@article{LiMillerWuestnecketal.1995, author = {Li, Junbai and Miller, Reinhard and W{\"u}stneck, Rainer and M{\"o}hwald, Helmuth and Neumann, A. W.}, title = {News of pendant drop technique as a film balance at liquid/liquid interfaces}, year = {1995}, language = {en} } @article{LiMillerKraegeletal.1995, author = {Li, Junbai and Miller, Reinhard and Kr{\"a}gel, J{\"u}rgen and Kretzschmar, G{\"u}nter and M{\"o}hwald, Helmuth}, title = {Dynamische Eigenschaften von Phospholipid-Monoschichten an Luft/Fl{\"u}ssig - und Fl{\"u}ssig/Fl{\"u}ssig Grenzfl{\"a}chen}, year = {1995}, language = {de} } @article{StruthDecherSchmittetal.1999, author = {Struth, Bernd and Decher, Gero and Schmitt, J. and Hofmeister, Wolfgang and Neißendorfer, Frank and Pietsch, Ullrich and Brezesinski, Gerald and M{\"o}hwald, Helmuth}, title = {Chemical modification of Topaz surfaces}, issn = {0928-4931}, year = {1999}, language = {en} } @article{NeissendorferPietschBreszisinskietal.1999, author = {Neißendorfer, Frank and Pietsch, Ullrich and Breszisinski, G. and M{\"o}hwald, Helmuth}, title = {Energy-dispersive reflectometry and diffractometry at the WLS of BESSY-I}, year = {1999}, language = {en} } @article{PietschGrenzerGeueetal.2001, author = {Pietsch, Ullrich and Grenzer, J{\"o}rg and Geue, Thomas and Neißendorfer, Frank and Brezesinski, Gerald and Symietz, Christian and M{\"o}hwald, Helmuth and Gudat, Wolfgang}, title = {The energy dispersive reflectometer at BESSY II : a challenge for thin film analysis}, issn = {0167- 5087}, year = {2001}, language = {en} } @article{BodenthinGrenzerLauteretal.2002, author = {Bodenthin, Yves and Grenzer, J{\"o}rg and Lauter, Robert and Pietsch, Ullrich and Lehmann, Pit and Kurth, Dirk G. and M{\"o}hwald, Helmuth}, title = {Temperature and time resolved x-ray scattering at thin organic films}, year = {2002}, language = {en} } @article{PietschPanznerLeitenbergeretal.2003, author = {Pietsch, Ullrich and Panzner, Tobias and Leitenberger, Wolfram and Grenzer, J{\"o}rg and Bodenthin, Th. and Geue, Thomas and M{\"o}hwald, Helmuth}, title = {Coherence experiments at the energy-dispersive reflectometry beamline at BESSY II}, year = {2003}, language = {en} } @article{BeissenhirtzSchellerStoeckleinetal.2004, author = {Beissenhirtz, Moritz Karl and Scheller, Frieder W. and St{\"o}cklein, Walter F. M. and Kurth, D. and M{\"o}hwald, Helmuth and Lisdat, Fred}, title = {Electroactive cytochrome c multilayers within a polyelectrolyte assembly}, year = {2004}, language = {en} } @article{TedeschiLiMoehwaldetal.2004, author = {Tedeschi, Concetta and Li, L. and M{\"o}hwald, Helmuth and Spitz, Christian and von Seggern, David and Menzel, Ralf and Kirstein, Stefan}, title = {Engineering of layer-by-layer coated capsules with the prospect of materials for efficient and directed electron transfer}, year = {2004}, abstract = {We show a Lefschetz fixed point formula for holomorphic functions in a bounded domain D with smooth boundary in the complex plane. To introduce the Lefschetz number for a holomorphic map of D, we make use of the Bergman kernel of this domain. The Lefschetz number is proved to be the sum of the usual contributions of fixed points of the map in D and contributions of boundary fixed points, these latter being different for attracting and repulsing fixed points}, language = {en} } @article{LiMoehwaldSpitzetal.2005, author = {Li, L. and M{\"o}hwald, Helmuth and Spitz, Christian and von Seggern, David and Mucke, M. and Menzel, Ralf}, title = {Long-lived photoinduced charge separation inside polarity gradient capsules}, year = {2005}, language = {en} } @article{PietschBodenthinGrenzeretal.2005, author = {Pietsch, Ullrich and Bodenthin, Yves and Grenzer, J{\"o}rg and Geue, Thomas and M{\"o}hwald, Helmuth and Kurth, Dirk G.}, title = {Structure and temperature behavior of metallo-supramolecular assemblies}, year = {2005}, abstract = {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}, language = {en} } @article{PietschBodenthinMoehwaldetal.2005, author = {Pietsch, Ullrich and Bodenthin, Yves and M{\"o}hwald, Helmuth and Kurth, Dirk G.}, title = {Inducing spin crossover in metallo-supramolecular polyelectrolytes through an amphiphilic phase transition}, year = {2005}, abstract = {A phase transition in an amphiphilic mesophase is explored to deliberately induce mechanical strain in an assembly of tightly coupled metal ion coordination centers. Melting of the alkyl chains in the amphiphilic mesophase causes distortion of the coordination geometry around the central transition metal ion. As a result, the crystal field splitting of the d-orbital subsets decreases resulting in a spin transition from a low-spin to a high-spin state. The diamagnetic-paramagnetic transition is reversible. This concept is demonstrated in a metallo-supramolecular coordination polyelectrolyte-amphiphile complex self-assembled from ditopic bis-terpyridines, Fe(II) as central transition metal, and dialkyl phosphates as amphiphiles. The magnetic properties are studied in a Langmuir-Blodgett multilayer. The modularity of this concept provides extensive control of structure and function from molecular to macroscopic length scales and gives access to a wide range of new molecular magnetic architectures such as nanostructures, thin films, and liquid crystals}, language = {en} } @article{KreftGeorgievaBaeumleretal.2006, author = {Kreft, Oliver and Georgieva, Radostina and B{\"a}umler, Hans and Steup, Martin and M{\"u}ller-R{\"o}ber, Bernd and Sukhorukov, Gleb B. and M{\"o}hwald, Helmuth}, title = {Red blood cell templated polyelectrolyte capsules : a novel vehicle for the stable encapsulation of DNA and proteins}, issn = {1022-1336}, doi = {10.1002/marc.200500777}, year = {2006}, abstract = {A novel method for the encapsulation of biomacromolecules, such as nucleic acids and proteins, into polyelectrolyte microcapsules is described. Fluorescence-labelled double-stranded DNA and human serum albumin (HSA) are used as model substances for encapsulation in hollow microcapsules templated on human erythrocytes. The encapsulation procedure involves an intermediate drying C, step. The accumulation of DNA and HSA in the capsules is observed by confocal laser scanning microscopy, UV spectroscopy, and flourimetry. The mechanism of encapsulation is discussed}, language = {en} } @article{LisdatDronovMoehwaldetal.2009, author = {Lisdat, Fred and Dronov, Roman and M{\"o}hwald, Helmuth and Scheller, Frieder W. and Kurth, Dirk G.}, title = {Self-assembly of electro-active protein architectures on electrodes for the construction of biomimetic signal chains}, issn = {1359-7345}, doi = {10.1039/B813559b}, year = {2009}, abstract = {The layer-by-layer adsorption technique based on the consecutive deposition of oppositely charged species is for the preparation of protein multilayers with fully electro-active protein molecules. The methodology was established with cytochrome c and the polyelectrolyte sulfonated polyaniline (PASA). The technique is also useful for the construction of bi-protein architectures confining protein-protein communication to an electrode. Following natural examples of protein complexes with defined signal transfer, cytochrome c was arranged with enzymes such as xanthine oxidase, bilirubin oxidase, laccase, and sulfite oxidase in self-assembled multilayer architectures. Thus, biomimetic signal chains from the enzyme substrate via the enzyme and cytochrome c towards the electrode can be established. Communication between proteins immobilised in multiple layers on the electrode can be achieved by in situ generation of small shuttle molecules or more advantageously by direct interprotein electron transfer. This allows the construction of new sensing electrodes, the properties of which can be tuned by the number of deposited protein layers. The mechanism of electron transfer within such protein assemblies on gold electrodes will be discussed.}, language = {en} } @article{RadziukSkirtachGessneretal.2011, author = {Radziuk, Darya and Skirtach, Andre and Gessner, Andre and Kumke, Michael Uwe and Zhang, Wei and M{\"o}hwald, Helmuth and Shchukin, Dmitry}, title = {Ultrasonic Approach for Formation of Erbium Oxide Nanoparticles with Variable Geometries}, series = {Langmuir}, volume = {27}, journal = {Langmuir}, number = {23}, publisher = {American Chemical Society}, address = {Washington}, issn = {0743-7463}, doi = {10.1021/la203622u}, pages = {14472 -- 14480}, year = {2011}, abstract = {Ultrasound (20 kHz, 29 W. cm(-2)) is employed to form three types of erbium oxide nanoparticles in the presence of multiwalled carbon nanotubes as a template material in water. The nanoparticles are (i) erbium carboxioxide nanoparticles deposited on the external walls of multiwalled carbon nanotubes and Er(2)O(3) in the bulk with (ii) hexagonal and (iii) spherical geometries. Each type of ultrasonically formed nanoparticle reveals Er(3+) photoluminescence from crystal lattice. The main advantage of the erbium carboxioxide nanoparticles on the carbon nanotubes is the electromagnetic emission in the visible region, which is new and not examined up to the present date. On the other hand, the photoluminescence of hexagonal erbium oxide nanoparticles is long-lived (mu s) and enables the higher energy transition ((4)S(3/2)-(4)I(15/2)), which is not observed for spherical nanoparticles. Our work is unique because it combines for the first time spectroscopy of Er(3+) electronic transitions in the host crystal lattices of nanoparticles with the geometry established by ultrasound in aqueous solution of carbon nanotubes employed as a template material. The work can be of great interest for "green" chemistry synthesis of photoluminescent nanoparticles in water.}, language = {en} } @article{KielMoehwaldBargheer2011, author = {Kiel, Mareike and M{\"o}hwald, Helmuth and Bargheer, Matias}, title = {Broadband measurements of the transient optical complex dielectric function of a nanoparticle/polymer composite upon ultrafast excitation}, series = {Physical review : B, Condensed matter and materials physics}, volume = {84}, journal = {Physical review : B, Condensed matter and materials physics}, number = {16}, publisher = {American Physical Society}, address = {College Park}, issn = {1098-0121}, doi = {10.1103/PhysRevB.84.165121}, pages = {6}, year = {2011}, abstract = {We determined experimentally the complex transient optical dielectric function of a well-characterized polyelectrolyte/gold-nanoparticle composite system over a broad spectral range upon short pulse laser excitation by simultaneously measuring the time-dependent reflectance and transmittance of white light pulses with femtosecond pump-probe spectroscopy. We extracted directly the ultrafast changes in the real and imaginary parts of the effective dielectric function, epsilon(eff)(r) (omega,t)and epsilon(eff)(i) (omega,t), from the experiment. This complete experimental set of information on the time-dependent complex dielectric function challenges theories modeling the transient dielectric function of gold particles and the effective medium.}, language = {en} } @article{LoebbickeChananaSchlaadetal.2011, author = {L{\"o}bbicke, Ruben and Chanana, Munish and Schlaad, Helmut and Pilz-Allen, Christine and G{\"u}nter, Christina and M{\"o}hwald, Helmuth and Taubert, Andreas}, title = {Polymer Brush Controlled Bioinspired Calcium Phosphate Mineralization and Bone Cell Growth}, series = {Biomacromolecules : an interdisciplinary journal focused at the interface of polymer science and the biological sciences}, volume = {12}, journal = {Biomacromolecules : an interdisciplinary journal focused at the interface of polymer science and the biological sciences}, number = {10}, publisher = {American Chemical Society}, address = {Washington}, issn = {1525-7797}, doi = {10.1021/bm200991b}, pages = {3753 -- 3760}, year = {2011}, abstract = {Polymer brushes on thiol-modified gold surfaces were synthesized by using terminal thiol groups for the surface initiated free radical polymerization of methacrylic acid and dimethylaminotheyl methacrylate, respectively. Atomic force microscopy shows that the resulting poly(methacrylic acid (PMAA) and poly(dimethylaminothyl methacrylate) (PDM- AEMA) brushes are homogeneous. Contact angle measurements show that the brushes are pH responsive and can reversibly be protonated and deprotonated. Mineralization of the brushes with calcium phosphate at different pH yields homogeneously mineralized surfaces, and preosteoblastic cells proliferate-on be number of living cells on the mineralized hybrid surface is ca. 3 times (P corresponding nonmineralized brushes.}, language = {en} } @article{LiBabuTurneretal.2013, author = {Li, Hongguang and Babu, Sukumaran Santhosh and Turner, Sarah T. and Neher, Dieter and Hollamby, Martin J. and Tomohito, Seki and Yagai, Shiki and deguchi, Yonekazu and M{\"o}hwald, Helmuth and Nakanishi, Takashi}, title = {Alkylated-C60 based soft materials: regulation of self-assembly and optoelectronic properties by chain branching}, doi = {10.1039/C3TC00066D}, year = {2013}, abstract = {Derivatization of fullerene (C60) with branched aliphatic chains softens C60-based materials and enables the formation of thermotropic liquid crystals and room temperature nonvolatile liquids. This work demonstrates that by carefully tuning parameters such as type, number and substituent position of the branched chains, liquid crystalline C60 materials with mesophase temperatures suited for photovoltaic cell fabrication and room temperature nonvolatile liquid fullerenes with tunable viscosity can be obtained. In particular, compound 1, with branched chains, exhibits a smectic liquid crystalline phase extending from 84°C to room temperature. Analysis of bulk heterojunction (BHJ) organic solar cells with a ca. 100 nm active layer of compound 1 and poly(3-hexylthiophene) (P3HT) as an electron acceptor and an electron donor, respectively, reveals an improved performance (power conversion efficiency, PCE: 1.6 {\~n} 0.1\%) in comparison with another compound, 10 (PCE: 0.5 {\~n} 0.1\%). The latter, in contrast to 1, carries linear aliphatic chains and thus forms a highly ordered solid lamellar phase at room temperature. The solar cell performance of 1 blended with P3HT approaches that of PCBM/P3HT for the same active layer thickness. This indicates that C60 derivatives bearing branched tails are a promising class of electron acceptors in soft (flexible) photovoltaic devices.}, language = {en} } @article{LiBabuTurneretal.2013, author = {Li, Hongguang and Babu, Sukumaran Santhosh and Turner, Sarah T. and Neher, Dieter and Hollamby, Martin J. and Seki, Tomohiro and Yagai, Shiki and Deguchi, Yonekazu and M{\"o}hwald, Helmuth and Nakanishi, Takashi}, title = {Alkylated-C-60 based soft materials regulation of self-assembly and optoelectronic properties by chain branching}, series = {Journal of materials chemistry : C, Materials for optical and electronic devices}, volume = {1}, journal = {Journal of materials chemistry : C, Materials for optical and electronic devices}, number = {10}, publisher = {Royal Society of Chemistry}, address = {Cambridge}, issn = {2050-7526}, doi = {10.1039/c3tc00066d}, pages = {1943 -- 1951}, year = {2013}, abstract = {Derivatization of fullerene (C-60) with branched aliphatic chains softens C-60-based materials and enables the formation of thermotropic liquid crystals and room temperature nonvolatile liquids. This work demonstrates that by carefully tuning parameters such as type, number and substituent position of the branched chains, liquid crystalline C-60 materials with mesophase temperatures suited for photovoltaic cell fabrication and room temperature nonvolatile liquid fullerenes with tunable viscosity can be obtained. In particular, compound 1, with branched chains, exhibits a smectic liquid crystalline phase extending from 84 degrees C to room temperature. Analysis of bulk heterojunction (BHJ) organic solar cells with a ca. 100 nm active layer of compound 1 and poly(3-hexylthiophene) (P3HT) as an electron acceptor and an electron donor, respectively, reveals an improved performance (power conversion efficiency, PCE: 1.6 + 0.1\%) in comparison with another compound, 10 (PCE: 0.5 + 0.1\%). The latter, in contrast to 1, carries linear aliphatic chains and thus forms a highly ordered solid lamellar phase at room temperature. The solar cell performance of 1 blended with P3HT approaches that of PCBM/P3HT for the same active layer thickness. This indicates that C-60 derivatives bearing branched tails are a promising class of electron acceptors in soft (flexible) photovoltaic devices.}, language = {en} } @misc{LiBabuTurneretal.2013, author = {Li, Hongguang and Babu, Sukumaran Santhosh and Turner, Sarah T. and Neher, Dieter and Hollamby, Martin J. and Seki, Tomohiro and Yagai, Shiki and Deguchi, Yonekazu and M{\"o}hwald, Helmuth and Nakanishi, Takashi}, title = {Alkylated-C60 based soft materials}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-95358}, pages = {1943 -- 1951}, year = {2013}, abstract = {Derivatization of fullerene (C60) with branched aliphatic chains softens C60-based materials and enables the formation of thermotropic liquid crystals and room temperature nonvolatile liquids. This work demonstrates that by carefully tuning parameters such as type, number and substituent position of the branched chains, liquid crystalline C60 materials with mesophase temperatures suited for photovoltaic cell fabrication and room temperature nonvolatile liquid fullerenes with tunable viscosity can be obtained. In particular, compound 1, with branched chains, exhibits a smectic liquid crystalline phase extending from 84 °C to room temperature. Analysis of bulk heterojunction (BHJ) organic solar cells with a ca. 100 nm active layer of compound 1 and poly(3-hexylthiophene) (P3HT) as an electron acceptor and an electron donor, respectively, reveals an improved performance (power conversion efficiency, PCE: 1.6 ± 0.1\%) in comparison with another compound, 10 (PCE: 0.5 ± 0.1\%). The latter, in contrast to 1, carries linear aliphatic chains and thus forms a highly ordered solid lamellar phase at room temperature. The solar cell performance of 1 blended with P3HT approaches that of PCBM/P3HT for the same active layer thickness. This indicates that C60 derivatives bearing branched tails are a promising class of electron acceptors in soft (flexible) photovoltaic devices.}, language = {en} }