4.7 Article

A universal method to easily design tough and stretchable hydrogels

Journal

NPG ASIA MATERIALS
Volume 13, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41427-021-00302-2

Keywords

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Funding

  1. Japan Society of the Promotion of Science (JSPS) [JP20H04539]
  2. Ministry of Education, Culture, Sports, Science and Technology (MEXT) Japan
  3. AMED S-innovation Program for the development of biofunctional materials for the realization of innovative medicine
  4. Canon Foundation
  5. [JP20H05236]

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This paper presents a universal strategy for preparing tough and stretchable hydrogels by adjusting polymerization conditions to increase polymer chain entanglements for energy dissipation. The balance between physical and chemical cross-links is optimized by utilizing entanglements and covalent bonds, respectively, leading to improved mechanical performance of hydrogels for wide practical use.
Hydrogels are flexible materials that have high potential for use in various applications due to their unique properties. However, their applications are greatly restricted by the low mechanical performance caused by high water content and inhomogeneous networks. This paper reports a universal strategy for easily preparing hydrogels that are tough and stretchable without any special structures or complicated processes. Our strategy involves tuning the polymerization conditions to form networks with many polymer chain entanglements to achieve energy dissipation. Tough and stretchable hydrogels can be prepared by free radical polymerization with a high monomer concentration and low cross-linker content to optimize the balance between physical and chemical cross-links by entanglements and covalent bonds, respectively. The strategy of using polymer chain entanglements for energy dissipation allows us to overcome the limitation of low mechanical performance, which leads to the wide practical use of hydrogels.

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