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T Thurn-Albrecht

Publications and source records attributed to T Thurn-Albrecht.

8 recordsLinked to original sources
PubMed2001

Direct visualization of random crystallization and melting in arrays of nanometer-size polymer crystals.

Using tapping mode atomic force microscopy, we visualized in direct space and time resolved the changes in viscoelastic properties during crystallization and melting of polyethyleneoxide in 12 nm spheres of a block copolymer mesophase. All spheres crystallized individually and independently, randomly distributed sphere by sphere. Melting of the confined crystals also proceeded in a stochastic manner. Not all spheres melted at the same temperature, indicating different degrees of order of the individual nanometer-size polymer crystals. The independence of the spheres opens the possibility to manipulate material properties of surfaces at the nanometer scale.

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PubMed2001

Size-selective electrochemical preparation of surfactant-stabilized Pd-, Ni- and Pt/Pd colloids.

A detailed study concerning the size-selective electrochemical preparation of R4N+Br- -stabilized palladium colloids is presented. Such colloids are readily accessible using a simple electrolysis cell in which the sacrificial anode is a commercially available Pd sheet, the surfactant serving as the electrolyte and stabilizer. It is shown that such parameters as solvent polarity, current density, charge flow, distance between electrodes and temperature can be used to control the size of the Pd nanoparticles in the range 1.2-5 nm. Characterization of the Pd colloids has been performed using transmission electron microscopy (TEM), small angle X-ray scattering (SAXS) and X-ray powder diffractometry (XRD) evaluated by Debye-function-analysis (DFA). Possible mechanisms of particle growth are discussed. Experiments directed towards the size-selective electrochemical fabrication of (n-C6H13)4N+Br- -stabilized nickel colloids are likewise described. Finally, a new strategy for preparing bimetallic colloids (e.g., Pt/Pd nanoparticles) electrochemically is presented, based on the use of a preformed colloid (e.g., (n-C8H17)4N+Br- -stabilized Pt particles) and a sacrificial anode (e.g., Pd sheet).

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PubMed2000

Ultrahigh-density nanowire arrays grown in self-assembled diblock copolymer templates.

We show a simple, robust, chemical route to the fabrication of ultrahigh-density arrays of nanopores with high aspect ratios using the equilibrium self-assembled morphology of asymmetric diblock copolymers. The dimensions and lateral density of the array are determined by segmental interactions and the copolymer molecular weight. Through direct current electrodeposition, we fabricated vertical arrays of nanowires with densities in excess of 1.9 x 10(11) wires per square centimeter. We found markedly enhanced coercivities with ferromagnetic cobalt nanowires that point toward a route to ultrahigh-density storage media. The copolymer approach described is practical, parallel, compatible with current lithographic processes, and amenable to multilayered device fabrication.

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PubMed2000

Self-assembly of nanoparticles into structured spherical and network aggregates

Multi-scale ordering of materials is central for the application of molecular systems in macroscopic devices. Self-assembly based on selective control of non-covalent interactions provides a powerful tool for the creation of structured systems at a molecular level, and application of this methodology to macromolecular systems provides a means for extending such structures to macroscopic length scale. Monolayer-functionalized nanoparticles can be made with a wide variety of metallic and non-metallic cores, providing a versatile building block for such approaches. Here we present a polymer-mediated 'bricks and mortar' strategy for the ordering of nanoparticles into structured assemblies. This methodology allows monolayer-protected gold particles to self-assemble into structured aggregates while thermally controlling their size and morphology. Using 2-nm gold particles as building blocks, we show that spherical aggregates of size 97 +/- 17 nm can be produced at 23 degrees C, and that 0.5-1 microm spherical assemblies with (5-40) x 10(5) individual subunits form at -20 degrees C. Intriguingly, extended networks of approximately 50-nm subunits are formed at 10 degrees C, illustrating the potential of our approach for the formation of diverse structural motifs such as wires and rods. These findings demonstrate that the assembly process provides control over the resulting aggregates, while the modularity of the 'bricks and mortar' approach allows combinatorial control over the constituents, providing a versatile route to new materials systems.

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PubMed2000

Electrically induced structure formation and pattern transfer

The wavelength of light represents a fundamental technological barrier to the production of increasingly smaller features on integrated circuits. New technologies that allow the replication of patterns on scales less than 100 nm need to be developed if increases in computing power are to continue at the present rate. Here we report a simple electrostatic technique that creates and replicates lateral structures in polymer films on a submicrometre length scale. Our method is based on the fact that dielectric media experience a force in an electric field gradient. Strong field gradients can produce forces that overcome the surface tension in thin liquid films, inducing an instability that features a characteristic hexagonal order. In our experiments, pattern formation takes place in polymer films at elevated temperatures, and is fixed by cooling the sample to room temperature. The application of a laterally varying electric field causes the instability to be focused in the direction of the highest electric field. This results in the replication of a topographically structured electrode. We report patterns with lateral dimensions of 140 nm, but the extension of the technique to pattern replication on scales smaller than 100 nm seems feasible.

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PubMed2000

Long-range density fluctuations in orthoterphenyl as studied by means of ultrasmall-angle x-ray scattering.

The structure factor of a fragile glass-forming liquid orthoterphenyl was measured in the previously inaccessible intermediate q range between the conventional light scattering (LS) and small-angle x-ray scattering (SAXS) q ranges using the low-angle scattering beam line at the European Synchrotron Radiation Facility. At low q the structure factor exhibits an excess scattering and matches well the LS data. This excess scattering is due to long-range density fluctuations also observed in the isotropic component of scattered light. At high q the structure factor decays to a plateau corresponding to the isothermal compressibility in agreement with the conventional SAXS data. In the intermediate q range, the structure factor exhibits a power law q dependence which indicates that the excess scattering is due to fractal aggregates of denser domains.

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PubMed1998

Self-Assembly of Ionically End-Capped Diblock Copolymers.

The self-assembly of ionically end-capped, symmetric polystyrene-polyisoprene diblock copolymers (PS-b-PI) has been studied. Structural data obtained from small-angle X-ray scattering (SAXS) and transmission electron microscopy (TEM) were correlated with the aggregation behavior of charged chain ends as evidenced by a spin probe using electron paramagnetic resonance (EPR) spectroscopy. The resulting mesomorphic structures were shown to be determined by the chain end topology, i.e., the site where the ionic chain end has been introduced chemically: For omega-functionalized diblock copolymers (monofunctional species) microphase separation is significantly stabilized due to the presence of ionic aggregates within the respective phase separated homopolymer domains. In contrast, for salt-free alpha,omega-macrozwitterionic diblock copolymers a marked perturbation of the block copolymer superstructure was found. In this case, the formation of a network of mixed ionic aggregates creates an additional microdomain interface by joining the chemically distinct blocks at their chain ends. The alteration of the degree of microphase separation as observed for the different functionalities can be attributed to conformational changes of the copolymer chain. Chain end association in the present system is reminiscent of certain covalently joined star and graft copolymers.

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