GLORIA

GEOMAR Library Ocean Research Information Access

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Online Resource  (2)
  • Wiley  (2)
  • Kong, Zhengyang  (2)
Material
  • Online Resource  (2)
Publisher
  • Wiley  (2)
Language
Years
  • 1
    In: Advanced Functional Materials, Wiley, Vol. 31, No. 10 ( 2021-03)
    Abstract: Polymeric elastomers play an increasingly important role in the development of stretchable electronics. A highly demanded elastic matrix is preferred to own not only excellent mechanical properties, but also additional features like high toughness and fast self‐healing. Here, a polyurethane (DA‐PU) is synthesized with donor and acceptor groups alternately distributed along the main chain to achieve both intra‐chain and inter‐chain donor‐acceptor self‐assembly, which endow the polyurethane with toughness, self‐healing, and, more interestingly, thermal repair, like human muscle. In detail, DA‐PU exhibits an amazing mechanical performance with elongation at break of 1900% and toughness of 175.9 MJ m −3 . Moreover, it shows remarkable anti‐fatigue and anti‐stress relaxation properties as manifested by cyclic tensile and stress relaxation tests, respectively. Even in case of large strain deformation or long‐time stretch, it can almost completely restore to original length by thermal repair at 60 °C in 60 s. The self‐healing speed of DA‐PU is gradually enhanced with the increasing temperature, and can be 1.0–6.15 µm min −1 from 60 to 80 °C. At last, a stretchable and self‐healable capacitive sensor is constructed and evaluated to prove that DA‐PU matrix can ensure the stability of electronics even after critical deformation and cut off.
    Type of Medium: Online Resource
    ISSN: 1616-301X , 1616-3028
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2021
    detail.hit.zdb_id: 2029061-5
    detail.hit.zdb_id: 2039420-2
    SSG: 11
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 2
    In: Advanced Functional Materials, Wiley, Vol. 32, No. 4 ( 2022-01)
    Abstract: Ionic skin (I‐Skin) has the advantage of feasible compatibility with biological systems. Nevertheless, developing a stable and durable ionic skin is challenging. Here, an ionic polyurethane (i‐PU) is synthesized, which is capable of self‐healing and able to lock the ionic liquids (ILs). In detail, an ionic chain extender containing an ammonium cationic group is synthesized, followed by the polymerization to obtain the target i‐PU. Through electrostatic interaction and chain diffusion, the i‐PU can be fully self‐healed at room temperature within 400 min. Afterward, low contact angle (37°) of the i‐PU against IL and the density functional theory (DFT) calculation prove their good compatibility and strong interaction, originating from the electrostatic interaction. The Raman intensity map shows the reversible process of the enrichment and restoration of ionic concentration on the i‐PU/IL surface when external pressure is applied or released, proving stable binding of ions by ionic polymer chains. Lastly, the self‐healing I‐Skin based on the i‐PU/IL is fabricated with a wide range of pressures (0–120 kPa), fast response time (32 ms), excellent antifatigue property (2% attenuation after 1000 cycles), and remarkable sensitivity (52.4 kPa –1 ).
    Type of Medium: Online Resource
    ISSN: 1616-301X , 1616-3028
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2022
    detail.hit.zdb_id: 2029061-5
    detail.hit.zdb_id: 2039420-2
    SSG: 11
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...