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Published on: August 15, 2019
Antibonding plasmon modes in colloidal gold nanorod clusters
Marek Grzelczak1, Stefano A Mezzasalma, Weihai Ni
1Department of Chemical and Pharmaceutical Sciences, University of Trieste, P.le Europa 1, 34127 Trieste Italy. grzelczak.marek@gmail.com
Langmuir : the ACS Journal of Surfaces and Colloids
|November 3, 2011
Summary
UV light induces self-assembly of gold nanorods (AuNRs) into ladderlike clusters. This process reveals antibonding plasmon modes in solution, previously only seen in simulations, paving the way for light-controlled nanoparticle assembly.
Area of Science:
- Nanotechnology
- Materials Science
- Physical Chemistry
Background:
- The optical properties of nanoplasmonic colloids depend on particle shape.
- Self-assembly of nanoparticles leads to new optical features like bonding/antibonding modes due to particle orientation.
- Observing these plasmon modes in liquid-phase self-assembly is challenging due to broad cluster size distributions.
Purpose of the Study:
- To demonstrate the observation of antibonding plasmon modes in low-symmetry nanoparticle clusters formed in solution.
- To investigate the mechanism of UV-light-induced self-assembly of gold nanorods (AuNRs).
Main Methods:
- Colloidal dispersions of AuNRs stabilized by poly(vinylpyrrolidone) (PVP) were irradiated with UV light.
- The morphology of the resulting AuNRs clusters was analyzed.
- Optical response of the clusters was measured to identify plasmon modes.
Main Results:
- UV-light irradiation of AuNRs in N-methyl-2-pyrrolidone (NMP) resulted in the formation of ladderlike AuNRs clusters.
- Antibonding plasmon modes were identified in these solution-phase clusters.
- A mechanism involving UV-induced radical formation and subsequent PVP cross-linking was proposed.
Conclusions:
- Low-symmetry clustering of AuNRs can reveal antibonding plasmon modes in solution.
- UV-light-induced self-assembly offers a route to control nanoparticle morphology and optical properties.
- This approach has potential applications in light-induced self-assembly for various nanomaterials.

