An understanding of the electrostatic interactions that exist between charged particles of dielectric materials has applications that span much of chemistry, physics, biology, and engineering. Areas of interest include cloud formation, ink-jet printing, and the stability of emulsions. A general solution to the problem of calculating electrostatic interactions between charged dielectric particles is presented. The solution converges very rapidly for low values of the dielectric constant and is stable up to the point where particles touch. Through applications to unspecified particles with a range of size and charge ratios, the model shows that there exist distinct regions of dielectric space where particles with the same sign of charge are strongly attracted to one another.

Direct preparation of long one-dimensional (1D) nanostructures with diameters <10 nm inside superfluid helium droplets is reported. Unlike conventional chemical synthetic techniques, where stabilizers, templates, or external fields are often required to induce 1D growth, here, we exploit the use of quantized vortices to guide the formation of ultrathin nanowires. A variety of elements have been added to the droplets to demonstrate that this is a general phenomenon, including Ni, Cr, Au, and Si. Control of the length and diameter of the nanowires is also demonstrated.

The formation of Ag nanoparticles by the addition of Ag atoms to helium droplets has been investigated. The resulting nanoparticles were then imaged by transmission electron microscopy after being deposited on a thin solid surface. In large helium droplets chains of Ag nanorods were observed similar to recently reported track-like deposits [Gomez et al., Phys. Rev. Lett., 2012, 108, 155302]. However, by adjusting the experimental conditions chains of spherical nanoparticles could also be seen with a nearly uniform inter-particle spacing. Given that spherical Ag nanoparticles have no intrinsic anisotropy, the only viable explanation is that these particles must

Helium droplets are large helium clusters that are capable of picking up individual atoms and molecules and show promise as nano-reactors for the synthesis of unique nanoparticles. In particular, the sequential addition of materials of different types offers opportunities for the fabrication of novel core-shell nanoparticles that cannot be synthesised by other methods. To exploit this potential, here we have carried out a mass spectrometry investigation on metal clusters in order to establish how to control the doping conditions for the fabrication of nanoparticles in superfluid helium droplets, and in particular to develop a recipe to control core and shell ratios in the case of core-shell nanoparticles. Several types of metal nanoparticles, including pure Ag, Au and Ni nanoparticles, and Ag/Au and Ni/Au core-shell systems, have been synthesised and then removed from the helium droplets by deposition on substrates for ex situ investigations using high-resolution transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). The TEM imaging has been used to estimate the sizes of nanoparticles, which show a bimodel distribution under the conditions employed. We also present the first evidence that crystalline metal nanoparticles are formed by self-assembly of metal atoms in helium droplets. The XPS investigation of Ni/Au core-shell nanoparticles shows an absence of any Au 4f core-level shift that would occur on alloying of Au and Ni, which provides the first direct evidence for the successful formation of core-shell nanoparticles using superfluid helium droplets.

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To explore how the ion-pair in a single salt molecule evolves with the addition of water, infrared (IR) spectra of complexes composed of NaCl and multiple water molecules have been recorded for the first time. The NaCl(H2O)n complexes were formed and probed in liquid helium nanodroplets, and IR spectra were recorded for n = 1 → 4. The spectra for n = 1, 2, and 3 are consistent with formation of the lowest energy contact-ion pair structures in which each water molecule forms a single ionic hydrogen bond to an intact Na+Cl− ion-pair. Alternative structures with hydrogen bonding between water molecules become energetically competitive for n = 4, and the IR spectrum indicates likely the coexistence of at least two isomers.

We have used X-Ray Magnetic Circular Dichroism (XMCD) and magnetometry to study isolated Fe@Cr core-shell nanoparticles with an Fe core diameter of 2.7 nm (850 atoms) and a Cr shell thickness varying between 1 and 2 monolayers. The addition of Cr shells significantly reduces the spin moment but does not change the orbital moment. At least two Cr atomic layers are required to stabilize a ferromagnetic/antiferromagnetic interface and generate the associated exchange bias and increase in coercivity.

Helium droplets provide a cold and confined environment where atomic and/or molecular dopants can aggregate into clusters and nanoparticles. In particular, the sequential addition of different materials to helium droplets can lead to the formation of a wide range of nanoparticles, including core-shell nanoparticles, which can then be deposited onto a surface. Here we briefly discuss the fundamental properties of helium droplets and then address their implications for the formation of clusters and nanoparticles. Several key experiments on atomic and molecular clusters will be highlighted and new results obtained for nanoparticles formed in this way will be presented. Finally, the versatility, the limitations and new possibilities provided by superfluid helium droplets in nanoscience and nanotechnology will be addressed.