P. Nagel
Karlsruhe Institute of Technology
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Publication
Featured researches published by P. Nagel.
Small | 2008
Sylwia Sekula; Jeanette Fuchs; Susanne Weg-Remers; P. Nagel; S. Schuppler; Joe Fragala; Nora Theilacker; Matthias Franzreb; Christer Wingren; Peter Ellmark; Carl Borrebaeck; Chad A. Mirkin; Harald Fuchs; Steven Lenhert
Molecular patterning processes taking place in biological systems are challenging to study in vivo because of their dynamic behavior, subcellular size, and high degree of complexity. In vitro patterning of biomolecules using nanolithography allows simplification of the processes and detailed study of the dynamic interactions. Parallel dip-pen nanolithography (DPN) is uniquely capable of integrating functional biomolecules on subcellular length scales due to its constructive nature, high resolution, and high throughput. Phospholipids are particularly well suited as inks for DPN since a variety of different functional lipids can be readily patterned in parallel. Here DPN is used to spatially pattern multicomponent micro- and nanostructured supported lipid membranes and multilayers that are fluid and contain various amounts of biotin and/or nitrilotriacetic acid functional groups. The patterns are characterized by fluorescence microscopy and photoemission electron microscopy. Selective adsorption of functionalized or recombinant proteins based on streptavidin or histidine-tag coupling enables the semisynthetic fabrication of model peripheral membrane bound proteins. The biomimetic membrane patterns formed in this way are then used as substrates for cell culture, as demonstrated by the selective adhesion and activation of T-cells.
Journal of Chemical Physics | 2007
I. Biswas; Heiko Peisert; M. Nagel; Maria Benedetta Casu; S. Schuppler; P. Nagel; E. Pellegrin; Thomas Chassé
The growth of copper phthalocyanine thin films evaporated on polycrystalline gold is examined in detail using near edge x-ray absorption fine structure spectroscopy and surface sensitive x-ray photoemission spectroscopy. The combination of both methods allows distinguishing between the uppermost layers and buried interface layers in films up to approximately 3 nm thickness. An interfacial layer of approximately 3 ML of molecules with an orientation parallel to the substrate surface was found, whereas the subsequent molecules are perpendicular to the metal surface. It was shown that even if the preferred molecular orientation in thin films is perpendicular, the buried interfacial layer can be oriented differently.
Physical Review Letters | 2012
D. K. Satapathy; M. A. Uribe-Laverde; I. Marozau; V. K. Malik; S. Das; Thomas Wagner; C. Marcelot; J. Stahn; Sebastian Brück; A. Rühm; S. Macke; T. Tietze; E. Goering; A. Frano; J. H. Kim; M. Wu; E. Benckiser; B. Keimer; A. Devishvili; B. P. Toperverg; M. Merz; P. Nagel; S. Schuppler; C. Bernhard
Using neutron reflectometry and resonant x-ray techniques we studied the magnetic proximity effect (MPE) in superlattices composed of superconducting YBa2Cu3O7 and ferromagnetic-metallic La0.67Ca0.33MnO3 or ferromagnetic-insulating LaMnO(3+δ). We find that the MPE strongly depends on the electronic state of the manganite layers, being pronounced for the ferromagnetic-metallic La0.67Ca0.33MnO3 and almost absent for ferromagnetic-insulating LaMnO(3+δ). We also detail the change of the magnetic depth profile due to the MPE and provide evidence for its intrinsic nature.
Physical Review Letters | 2001
C. Meingast; Volker Pasler; P. Nagel; A. I. Rykov; S. Tajima; Peter Olsson
: The thermodynamics of the superconducting transition is studied as a function of doping using high-resolution expansivity data of YBa(2)Cu(3)O (x) single crystals and Monte Carlo simulations of the anisotropic 3D- XY model. We directly show that T(c) of underdoped YBa(2)Cu(3)O (x) is strongly suppressed from its mean-field value (T(MF)(c)) by phase fluctuations of the superconducting order parameter. For overdoped YBa(2)Cu(3)O (x) fluctuation effects are greatly reduced and T(c) approximately T(MF)(c). We find that T(MF)(c) exhibits a similar doping dependence as the pseudogap energy, naturally suggesting that the pseudogap arises from phase-incoherent Cooper pairing.
Physical Review B | 2010
M. Merz; P. Nagel; C. Pinta; A. Samartsev; H. v. Löhneysen; M. Wissinger; S. Uebe; A. Assmann; D. Fuchs; S. Schuppler
Epitaxial thin films of undoped LaCoO
ACS Applied Materials & Interfaces | 2015
Karin Kleiner; Julia Melke; M. Merz; Peter Jakes; P. Nagel; S. Schuppler; Verena Liebau; Helmut Ehrenberg
_{3}
Applied Physics Letters | 2008
Maria Benedetta Casu; I. Biswas; B.-E. Schuster; M. Nagel; P. Nagel; S. Schuppler; Thomas Chassé
\@, of electron-doped La
Physical Review Letters | 2000
P. Nagel; Volker Pasler; C. Meingast; Alexandre I. Rykov; S. Tajima
_{0.7}
Physical Review B | 2010
R. Werner; C. Raisch; A. Ruosi; B. A. Davidson; P. Nagel; M. Merz; S. Schuppler; M. Glaser; J. Fujii; Thomas Chassé; R. Kleiner; D. Koelle
Ce
Physical Review B | 2008
C. Pinta; D. Fuchs; M. Merz; M. Wissinger; E. Arac; H. v. Löhneysen; A. Samartsev; P. Nagel; S. Schuppler
_{0.3}