Stephen Berkebile
University of Graz
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Featured researches published by Stephen Berkebile.
Physical Chemistry Chemical Physics | 2012
L. D. Sun; Stephen Berkebile; Günther Weidlinger; Mariella Denk; Richard Denk; M. Hohage; Georg Koller; F.P. Netzer; M.G. Ramsey; P. Zeppenfeld
We report a combined reflectance difference spectroscopy and scanning tunneling microscopy study of ultrathin α-sexithiophene (6T) films deposited on the Cu(110)-(2×1)O surface. The correlation between the layer resolved crystalline structure and the corresponding optical spectra data reveals a highly sensitive dependence of the excitonic optical properties on the layer thickness and crystalline structure of the 6T film.
Physical Chemistry Chemical Physics | 2010
L. D. Sun; Stephen Berkebile; Günther Weidlinger; Georg Koller; M. Hohage; F.P. Netzer; M.G. Ramsey; P. Zeppenfeld
The thickness dependent optical and electronic structure of para-sexiphenyl thin films grown on TiO(2)(110) at around 400 K reveals that the substrate is first wet by one monolayer of molecules lying with their long axis parallel to the [001] direction of the substrate, while the molecules in subsequent layers are almost standing upright. Whilst ultraviolet photoemission spectroscopy (UPS) is sensitive to the molecules in the outermost layer, reflection difference spectroscopy (RDS) shows that the molecules at the buried interface do not dewet and maintain the orientation of the original wetting monolayer.
42nd International Conference on Environmental Systems | 2012
Stephen Berkebile; James R. Gaier
During the Apollo missions, the adhesion of dust to critical spacecraft systems was a greater problem than anticipated and resulted in functional degradation of thermal control surfaces, spacesuit seals, and other spacecraft components. Notably, Earth-based simulation efforts did not predict the magnitude and effects of dust adhesion in the lunar environment. Forty years later, we understand that the ultrahigh vacuum (UHV) environment, coupled with micrometeorite impacts and constant ion and photon bombardment from the sun result in atomically clean and high surface energy dust particles and spacecraft surfaces. However, both the dominant mechanism of adhesion in airless environments and the conditions for high fidelity simulation tests have still to be determined. The experiments presented in here aim to aid in the development of dust mitigation techniques for airless bodies (e.g. lunar surface, asteroids, moons of outer planets). The approach taken consists of (a) quantifying the adhesion between common polymer and metallic spacecraft materials and a synthetic noritic volcanic glass, as a function of surface cleanliness and of triboelectric charge transfer in a UHV environment, and (b) determining parameters for high fidelity tests through investigation of adhesion dependence on vacuum environment and sample treatment. Adhesion force has been measured between pins of spacecraft materials and a plate of synthetic volcanic glass by determining the pull-off force with a torsion balance. Although no significant adhesion is generally observed directly as a result of high surface energies, the adhesion due to induced electrostatic charge is observed to increase with spacecraft material cleanliness, in some cases by over a factor of 10. Furthermore, electrostatically-induced adhesion is found to decrease rapidly above pressures of 10 -6 Torr. It is concluded that highfidelity tests should be conducted in high to ultrahigh vacuum and include an ionized surface cleaning process.
ACS Nano | 2015
Margareta Wagner; Stephen Berkebile; F.P. Netzer; M.G. Ramsey
With the use of molecular manipulation in a cryogenic scanning tunneling microscope, the structure and rearrangement of sexiphenyl molecules at the buried interface of the organic film with the Cu(110) substrate surface have been revealed. It is shown that a reconstruction of the first monolayer of flat lying molecules occurs due to the van der Waals pressure from subsequent layers. In this rearrangement, additional sexiphenyl molecules are forced into the established complete monolayer and adopt an edge-on configuration. Incorporation of second layer molecules into the first layer is also demonstrated by purposely pushing sexiphenyl molecules with the STM tip. The results indicate that even chemisorbed organic layers at interfaces can be significantly influenced by external stress from van der Waals forces of subsequent layers.
3rd AIAA Atmospheric Space Environments Conference | 2011
Stephen Berkebile; Kenneth W. Street; James R. Gaier
The successful exploration of airless bodies, such as the Earth’s moon, many smaller moons of the outer planets (including those of Mars) and asteroids, will depend on the development and implementation of effective dust mitigation strategies. The ultrahigh vacuum environment (UHV) on the surfaces of these bodies, coupled with constant ion and photon bombardment from the Sun and micrometeorite impacts (space weathering), makes dust adhesion to critical spacecraft systems a severe problem. As a result, the performance of thermal control surfaces, photovoltaics and mechanical systems can be seriously degraded even to the point of failure. The severe dust adhesion experienced in these environments is thought to be primarily due to two physical mechanisms, electrostatic attraction and high surface energies, but the dominant of these has yet to be determined. The experiments presented here aim to address which of these two mechanisms is dominant by quantifying the adhesion between common spacecraft materials (polycarbonate, FEP and PTFE Teflon®, Ti-6-4) and a synthetic noritic volcanic glass, as a function of surface cleanliness and triboelectric charge transfer in a UHV environment. Adhesion force has been measured between pins of spacecraft materials and a plate of synthetic volcanic glass by determining the pull-off force with a torsion balance. Although no significant adhesion is observed directly as a result of high surface energies, the adhesion due to induced electrostatic charge is observed to increase with spacecraft material cleanliness, in some cases by over a factor of 10, although the increase is dependent on the particular material pair. The knowledge gained by these studies is envisioned to aid the development of new dust mitigation strategies and improve existing strategies by helping to identify and characterize mechanisms of glass to spacecraft adhesion for norite volcanic glass particles. Furthermore, the experience of the Apollo missions revealed that dust mitigation strategies must be subjected to high fidelity tests. To facilitate the effectiveness of ground-based testing of mitigation strategies, the issue of a pressure limit for high fidelity tests will be addressed.
50th AIAA Aerospace Sciences Meeting including the New Horizons Forum and Aerospace Exposition | 2012
James R. Gaier; Stephen Berkebile
Abstract Experiments measuring the adhesion forces under ultrahigh vacuum conditions (10 –10 torr) between a synthetic volcanic glass and commonly used space exploration materials have recently been described. The glass has a chemistry and surface structure typical of the lunar regolith. It was found that Van der Waals forces between the glass and common spacecraft materials was negligible. Charge transfer between the materials was induced by mechanically striking the spacecraft material pin against the glass plate. No measurable adhesion occurred when striking the highly conducting materials, however, on striking insulating dielectric materials the adhesion increased dramatically. This indicates that electrostatic forces dominate over Van der Waals forces under these conditions. The presence of small amounts of surface contaminants was found to lower adhesive forces by at least two orders of magnitude, and perhaps more. Both particle and space exploration material surfaces will be cleaned by the interaction with the solar wind and other energetic processes and stay clean because of the extremely high vacuum (10
Archive | 2009
Martin Oehzelt; Stephen Berkebile; Georg Koller; Thomas Haber; Markus Koini; Oliver Werzer; Roland Resel; M.G. Ramsey
The growth of a-sexithiophene (6T) on copper (110) and oxygen reconstructed Cu(110) is studied by multiple techniques such as STM (scanning tunnelling microscopy), XRD (X-ray diffraction), XPS (X-ray photoelectron spectroscopy) and NEXAFS (near edge X-ray absorption fine structure). Selected data will be presented here and we will show that the long axes of the molecules on Cu(110) and Cu(110)-(2x1)O (CuO) are aligned along the valleys of the surface corrugations, i.e. along [1–10] and [001], respectively. With GIXD (grazing incidence X-ray diffraction) measurements the monolayer structure of 6T on Cu-O could be determined. Thicker films were studied by the X-ray diffraction pole figure technique. On all surfaces the (010) net planes of the bulk crystal structure are parallel to the surface i.e. the films grow exclusively (on Cu-O) or pre- dominantly (on Cu) in the (010) orientation. In the thick film the long molecular axes of the 6T molecules are found to be parallel to those of the monolayer. To study the transition from the monolayer to the multilayer structures NEXAFS measurements were carried out.
Advanced Functional Materials | 2008
Christopher R. McNeill; Jonathan Halls; Richard Wilson; Gregory L. Whiting; Stephen Berkebile; M.G. Ramsey; Richard H. Friend; Neil C. Greenham
Science | 2009
Peter Puschnig; Stephen Berkebile; Alexander J. Fleming; Georg Koller; Konstantin V. Emtsev; Thomas Seyller; J.D. Riley; Claudia Ambrosch-Draxl; F.P. Netzer; M.G. Ramsey
Advanced Materials | 2004
Georg Koller; Stephen Berkebile; Joachim R. Krenn; George Tzvetkov; Gregor Hlawacek; O. Lengyel; F.P. Netzer; Christian Teichert; Roland Resel; M.G. Ramsey