Abstract
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.
Original language | English |
---|---|
Pages (from-to) | 6696-6702 |
Number of pages | 7 |
Journal | Journal of Materials Chemistry |
Volume | 20 |
Issue number | 32 |
DOIs | |
Publication status | Published - 28 Aug 2010 |
Keywords
- FUNCTIONALIZED GOLD NANOPARTICLES
- METAL NANOPARTICLES
- SILVER NANOPARTICLES
- SUPRAMOLECULAR GELS
- INORGANIC MATERIALS
- PHYSICAL GELS
- CAPPING AGENT
- SHORT-PEPTIDE
- QUANTUM DOTS
- GELATORS