Dynamics of Diblock Copolymers in Dilute Solutions

We consider the dynamics of freely translating and rotating diblock (A-B), Gaussian copolymers, in dilute solutions. Using the multiple scattering technique, we have computed the diffusion and the friction coefficients D_AB and Zeta_AB, and the change Eta_AB in the viscosity of the solution as functions of x = N_A/N and t = l_B/l_A, where N_A, N are the number of segments of the A block and of the whole copolymer, respectively, and l_A, l_B are the Kuhn lengths of the A and B blocks. Specific regimes that maximize the efficiency of separation of copolymers with distinct "t" values, have been identified.Comment: 20 pages Revtex, 7 eps figures, needs epsf.tex and amssymb.sty, submitted to Macromolecule

Determining the underlying Fermi surface of strongly correlated superconductors

The notion of a Fermi surface (FS) is one of the most ingenious concepts developed by solid state physicists during the past century. It plays a central role in our understanding of interacting electron systems. Extraordinary efforts have been undertaken, both by experiment and by theory, to reveal the FS of the high temperature superconductors (HTSC), the most prominent strongly correlated superconductors. Here, we discuss some of the prevalent methods used to determine the FS and show that they lead generally to erroneous results close to half filling and at low temperatures, due to the large superconducting gap (pseudogap) below (above) the superconducting transition temperature. Our findings provide a perspective on the interplay between strong correlations and superconductivity and highlight the importance of strong coupling theories for the characterization as well as the determination of the underlying FS in ARPES experiments

The J_1-J_2 model revisited : Phenomenology of CuGeO_3

We present a mean field solution of the antiferromagnetic Heisenberg chain with nearest (J_1) and next to nearest neighbor (J_2) interactions. This solution provides a way to estimate the effects of frustration. We calculate the temperature-dependent spin-wave velocity, v_s(T) and discuss the possibility to determine the magnitude of frustration J_2/J_1 present in quasi 1D compounds from measurements of v_s(T). We compute the thermodynamic susceptibility at finite temperatures and compare it with the observed susceptibility of the spin-Peierls compound CuGeO_3. We also use the method to study the two-magnon Raman continuum observed in CuGeO_3 above the spin-Peierls transition.Comment: Phys. Rev.

Anomalous Dynamics of Translocation

We study the dynamics of the passage of a polymer through a membrane pore (translocation), focusing on the scaling properties with the number of monomers $N$. The natural coordinate for translocation is the number of monomers on one side of the hole at a given time. Commonly used models which assume Brownian dynamics for this variable predict a mean (unforced) passage time $\tau$ that scales as $N^2$, even in the presence of an entropic barrier. However, the time it takes for a free polymer to diffuse a distance of the order of its radius by Rouse dynamics scales with an exponent larger than 2, and this should provide a lower bound to the translocation time. To resolve this discrepancy, we perform numerical simulations with Rouse dynamics for both phantom (in space dimensions $d=1$ and 2), and self-avoiding (in $d=2$) chains. The results indicate that for large $N$, translocation times scale in the same manner as diffusion times, but with a larger prefactor that depends on the size of the hole. Such scaling implies anomalous dynamics for the translocation process. In particular, the fluctuations in the monomer number at the hole are predicted to be non-diffusive at short times, while the average pulling velocity of the polymer in the presence of a chemical potential difference is predicted to depend on $N$.Comment: 9 pages, 9 figures. Submitted to Physical Review

Electronic structure of strongly correlated d-wave superconductors

We study the electronic structure of a strongly correlated d-wave superconducting state. Combining a renormalized mean field theory with direct calculation of matrix elements, we obtain explicit analytical results for the nodal Fermi velocity, v_F, the Fermi wave vector, k_F, and the momentum distribution, n_k, as a function of hole doping in a Gutzwiller projected d-wave superconductor. We calculate the energy dispersion, E_k, and spectral weight of the Gutzwiller-Bogoliubov quasiparticles, and find that the spectral weight associated with the quasiparticle excitation at the antinodal point shows a non monotonic behavior as a function of doping. Results are compared to angle resolved photoemission spectroscopy (ARPES) of the high temperature superconductors.Comment: final version, comparison to experiments added, 4+ pages, 4 figure

An overview of the ciao multiparadigm language and program development environment and its design philosophy

We describe some of the novel aspects and motivations behind the design and implementation of the Ciao multiparadigm programming system. An important aspect of Ciao is that it provides the programmer with a large number of useful features from different programming paradigms and styles, and that the use of each of these features can be turned on and off at will for each program module. Thus, a given module may be using e.g. higher order functions and constraints, while another module may be using objects, predicates, and concurrency. Furthermore, the language is designed to be extensible in a simple and modular way. Another important aspect of Ciao is its programming environment, which provides a powerful preprocessor (with an associated assertion language) capable of statically finding non-trivial bugs, verifying that programs comply with specifications, and performing many types of program optimizations. Such optimizations produce code that is highly competitive with other dynamic languages or, when the highest levéis of optimization are used, even that of static languages, all while retaining the interactive development environment of a dynamic language. The environment also includes a powerful auto-documenter. The paper provides an informal overview of the language and program development environment. It aims at illustrating the design philosophy rather than at being exhaustive, which would be impossible in the format of a paper, pointing instead to the existing literature on the system

Substitution effects on spin fluctuations in the spin-Peierls compound CuGeO_3

Using Raman scattering we studied the effect of substitutions on 1D spin fluctuations in CuGeO_3 observed as a spinon continuum in frustration induced exchange scattering. For temperatures below the spin-Peierls transition (T_{SP}=14K) the intensity of this continuum at 120-500 cm^{-1} is exponentially suppressed and transferred into a 3D two-magnon density of states. Besides a spin-Peierls gap-induced mode at 30 cm^{-1} and additional modes at 105 and 370 cm^{-1} are observed. Substitution of Zn on the Cu-site and Si on the Ge-site of CuGeO_3 quenches easily the spin-Peierls state. Consequently a suppression of the spin-Peierls gap observable below T_{SP}=14K as well as a change of the temperature dependence of the spinon continuum are observed. These effects are discussed in the context of a dimensional crossover of this compound below T_{SP} and strong spin-lattice interaction.Comment: 9 pages, 2 eps figures include

Anomalous Dynamics of Forced Translocation

We consider the passage of long polymers of length N through a hole in a membrane. If the process is slow, it is in principle possible to focus on the dynamics of the number of monomers s on one side of the membrane, assuming that the two segments are in equilibrium. The dynamics of s(t) in such a limit would be diffusive, with a mean translocation time scaling as N^2 in the absence of a force, and proportional to N when a force is applied. We demonstrate that the assumption of equilibrium must break down for sufficiently long polymers (more easily when forced), and provide lower bounds for the translocation time by comparison to unimpeded motion of the polymer. These lower bounds exceed the time scales calculated on the basis of equilibrium, and point to anomalous (sub-diffusive) character of translocation dynamics. This is explicitly verified by numerical simulations of the unforced translocation of a self-avoiding polymer. Forced translocation times are shown to strongly depend on the method by which the force is applied. In particular, pulling the polymer by the end leads to much longer times than when a chemical potential difference is applied across the membrane. The bounds in these cases grow as N^2 and N^{1+\nu}, respectively, where \nu is the exponent that relates the scaling of the radius of gyration to N. Our simulations demonstrate that the actual translocation times scale in the same manner as the bounds, although influenced by strong finite size effects which persist even for the longest polymers that we considered (N=512).Comment: 13 pages, RevTeX4, 16 eps figure