Indium coverage of the Si(111)- 7×3 -in surface

The indium coverage of the Si(111)-√7 × √3-In surface is investigated by means of x-ray photoelectron spectroscopy and first-principles density functional theory calculations. Both experimental and theoretical results indicate that the In coverage is a double layer rather than a single layer. Moreover, the atomic structure of the Si(111)-√7 × √3-In surface is discussed by comparing experimental with simulated scanning tunneling microscopy (STM) images and scanning tunneling spectra with the calculated density of states. Our structural assignment agrees with previous studies, except for the interpretation of experimental STM images

Measuring Electric Charge and Molecular Coverage on Electrode Surface from Transient Induced Molecular Electronic Signal (TIMES).

Charge density and molecular coverage on the surface of electrode play major roles in the science and technology of surface chemistry and biochemical sensing. However, there has been no easy and direct method to characterize these quantities. By extending the method of Transient Induced Molecular Electronic Signal (TIMES) which we have used to measure molecular interactions, we are able to quantify the amount of charge in the double layers at the solution/electrode interface for different buffer strengths, buffer types, and pH values. Most uniquely, such capabilities can be applied to study surface coverage of immobilized molecules. As an example, we have measured the surface coverage for thiol-modified single-strand deoxyribonucleic acid (ssDNA) as anchored probe and 6-Mercapto-1-hexanol (MCH) as blocking agent on the platinum surface. Through these experiments, we demonstrate that TIMES offers a simple and accurate method to quantify surface charge and coverage of molecules on a metal surface, as an enabling tool for studies of surface properties and surface functionalization for biochemical sensing and reactions

Gestufte Oberflächen und Quasieindimensionale Strukturen - Photoemission an 3d Metallen auf W(110)

The coverage dependent electronic structure of Cu and Co an vicinal W(110) surfaces has been investigated with angle resolved photoelectron spectroscopy. To prepare the quasi-one-dimensional Cu and Co systems the method of step edge decoration of the vicinal W(110) surfaces has been used. The vicinal surfaces with step edges in (110), (100) and (111) direction has been investigated using LEED. From the characteristic spot splitting a terrace width of 11 atom rows was determined. The band structures of the flat and the vicinal surfaces have indicated that the step edges have no bearing an the bulk band structure at k$_{\parallel}$=0. But the surface band structure shows a different dispersion and different energy positions of surface states. An analysis of the W 4$\int_{\frac{\tau}{2}}$ core level spectra has resulted in an additional contribution of the step edges in the spectra of the vicinal surfaces wich a surface core level shift between 120 and 150meV. A Cu and Co coverage dependent investigation of the core levels shows that there is no Co induced surface reconstruction and up to 0.15 monolayer no Cu induced surface reconstruction. In the range of 0.15 and 0.3 monolayer Cu the surface peak shifts to higher binding energies. This is probably a result of a surface reconstruction of the W substrat. In the core level spectra wich Co coverage the intensity of the surface peak decreases linear with Co coverage and the intensity of a new contribution, the interface structure, increases with Co coverage. With Co respectively Cu coverage the contribution of the step edge shifts to lower respectively higher binding energies. This can be attributed to a charge transfer between the adsorbat and the substrat in different directions. For coverages of 0.1 monolayer Co respectively Cu electronic states near the fermi edge has been observed. These states show a dispersion with k$_{\parallel}$ along the step edges but they show no dispersion perpendicular to the step edges. This is the first evidence of a quasi-one-dimensional structure (Co respectively Cu quantum wire) an vicinal W(110) surfaces

Energetics of hydrogen coverage on group VIII transition metal surfaces and a kinetic model for adsorption/desorption

We determined the binding energy of hydrogen to the closest packed surface for all nine group VIII transition metals as a function of surface coverage using quantum mechanics (density functional theory with the generalized gradient approximation) with periodic boundary conditions. The study provides a systematic comparison of the most stable surfaces of the nine group VIII transition metals, leading to results consistent with available surface science studies. We then use these to develop a simple thermodynamic model useful in estimating the surface coverage under typical heterogeneous catalysis conditions and compare these results to temperature programmed desorption experiments

In situ surface coverage analysis of RuO₂-catalysed HCl oxidation reveals the entropic origin of compensation in heterogeneous catalysis

In heterogeneous catalysis, rates with Arrhenius-like temperature dependence are ubiquitous. Compensation phenomena, which arise from the linear correlation between the apparent activation energy and the logarithm of the apparent pre-exponential factor, are also common. Here, we study the origin of compensation and find a similar dependence on the rate-limiting surface coverage term for each Arrhenius parameter. This result is derived from an experimental determination of the surface coverage of oxygen and chlorine species using temporal analysis of products and prompt gamma activation analysis during HCl oxidation to Cl2 on a RuO2 catalyst. It is also substantiated by theory. We find that compensation phenomena appear when the effect on the apparent activation energy caused by changes in surface coverage is balanced out by the entropic configuration contributions of the surface. This result sets a new paradigm in understanding the interplay of compensation effects with the kinetics of heterogeneously catalysed processes

The Effect of EDTA in Attachment Gain and Root Coverage

Root surface biomodification using low pH agents such as citric acid and tetracycline has been proposed to enhance root coverage following connective tissue grafting. The authors hypothesized that root conditioning with neutral pH edetic acid would improve vertical recession depth, root surface coverage, pocket depth, and clinical attachment levels. Twenty teeth in 10 patients with Miller class I and II recession were treated with connective tissue grafting. The experimental sites received 24% edetic acid in sterile distilled water applied to the root surface for 2 minutes before grafting. Controls were pretreated with only sterile distilled water. Measurements were evaluated before surgery and 6 months after surgery. Analysis of variance was used to determine differences between experimental and control groups. We found significant postoperative improvements in vertical recession depth, root surface coverage, and clinical attachment levels in test and control groups, compared to postoperative data. Pocket depth differences were not significant (P\u3c.01)

Theory of alkali metal adsorption on close-packed metal surfaces

Results of recent density functional theory calculations for alkali metal adsorbates on close-packed metal surfaces are discussed. Single adatoms on the (111) surface of Al and Cu are studied with the self-consistent surface Green-function method by which the pure adsorbate-substrate interaction may be analyzed. Higher coverage ordered adlayers of K on Al(111), Na on Al(111), and Na on Al(001) are treated using the ab-initio pseudopotential plane wave method which affords the prediction of coverage dependent stable and metastable adsorbate geometries and phase transitions of the adsorbate layers. Together, these studies give insight and understanding into current key issues in alkali metal adsorption, namely, the nature of the adsorbate-substrate bond at low coverage and the occurrence of hitherto unanticipated adsorbate geometries, and the associated electronic properties.Comment: to be published in Surface Reviews and Letters, 18 pages, 18 figure