4.7 Review

Progress in Utilizing Dynamic Bonds to Fabricate Structurally Adaptive Self-Healing, Shape Memory, and Liquid Crystal Polymers

Journal

MACROMOLECULAR RAPID COMMUNICATIONS
Volume 43, Issue 5, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/marc.202100768

Keywords

dynamic bonds; liquid crystal elastomers; self-healing; shape memory; structurally adaptive polymers

Funding

  1. National Natural Science Foundation of China [52103145, 51973137]
  2. Fundamental Research Funds for the Central Universities [1082204112682]
  3. State Key Laboratory of Polymer Materials Engineering [sklpme2020-1-06]

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Stimuli-responsive structurally dynamic polymers have gained significant attention due to their potential applications and ability to exhibit various responses such as self-healing and shape-morphing. This review article focuses on recent advances and challenges in the development of dynamic polymers, specifically dynamic self-healing polymers, shape-memory polymers, and liquid crystal elastomers. The authors discuss the chemistry strategies and dynamic reaction mechanisms that enhance the materials' performances, including self-healing, reprocessing, and reprogramming. The article also provides an outline of unresolved issues and future perspectives in this field.
Stimuli-responsive structurally dynamic polymers are capable of mimicking the biological systems to adapt themselves to the surrounding environmental changes and subsequently exhibiting a wide range of responses ranging from self-healing to complex shape-morphing. Dynamic self-healing polymers (SHPs), shape-memory polymers (SMPs), and liquid crystal elastomers (LCEs), which are three representative examples of stimuli-responsive structurally dynamic polymers, have been attracting broad and growing interest in recent years because of their potential applications in the fields of electronic skin, sensors, soft robots, artificial muscles, and so on. Recent advances and challenges in the developments toward dynamic SHPs, SMPs, and LCEs are reviewed, focusing on the chemistry strategies and the dynamic reaction mechanisms that enhance the performances of the materials including self-healing, reprocessing, and reprogramming. The different dynamic chemistries and their mechanisms on the enhanced functions of the materials are compared and discussed, where three summary tables are presented: A library of dynamic bonds and the resulting characteristics of the materials. Finally, a critical outline of the unresolved issues and future perspectives on the emerging developments is provided.

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