@article{FumaniNematiMahdavifar2020,
  author    = {Fumani, F. Khastehdel and Nemati, Somayyeh and Mahdavifar, Saeed},
  title     = {Quantum critical lines in the ground state phase diagram of spin-1/2 frustrated transverse-field ising chains},
  series = {Annalen der Physik},
  volume    = {533},
  journal   = {Annalen der Physik},
  number    = {2},
  publisher = {Wiley-VCH},
  address   = {Weinheim},
  issn      = {0003-3804},
  doi       = {10.1002/andp.202000384},
  pages     = {8},
  year      = {2020},
  abstract  = {This paper focuses on the ground state phase diagram of a 1D spin-1/2 quantum Ising model with competing first and second nearest neighbour interactions known as the axial next nearest neighbour Ising model in the presence of a transverse magnetic field. Here, using quantum correlations, both numerically and analytically, some evidence is provided to clarify the identification of the ground state phase diagram. Local quantum correlations play a crucial role in detecting the critical lines either revealed or hidden by symmetry-breaking. A non-symmetry-breaking disorder transition line can be identified by the first derivative of both entanglement of formation and quantum discord between nearest neighbour spins. In addition, the quantum correlations between the second neighbour spins can also be used to reveal Kosterlitz-Thouless phase transition when their interaction strength grows and becomes closer to the first nearest neighbour one. The results obtained using the Jordan-Wigner transformation confirm the accuracy of the numerical case.},
  language  = {en}
}
@article{XieTaubert2011,
  author    = {Xie, Zai-Lai and Taubert, Andreas},
  title     = {Thermomorphic behavior of the ionic liquids [C(4)mim][FeCl4] and [C(12)mim][FeCl4]},
  series = {ChemPhysChem : a European journal of chemical physics and physical chemistry},
  volume    = {12},
  journal   = {ChemPhysChem : a European journal of chemical physics and physical chemistry},
  number    = {2},
  publisher = {Wiley-VCH},
  address   = {Weinheim},
  issn      = {1439-4235},
  doi       = {10.1002/cphc.201000808},
  pages     = {364 -- 368},
  year      = {2011},
  abstract  = {The iron-containing ionic liquids 1-butyl-3-methylimidazolium tetrachloroferrate(III) [C(4)mim][FeCl4] and 1-dodecyl-3-methylimidazolium tetrachloroferrate(III) [C(12)mim][FeCl4] exhibit a thermally induced demixing with water (thermomorphism). The phase separation temperature varies with IL weight fraction in water and can be tuned between 100 degrees C and room temperature. The reversible lower critical solution temperature (LCST) is only observed at IL weight fractions below ca. 35\% in water. UV/Vis, IR, and Raman spectroscopy along with elemental analysis prove that the yellow-brown liquid phase recovered after phase separation is the starting IL [C(4)mim][FeCl4] and [C(12)mim][FeCl4], respectively. Photometry and ICP-OES show that about 40\% of iron remains in the water phase upon phase separation. Although the process is thus not very efficient at the moment, the current approach is the first example of an LCST behavior of a metal-containing IL and therefore, although still inefficient, a prototype for catalyst removal or metal extraction.},
  language  = {en}
}
@article{InalKoelschChiappisietal.2013,
  author    = {Inal, Sahika and Koelsch, Jonas D. and Chiappisi, Leonardo and Kraft, Mario and Gutacker, Andrea and Janietz, Dietmar and Scherf, Ullrich and Gradzielski, Michael and Laschewsky, Andr{\´e} and Neher, Dieter},
  title     = {Temperature-Regulated Fluorescence Characteristics of Supramolecular Assemblies Formed By a Smart Polymer and a Conjugated Polyelectrolyte},
  series = {MACROMOLECULAR CHEMISTRY AND PHYSICS},
  volume    = {214},
  journal   = {MACROMOLECULAR CHEMISTRY AND PHYSICS},
  number    = {4},
  publisher = {WILEY-V C H VERLAG GMBH},
  address   = {WEINHEIM},
  issn      = {1022-1352},
  doi       = {10.1002/macp.201200493},
  pages     = {435 -- 445},
  year      = {2013},
  abstract  = {Aqueous mixtures of a coumarin-labeled non-ionic thermoresponsive copolymer and a cationic polythiophene exhibit marked changes in their fluorescence properties upon heating. At room temperature, emission from the label is significantly quenched due to energy transfer to the conjugated polyelectrolyte. Heating the mixture reduces the energy-transfer efficiency markedly, resulting in a clearly visible change of the emission color. Although the two macromolecules associate strongly at room temperature, the number of interacting sites is largely reduced upon the phase transition. Crucially, the intermolecular association does not suppress the responsiveness of the smart polymer, meaning that this concept should be applicable to chemo- or bioresponsive polymers with optical read-out, for example, as a sensor device.},
  language  = {en}
}
@phdthesis{Trabant2014,
  author    = {Trabant, Christoph},
  title     = {Ultrafast photoinduced phase transitions in complex materials probed by time-resolved resonant soft x-ray diffraction},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-71377},
  school      = {Universit{\"a}t Potsdam},
  year      = {2014},
  abstract  = {In processing and data storage mainly ferromagnetic (FM) materials are being used. Approaching physical limits, new concepts have to be found for faster, smaller switches, for higher data densities and more energy efficiency. Some of the discussed new concepts involve the material classes of correlated oxides and materials with antiferromagnetic coupling. Their applicability depends critically on their switching behavior, i.e., how fast and how energy efficient material properties can be manipulated. This thesis presents investigations of ultrafast non-equilibrium phase transitions on such new materials. In transition metal oxides (TMOs) the coupling of different degrees of freedom and resulting low energy excitation spectrum often result in spectacular changes of macroscopic properties (colossal magneto resistance, superconductivity, metal-to-insulator transitions) often accompanied by nanoscale order of spins, charges, orbital occupation and by lattice distortions, which make these material attractive. Magnetite served as a prototype for functional TMOs showing a metal-to-insulator-transition (MIT) at T = 123 K. By probing the charge and orbital order as well as the structure after an optical excitation we found that the electronic order and the structural distortion, characteristics of the insulating phase in thermal equilibrium, are destroyed within the experimental resolution of 300 fs. The MIT itself occurs on a 1.5 ps timescale. It shows that MITs in functional materials are several thousand times faster than switching processes in semiconductors. Recently ferrimagnetic and antiferromagnetic (AFM) materials have become interesting. It was shown in ferrimagnetic GdFeCo, that the transfer of angular momentum between two opposed FM subsystems with different time constants leads to a switching of the magnetization after laser pulse excitation. In addition it was theoretically predicted that demagnetization dynamics in AFM should occur faster than in FM materials as no net angular momentum has to be transferred out of the spin system. We investigated two different AFM materials in order to learn more about their ultrafast dynamics. In Ho, a metallic AFM below T ≈ 130 K, we found that the AFM Ho can not only be faster but also ten times more energy efficiently destroyed as order in FM comparable metals. In EuTe, an AFM semiconductor below T ≈ 10 K, we compared the loss of magnetization and laser-induced structural distortion in one and the same experiment. Our experiment shows that they are effectively disentangled. An exception is an ultrafast release of lattice dynamics, which we assign to the release of magnetostriction. The results presented here were obtained with time-resolved resonant soft x-ray diffraction at the Femtoslicing source of the Helmholtz-Zentrum Berlin and at the free-electron laser in Stanford (LCLS). In addition the development and setup of a new UHV-diffractometer for these experiments will be reported.},
  language  = {en}
}
@phdthesis{Lazar2005,
  author    = {Lazar, Paul},
  title     = {Transport mechanisms and wetting dynamics in molecularly thin films of long-chain alkanes at solid/vapour interface : relation to the solid-liquid phase transition},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-5275},
  school      = {Universit{\"a}t Potsdam},
  year      = {2005},
  abstract  = {Wetting and phase transitions play a very important role our daily life. Molecularly thin films of long-chain alkanes at solid/vapour interfaces (e.g. C30H62 on silicon wafers) are very good model systems for studying the relation between wetting behaviour and (bulk) phase transitions. Immediately above the bulk melting temperature the alkanes wet partially the surface (drops). In this temperature range the substrate surface is covered with a molecularly thin ordered, solid-like alkane film ("surface freezing"). Thus, the alkane melt wets its own solid only partially which is a quite rare phenomenon in nature. The thesis treats about how the alkane melt wets its own solid surface above and below the bulk melting temperature and about the corresponding melting and solidification processes. Liquid alkane drops can be undercooled to few degrees below the bulk melting temperature without immediate solidification. This undercooling behaviour is quite frequent and theoretical quite well understood. In some cases, slightly undercooled drops start to build two-dimensional solid terraces without bulk solidification. The terraces grow radially from the liquid drops on the substrate surface. They consist of few molecular layers with the thickness multiple of all-trans length of the molecule. By analyzing the terrace growth process one can find that, both below and above the melting point, the entire substrate surface is covered with a thin film of mobile alkane molecules. The presence of this film explains how the solid terrace growth is feeded: the alkane molecules flow through it from the undercooled drops to the periphery of the terrace. The study shows for the first time the coexistence of a molecularly thin film ("precursor") with partially wetting bulk phase. The formation and growth of the terraces is observed only in a small temperature interval in which the 2D nucleation of terraces is more likely than the bulk solidification. The nucleation mechanisms for 2D solidification are also analyzed in this work. More surprising is the terrace behaviour above bulk the melting temperature. The terraces can be slightly overheated before they melt. The melting does not occur all over the surface as a single event; instead small drops form at the terrace edge. Subsequently these drops move on the surface "eating" the solid terraces on their way. By this they grow in size leaving behind paths from were the material was collected. Both overheating and droplet movement can be explained by the fact that the alkane melt wets only partially its own solid. For the first time, these results explicitly confirm the supposed connection between the absence of overheating in solid and "surface melting": the solids usually start to melt without an energetic barrier from the surface at temperatures below the bulk melting point. Accordingly, the surface freezing of alkanes give rise of an energetic barrier which leads to overheating.},
  subject      = {Benetzung},
  language  = {en}
}
@phdthesis{Klumpp2003,
  author    = {Klumpp, Stefan},
  title     = {Movements of molecular motors : diffusion and directed walks},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-0000806},
  school      = {Universit{\"a}t Potsdam},
  year      = {2003},
  abstract  = {Bewegungen von prozessiven molekularen Motoren des Zytoskeletts sind durch ein Wechselspiel von gerichteter Bewegung entlang von Filamenten und Diffusion in der umgebenden L{\"o}sung gekennzeichnet. Diese eigent{\"u}mlichen Bewegungen werden in der vorliegenden Arbeit untersucht, indem sie als Random Walks auf einem Gitter modelliert werden. Ein weiterer Gegenstand der Untersuchung sind Effekte von Wechselwirkungen zwischen den Motoren auf diese Bewegungen. Im einzelnen werden vier Transportph{\"a}nomene untersucht: (i) Random Walks von einzelnen Motoren in Kompartimenten verschiedener Geometrien, (ii) station{\"a}re Konzentrationsprofile, die sich in geschlossenen Kompartimenten infolge dieser Bewegungen einstellen, (iii) randinduzierte Phasen{\"u}berg{\"a}nge in offenen r{\"o}hrenartigen Kompartimenten, die an Motorenreservoirs gekoppelt sind, und (iv) der Einfluß von kooperativen Effekten bei der Motor-Filament-Bindung auf die Bewegung. Alle diese Ph{\"a}nomene sind experimentell zug{\"a}nglich, und m{\"o}gliche experimentelle Realisierungen werden diskutiert.},
  language  = {en}
}