Publications by authors named "Burebi Yiming"

Stretchable elastic materials with high strength, toughness, and good ionic conductivity are highly desirable for wearable devices and stretchable batteries. Unfortunately, limited success has been reported to attain all of these properties simultaneously. Here, we report a family of ionically conductive elastomers (ICEs) without compromise between mechanical properties (high stiffness, reversible elasticity, fracture resistance) and ionic conductivity, by introducing a multiple network elastomer (MNE) architecture into a low polymer.

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Article Synopsis
  • - Endotracheal intubation is crucial for critically ill patients but can lead to tissue damage and ventilator-associated pneumonia (VAP) due to biofilms created by drug-resistant pathogens.
  • - A new hydrogel catheter made from quaternary phosphonium salts is designed to be more tissue-friendly and prevent infections by inhibiting stubborn bacteria and fungi.
  • - This hydrogel displays strong antimicrobial properties, effectively killing most multi-drug resistant bacteria and fungi, and successfully prevents biofilm formation, thereby reducing the risk of VAP.
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Soft ionic conductors, such as hydrogels and ionogels, have enabled stretchable and transparent ionotronics, but they suffer from key limitations inherent to the liquid components, which may leak and evaporate. Here, novel liquid-free ionic conductive elastomers (ICE) that are copolymer networks hosting lithium cations and associated anions via lithium bonds and hydrogen bonds are demonstrated, such that they are intrinsically immune from leakage and evaporation. The ICEs show extraordinary mechanical versatility including excellent stretchability, high strength and toughness, self-healing, quick self-recovery, and 3D-printability.

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As one of the most promising drug delivery carriers, hydrogels have received considerable attention in recent years. Many previous efforts have focused on diffusion-controlled release, which allows hydrogels to load and release drugs in vitro and/or in vivo. However, it hardly applies to lipophilic drug delivery due to their poor compatibility with hydrogels.

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