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Peter Reineker

Publications and source records attributed to Peter Reineker.

5 recordsLinked to original sources

The formation of planar ribbonlike aggregates from stiff polyanions in the presence of anisotropic cations.

A dilute salt-free solution of rodlike polyanions in the presence of anisotropic (chain) cations consisting of neutral tails and charged heads is studied. Using Monte Carlo simulation within the framework of the primitive model, different Coulomb coupling regimes were considered. While aggregation in the strong coupling limit is expected, we report new morphology, namely, the formation of ribbonlike nanostructures. At strong electrostatic interaction, the system is found to undergo the self-organization resulting in the formation of planar aggregates that look like a "ladder" of polyanions sandwiched between cationic chains. We investigate the stability of different morphologies and find that these aggregates are thermodynamically stable. Focus has been made on how the chemical structure of anisotropic cations affects the morphology of the aggregates.

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Mori-Zwanzig memory analysis in single-molecule spectroscopy.

We study the dynamical behavior of the Rhodospirillum molischianum LH2 complex based on intensity time series obtained from single-molecule spectroscopy experiments. This is achieved by reconstructing the memory function describing the time-dependent fluctuations of the excited states. We conclude that the apparent stochastic evolution of the dynamics is controlled by at least two different non-Markovian main processes.

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Effect of low-molecular-weight salt on the nematic ordering in solutions of rodlike polyelectrolytes.

Nematic ordering is studied in solutions of rodlike macroions in the presence of monovalent salt ions. The correlation free energy of electrostatic interactions is calculated within the framework of the Debye-Hückel approach. The phase diagram of the system is obtained. We have shown that the addition of salt destroys the weakly ordered nematic phase which is stable at small polymer concentrations. On the other hand, the salt widens the region of the phase separation between the isotropic (or weakly ordered nematic) and the highly ordered nematic phases at high polymer concentrations. An explanation of these effects is proposed.

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Analysis of stochastic resonances.

We investigate the one-dimensional diffusion of a particle in a piecewise linear potential superimposed with a step of a harmonically modulated height. Employing the matching conditions, we solve the corresponding Fokker-Planck equation and we analyze nonlinear features of the particle's mean position as a function of time. We present detailed results in two physically relevant cases. First, we take the unperturbed potential as a symmetrical up-oriented tip, which is placed between two reflecting boundaries and we add the jump at the tip coordinate. The setting yields resonance-like behavior of the stationary-response amplitude. Second, if the discontinuity at origin is combined with the constant force in the symmetrical region between the boundaries, the stationary response displays a time-independent shift against the potential slope. The driving-induced force exhibits a resonance-like behavior both with respect to the diffusion constant and the slope of the unperturbed potential.

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Complex formation in systems of oppositely charged polyelectrolytes: a molecular dynamics simulation study.

Results of molecular dynamics simulations for systems with two flexible, oppositely charged polymer chains are presented. The lengths N and interaction strength lambda of the chains are varied. We find that the chains remain separated for small values of lambda. For large interaction strengths, i.e., large Bjerrum lengths, we find glasslike structures and order on the length scale of a few monomer diameters. Between these two limits of the interaction strengths, the chains of various lengths collapse into compact complexes that exhibit self-similar structures. The scaling behavior of the radius of gyration is discussed as a function of chain length and interaction strength. In addition, the local structure of the collapsed systems is analyzed and the dependence of the density of the aggregate on the interaction strength is discussed.

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