Directed organization of C70 kagome lattice by titanyl phthalocyanine monolayer template

Controlled deposition of titanyl phthalocyanine (TiOPc) on Ag(111) produces a honeycomb monolayer phase consisting of TiOPc molecules with two distinctive tilt angles. This periodic arrangement of polar molecules is used to direct C(70) growth into low-density 3D films with novel C(70) kagome lattice arrangements. Structural models for the C(70) kagome lattice are determined from layer-by-layer scanning tunneling microscopy images and related to the dipolar TiOPc template and C(70)'s anisotropic polarizability. Molecular templates with designed electrostatic features offer a practical method to control 3D film organization on the nanoscale by harnessing anisotropic molecular interactions at the growth interface.     

Steps as adatom sources for surface chemistry: oxygen overlayer formation on Ag(110)

Surface chemical reactions often require a ready supply of substrate atoms to occur. In principle, steps serve as an efficient source of these atoms, provided that detachment rates from the step edges are sufficiently large. In this paper, we characterize atomic detachment rates from steps on clean Ag(110) by examining step fluctuations. We show that these rates are sufficient to supply atoms to form the added-row reconstruction of oxidized Ag(110) when the oxygen partial pressure is low. For high oxygen pressures, however, we find that step detachment rates are slow compared with oxidation rates, and the step source of Ag is supplemented by vacancy-island generation on the terraces. These results are compared to those obtained for the similar O/Cu(110) and O/Ni(110) systems.     

The influence of crystallographic steps on coadsorption: CO---O/Ni(119)

On low index nickel surfaces, repulsive interactions between atomic oxygen and CO drive the phase separation of these species into oxygen-rich and CO-rich islands. Because these adsorbates interact differently with crystallographic steps, the size and the structure of these islands are modified on stepped surfaces. We have monitored coadsorption-induced changes in the distribution of CO with IRRAS, observing six different CO stretching bands which are assigned to distinct local chemisorption environments. When oxygen fully saturates sites along the step edge, the steps are completely blocked from CO adsorption and virtually all the CO population on the terraces shifts from atop to bridge sites. This terrace site shift is similarly accomplished by atomic oxygen chemisorbed at terrace sites. From these coadsorption-induced changes in CO site distributions, constrained by the 10 Å terrace width, we conclude the through-metal O---CO interaction responsible for this CO site shift must be operative over a range of 5 Å. At θ_o = 0.18 ML, when oxygen occupies, but does not fully saturate the step edge, a new CO adsorption site is created, with a characteristic frequency of 1750 cm⁻¹. This new site is assigned to CO bonded to kinks along the step edge based upon its low intensity ( geometric kink density), enhanced binding strength and sensitivity to oxygen coverage. At higher oxygen coverages, compression of the CO adlayer is observed, with CO shifting to asymmetric bridge sites. As saturation coverage is approached, CO occupies weakly bound sites in close proximity ( 3 Å) to O adatoms, with high characteristic frequencies of 2100 cm⁻¹.