AI Article Synopsis

  • - Biological tissues exhibit multiple responses and functions, and integrating responsive polymers into hierarchical soft architectures could mimic these properties in synthetic systems.
  • - The newly developed nanoparticle-in-micropore (NP-MP) architecture in mechanochromic polymers enhances the sensitivity and stretchability of electronic skins (e-skins), effectively responding to force with improved mechanochemical activation.
  • - This innovative structure allows for a dual-mode functionality in e-skins, enabling the detection of both static and dynamic forces, and demonstrates high sensitivity under various strains, making it a versatile platform for future mechanochromic composites.

Article Abstract

Biological tissues are multiresponsive and functional, and similar properties might be possible in synthetic systems by merging responsive polymers with hierarchical soft architectures. For example, mechanochromic polymers have applications in force-responsive colorimetric sensors and soft robotics, but their integration into sensitive, multifunctional devices remains challenging. Herein, a hierarchical nanoparticle-in-micropore (NP-MP) architecture in porous mechanochromic polymers, which enhances the mechanosensitivity and stretchability of mechanochromic electronic skins (e-skins), is reported. The hierarchical NP-MP structure results in stress-concentration-induced mechanochemical activation of mechanophores, significantly improving the mechanochromic sensitivity to both tensile strain and normal force (critical tensile strain: 50% and normal force: 1 N). Furthermore, the porous mechanochromic composites exhibit a reversible mechanochromism under a strain of 250%. This architecture enables a dual-mode mechanochromic e-skin for detecting static/dynamic forces via mechanochromism and triboelectricity. The hierarchical NP-MP architecture provides a general platform to develop mechanochromic composites with high sensitivity and stretchability.

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Source
http://dx.doi.org/10.1002/adma.201808148DOI Listing

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