Intrinsically Self-Healing Polymers: From Mechanistic Insight to Current Challenges

被引:277
作者
Li, Bingrui [1 ,2 ]
Cao, Peng-Fei [3 ]
Saito, Tomonori [2 ]
Sokolov, Alexei P. [4 ]
机构
[1] Univ Tennessee, Bredesen Ctr Interdisciplinary Res & Grad Educ, Knoxville, TN 37996 USA
[2] Oak Ridge Natl Lab, Chem Sci Div, Oak Ridge, TN 37830 USA
[3] Beijing Univ Chem Technol, State Key Lab Organ Inorgan Composites, Beijing 100029, Peoples R China
[4] Univ Tennessee, Dept Chem, Knoxville, TN 37996 USA
关键词
CROSS-LINKED POLYMER; SHAPE-MEMORY; ASSOCIATING POLYMERS; COORDINATION BONDS; METAL BATTERIES; DISULFIDE BOND; CARBON-DIOXIDE; DYNAMIC BONDS; NETWORKS; ELASTOMERS;
D O I
10.1021/acs.chemrev.2c00575
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Self-healing materials open new prospects for more sustainable technologies with improved material performance and devices' longevity. We present an overview of the recent developments in the field of intrinsically self-healing polymers, the broad class of materials based mostly on polymers with dynamic covalent and noncovalent bonds. We describe the current models of self-healing mechanisms and discuss several examples of systems with different types of dynamic bonds, from various hydrogen bonds to dynamic covalent bonds. The recent advances indicate that the most intriguing results are obtained on the systems that have combined different types of dynamic bonds. These materials demonstrate high toughness along with a relatively fast self-healing rate. There is a clear trade-off relationship between the rate of self-healing and mechanical modulus of the materials, and we propose design principles of polymers toward surpassing this trade-off. We also discuss various applications of intrinsically self-healing polymers in different applications intrinsically-healing polymers technologies and summarize the current challenges in the field. This review intends to provide guidance for the design of intrinsic self-healing polymers with required properties.
引用
收藏
页码:701 / 735
页数:35
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