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 language | English |
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Article number | 2503910 |
Journal | Advanced Materials |
Volume | 37 |
Issue number | 30 |
DOIs | |
Publication status | Published - Jul 29 2025 |
Externally published | Yes |
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