ABSTRACT
We have investigated the thickness and surface structure of surface freezing films in Ga-Bi and Ga-Pb alloys over a wide temperature range between room temperature and the respective surface freezing transitions by x-ray photoelectron spectroscopy (XPS) and scanning tunnelling microscopy (STM). For the example of a Ga-Bi alloy dilute in Bi, XPS measurements show that the surface freezing film has a nearly constant value of approximately 25 A between the surface freezing temperature of 130 degrees C and room temperature if the sample is cooled slowly (5 Kh). On heating to 130 degrees C the film thickness exhibits a clear hysteresis on melting. On quenching the alloy sample (>100 Kh) the film thickness increases by almost a factor of 10. These observations indicate that the surface freezing films are metastable. The surface structure of the surface freezing films of various Ga-rich Ga-Bi and Ga-Pb alloys has been probed for the first time by STM at different temperatures below and above the bulk eutectic point. Atomically resolved STM images show the surface structures of pure Bi (0001) and Pb (111), respectively, at room temperature. On heating above the eutectic temperature the surface structure of the films does not change significantly as judged from the size and thickness of Pb or Bi terraces. These observations together with the film thickness variation with temperature indicate that the surface freezing films behave like a metastable independent surface phase. These results together with the wetting characteristics of these alloys suggest that surface freezing in these systems is a first order surface phase transition between wetting and metastable surface freezing films. The energy barrier for nucleation is strongly reduced due to a lowering of the interfacial energy if the nucleus is completely immersed in the respective wetting layer.
ABSTRACT
We have measured the surface tension and the capillary wave spectra at the liquid/vapour interface of the ionic liquid 1-butyl-3-methylimidazolium hexafluorophosphate at various temperatures up to 400 K. From the weak temperature dependence of the surface tension a low value of the surface excess entropy of approximately 3.5 x 10(5) J K(-1) m(-2) results which is consistent with a strongly aligned surface layer of imidazolium cations previously predicted by MD-calculations. The capillary wave spectra recorded at different wave numbers in the range 170 cm(-1) < or = q < or =500 cm(-1) exhibit strong deviations from the behaviour expected for the free surface of simple liquids. With an extended dispersion relation including the contributions of surface dipole moment density gamma and shear surface excess viscosity mu the spectra have been analyzed. It is found that mu is negligibly small, whereas gamma substantially influences the capillary wave spectra. The electrostatic potential across the interface, which corresponds to the measured dipole moment densities, qualitatively agrees with simulation calculations. The distinct temperature dependence of gamma suggests that with increasing temperature an order-disorder transformation occurs in the surface layer.