Inorganic Hydrogels can be Flexible and Highly Extensible

Tongtong Zhou, Yan Wang, Jiulong Zhou, Lifeng Yao, Ke He, Lixun Chen, Song Zhang, Hong Liu, Xiaodong Chen*, Shuxun Cui*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Inorganic hydrogels have great potential in many applications as sustainable materials, but lack flexibility due to rigid network structures. Here, a novel strategy is proposed—an inorganic polymer hydrogel, prepared by crosslinking long-chain polyphosphate (LPP) with M2+ ions (Ca2+, Mn2+, Mg2+, Ni2+), which effectively address the rigidity and fragility issues commonly associated with traditional inorganic gels. With the most stable hydration shell among those ions, Ni2+ tends to interact indirectly with LPP through hydrogen bonds rather than coordination bonds. The unique Ni2+-phosphate interaction endows the Ni-LPP hydrogels with ultrahigh elongation at break (≈15 000×). Further experiments reveal that the Ni2+-phosphate motif can be applied to other hydrogels as an extension enhancement factor. The highly extensible, good conductive (1.06 ± 0.08 S m−1), self-healing (within 30 s and without stimulation), arbitrarily shapeable, and nonflammable Ni-LPP inorganic hydrogel indicates a bright future in flexible electronics, environmental remediation, and beyond.

Original languageEnglish
Article number2503910
JournalAdvanced Materials
Volume37
Issue number30
DOIs
Publication statusPublished - Jul 29 2025
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2025 Wiley-VCH GmbH.

ASJC Scopus Subject Areas

  • General Materials Science
  • Mechanics of Materials
  • Mechanical Engineering

Keywords

  • high elongation
  • inorganic polymer hydrogel
  • Ni ion
  • polyphosphate
  • self-healing

Cite this