Surface plasmon resonance of gold nanoparticle aggregates induced by halide ions

The localized surface plasmon resonance (LSPR) of metal nanoparticles is strongly dependent on geometrical and environmental factors, as well as the nanoparticle aggregation phenomena, which are exploited in a range of applications. In this work we investigate the LSPR of gold nanoparticles, produced by laser ablation in liquid (LAL), and their agglomeration induced by halides after LAL. We study the aggregation process under a range of factors like bromide concentration, temperature, and different halides. By absorption spectroscopy and electron microscopy we show that increasing bromide concentration leads to longer and more complex aggregates, with consequent red-shift and broadening of the LSPR. Simulations, in agreement with experiments, show that a redshift of the LSPR is expected as AuNP linear chains become longer and validate this trend for different particle size and gap between particles. By using real-time absorption spectroscopy, we observe immediate growth of nanoparticles after salt addition. We also demonstrate that higher temperatures tend to suppress the aggregation process, while lower temperatures promote it. We then observe that a heavier halide like iodide tends to form a very broad LSPR indicating complex nanoparticle architectures. Finally, we show that the aggregates are disrupted by re-irradiating the colloid. These findings provide an expanded understanding into the factors ruling the aggregation phenomena, and will help developing existing applications while stimulating new ones.