Gold nanoparticle Created 2026-10-20 Updated 2026-11-05
A gold nanoparticle is a small particle of gold whose optical and surface chemistry depend on its geometry and surroundings. A dispersion of such particles can appear red or purple rather than resembling a piece of bulk gold.[ref]
In 1857, Michael Faraday described ruby-coloured fluids containing finely divided gold. He compared the transmitted colour of these fluids with coloured glass and observed changes toward blue or violet under conditions that altered the dispersed particles. These observations established a striking connection between the physical state of gold and its interaction with light.[ref]
A modern explanation involves localized surface plasmon resonance: the collective response of conduction electrons to an incident electromagnetic field changes absorption and scattering. The resulting spectrum depends on particle shape and the surrounding dielectric, as well as size. Thus colour alone is not a universal measure of nanoparticle diameter.
Experiments on gold nanorings show how geometry changes the response: varying the ratio of ring thickness to radius shifts the localized surface plasmon resonance. This is evidence for control through particle shape rather than a change of chemical element.[ref]
Nanoparticle Created 2026-10-20 Updated 2026-11-05
A nanoparticle is a particle whose external dimensions lie on the nanoscale. Its behaviour can depend strongly on its size, shape and surface chemistry, even when its overall chemical chemical composition is fixed.
For a sphere of radius , the ratio of surface area to volume is
Halving therefore doubles the surface area exposed per unit volume. At fixed total volume, making many smaller particles exposes more material to the surrounding medium. This helps explain why surface reactions and attached molecules can have a large effect on nanoparticles.[ref]
The size of an individual nanoparticle also differs from the size of an particle aggregate containing many particles. Reports of particle size consequently need to identify what was measured. Gold nanoparticles provide a visible example: their interaction with light can differ markedly from bulk gold.
The stabilizing outer groups should be compatible with the solvent, while the thiol-derived sulfur anchors the ligand shell to the gold nanoparticle.
SolventThiol numberReason
Acidic water1The terminal amine is protonated, favoring hydration and electrostatic repulsion between similarly charged particles.
Basic water2The carboxylic acid becomes carboxylate, giving a hydrated negatively charged outer group.
Hexane4The long hydrocarbon tail is well solvated by a hydrocarbon solvent and can provide steric protection.
Perfluorohexane5The fluorinated tail is compatible with the fluorous solvent, unlike a conventional hydrocarbon shell.
Toluene3The aromatic-containing ligand is compatible with the aromatic organic solvent.
These choices concern colloidal stability, not merely whether a free ligand dissolves. Coverage, chain packing and particle separation also matter. In the aqueous cases, high electrolyte concentrations can screen electrostatic repulsion, so ionization alone does not guarantee stability at every acid or base concentration.