Nanoparticles form supercrystals under pressure
Investigations at Diamond may lead to easier ways to synthesise nanoparticle supercrystals
Over the last few decades, there has been considerable interest in the formation of nanoparticle (NP) supercrystals, which can exhibit tunable and collective properties that are different from that of their component parts, and which have potential applications in areas such as optics, electronics, and sensor platforms. Whilst the formation of high-quality supercrystals is normally a slow and complex process, recent research has shown that applying pressure can induce gold nanoparticles to form supercrystals. Building on this and the established effect of salts on the solubility of gold nanoparticles (AuNP) coated with PEG-based ligands, Dr Martin Schroer and his team carried out a series of experiments investigating the effect of varying pressure on gold nanoparticles in aqueous solutions. They made an unexpected observation – when a salt is added to the solution, the nanoparticles crystallise at a certain pressure. The phase diagram is very sensitive, and the crystallisation can be tuned by varying the type of salt added, and its concentration.
I22 is one of the few beamlines to offer a high-pressure environment, and it is unusual because the experimental setup is easily managed by the users themselves. The beamline staff are excellent, and we are particularly grateful for their expertise in data processing, which was invaluable.”
The resulting pressure-salt concentration phase diagram shows that the crystallisation is a result of the combined effect of salt and pressure on the PEG coatings. Supercrystal formation occurs only at high salt concentrations, and is reversible. Increasing the salt concentration leads to a continuous decrease of the crystallisation pressure, whereas the lattice structure and degree of crystallinity is independent of the salt type and concentration.
The NP crystallisation appears to be instantaneous, but in this set of experiments there was a delay of around 30 seconds between applying the pressure and taking the SAXS measurements. Dr Schroer and his team are returning to Diamond later this year to carry out time-resolved studies to further investigate this phenomenon.