4.6 Article

An in situ and rapid self-healing strategy enabling a stretchable nanocomposite with extremely durable and highly sensitive sensing features

Journal

MATERIALS HORIZONS
Volume 8, Issue 1, Pages 250-258

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0mh01539c

Keywords

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Funding

  1. National Key R&D Program of China [2016YFA0200200]
  2. NSFC [51872146, 51673099, 51633002, 21421001]

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This study presents a reliable approach for constructing a mechanically stretchable and structurally healable sensing nanocomposite by nano-confining a dynamic host-guest supramolecular polymer network in a graphene-based multilevel nanocomposite matrix. The resulting material exhibits high durability, sensitivity, and stability, allowing it to undergo over one million stretching-releasing cycles at large strains.
Progress toward the development of wearable electromechanical sensors with durable and reliable sensing performance is critical for emerging wearable integrated electronic applications. However, it remains a long-standing challenge to realize mechanically stretchable sensing materials with extremely durable and high-performing sensing ability due to the fundamental dilemma lying in the sensing mechanism. In this work, we proposed an in situ and rapid self-healing strategy through nano-confining a dynamic host-guest supramolecular polymer network in a graphene-based multilevel nanocomposite matrix to fabricate a mechanically stretchable and structurally healable sensing nanocomposite which is provided with intriguing sensing durability and sensitivity simultaneously. When repeatedly stretching and releasing the nanocomposite sensing film, the fast association kinetics of cyclodextrin and adamantane host-guest inclusion complexes and good polymer chain dynamics in the supramolecular polymer network endowed by the nanoconfinement effect enable autonomous and rapid repair of the micro-cracks in situ generated in the sensing material. As a result, our strain sensing devices can achieve an extremely high durability and retain stable sensing performance even after over 100 000 stretching-releasing cycles at large strain of 50%. Moreover, the brittle nature originated from the inorganically dominated structure in conjunction with the thermodynamically stable host-guest interactions and dynamic hydrogen bonds inside the multilevel nanocomposite allow the sensing material to exhibit an ultrahigh gauge factor over 1500 with a large working strain of 58%. This work presents a reliable approach for the construction of ultradurable and high-performing wearable electronics.

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