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Dive into the research topics where Georgeta Salvan is active.

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Featured researches published by Georgeta Salvan.


Journal of Applied Physics | 2013

Optical and magneto-optical study of nickel and cobalt ferrite epitaxial thin films and submicron structures

Cameliu Himcinschi; Georgeta Salvan; Michael Fronk; Andreas Talkenberger; D. R. T. Zahn; David Rafaja; Jens Kortus

Epitaxial films and ordered arrays of submicron structures of nickel and cobalt ferrites were deposited on Nb doped SrTiO3 by pulsed laser deposition. X-Ray diffraction and atomic force microscopy showed that the films have a good crystalline quality and smooth surfaces. A larger number of phonon bands was observed in the polarization dependent Raman spectra of the ferrite films than expected for the cubic spinel structures. This is explained by short range ordering of the Ni2+ (or Co2+) and Fe3+ cations at the octahedral sites inducing a lowering of the symmetry. The same behavior was also observed in the Raman spectra measured for the submicron structures, suggesting the same cation distribution as in the films. The diagonal components of the dielectric function for nickel and cobalt ferrites are determined from ellipsometry in the 0.73–5 eV photon energy range. The absorption edge was analyzed using a bandgap model and the energies for the indirect and direct optical transitions were calculated. It was...


Journal of Applied Physics | 2004

Study of the interaction of tris-(8-hydroxyquinoline) aluminum (Alq3) with potassium using vibrational spectroscopy: Examination of possible isomerization upon K doping

Yoko Sakurai; Yoshinobu Hosoi; Hisao Ishii; Yukio Ouchi; Georgeta Salvan; A. Kobitski; Thorsten U. Kampen; D. R. T. Zahn; Kazuhiko Seki

The geometrical structure of potassium-doped Alq3 [tris-(8-hydroxyquinoline) aluminum] and the interaction between the Alq3 molecule and potassium were studied using infrared reflection absorption spectroscopy (IRRAS), surface-enhanced Raman scattering (SERS), and density functional theory calculations. A major aim of this study was to examine the theoretically predicted isomerization of Alq3 molecules from the meridional form to the facial form upon alkali-metal doping. The observed spectra show significant changes with the deposition of potassium on a thin Alq3 film. The calculated IR spectra of the K-Alq3 complex differ significantly between the meridional and facial forms, and the calculation for the meridional form agrees fairly well with the observed spectrum. This demonstrates that (1) the Alq3 molecule does not change to a facial isomer with the deposition of potassium, but retains the meridional form, in contrast to the reported theoretical prediction, and (2) the structure of the complex as eval...


Journal of Physics: Condensed Matter | 2003

Optical properties and molecular orientation in organic thin films

M. Friedrich; G. Gavrila; Cameliu Himcinschi; Thorsten U. Kampen; A.Yu. Kobitski; H. Méndez; Georgeta Salvan; Javier Méndez; N Nicoara; A. M. Baró; D. R. T. Zahn

The optical properties and the molecular orientation in thin films of 3,4,9,10perylenetetracarboxylic dianhydride (PTCDA) and N,N � -dimethyl-3,4,9,10perylenetetracarboxylic diimide (DiMePTCDI) were studied by means of variable angle spectroscopic ellipsometry (VASE), atomic force microscopy (AFM), near edge x-ray absorption fine structure (NEXAFS) spectroscopy, and infrared (IR) and Raman spectroscopy. VASE reveals that both kinds of film exhibit a strong optical anisotropy. For PTCDA, the optical constants are found to have much higher values in the substrate plane than perpendicular to it. While th ea nisotropy measured in the substrate plane on passivated GaAs(100) is very small for PTCDA a giant anisotropy is observed for DiMePTCDI. This difference in the optical properties is attributed to the different orientation of molecules in the thin organic films. While the PTCDA molecules lie flat on the substrate with their molecular plane parallel to the substrate surface, the DiMePTCDI molecules are tilted with respect to the substrate surface and are predominantly oriented with their long axis parallel to the [011] direction of the substrate as confirmed by VASE, NEXAFS, and Raman and IR results.


Applied Surface Science | 2000

Optical characterisation of PTCDA films grown on passivated semiconductor substrates

Thorsten U. Kampen; Georgeta Salvan; M. Friedrich; D. A. Tenne; Sunggook Park; D. R. T. Zahn

3,4,9,10-Perylenetetracarboxylic dianhydride (PTCDA) was deposited on passivated Si(111) and GaAs(001) surfaces using organic molecular beam deposition (OMBD). The growth of the PTCDA films was monitored in situ and on-line by means of Raman spectroscopy. In addition, ex situ infrared (IR) spectra were recorded in order to observe the non-Raman active modes. Raman and IR spectra reveal molecular vibrational modes, allowing us to characterize the structural quality of the PTCDA films and the interaction with the substrate.


Diamond and Related Materials | 2002

Detection of nanophase at the surface of HFCVD grown diamond films using surface enhanced Raman spectroscopic technique

Mainak Roy; V.C. George; A.K. Dua; P Raj; Steffen Schulze; D.A Tenne; Georgeta Salvan; D. R. T. Zahn

Abstract Diamond films prepared by hot filament chemical vapour deposition technique were characterised using X-ray diffraction, scanning electron microscopy and surface enhanced Raman spectroscopic technique. Silver was deposited on to diamond thin film under ultra high vacuum conditions and macro-Raman spectra were recorded during the deposition. An asymmetric broadening of the Raman peak at 1332 cm−1 and gradual emergence of a new peak at 1240 cm−1 with increasing thickness of the silver layer were observed. These observations were explained on the basis of phonon confinement in nanometer-sized crystals. It is proposed that the detected nanophase is present only at the surface and is not a bulk property. The average particle size of the film was estimated from X-ray analysis and also from the symmetric broadening of the 1332 cm−1 line in the Raman spectra of the bare sample. The presence of the nanophase was further evidenced by high resolution scanning electron microscopy. The probable mechanism of formation was briefly explored.


Advanced Materials | 2016

Fully Integrated Organic Nanocrystal Diode as High Performance Room Temperature NO2 Sensor

Abdur Rehman Jalil; Hao Chang; Vineeth Kumar Bandari; Peter Robaschik; Jian Zhang; Pablo F. Siles; Guodong Li; Danilo Bürger; Daniel Grimm; Xingyuan Liu; Georgeta Salvan; D. R. T. Zahn; Feng Zhu; Haibo Wang; Donghang Yan; Oliver G. Schmidt

Organic diodes consisting of molecular nano-pyramid structures sandwiched between metal and strained nano-membrane electrodes are created. The robust and smooth contacts provided by self-curled metal layers render the molecular nano-pyramids efficent channels for detecting nitrogen dioxide airflow.


Journal of Physical Chemistry B | 2009

Magneto-Optical Kerr Effect Spectroscopy—A Sensitive Tool for Investigating the Molecular Orientation in Organic Semiconductor Films

Björn Bräuer; Michael Fronk; Daniel Lehmann; D. R. T. Zahn; Georgeta Salvan

The detection and control of the molecular growth mode is a key prerequisite for fabricating opto-electronic devices. In this work we present the magneto-optical Kerr effect (MOKE) spectroscopy to be a highly sensitive method for the detection of the molecular orientation. On the example of metal free phthalocyanine (H(2)Pc) in thin films, it will be shown that also for diamagnetic molecules a strong magneto-optical response can be expected. The growth mode and thus the intensity of the MOKE signal of H2Pc is strongly influenced by a templating effect using ultrathin layers of 3,4,9,10-perylenetetracarboxylic dianhydride (PTCDA). From the MOKE spectra in the energy range from 1.5 to 5.0 eV and the optical constants, the Voigt constant of thin organic films was determined. From the strong in-plane/out-of-plane anisotropy of the optical constants and the value of the Voigt constant the average molecular tilt angle of H2Pc molecules with respect to the substrate plane can be obtained.


Journal of Physics: Condensed Matter | 2003

Infrared spectroscopic study of the morphology of 3,4,9,10-perylene tetracarboxylic dianhydride films grown on H-passivated Si(111)

Reinhard Scholz; M. Friedrich; Georgeta Salvan; Thorsten U. Kampen; D. R. T. Zahn; Thomas Frauenheim

Infrared spectroscopy is applied to the characterization of 3,4,9,10-perylene tetracarboxylic dianhydride (PTCDA) films grown with organic molecular beam deposition (OMBD) on hydrogen-passivated Si(111). Comparing these films with powder spectra, the films show a preferential orientation of the PTCDA molecules close to coplanar with the substrate surface. For deposition of PTCDA films using laser ablation at 1064 nm, the average orientation of the molecules is more random than in the OMBD-grown films, but we still find some degree of preferential order of the molecules with respect to the substrate surface. The experimental findings are compared to density functional calculations of the single molecule and the two crystalline phases.


Applied Surface Science | 2001

Raman spectroscopy: a powerful tool for characterisation of Ag/3,4,9,10-perylene-tetracarboxylic-dianhydride/GaAs heterostructures

Georgeta Salvan; D. A. Tenne; Thorsten U. Kampen; Reinhard Scholz; G. Jungnickel; Th. Frauenheim; D. R. T. Zahn

Abstract The present contribution emphasises the capabilities of Raman spectroscopy for the characterisation of chemical and structural properties of thin organic films. As an example, a perylene derivative is presented, namely 3,4,9,10-perylene-tetracarboxylic-dianhydride (PTCDA). The focus will be directed to the Raman monitoring of dynamic processes. First, the PTCDA film formation on GaAs substrates by organic molecular beam deposition will be followed. The changes in the GaAs bands and PTCDA internal and external vibrational modes will be investigated as indicators for the interface formation. Secondly, the PTCDA internal modes will be monitored upon the deposition of silver onto the PTCDA/GaAs heterostructure.


Journal of Physics: Condensed Matter | 2014

Optical and magneto-optical properties of metal phthalocyanine and metal porphyrin thin films

Tobias Birnbaum; Torsten Hahn; Claudia Martin; Jens Kortus; Michael Fronk; Frank Lungwitz; D. R. T. Zahn; Georgeta Salvan

The optical constants together with the magneto-optical Voigt constants of several phthalocyanine (Pc) and methoxy functionalized tetraphenylporphyrin (TMPP) thin films prepared on silicon substrates are presented. The materials investigated are MePc with Me = Fe, Co, Ni, Cu, Zn and MeTMPP with Me = Cu, Ni. We also compared our results to the metal-free H2Pc, H2TPP and H2TMPP. The experimental results will be supported by electronic structure calculations based on density functional theory (DFT) and interpreted using the perimeter model initially proposed by Platt. The model allows for qualitative understanding of the forbidden character of transitions in planar, aromatic molecules, and is able to qualify differences between Pc and TMPP type materials.

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D. R. T. Zahn

Chemnitz University of Technology

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Michael Fronk

Chemnitz University of Technology

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Reinhard Scholz

Dresden University of Technology

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Björn Bräuer

Chemnitz University of Technology

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M. Friedrich

Chemnitz University of Technology

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Beynor A. Paez

Chemnitz University of Technology

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Oliver G. Schmidt

Chemnitz University of Technology

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Tobias Rüffer

Chemnitz University of Technology

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Cameliu Himcinschi

Freiberg University of Mining and Technology

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