Elias Vlieg
Radboud University Nijmegen
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Publication
Featured researches published by Elias Vlieg.
Journal of Applied Crystallography | 2000
Elias Vlieg
A brief description is given of the C-program ROD with which surface structures can be refined on the basis of X-ray data. All main features one encounters on surfaces, like roughness, relaxations, reconstructions and multiple domains, are taken into account. The program has proven to be a useful tool over the past ten years.
Journal of Applied Crystallography | 1997
Elias Vlieg
The geometrical and resolution corrections are derived that occur in the measurement of the integrated intensities of surface diffraction rods for the case of a six-circle diffractometer. Since the six-circle geometry entails as special cases the five-circle and the z-axis diffractometers, the results are valid for these geometries as well. The derivations are valid for any incoming or outgoing angle of the X-ray beam, and are particularly important for measurements at large perpendicular momentum transfer. Expressions are derived for the integrated intensity from rocking scans, from stationary measurements and from reflectivity data. With all correction factors known, it is possible to derive the structure factors with a common scale factor from all these types of scans. It is expected that area detectors combined with stationary measurements will find widespread use in the surface X-ray diffraction community.
ACS Applied Materials & Interfaces | 2015
Michiel W. Pot; Kaeuis A. Faraj; Alaa Adawy; Willem J. P. van Enckevort; Herman T.B. van Moerkerk; Elias Vlieg; Willeke F. Daamen; Toin H. van Kuppevelt
Aligned unidirectional collagen scaffolds may aid regeneration of those tissues where alignment of cells and extracellular matrix is essential, as for instance in cartilage, nerve bundles, and skeletal muscle. Pores can be introduced by ice crystal formation followed by freeze-drying, the pore architecture reflecting the ice crystal morphology. In this study we developed a wedge-based system allowing the production of a wide range of collagen scaffolds with unidirectional pores by directional freezing. Insoluble type I collagen suspensions were frozen using a custom-made wedge system, facilitating the formation of a horizontal as well as a vertical temperature gradient and providing a controlled solidification area for ice dendrites. The system permitted the growth of aligned unidirectional ice crystals over a large distance (>2.5 cm), an insulator prolonging the freezing process and facilitating the construction of crack-free scaffolds. Unidirectional collagen scaffolds with tunable pore sizes and pore morphologies were constructed by varying freezing rates and suspension media. The versatility of the system was indicated by the construction of unidirectional scaffolds from albumin, poly(vinyl alcohol) (a synthetic polymer), and collagen-polymer blends producing hybrid scaffolds. Macroscopic observations, temperature measurements, and scanning electron microscopy indicated that directed horizontal ice dendrite formation, vertical ice crystal nucleation, and evolutionary selection were the basis of the aligned unidirectional ice crystal growth and, hence, the aligned unidirectional pore structure. In conclusion, a simple, highly adjustable freezing system has been developed allowing the construction of large (hybrid) bioscaffolds with tunable unidirectional pore architecture.
Nano Letters | 2011
Rienk E. Algra; Vedran Vonk; D. Wermeille; Wiesiek Szweryn; Marcel A. Verheijen; Willem J. P. van Enckevort; Arno A. C. Bode; Wim L. Noorduin; Erik Tancini; Aryan E. F. de Jong; Erik P. A. M. Bakkers; Elias Vlieg
We report an in situ surface X-ray diffraction study of liquid AuIn metal alloys in contact with zinc-blende InP (111)(B) substrates at elevated temperatures. We observe strong layering of the liquid metal alloy in the first three atomic layers in contact with the substrate. The first atomic layer of the alloy has a higher indium concentration than in bulk. In addition, in this first layer we find evidence for in-plane ordering at hollow sites, which could sterically hinder nucleation of zinc-blende InP. This can explain the typical formation of the wurtzite crystal structure in InP nanowires grown from AuIn metal particles.
Langmuir | 2017
Vedran Vonk; Diego Pontoni; Melissa Cremers; Anne M. Kerkenaar; Arno A. C. Bode; Wiesiek Szweryn; Gregor Nowak; Aryan E. F. de Jong; H. Dosch; Elias Vlieg
Our in situ X-ray study shows that a silicon substrate in contact with an undersaturated In(Ge) solution is wetted by an approximately 1 nm thin germanium film, which does not grow any thicker. The results can be understood by the use of thickness-dependent correlated interfacial energies. This near-equilibrium heterogeneous interface structure marks the initial stage of crystal growth before the formation of bulk material, which can only form under conditions of supersaturation. This finding uncovers a fundamental aspect of the thermodynamics at solid-liquid interfaces relevant for understanding the transition from equilibrium to supersaturation and is of importance for nanoscale solution growth methods.
Langmuir | 2014
Wester de Poel; Stelian Pintea; Aryan de Jong; Jakub Drnec; Francesco Carlà; Roberto Felici; Huub J. M. Op den Camp; Johannes A. A. W. Elemans; Willem J. P. van Enckevort; Alan E. Rowan; Elias Vlieg
Stable layers of crown ethers were grown on muscovite mica using the potassium-crown ether interaction. The multilayers were grown from solution and from the vapor phase and were analyzed with atomic force microscopy (AFM), matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry, and surface X-ray diffraction (SXRD). The results show that the first molecular layer of the three investigated dibenzo crown ethers is more rigid than the second because of the strong interaction of the first molecular layer with the potassium ions on the surface of muscovite mica. SXRD measurements revealed that for all of the investigated dibenzo crown ethers the first molecule lies relatively flat whereas the second lies more upright. The SXRD measurements further revealed that the molecules of the first layer of dibenzo-15-crown-5 are on top of a potassium atom, showing that the binding mechanism of this layer is indeed of the coordination complex form. The AFM and SXRD data are in good agreement, and the combination of these techniques is therefore a powerful way to determine the molecular orientation at surfaces.
Surface Science | 2014
Wester de Poel; Stelian Pintea; Jakub Drnec; Francesco Carlà; Roberto Felici; P. Mulder; Johannes A. A. W. Elemans; Willem J. P. van Enckevort; Alan E. Rowan; Elias Vlieg
Diamond and Related Materials | 2009
G.W.G. van Dreumel; Josephus Gerardus Buijnsters; T. Bohnen; J. J. ter Meulen; P.R. Hageman; W.J.P. van Enckevort; Elias Vlieg
Crystal Growth & Design | 2015
Alaa Adawy; Esther G. G. van der Heijden; Johan Hekelaar; Willem J. P. van Enckevort; Willem J. de Grip; Elias Vlieg
Journal of Crystal Growth | 2009
T. Bohnen; Gholamreza Yazdi; Rositsa Yakimova; G.W.G. van Dreumel; P.R. Hageman; Elias Vlieg; Rienk E. Algra; Marcel A. Verheijen; James H. Edgar