A new insight into the temperature induced molecular aggregations in tris(8-hydroxyquinoline) metals

Abstract Annealing of tris(8-hydroxyquinoline) gallium (Gaq3) film at various temperatures in dry N2 atmosphere has shown the existences of four different phases of molecular aggregations before the burning out of the film at about 310 °C. The first three phases, up to 235 °C, are amorphous molecular aggregations, while the fourth one at 255 °C is a crystalline structure, very likely α-polymorph. The photoluminescence (PL) intensity was increased to about five times greater than that of the pristine film at 235 °C, while the PL peak was blue shifted consistently. Although a small contribution of Rayleigh scattering cannot be excluded at high temperatures when crystallites appear, the PL blueshift was mainly attributed to the nanostructured molecular aggregations followed by enhanced PL intensity. These new findings can be a common characteristic of organometallic complexes at varied annealing temperatures. The presented results open a new route of fabricating highly emissive thin films of amorphous nanostructure, which are specifically important for organic light emitting diode (OLED) based displays

Phase transitions in thermally annealed films of Alq₃

Organic light emitting devices have been so very much improved lately that they are being widely applied for displays and lighting. Among many improving technologies, annealing processes in different atmospheres affect greatly their performance, for instance when the active material is the small molecule Alq3. In particular, a significant increase of the photoluminescence is observed in thin films of this molecule between 150 and 180 °C, before the physical destruction of the films occurs at higher temperatures. This phenomenon is attributed to a phase transition towards a novel morphological aggregation of the molecules in the film, which proved to be a much improved optical material for luminescent applications, and which seems common to other molecules as well

Symmetry lowering of pentacene molecular states interacting with a Cu surface

Pentacene adsorbed on the Cu(119) vicinal surface forms long-range ordered chain structures. Photoemission spectroscopy measurements and ab initio density functional theory simulations provide consistent evidences that pentacene molecular orbitals mix with the copper bands, giving rise to interaction states localized at the interface. Angular-resolved and polarization dependent photoemission spectroscopy shows that most of the pentacene derived intensity is strongly dichroic. The symmetry of the molecular states of the free pentacene molecules is reduced upon adsorption on Cu(119), as a consequence of the molecule-metal interaction. Theoretical results show a redistribution of the charge density in \u3c0 molecular states close to the Fermi level, consistent with the photoemission intensities (density of states) and polarization dependence (orbital symmetry)

High resolution and high efficiency coloration of lithium fluoride by soft X-rays irradiation

The efficient coloration of LiF material, in the form of bulk and films, by EUV and soft X-rays emitted by a laser-plasma source is demonstrated. The short penetration depth of soft-X-rays is exploited to obtain high spatial resolution luminescent patterns while the high dynamic range of proportionality between X-ray dose and coloration is exploited for using LiF as image detector in micro-radiography and soft X-ray microscopy applications

Spallative ablation of dielectrics by X-ray laser

Short laser pulse in wide range of wavelengths, from infrared to X-ray, disturbs electron-ion equilibrium and rises pressure in a heated layer. The case where pulse duration $\tau_L$ is shorter than acoustic relaxation time $t_s$ is considered in the paper. It is shown that this short pulse may cause thermomechanical phenomena such as spallative ablation regardless to wavelength. While the physics of electron-ion relaxation on wavelength and various electron spectra of substances: there are spectra with an energy gap in semiconductors and dielectrics opposed to gapless continuous spectra in metals. The paper describes entire sequence of thermomechanical processes from expansion, nucleation, foaming, and nanostructuring to spallation with particular attention to spallation by X-ray pulse

Influence of steps on the tilting and adsorption dynamics of ordered Pn films on vicinal Ag(111) surfaces

Here we present a structural study of pentacene (Pn) thin films on vicinal Ag(111) surfaces by He atom diffraction measurements and density functional theory (DFT) calculations supplemented with van der Waals (vdW) interactions. Our He atom diffraction results suggest initial adsorption at the step edges evidenced by initial slow specular reflection intensity decay rate as a function of Pn deposition time. In parallel with the experimental findings, our DFT+vdW calculations predict the step edges as the most stable adsorption site on the surface. An isolated molecule adsorbs as tilted on the step edge with a binding energy of 1.4 eV. In addition, a complete monolayer (ML) with pentacenes flat on the terraces and tilted only at the step edges is found to be more stable than one with all lying flat or tilted molecules, which in turn influences multilayers. Hence our results suggest that step edges can trap Pn molecules and act as nucleation sites for the growth of ordered thin films with a crystal structure similar to that of bulk Pn.Comment: 4 pages, 4 figures, 1 tabl

Molecular charge distribution and dispersion of electronic states in the contact layer between pentacene and Cu(119) and beyond

The interaction of pentacene molecules in contact with the Cu(119) stepped surface has been directly imaged by scanning tunneling microscopy and analyzed by angle resolved photoemission spectroscopy. Interacting molecules, which are in contact with copper, generate dispersive electronic states associated with a perturbed electron charge density distribution of the molecular orbitals. In contrast, the electron charge density of molecules of the pentacene on top of the first layer, which is not in direct contact with the Cu surface, shows an intramolecular structure very similar to that of the free molecule. Our results indicate that the delocalization of the molecular states in the pentacene/Cu system is confined to the very first molecular layer at the interface