4.6 Article

Superior stretchable, low thermal resistance and efficient self-healing composite elastomers for thermal management

Journal

JOURNAL OF MATERIALS CHEMISTRY A
Volume 10, Issue 41, Pages 21923-21932

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2ta05781f

Keywords

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Funding

  1. National Natural Science Foundation of China [52073300]
  2. Guangdong Province Key Field R&D Program Project [2020B010190004]
  3. Key Project of Science and Technology of Changsha [kq2102005]
  4. Youth Innovation Promotion Association of the Chinese Academy of Sciences [2019354]
  5. Shenzhen Science and Technology Research Fund [JCYJ20200109114401708, JCYJ20180507182530279]

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In this study, a poly(thioctic acid)/aluminum composite elastomer was successfully fabricated with enhanced stretchability, high thermal conductivity, and excellent self-healing efficiency. The combination of supramolecular interactions and covalent adaptable networks contributed to the superior properties of the composite. This research provides a practical method for designing thermally conductive self-healing composites with stretchability and recyclability, which are essential for heat dissipation in advanced electronic devices.
Thermally conductive polymer-based composites with the combination of superior stretchability, efficient self-healing, recyclability and high thermal conductivity have long been pursued in the modern electronics industry. However, integrating these attractive properties remains challenging due to the complexity of the composite structure and composition. In this work, by fabricating covalent adaptable networks and introducing supramolecular interactions, we prepared a poly(thioctic acid)/aluminum (poly(TA)/Al) composite elastomer. The prevalent supramolecular interactions provide the poly(TA)/Al with enhanced interfacial interaction and a stretchable covalent adaptable network, leading to superior stretchability (1640%), enhanced thermal conductivity (1.83 W mK(-1)) and excellent self-healing efficiency (96% and 98% at 80 degrees C for tensile elongation and thermal conductivity, respectively). Moreover, the dynamically reversible covalent adaptable network ensures solid-state plasticity and thermally induced recyclability of the poly(TA)/Al, which can maintain desirable mechanical and thermal conductivity. The current work provides a practical method to design thermally conductive self-healing composites with stretchability and recyclability, which are needed for the heat dissipation of advanced electronic devices.

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