hamley, Ian W. ;
Rowan, Stuart J. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2010, 132 (34) :12051-12058
[6]   Optically healable supramolecular polymers [J].
Burnworth, Mark ;
Tang, Liming ;
Kumpfer, Justin R. ;
Duncan, Andrew J. ;
Beyer, Frederick L. ;
Fiore, Gina L. ;
Rowan, Stuart J. ;
Weder, Christoph .
NATURE, 2011, 472 (7343) :334-U230
[7]   Self-healing electronic skins for aquatic environments [J].
Cao, Yue ;
Tan, Yu Jun ;
Li, Si ;
Lee, Wang Wei ;
Guo, Hongchen ;
Cai, Yongqing ;
Wang, Chao ;
Tee, Benjamin C. -K. .
NATURE ELECTRONICS, 2019, 2 (02) :75-82
[8]   A Transparent, Self-Healing, Highly Stretchable Ionic Conductor [J].
Cao, Yue ;
Morrissey, Timothy G. ;
Acome, Eric ;
Allec, Sarah I. ;
Wong, Bryan M. ;
Keplinger, Christoph ;
Wang, Chao .
ADVANCED MATERIALS, 2017, 29 (10)
[9]   A Novel Design Strategy for Fully Physically Linked Double Network Hydrogels with Tough, Fatigue Resistant, and Self-Healing Properties [J].
Chen, Qiang ;
Zhu, Lin ;
Chen, Hong ;
Yan, Hongli ;
Huang, Lina ;
Yang, Jia ;
Zheng, Jie .
ADVANCED FUNCTIONAL MATERIALS, 2015, 25 (10) :1598-1607
[10]   A thermally re-mendable cross-linked polymeric material [J].
Chen, XX ;
Dam, MA ;
Ono, K ;
Mal, A ;
Shen, HB ;
Nutt, SR ;
Sheran, K ;
Wudl, F .
SCIENCE, 2002, 295 (5560) :1698-1702