Polymer adsorption on a fractal substrate: numerical study

We study the adsorption of flexible polymer macromolecules on a percolation cluster, formed by a regular two-dimensional disordered lattice at critical concentration p_c of attractive sites. The percolation cluster is characterized by a fractal dimension d_s^{p_c}=91/49. The conformational properties of polymer chains grafted to such a fractal substrate are studied by means of the pruned-enriched Rosenbluth method (PERM). We find estimates for the surface crossover exponent governing the scaling of the adsorption energy in the vicinity of the transition point, \phi_s^{p_c}=0.425\pm0.009, and for the adsorption transition temperature, T_A^{p_c}=2.64\pm0.02. As expected, the adsorption is diminished when the fractal dimension of the substrate is smaller than that of a plain Euclidean surface. The universal size and shape characteristics of a typical spatial conformation which attains a polymer chain in the adsorbed state are analyzed as well.Comment: 11 pages, 16 figure

Shape anisotropy of polymers in disordered environment

We study the influence of structural obstacles in a disordered environment on the size and shape characteristics of long flexible polymer macromolecules. We use the model of self-avoiding random walks on diluted regular lattices at the percolation threshold in space dimensions d=2, 3. Applying the Pruned-Enriched Rosenbluth Method (PERM), we numerically estimate rotationally invariant universal quantities such as the averaged asphericity A_d and prolateness S of polymer chain configurations. Our results quantitatively reveal the extent of anisotropy of macromolecules due to the presence of structural defects.Comment: 8 page

Multifractality of self-avoiding walks on percolation clusters

We consider self-avoiding walks (SAWs) on the backbone of percolation clusters in space dimensions d=2, 3, 4. Applying numerical simulations, we show that the whole multifractal spectrum of singularities emerges in exploring the peculiarities of the model. We obtain estimates for the set of critical exponents, that govern scaling laws of higher moments of the distribution of percolation cluster sites visited by SAWs, in a good correspondence with an appropriately summed field-theoretical \varepsilon=6-d-expansion (H.-K. Janssen and O. Stenull, Phys. Rev. E 75, 020801(R) (2007)).Comment: 4 page

The size and shape of snowflake star polymers in dilute solutions: analytical and numerical approaches

We investigate the conformational properties of a multi-branched polymer structure with a dendrimer-like topology, known as a snowflake polymer. This polymer is characterized by two parameters: $f_s$, which represents the functionality of the central star-like core, and $f$, which represents the functionality of the side branching points. To analyze the conformational properties, we have employed various approaches, including analytical methods based on direct polymer renormalization and the Wei's approach as well as numerical molecular dynamics simulations. These methods have allowed us to estimate a size and shape characteristics of the snowflake polymer as functions of $f$ and $f_s$. Our findings consistently demonstrate the effective compactification of the typical polymer conformation as the number of branching points increases. Overall, our study provides valuable insights into the conformational behavior of the snowflake polymer and highlights the impact of branching parameters on its overall compactness

Survival in two-species reaction-superdiffusion system: Renormalization group treatment and numerical simulations

We analyze the two-species reaction-diffusion system including trapping reaction $A + B \to A$ as well as coagulation/annihilation reactions $A + A \to (A,0)$ where particles of both species are performing L\'evy flights with control parameter $0 < \sigma < 2$, known to lead to superdiffusive behaviour. The density, as well as the correlation function for target particles $B$ in such systems, are known to scale with nontrivial universal exponents at space dimension $d \leq d_{c}$. Applying the renormalization group formalism we calculate these exponents in a case of superdiffusion below the critical dimension $d_c=\sigma$. The numerical simulations in one-dimensional case are performed as well. The quantitative estimates for the decay exponent of the density of survived particles $B$ are in good agreement with our analytical results. In particular, it is found that the surviving probability of the target particles in a superdiffusive regime is higher than that in a system with ordinary diffusion.Comment: 24 pages, 11 figure

Critical behavior of the 2D Ising model with long-range correlated disorder

We study critical behavior of the diluted 2D Ising model in the presence of disorder correlations which decay algebraically with distance as $\sim r^{-a}$. Mapping the problem onto 2D Dirac fermions with correlated disorder we calculate the critical properties using renormalization group up to two-loop order. We show that beside the Gaussian fixed point the flow equations have a non trivial fixed point which is stable for $0.995<a<2$ and is characterized by the correlation length exponent $\nu= 2/a + O((2-a)^3)$. Using bosonization, we also calculate the averaged square of the spin-spin correlation function and find the corresponding critical exponent $\eta_2=1/2-(2-a)/4+O((2-a)^2)$.Comment: 14 pages, 3 figures, revtex

Universal size ratios of Gaussian polymers with complex architecture: radius of gyration vs hydrodynamic radius

We study the impact of arm architecture of polymers with a single branch point on their structure in solvents. Many physical properties of polymer liquids strongly dependent on the size and shape measures of individual macromolecules, which in turn are determined by their topology. Here, we use combination of analytical theory, based on path integration method, and molecular dynamics simulations to study structural properties of complex Gaussian polymers containing fc linear branches and fr closed loops grafted to the central core. We determine size measures such as the gyration radius Rg and the hydrodynamic radii RH, and obtain the estimates for the size ratio Rg/RH with its dependence on the functionality f=fc+fr of grafted polymers. In particular, we obtain the quantitative estimate of the degree of compactification of these polymers with increasing number of closed loops fr as compared to linear or star-shape molecules of the same total molecular weight. Numerical simulations corroborate theoretical prediction that Rg/RH decreases towards unity with increasing f. These findings provide qualitative description of polymers with complex architecture in θ solvents

Percolation thresholds and fractal dimensions for square and cubic lattices with long-range correlated defects

We study long-range power-law correlated disorder on square and cubic lattices. In particular, we present high-precision results for the percolation thresholds and the fractal dimension of the largest clusters as function of the correlation strength. The correlations are generated using a discrete version of the Fourier filtering method. We consider two different metrics to set the length scales over which the correlations decay, showing that the percolation thresholds are highly sensitive to such system details. By contrast, we verify that the fractal dimension $d_{\rm f}$ is a universal quantity and unaffected by the choice of metric. We also show that for weak correlations, its value coincides with that for the uncorrelated system. In two dimensions we observe a clear increase of the fractal dimension with increasing correlation strength, approaching $d_{\rm f}\rightarrow 2$. The onset of this change does not seem to be determined by the extended Harris criterion.Comment: 12 pages, 8 figure