Journal
JOURNAL OF MATERIALS CHEMISTRY
Volume 20, Issue 32, Pages 6696-6702Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c0jm01166e
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This article reports the interaction between cysteine-functionalised organogelators and gold nanoparticles. It is clearly demonstrated by transmission electron microscopy that for these gelators, where S-Au interactions can form, the nanoparticles align directly on top of, inside, and along the gel fibres. On the other hand, for a tryptophan functionalised gelator, which cannot form direct interactions with gold nanoparticles, the nanoparticles tend instead to simply cluster loosely around the fibrillar objects as a consequence of sample drying effects. Dependent on the ligand initially present as a stabiliser on the nanoparticle surface, some rearrangement of the nanoparticles on exposure to the gelator and sonication conditions can be observed. On thermal treatment, the nanoparticle-doped xerogel undergoes significant rearrangement: the gel fibres become smaller in diameter and the gold nanoparticles undergo enlargement by Ostwald ripening. This demonstrates how supramolecular nanohybrid assembled materials can evolve in response to stimulus as a consequence of the non-covalent interactions which underpin them, and their resulting dynamic nature.
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