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Organic Thin Films (organic + thin_film)
Selected Abstractsn-Type Doping of Organic Thin Films Using Cationic Dyes,ADVANCED FUNCTIONAL MATERIALS, Issue 3 2004A. Werner Abstract We present an approach to stable n-type doping of organic matrices using organic dopants. In order to circumvent stability limitations inherent to strong organic donors, we produce the donor from a stable precursor compound in situ. As an example, the cationic dye pyronin B chloride is studied as a dopant in a 1,4,5,8-naphthalene tetracarboxylic dianhydride (NTCDA) matrix. Conductivities of up to 1.9,×,10,4,S,cm,1 are obtained for doped NTCDA, two orders of magnitude higher than the conductivity of NTCDA doped with bis(ethylenedithio)-tetrathiafulvalene as investigated previously, and four orders of magnitude higher than nominally undoped NTCDA films. Field-effect measurements are used to prove n-type conduction and to study the doping effect further. The findings are interpreted using a model of transport in disordered solids using a recently published model. Combined FTIR, UV-vis, and mass spectroscopy investigations suggest the formation of leuco pyronin B during sublimation of pyronin B chloride. [source] Generation of paramagnetic hybrid inorganic/organic thin filmsAPPLIED ORGANOMETALLIC CHEMISTRY, Issue 7 2010Abhinav Bhushan Abstract There is a growing interest in developing advanced materials for thin film applications in biology, electronics, photonics and engineering. We report the development of hybrid inorganic/organic thin films containing nickel, iron and cobalt paramagnetic materials. By etching the resist in oxygen plasma after processing, most of the organic component of the resist was removed. The elemental chemical composition of the films was confirmed by energy dispersive X-ray spectroscopy. This process can potentially lead to patterning paramagnetic thin films containing paramagnetic materials by following standard photolithography protocols, obviating the need for a wet or vacuum metal deposition. Copyright © 2010 John Wiley & Sons, Ltd. [source] A Computational Study of the Sub-monolayer Growth of PentaceneADVANCED FUNCTIONAL MATERIALS, Issue 13 2006D. Choudhary Abstract A computational study of organic thin-film growth using a combination of ab,initio based energy calculations and kinetic Monte Carlo (KMC) simulations is provided. A lattice-based KMC model is used in which binding energies determine the relative rates of diffusion of the molecules. This KMC approach is used to present "landscapes" or "maps" that illustrate the possible structural outcomes of growing a thin film of small organic molecules, represented as a two-site dimer, on a substrate in which the strength of organic,substrate interactions is allowed to vary. KMC provides a mesoscopic-scale view of sub-monolayer deposition of organic thin films on model substrates, mapped out as a function of the flux of depositing molecules and the temperature of the substrate. The morphology of the crystalline thin films is shown to be a strong function of the molecule,molecule and molecule,substrate interactions. A rich variety of maps is shown to occur in which the small organic molecules either stand up or lie down in a variety of different patterns depending on the nature of the binding to the surface. In this way, it is possible to suggest how to tailor the substrate or the small organic molecule in order to create a desired growth habit. In order to demonstrate how this set of allowable maps is reduced in the case where the set of energy barriers between substrate and organic molecule are reliably known, we have used Gaussian,98 calculations to establish binding energies for the weak van der Waals interactions between a),pairs of pentacene molecules as a function of orientation and b),pentacene and two substrates, silicon surfaces passivated with cyclopentene molecules and a crystalline model of silicon dioxide. The critical nucleation size and the mode of diffusion of this idealized two-site dimer model for pentacene molecules are found to be in good agreement with experimental data. [source] Hybrid Light-Emitting Diodes from Microcontact-Printing Double-Transfer of Colloidal Semiconductor CdSe/ZnS Quantum Dots onto Organic Layers,ADVANCED MATERIALS, Issue 10 2008Aurora Rizzo A novel dry deposition approach is developed to transfer arrays of colloidal quantum dots onto organic thin films, as illustrated in the figure. A red light-emitting device combining inorganic and organic components is fabricated based on this simple transfer protocol. [source] Vacuum-Ultraviolet Photopolymerisation of Amine-Rich Thin FilmsMACROMOLECULAR CHEMISTRY AND PHYSICS, Issue 10 2008Florina Truica-Marasescu Abstract Nitrogen-rich organic thin films were deposited by VUV-assisted photochemical polymerisation of flowing C2H4/NH3 mixtures. The fundamental reaction mechanisms of these binary gas mixtures were investigated as a function of the wavelength of two almost monochromatic VUV sources. Compositions of these "UV-PE:N" films close to the surface were determined by XPS, and the amine concentrations and selectivities were quantified via chemical derivatisation. The UV-PE:N films were compared with plasma polymers deposited using low-pressure glow discharges in similar gas flow mixtures, "L-PPE:N"; it is shown that VUV photochemistry is superior to plasma chemistry in producing almost monofunctional organic thin films. [source] Influence of top layer geometries on the electronic properties of pentacene and diindenoperylene thin filmsPHYSICA STATUS SOLIDI (A) APPLICATIONS AND MATERIALS SCIENCE, Issue 3 2008M. Scharnberg Abstract Top layers have a pronounced influence on the electronic properties of molecular organic thin films. Here, we report about the changes induced by metallic and polymeric top layers and contacts. As test structures, model systems of diindenoperylene and pentacene crystalline molecular organic thin films are used. A very sensitive radiotracer technique is introduced to study the details of metal penetration during top contact formation. The influence of temperature, evaporation time, adhesion promoter and grain size of the organic film were examined. The electric currents passing through metal top contacts were found to vary by more than a factor of three, depending on the preparation conditions of the metal contact. Furthermore, the series resistance of chemically identical contacts that only differed in the morphology of the interface were found to show pronounced asymmetric conductivity behaviour. We also show that with the help of electret top layers, based on the Teflon-AF fluropolymer, the threshold voltage of an organic field effect transistor can be tuned by several volts. (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Measuring carrier mobility in conventional multilayer organic light emitting devices by delayed exciton generationPHYSICA STATUS SOLIDI (B) BASIC SOLID STATE PHYSICS, Issue 5 2008S. Reineke Abstract The authors present an alternative method for the determination of the charge carrier mobility of organic thin films. In contrast to known methods like space charge limited current, field effect transistor and time of flight approaches, we determine the charge carrier mobility of a mixed film, serving as emission layer, within the conventional multilayer device architecture. We make use of a strong delayed generation feature in the electroluminescent decay, following a short voltage pump pulse in a time-resolved set-up. Taking into account the preferentially electron transporting properties of the film, the mobility of a N,N ,-di(naphthalen-2-yl)- N,N ,-diphenyl-benzidine (NPB):tris(1-phenylisoquinoline) iridium [Ir(piq)3] mixed film is found to be on the order of 10,5 cm2 (Vs),1. (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Enhanced surface sensitivity in secondary ion mass spectrometric analysis of organic thin films using size-selected Ar gas-cluster ion projectilesRAPID COMMUNICATIONS IN MASS SPECTROMETRY, Issue 10 2010Motohiro Tanaka A size-selected argon (Ar) gas-cluster ion beam (GCIB) was applied to the secondary ion mass spectrometry (SIMS) of a 1,4-didodecylbenzene (DDB) thin film. The samples were also analyzed by SIMS using an atomic Ar+ ion projectile and X-ray photoelectron spectroscopy (XPS). Compared with those in the atomic-Ar+ SIMS spectrum, the fragment species, including siloxane contaminants present on the sample surface, were enhanced several hundred times in the Ar gas-cluster SIMS spectrum. XPS spectra during beam irradiation indicate that the Ar GCIB sputters contaminants on the surface more effectively than the atomic Ar+ ion beam. These results indicate that a large gas-cluster projectile can sputter a much shallower volume of organic material than small projectiles, resulting in an extremely surface-sensitive analysis of organic thin films. Copyright © 2010 John Wiley & Sons, Ltd. [source] | ||||||||||||||||