Click-Gelable and Self-Healing Organogels Based on Inorganic Sub-Nanowires

The fabrication of self-healing gels typically relies on dynamic covalent bonds, which prove particularly challenging in organic systems. Inorganic subnanowires (SNWs) exhibit excellent structural flexibility and enhanced interactions beyond molecular levels, enabling click-gelation and self-healing of organogels different from polymers and biomaterials. In this study, we synthesize Na-PMo 12 SNWs bridged by Na + and polyoxometalate clusters, which can lock various organic solvents into transparent organogels within 5 s. These organogels exhibit remarkable self-healing capabilities, with visually complete morphological recovery within 20 min even after mechanical disruption. The framework formed by the linkage of Na + and clusters significantly augments the flexibility of SNWs, and the dense surface ligands of SNWs bring enhanced interactions and entanglements, facilitating the click gelation and self-healing of organogels. The shear-thinning property of the organogel enables its facile injection, making it a promising candidate for applications, such as transarterial chemoembolization (TACE) for liver cancer and injectable drug delivery systems.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2026-06-13
DOI
https://doi.org/10.1021/jacs.6c02390
Primary Topic
Supramolecular Self-Assembly in Materials
Type
article
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article

Click-Gelable and Self-Healing Organogels Based on Inorganic Sub-Nanowires

Qingda Liu, Wenxiong Shi, Feng Yuan, Tongjin Zhang et al.
Journal of the American Chemical Society
Supramolecular Self-Assembly in Materials
article

Click-Gelable and Self-Healing Organogels Based on Inorganic Sub-Nanowires

Qingda Liu, Wenxiong Shi, Feng Yuan, Tongjin Zhang, Xun Wang, Fenghua Zhang, Dongzheng Zhang
article en

Abstract

The fabrication of self-healing gels typically relies on dynamic covalent bonds, which prove particularly challenging in organic systems. Inorganic subnanowires (SNWs) exhibit excellent structural flexibility and enhanced interactions beyond molecular levels, enabling click-gelation and self-healing of organogels different from polymers and biomaterials. In this study, we synthesize Na-PMo 12 SNWs bridged by Na + and polyoxometalate clusters, which can lock various organic solvents into transparent organogels within 5 s. These organogels exhibit remarkable self-healing capabilities, with visually complete morphological recovery within 20 min even after mechanical disruption. The framework formed by the linkage of Na + and clusters significantly augments the flexibility of SNWs, and the dense surface ligands of SNWs bring enhanced interactions and entanglements, facilitating the click gelation and self-healing of organogels. The shear-thinning property of the organogel enables its facile injection, making it a promising candidate for applications, such as transarterial chemoembolization (TACE) for liver cancer and injectable drug delivery systems.

Journal of the American Chemical Society
Tianjin University of Technology (CN), Materials Technologies (United States) (US), Tsinghua University (CN)
Openalex Percentile: Top 12%
Supramolecular Self-Assembly in Materials
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Click-Gelable and Self-Healing Organogels Based on Inorganic Sub-Nanowires — Qingda Liu, Wenxiong Shi, et al. · Journal of the American Chemical Society (2026) | TGRS Research Map | TGRS