TY - JOUR A1 - Schwarz, Guntram A1 - Sievers, Torsten K. A1 - Bodenthin, Yves A1 - Hasslauer, Ires A1 - Geue, Thomas A1 - Koetz, Joachim A1 - Kurth, Dirk G. T1 - The structure of metallo-supramolecular polyelectrolytes in solution and on surfaces N2 - Metal ion induced self-assembly of the rigid ligand 1,4-bis(2,2':6',2 ''-terpyridine- 4'-yl) benzene (1) with Fe(II), Co(II), Ni(II) and Zn(II) acetate in aqueous solution results in extended, rigid- rod like metallosupramolecular coordination polyelectrolytes (MEPE-1). Under the current experimental conditions the molar masses range from 1000 g mol(-1) up to 500 000 g mol(-1). The molar mass depends on concentration, stoichiometry, metal-ion and time. In addition, we present viscosity measurements, small angle neutron scattering and AFM data. We introduce a protocol to precisely control the stoichiometry during self-assembly using conductometry. The protocol can be used with different terpyridine ligands and the above-mentioned metal ions and is of paramount importance to obtain meaningful and reproducible results. As a control experiment we studied the mononuclear 4'- (phenyl)2,2':6',2 ''-terpyridine (3) complex with Ni(II) and Zn(II) and the flexible ligand 1,3- bis[4'-oxa(2,2': 6',2 ''-terpyridinyl)] propane (2) with Ni(II) acetate (Ni-MEPE-2). This ligand does not form extended macroassemblies but likely ring-like structures with 3 to 4 repeat units. Through spin- coating of Ni-MEPE-1 on a solid surface we can image the MEPEs in real space by AFM. SANS measurements of Fe-MEPE-1 verify the extended rigid-rod type structure of the MEPEs in aqueous solution. Y1 - 2010 UR - http://pubs.rsc.org/en/content/articlehtml/2010/jm/b926783b U6 - https://doi.org/10.1039/B926783b SN - 0959-9428 ER - TY - JOUR A1 - Schwarz, Guntram A1 - Bodenthin, Yves A1 - Geue, Thomas A1 - Koetz, Joachim A1 - Kurth, Dirk G. T1 - Structure and properties of dynamic rigid rod-like metallo-supramolecular polyelectrolytes in solution N2 - Metal-ion-induced self-assembly in aqueous solution of the rigid ligand 1,4-bis(2,2':6',2 ''-terpyridine-4'-yl)benzene (1) with Fe(OAc)(2) and Ni(OAc)(2) is investigated with viscosimetry, SANS, and AFM. Ligand 1 forms extended, rigid-rod like metallo-supramolecular coordination polyeectrolytes (MEPEs) with a molar mass of up to 200 000 g mol(-1) under the Current experimental conditions. The molar mass depends oil concentration, stoichiometry, and time. By spin-coating MEPEs oil a solid surface, we call image the MEPEs in real space by AFM. Both AFM and SANS confirm the extended rigid-rod-type structure of the MEPEs. As a control experiment, we also studied the flexible ligand 1,3-bis[4'-oxa(2,2':6',2 ''-terpyridinyl)]propane (2). Ligand 2 does not form extended macro-assemblies but likely ringlike structures with three 10 four repeat units. Finally, we present it protocol to control the stoichiometry during self-assembly using conductometry, which is of paramount importance to obtain meaningful and reproducible results. Y1 - 2010 UR - http://pubs.acs.org/doi/full/10.1021/ma902057f U6 - https://doi.org/10.1021/Ma902057f SN - 0024-9297 ER - TY - JOUR A1 - Pietsch, Ullrich A1 - Bodenthin, Yves A1 - Grenzer, Jörg A1 - Geue, Thomas A1 - Möhwald, Helmuth A1 - Kurth, Dirk G. T1 - Structure and temperature behavior of metallo-supramolecular assemblies N2 - A detailed structural analysis of a Langmuir-Blodgett (LB) multilayer composed of a polyelectrolyte-amphiphile complex (PAC) is presented. The PAC is self-assembled from metal ions, ditopic bis-terpyridines, and amphiphiles. The vertical structure of the LB multilayer is investigated by X-ray reflectometry. The multilayer has a periodicity of 57 A, which corresponds to an architecture of flat lying metallo-supramolecular coordination polyelectrolyte (MEPE) rods and upright-standing amphiphiles (dihexadecyl phosphate, DHP). In-plane diffraction reveals hexagonal packing of the DHP molecules. Using extended X-ray absorption fine structure (EXAFS) experiments, we prove that the central metal ion is coordinated to the terpyridine moieties in a pseudo-octahedral coordination environment. The Fe-N bond distances are 1.82 and 2.0 angstrom, respectively. Temperature resolved measurements indicate a reversible phase transition in a temperature range up to 55 degrees C. EXAFS measurements indicate a lengthening of the average Fe-N bond distance from 1.91 to 1.95 angstrom. The widening of the coordination cage upon heating is expected to lower the ligand field stabilization, thus giving rise to spin transitions in these composite materials Y1 - 2005 ER - TY - JOUR A1 - Pietsch, Ullrich A1 - Bhattacharya, M. K. A1 - Sanyal, M. K. A1 - Geue, Thomas T1 - Glass transition in Ultrathin Polymer Films : a Thermal Expansion Study N2 - The glass transition process gets affected in ultrathin films having thickness comparable to the size of the molecules. We observe systematic broadening of the glass transition temperature (T-g) as the thickness of an ultrathin polymer film reduces below the radius of gyration but the change in the average T-g was found to be very small. The existence of reversible negative and positive thermal expansion below and above T-g increased the sensitivity of our thickness measurements performed using energy-dispersive x-ray reflectivity. A simple model of the T-g variation as a function of depth expected from sliding motion could explain the results Y1 - 2005 ER - TY - JOUR A1 - Henneberg, Oliver A1 - Rochon, Paul A1 - Panzner, Tobias A1 - Finkelstein, Kenneth D. A1 - Geue, Thomas A1 - Saphiannikova, Marina A1 - Pietsch, Ullrich T1 - In-situ Investigation of Surface Relief Grating Formation in Photosensitive Polymers Y1 - 2004 UR - http://www.chess.cornell.edu/pubs/csnm2004/research/insitu.pdf ER - TY - JOUR A1 - Pietsch, Ullrich A1 - Saphiannikova, Marina A1 - Henneberg, Oliver A1 - Geue, Thomas T1 - Non-linear effects during inscription of azobenzene surface relief gratings Y1 - 2004 ER - TY - JOUR A1 - Henneberg, Oliver A1 - Geue, Thomas A1 - Pietsch, Ullrich A1 - Winter, Bernd T1 - Investigation of azobenzene side group orientation in polymer surface relief gratings by means of photoelectron spectroscopy N2 - The molecular orientation of azobenzene side groups in polymer films before (nonpatterned) and after (patterned) development of a surface relief grating has been investigated by photoelectron spectroscopy using synchrotron radiation. The photoemission spectra obtained for 60-100 eV photons of a patterned and a nonpatterned surface are similar when the polarization vector of the synchrotron light is parallel to the grating vector. However, for perpendicular excitation, considerable spectral intensity differences can be observed for 9-14 eV electron binding energy. The observed changes are attributed to the formation of well-oriented azobenzenes at the surface. (C) 2004 American Institute of Physics Y1 - 2004 UR - http://scitation.aip.org/journals/doc/APPLAB-ft/vol_84/iss_9/1561_1.html ER - TY - JOUR A1 - Pietsch, Ullrich A1 - Mukhopadhyay, M. K. A1 - Sanyal, M. K. A1 - Datta, A. A1 - Mukherjee, M. A1 - Geue, Thomas A1 - Grenzer, Jörg T1 - Transition from two-dimensional to three-dimensional melting in Langmuir-Blodgett films N2 - Results of energy-dispersive x-ray reflectivity and grazing incidence diffraction studies of Langmuir-Blodgett films exhibited evolution of conventional three-dimensional melting from continuous melting, characteristic of two- dimensional systems, as a function of deposited monolayers. Continuous expansion followed by a sharp phase transition of the in-plane lattice was observed before the melting point and found to be independent of number of deposited layers. Evolution of conventional melting with an increase in the number of monolayers could be quantified by measuring stiffness against tilting of the vertical stack of molecules, which are kept together by an internal field. The internal field as defined in this model reduces as the in-plane lattice expands and the sample temperature approaches melting point. The sharpness of the melting transition, which has been approximated by a Langevin function, increases with the number of deposited monolayers Y1 - 2004 ER - TY - JOUR A1 - Stiller, Burkhard A1 - Karageorgiev, Peter A1 - Buchsteiner, Andrea A1 - Geue, Thomas A1 - Henneberg, Oliver A1 - Brehmer, Ludwig A1 - Natansohn, Almeria A1 - Hollricher, Olga T1 - Using light as a tool : optically Induced mass transport generated in Near-Fields Y1 - 2003 SN - 0038-7355 - ER - TY - JOUR A1 - Pietsch, Ullrich A1 - Panzner, Tobias A1 - Leitenberger, Wolfram A1 - Grenzer, Jörg A1 - Bodenthin, Th. A1 - Geue, Thomas A1 - Möhwald, Helmuth T1 - Coherence experiments at the energy-dispersive reflectometry beamline at BESSY II Y1 - 2003 ER - TY - JOUR A1 - Pietsch, Ullrich A1 - Bhattacharya, M. K. A1 - Mukherjee, M. A1 - Sanyal, M. K. A1 - Geue, Thomas A1 - Grenzer, Jörg T1 - Energy dispersive x-ray reflectivity technique to study thermal properties of polymer films Y1 - 2003 ER - TY - JOUR A1 - Geue, Thomas A1 - Henneberg, Oliver A1 - Grenzer, Jörg A1 - Pietsch, Ullrich A1 - Natansohn, Almeria A1 - Rochon, Paul A1 - Finkelstein, Kenneth D. T1 - Formation of a buried density grating on thermal erasure of azobenzene polymer surface gratings Y1 - 2002 SN - 0927-7757 ER - TY - JOUR A1 - Geue, Thomas A1 - Henneberg, Oliver A1 - Pietsch, Ullrich T1 - X-ray reflectivity from sinusoidal surface relief gratings Y1 - 2002 SN - 0023-4753 ER - TY - JOUR A1 - Reiche, Jürgen A1 - Penacorada, Florencio A1 - Geue, Thomas A1 - Pietsch, Ullrich A1 - Brehmer, Ludwig T1 - In-plane structure of uranylarachidate multilayers Y1 - 1995 ER - TY - JOUR A1 - Geue, Thomas A1 - Katholy, Stefan A1 - Reiche, Jürgen A1 - Brehmer, Ludwig A1 - Caliebe, W. T1 - Grazing incidence x-ray diffraction (GIXD) measurements of uranyl arachidate (UO2A2) LB films Y1 - 1998 ER - TY - JOUR A1 - Date, R. W. A1 - Fawcett, A. H. A1 - Geue, Thomas A1 - Haferkorn, J. A1 - Malcolm, R. K. A1 - Stumpe, Joachim T1 - Self-ordering within thin films of poly(olefin sulfone)s. Y1 - 1998 ER - TY - JOUR A1 - Haferkorn, J. A1 - Geue, Thomas A1 - Date, R. W. A1 - Fawcett, A. H. A1 - Stumpe, Joachim T1 - Aggregation and orientation phenomena in constrained films of Poly(olefine sulfone)s. Y1 - 1998 ER - TY - JOUR A1 - Paschke, K. A1 - Geue, Thomas A1 - Barberka, Thomas Andreas A1 - Bolm, A. A1 - Pietsch, Ullrich A1 - Rösch, M. A1 - Batke, Edwin A1 - Faller, F. A1 - Kerkel, K. A1 - Oshiniwo, J. A1 - Forchel, Alfred T1 - Characterization of lateral semiconductor nano structures by means of x-ray grazing-incidence diffraction Y1 - 1997 ER - TY - JOUR A1 - Herrmann, A. A1 - Kaupp, G. A1 - Geue, Thomas A1 - Pietsch, Ullrich T1 - AFM and GID investigations of the gas-solid diazotation of 4-sulfanil-acid-monohydrat single crystals Y1 - 1997 ER - TY - JOUR A1 - Reiche, Jürgen A1 - Knochenhauer, Gerald A1 - Barberka, Thomas Andreas A1 - Geue, Thomas A1 - Pietsch, Ullrich A1 - Brehmer, Ludwig A1 - Hodge, P. A1 - Tredgold, Richard H. T1 - In-plane structure of perfluorotetra decanoic acid Langmuir-Blodgett films and films formed by vacuum deposition Y1 - 1995 ER - TY - JOUR A1 - Reiche, Jürgen A1 - Dietzel, Birgit A1 - Freydank, Anke-Christine A1 - Geue, Thomas A1 - Pietsch, Ullrich A1 - Brehmer, Ludwig T1 - Lateral structure of thermally treated oxadiazole Langmuir-Blodgett films Y1 - 1995 ER - TY - JOUR A1 - Stumpe, Joachim A1 - Geue, Thomas A1 - Fischer, Thomas M. A1 - Menzel, Henning T1 - Photochemically induced changes of structures in LB-multilayers of amphotropic polymers Y1 - 1995 ER - TY - JOUR A1 - Geue, Thomas A1 - Stumpe, Joachim A1 - Pietsch, Ullrich A1 - Haak, M. A1 - Kaupp, G. T1 - Photochemically induced changes of optical anisotropy and surface of LB-multilayers built up by an amphiphilic and liquid crystalline copolymer conating azobenzene moieties Y1 - 1995 ER - TY - JOUR A1 - Reinhold, Beate A1 - Geue, Thomas A1 - Huber, Patrick A1 - Sant, Tushar A1 - Pietsch, Ullrich A1 - Sztucki, Michael T1 - In situ and ex situ SAXS investigation of colloidal sedimentation onto laterally patterned support N2 - We report on in situ investigations of colloidal ordering during gravity sedimentation from a colloidal suspension onto a prepatterned support using a polymeric surface relief grating (SRG) as the support. The ordering of colloids with a diameter of 420 nm was investigated by means of grazing-incidence small-angle X-ray scattering (GISAXS) and transmission SAXS using a preparation cell guaranteeing stable temperature and humidity. GISAXS was used for in situ monitoring of the time evolution of colloidal ordering within the whole illuminated sample area. The onset of ordering was indicated by the increase of integrated intensity within a small time frame shortly before complete evaporation of the dispersant. Single domains of coated samples were investigated ex situ by SAXS in transmission geometry where the irradiated sample area was 200 x 200 mu m(2) only. Domains with the typical size of a few millimeters were observed varying in orientation and crystallographic structure for various positions at the sample. They were mainly oriented along the grooves of the grating, confirming the influence of the underlying grating on colloidal ordering. Y1 - 2009 UR - http://pubs.acs.org/journal/langd5 U6 - https://doi.org/10.1021/La803078b SN - 0743-7463 ER - TY - JOUR A1 - Pietsch, Ullrich A1 - Barberka, Thomas Andreas A1 - Geue, Thomas A1 - Stömmer, Ralph T1 - X-ray scattering from thin organic films and multilayers Y1 - 1997 ER - TY - JOUR A1 - Stömmer, Ralph A1 - Martin, C. R. A1 - Geue, Thomas A1 - Göbel, H. A1 - Hub, W. A1 - Pietsch, Ullrich T1 - Comparative studies of fractal parameters of Si(100) surfaces measured by X-ray scattering and atomic force microscopy Y1 - 1998 ER - TY - JOUR A1 - Stahn, Jochen A1 - Pucher, Andreas A1 - Geue, Thomas A1 - Daniel, A. A1 - Pietsch, Ullrich T1 - Electric field induced electron density response of GaAs and ZnSe Y1 - 1998 ER - TY - JOUR A1 - Reiche, Jürgen A1 - Penacorada, Florencio A1 - Geue, Thomas A1 - Pietsch, Ullrich A1 - Brehmer, Ludwig T1 - Monolayers and multilayers of uranyl arachidate : in-plane structure of uranyl arachidate multilayers N2 - The molecular in-plane structure of uranyl arachidate Langmuir-Blodgett (LB) films formed at different subphase pH values was analysed by means of X-ray grazing-incidence diffraction. For multilayers formed at low subphase pH a reorganisation of the arachidic acid film structure is confirmed. At appropriate subphase pH values, reorganisation of the film structure, e.g. via the formation of three-dimensional crystallites, is prevented by the presence of the uranyl ions and by the subsequent introduction of conformational disorder (gauche defects) in the alkyl chains. The observation of a macroscopic flow-induced in-plane texture in these uranyl arachidate LB films has profound implications for the design of ordered, supramolecular structures by the Langmuir-Blodgett technique. Y1 - 1997 ER - TY - JOUR A1 - Reiche, Jürgen A1 - Knochenhauer, Gerald A1 - Dietel, Reinhard A1 - Freydank, Anke-Christine A1 - Zetzsche, Thomas A1 - Pietsch, Ullrich A1 - Brehmer, Ludwig A1 - Barberka, Thomas Andreas A1 - Geue, Thomas T1 - Structure of thermally treated oxadiazoleamide Langmuir-Blodgett films N2 - The thermal treatment of Y-type Langmuir-Blodgett (LB) films formed from the amphiphilic derivative of 2,5- diphenyl-1,3,4-oxadiazole 1 results in changes of the molecular packing. These changes have been analysed by a combination of X-ray specular reflectivity data, X-ray grazing incidence diffraction data and scanning force microscopy images, On the basis of these experimental data we have simulated possible supramolecular structures, These simulations provide insight into the intermolecular interactions giving rise to the observed structural transitions. The crystalline structure induced by thermal treatment of the LB films is characterized by a uniaxial texture, which is correlated with the dipping direction during deposition of the LB film. Y1 - 1997 ER - TY - JOUR A1 - Henneberg, Oliver A1 - Pietsch, Ullrich A1 - Panzner, Tobias A1 - Geue, Thomas A1 - Finkelstein, Kenneth D. T1 - Simultaneous X-ray and visible light diffraction for the investigation of surface relief and density grating formation in azobenzene containing polymer films N2 - The development of surface relief and density patterns in azobenzene polymer films was studied by diffraction at two different wavelengths. We used x-ray diffraction of synchrotron radiation at 0.124 nm in combination with visible light diffraction at a wavelength of 633 nm. In contrast to visible light scattering x-ray diffraction allows the separation of a surface relief and a density grating contribution due to the different functional dependence of the scattering power. Additionally, the x-ray probe is most sensitive for the onset of the surface grating formation Y1 - 2006 UR - http://www.informaworld.com/smpp/title~content=t713644168~db=all U6 - https://doi.org/10.1080/15421400500383345 SN - 1542-1406 ER - TY - JOUR A1 - Kopec, Maciej A1 - Rozpedzik, Anna A1 - Lapok, Lukasz A1 - Geue, Thomas A1 - Laschewsky, Andre A1 - Zapotoczny, Szczepan T1 - Stratified Micellar Multilayers-Toward Nanostructured Photoreactors JF - Chemistry of materials : a publication of the American Chemical Society N2 - Polyelectrolyte multilayers (PEMs) with stratification of the internal structure were assembled from statistical amphiphilic copolyelectrolytes of opposite charges. These polyelectrolytes organize in aqueous solutions into micellar structures with fluoroalkyl and aromatic nanodomains, respectively, that were also preserved after deposition as thin films via layer-by-layer (LbL) electrostatic self-assembly. The unimolecular micelles, formed due to statistical compositions of amphiphilic polyelectrolytes used, were shown to suppress chain interdiffusion between adjacent layers in resulting micellar PEMs, as evidenced by spectroscopic ellipsometry, atomic force microscopy (AFM), and neutron reflectometry (NR) measurements. Additionally, hydrophobic cores of the micelles were used as hosts for photoactive molecules, namely, ferrocene and perfluorinated magnesium phthalocyanine. Stratified micellar multilayers were then deposited as hollow capsules using CaCO3 microparticles as templates. Photoinduced electron transfer (PET) between ferrocene and phthalocyanine solubilized in the polymer micelles was demonstrated to occur efficiently inside the stratified, polyelectrolyte walls of the capsules, due to the polarity gradient created by the incompatible aromatic and fluoroalkyl domains. The obtained results present a new approach to construct well-organized, self-assembled nanostructured materials for solar energy conversion. Y1 - 2016 U6 - https://doi.org/10.1021/acs.chemmater.6b00161 SN - 0897-4756 SN - 1520-5002 VL - 28 SP - 2219 EP - 2228 PB - American Chemical Society CY - Washington ER - TY - JOUR A1 - Poloucek, P. A1 - Pietsch, Ullrich A1 - Geue, Thomas A1 - Symietz, Christian A1 - Brezesinski, Gerald T1 - X-ray reflectivity analysis of thin complex Langmuir-Blodgett films Y1 - 2001 ER - TY - JOUR A1 - Pietsch, Ullrich A1 - Grenzer, Jörg A1 - Geue, Thomas A1 - Neißendorfer, Frank A1 - Brezesinski, Gerald A1 - Symietz, Christian A1 - Möhwald, Helmuth A1 - Gudat, Wolfgang T1 - The energy dispersive reflectometer at BESSY II : a challenge for thin film analysis Y1 - 2001 SN - 0167- 5087 ER - TY - JOUR A1 - Grenzer, Jörg A1 - Darowski, Nora A1 - Geue, Thomas A1 - Pietsch, Ullrich A1 - Daniel, A. A1 - Rennon, Siegfried A1 - Reithmaier, Johann-Peter A1 - Forchel, Alfred T1 - Strain analysis and quantum well intermixing of a laterally modulated multiquantum well system produced by focused ion beam implantation Y1 - 2001 ER - TY - JOUR A1 - Eichhorn, Holger A1 - Bruce, Duncan W. A1 - Guillon, D. A1 - Gallani, Jean Louis A1 - Fischer, Thomas A1 - Stumpe, Joachim A1 - Geue, Thomas T1 - Metal ion mediated mesomorphism and thin film behaviour of amphitropic tetraazaporphyrin complexes Y1 - 2001 ER - TY - JOUR A1 - Mukhopadhyay, M. K. A1 - Datta, A. A1 - Sanyal, M. K. A1 - Geue, Thomas A1 - Pietsch, Ullrich T1 - Synchrotron Studies of Melting of Langmuir-Blodgett Films Y1 - 2001 ER - TY - JOUR A1 - Neumann, Werner A1 - Buchsteiner, Alexandra A1 - Mahler, Willy A1 - Geue, Thomas A1 - Pietsch, Ullrich T1 - Dielectric loss spectroscopy at fatty acid salt multilayers N2 - Dielectric loss spectroscopy (DLS) was performed at compact samples and lamellary organized Langmuir-Blodgett (LB) films from various fatty acid salts. Previous thermoanalytical measurements at compact samples revealed the appearance of two different phase transition temperatures; the lower one is related to the acid the second one to the acid salt molecules. In spite of ill defined electrical contacts with the film the characteristic DLS frequencies obtained from about 100nm thick multilayer films are similar to those recorded from bulk samples. No significant variations of frequencies were found changing the counter ions. Besides conductivity influence at low frequncies we found two relaxations related to the mobility of the dipolar carboxylat-metal group at about 100 and 10000Hz. One of these frequencies is related to the rotation around the chain axis. The strength of this relaxation increases significantly with increasing the sample temperature above 105°C. This temperature is connected with a structural phase transition observed by X-ray reflectometry. In case of Pb-stearate the results of the dielectric measurements help to interprete this structural change as a transition from an orthorhombic into a free-rotator phase. The uncorrelated rotation of molecules around their molecular axes initiates a much increased relaxation strength at the carboxylat-metal sites. Y1 - 2000 ER - TY - JOUR A1 - Stahn, Jochen A1 - Geue, Thomas A1 - Grenzer, Jörg A1 - Pietsch, Ullrich T1 - Interaction of short-chain alkanes with surface and interfaces of multilayer films built from amphiphilic molecules: an in-situ X-ray and neutron scattering probe Y1 - 2000 ER - TY - JOUR A1 - Karcenko, Anatolij V. A1 - Englisch, Uwe A1 - Grenzer, Jörg A1 - Geue, Thomas A1 - Pietsch, Ullrich A1 - Siebrecht, R. T1 - Investigation of partially deuterated multilayers by means of X-ray and polarized neutron reflectometry Y1 - 2000 SN - 1044-8632 ER - TY - JOUR A1 - Mukherjee, M. A1 - Bhattacharya, M. K. A1 - Sanyal, M. K. A1 - Geue, Thomas A1 - Grenzer, Jörg A1 - Pietsch, Ullrich T1 - Temperature dependent thickness and surface tension of polymer films Y1 - 2000 SN - 81-7371295-6 ER - TY - JOUR A1 - Geue, Thomas A1 - Schultz, Michael A1 - Grenzer, Jörg A1 - Natansohn, Almeria A1 - Rochon, Paul T1 - X-ray investigations of the molecular mobility with polymer surface gratings Y1 - 2000 ER - TY - JOUR A1 - Geue, Thomas A1 - Pietsch, Ullrich A1 - Haferkorn, J. A1 - Stumpe, Joachim A1 - Date, R. W. A1 - Fawcett, A. H. T1 - Competition of alignment and aggregation? : Phenomena in constrained films of LC poly(olefin ulfone)s and maleic anhydride co- and terpolymers Y1 - 1999 ER - TY - JOUR A1 - Reiche, Jürgen A1 - Freydank, Anke-Christine A1 - Helms, Andreas A1 - Geue, Thomas A1 - Schulz, Burkhard A1 - Brehmer, Ludwig A1 - Stiller, Burkhard A1 - Knochenhauer, Gerald T1 - Vacuum deposition films of oxadiazole compounds : formation and structure investigation N2 - The search for alternative routes of organic thin film formation is stimulated by the outstanding properties of these films in such fields as nonlinear optics, photonic data processing and molecular electronics. The formation of highly ordered multilayer structures by thermal vacuum deposition (VD) of organic compounds is an essential step toward the application of supramolecular organic architectures in technical systems. The VD of an amphiphilic substituted 2,5- diphenylene-1,3,4-oxadiazole 1 onto silicon substrates at defined temperature was used for the formation of ultrathin films. The structural data obtained for the VD-films of oxadiazole 1 by means of X-ray reflectivity, X-ray grazing incidence diffraction and atomic force microscopy (AFM) investigations indicate the formation of well ordered oxadiazole multilayers. The structure of the VD-multilayers is compared with that of Langmuir-Blodgett (LB) films and thermally treated LB-multilayers prepared from the same compound. Y1 - 1999 ER - TY - JOUR A1 - Geue, Thomas A1 - Schultz, M. A1 - Englisch, Uwe A1 - Stömmer, Ralph A1 - Pietsch, Ullrich A1 - Meine, Kerstin A1 - Vollhard, D. T1 - Investigation of pH-dependent domain structure of fatty acid salt Langmuir-Blodgett films by means of X-ray diffuse scattering and Atomic Force Microscopy Y1 - 1999 ER - TY - JOUR A1 - Pietsch, Ullrich A1 - Kubowicz, Stephan A1 - Thünemann, Andreas F. A1 - Geue, Thomas A1 - Watson, M. D. A1 - Tchebotareva, N. A1 - Müllen, K. T1 - X-ray reflectivity study of an amphiphilic hex-peri-hexabenzocoronene at a structured silicon wafer surface Y1 - 2003 ER - TY - JOUR A1 - Henneberg, Oliver A1 - Geue, Thomas A1 - Saphiannikova, Marina A1 - Pietsch, Ullrich A1 - Rochon, Paul A1 - Natansohn, Almeria T1 - Formation and dynamics of polymer surface relief gratings Y1 - 2001 SN - 0378-5963 ER - TY - JOUR A1 - Henneberg, Oliver A1 - Chi, Li Feng A1 - Geue, Thomas A1 - Saphiannikova, Marina A1 - Pietsch, Ullrich A1 - Rochon, Paul A1 - Natansohn, Almeria T1 - Atomic force microscopy inspection of the early state of formation of polymer surface relief grating Y1 - 2001 ER - TY - JOUR A1 - Geue, Thomas A1 - Saphiannikova, Marina A1 - Henneberg, Oliver A1 - Pietsch, Ullrich A1 - Rochon, Paul A1 - Natansohn, Almeria T1 - Formation mechanism and dynamics in polymer surface gratings Y1 - 2002 ER - TY - JOUR A1 - Stiller, Burkhard A1 - Geue, Thomas A1 - Morawetz, Knut A1 - Saphiannikova, Marina T1 - Optical patterning in azobenzene polymer films N2 - Thin azobenzene polymer films show a very unusual property, namely optically induced material transport. The underlying physics for this phenomenon has not yet been thoroughly explained. Nevertheless, this effect enables one to inscribe different patterns onto film surfaces, including one- and two-dimensional periodic structures. Typical sizes of such structures are of the order of micrometers, i.e. related to the interference pattern made by the laser used for optical excitation. In this study we have measured the mechanical properties of one- and two-dimensional gratings, with a high lateral resolution, using force-distance curves and pulse force mode of the atomic force microscope. We also report on the generation of considerably finer structures, with a typical size of 100 nm, which were inscribed onto the polymer surface by the tip of a scanning near-field optical microscope used as an optical pen. Such inscription not only opens new application possibilities but also gives deeper insight into the fundamentals physics underlying optically induced material transport Y1 - 2005 SN - 0022-2720 ER - TY - JOUR A1 - Saphiannikova, Marina A1 - Geue, Thomas A1 - Henneberg, Oliver A1 - Morawetz, Knut A1 - Pietsch, Ullrich T1 - Linear viscoelastic analysis of formation and relaxation of azobenzene polymer gratings N2 - Surface relief gratings on azobenzene containing polymer films were prepared under irradiation by actinic light. Finite element modeling of the inscription process was carried out using linear viscoelastic analysis. It was assumed that under illumination the polymer film undergoes considerable plastification, which reduces its original Young's modulus by at least three orders of magnitude. Force densities of about 10(11) N/m(3) were necessary to reproduce the growth of the surface relief grating. It was shown that at large deformations the force of surface tension becomes comparable to the inscription force and therefore plays an essential role in the retardation of the inscription process. In addition to surface profiling the gradual development of an accompanying density grating was predicted for the regime of continuous exposure. Surface grating development under pulselike exposure cannot be explained in the frame of an incompressible fluid model. However, it was easily reproduced using the viscoelastic model with finite compressibility. (C) 2004 American Institute of Physics Y1 - 2004 U6 - https://doi.org/10.1063/1.1642606 ER - TY - JOUR A1 - Henneberg, Oliver A1 - Geue, Thomas A1 - Saphiannikova, Marina A1 - Pietsch, Ullrich A1 - Rochon, Paul T1 - X-ray and VIS light scattering from light-induced polymer gratings Y1 - 2003 UR - http://stacks.iop.org/0022-3727/36/A241 U6 - https://doi.org/10.1088/0022-3727/36/10A/350 ER - TY - JOUR A1 - Henneberg, Oliver A1 - Panzner, Tobias A1 - Pietsch, Ullrich A1 - Geue, Thomas A1 - Saphiannikova, Marina A1 - Rochon, Paul A1 - Finkelstein, Kenneth D. T1 - X-ray and VIS light scattering from light-induced polymer gratings N2 - Sinusoidally shaped surface relief gratings made of polymer films containing, azobenzene moieties can be created by holographic illumination with laser light of about lambda approximate to 500 nm. The remarkable material transport takes place at temperatures far (100 K) below the glass transition temperature of the material. As probed by visible light scattering the efficiency of grating formation crucially depends on the polarization state of the laser light and is maximal when circular polarization is used. In contrast to VIS light scattering X-ray diffraction is most sensitive for periodic surface undulations with amplitudes below 10 nm. Thus, combined in-situ X-ray and visible light scattering at CHESS were used to investigate the dynamics of surface relief grating formations upon laser illumination. The time development of grating peaks up to 9th order at laser power of P = 20 mW/cm(2) could be investigated, even the onset of grating formation as a function of light polarization. A linear growth of grating amplitude was observed for all polarizations. The growth velocity is maximal using circularly polarized light but very small for s-polarized light Y1 - 2004 UR - 1960 = doi:10.1524/zkri.219.4.218.30438 SN - 0044-2968 ER - TY - JOUR A1 - Stiller, Burkhard A1 - Karageorgiev, Peter A1 - Geue, Thomas A1 - Morawetz, Knut A1 - Saphiannikova, Marina A1 - Mechau, Norman A1 - Neher, Dieter T1 - Optically induced mass transport studied by scanning near-field optical- and atomic force microscopy N2 - Some functionalised thin organic films show a very unusual property, namely the light induced material transport. This effect enables to generate three-dimensional structures on surfaces of azobenzene containing films only caused by special optical excitation. The physical mechanisms underlying this phenomenon have not yet been fully understood, and in addition, the dimensions of structures created in that way are macroscopic because of the optical techniques and the wavelength of the used light. In order to gain deeper insight into the physical fundamentals of this phenomenon and to open possibilities for applications it is necessary to create and study structures not only in a macroscopic but also in nanometer range. We first report about experiments to generate optically induced nano structures even down to 100 nm size. The optical stimulation was therefore made by a Scanning Near-field Optical Microscope (SNOM). Secondly, physical conditions inside optically generated surface relief gratings were studied by measuring mechanical properties with high lateral resolution via pulse force mode and force distance curves of an AFM Y1 - 2004 SN - 0204-3467 ER - TY - JOUR A1 - Henneberg, Oliver A1 - Geue, Thomas A1 - Saphiannikova, Marina A1 - Natansohn, Almeria A1 - Rochon, Paul A1 - Finkelstein, Kenneth D. T1 - Investigation of material flow on inscribing a polymer surface grating probing X-ray and VIS light scattering Y1 - 2002 SN - 0927-7757 ER - TY - JOUR A1 - Pietsch, Ullrich A1 - Geue, Thomas A1 - Henneberg, Oliver A1 - Saphiannikova, Marina T1 - X-ray investigations of formation efficiency of buried azobenzene polymer density gratings Y1 - 2003 UR - http://scitation.aip.org/journals/doc/JAPIAU-ft/vol_93/iss_6/3161_1.html U6 - https://doi.org/10.1063/1.1554753 ER -