Exact diffusion coefficient of self-gravitating Brownian particles in two dimensions

We derive the exact expression of the diffusion coefficient of a self-gravitating Brownian gas in two dimensions. Our formula generalizes the usual Einstein relation for a free Brownian motion to the context of two-dimensional gravity. We show the existence of a critical temperature T_c at which the diffusion coefficient vanishes. For T < T_c, the diffusion coefficient is negative and the gas undergoes gravitational collapse. This leads to the formation of a Dirac peak concentrating the whole mass in a finite time. We also stress that the critical temperature T_c is different from the collapse temperature T_* at which the partition function diverges. These quantities differ by a factor 1-1/N where N is the number of particles in the system. We provide clear evidence of this difference by explicitly solving the case N = 2. We also mention the analogy with the chemotactic aggregation of bacteria in biology, the formation of “atoms” in a two-dimensional (2D) plasma and the formation of dipoles or “supervortices” in 2D point vortex dynamics.     

Dynamical models for fragment formation

The various dynamical models for fragment formation in nuclear collisions are discussed in order to bring out their relative advantages and shortcomings. After discussing the general requirements for dynamical models that aim to describe fragment formation, we consider the various mean-field models that incorporate fluctuations and then turn to models based on molecular dynamics.     

Thermal multifragmentation in p + Au interactions at 2.16, 3.6 and 8.1 GeV incident energies

Multiple emission of intermediate-mass fragments has been studied for the collisions p + Au at 2.16, 3.6 and 8.1 GeV with the FASA setup. The mean IMF multiplicities for events with at least one IMF are equal to 1.7, 1.9 and 2.1 (±0.2) respectively. The multiplicity, charge distributions and kinetic energy spectra of IMF are described in the framework of a intranuclear cascade model followed by the statistical multifragmentation model. However, between the two parts of the calculation the excitation energies and the residual masses and charges are modified to take into account the losses during expansion. The results support a scenario of true thermal multifragmentation of a hot and expanded target spectator. Received: 15 December 1997 / Revised version: 24 April 1998     

Renormalization group analysis of weakly charged polyelectrolytes

We present a field-theoretic Renormalization Group (RG) analysis of the statistical mechanics of long flexible, screened polyelectrolyte chains (Debye-Hückel chains) in polar solvents where the screening length is of the order of the chain size. A systematic analysis of the resulting field theory shows that the system is one with two length-scales requiring the calculation of scaling functions as well as exponents to fully describe its physical behaviour. This means that care must be taken to understand the interplay of the length-scales. Using the RG we identify the relevant scaling variables and explicitly calculate the scaling behaviour of the end-to-end distance for single chains. In addition we consider the many-chain system and calculate the scaling behaviour of the osmotic pressure of a dilute solution of chains. Received 16 December 1999 and Received in final form 13 December 2000     

From molecular flexibility to shape, curvature and thermotropic transitions in pure surfaces

A material surface of pure constituents with a flexible molecular chain (amphiphilics) is considered; thermodynamic behaviour is studied in the chain length-temperature plane. The Hamiltonian of the system is modelled as the sum of a formation term which refers to the polymer nature of the chain, and of a fluctuation term with a specific elastic form. For closed systems the model exhibits phases with uniform curvature and conformational order/disorder or, alternatively, modulated phases; a critical chain length is found for the existence of modulated phases; the dependence of transition temperature on energy parameters is determined. A critical region is found for open systems, where conformational disorder drives spontaneous generation of curvature; this lies above a characteristic chain length and around the shape transition temperature. Received: 13 November 1996 / Revised: 9 May 1997 / Received in final form: 4 November 1997 / Accepted: 10 November 1997     

Phase transitions in “small” systems

Traditionally, phase transitions are defined in the thermodynamic limit only. We discuss how phase transitions of first order (with phase separation and surface tension), continuous transitions and (multi)-critical points can be seen and classified for small systems. “Small” systems are systems where the linear dimension is of the characteristic range of the interaction between the particles; i.e. also astrophysical systems are “small” in this sense. Boltzmann defines the entropy as the logarithm of the area of the surface in the mechanical N-body phase space at total energy E. The topology of S(E,N) or more precisely, of the curvature determinant allows the classification of phase transitions without taking the thermodynamic limit. Micro-canonical thermo-statistics and phase transitions will be discussed here for a system coupled by short range forces in another situation where entropy is not extensive. The first calculation of the entire entropy surface S(E,N) for the diluted Potts model (ordinary (q=3)-Potts model plus vacancies) on a square lattice is shown. The regions in {E,N} where D>0 correspond to pure phases, ordered resp. disordered, and D<0 represent transitions of first order with phase separation and “surface tension”. These regions are bordered by a line with D=0. A line of continuous transitions starts at the critical point of the ordinary (q=3)-Potts model and runs down to a branching point P_m. Along this line vanishes in the direction of the eigenvector of D with the largest eigen-value . It characterizes a maximum of the largest eigenvalue . This corresponds to a critical line where the transition is continuous and the surface tension disappears. Here the neighboring phases are indistinguishable. The region where two or more lines with D=0 cross is the region of the (multi)-critical point. The micro-canonical ensemble allows to put these phenomena entirely on the level of mechanics. Received 18 October 1999 and received in final form 17 November 1999     

Scaling with respect to disorder in time-to-failure

We revisit a simple dynamical model of rupture in random media with long-range elasticity to test whether rupture can be seen as a first-order or a critical transition. We find a clear scaling of the macroscopic modulus as a function of time-to-rupture and of the amplitude of the disorder, which allows us to collapse neatly the numerical simulations over more than five decades in time and more than one decade in disorder amplitude onto a single master curve. We thus conclude that, at least in this model, dynamical rupture in systems with long-range elasticity is a genuine critical phenomenon occurring as soon as the disorder is non-vanishing. Received: 11 July 1997 / Revised: 6 November 1997 / Accepted: 10 November 1997     

The secondary structure of RNA under tension

We study the force-induced unfolding of random disordered RNA or single-stranded DNA polymers. The system undergoes a second-order phase transition from a collapsed globular phase at low forces to an extensive necklace phase with a macroscopic end-to-end distance at high forces. At low temperatures, the sequence inhomogeneities modify the critical behaviour. We provide numerical evidence for the universality of the critical exponents which, by extrapolation of the scaling laws to zero force, contain useful information on the ground-state (f = 0) properties. This provides a good method for quantitative studies of scaling exponents characterizing the collapsed globule. In order to get rid of the blurring effect of thermal fluctuations, we restrict ourselves to the ground state at fixed external force. We analyze the statistics of rearrangements, in particular below the critical force, and point out its implications for force-extension experiments on single molecules. Received 18 June 2002 and Received in final form 23 September 2002 RID="a" ID="a"e-mail: muller@ipno.in2p3.fr     

One-dimensional Ising-like systems: an analytical investigation of the static and dynamic properties, applied to spin-crossover relaxation

We investigate the dynamical properties of the 1-D Ising-like Hamiltonian taking into account short and long range interactions, in order to predict the static and dynamic behavior of spin crossover systems. The stochastic treatment is carried out within the frame of the local equilibrium method [1]. The calculations yield, at thermodynamic equilibrium, the exact analytic expression previously obtained by the transfer matrix technique [2]. We mainly discuss the shape of the relaxation curves: (i) for large (positive) values of the short range interaction parameter, a saturation of the relaxation curves is observed, reminiscent of the behavior of the width of the static hysteresis loop [3]; (ii) a sigmoidal (self-accelerated) behavior is obtained for large enough interactions of any type; (iii) the relaxation curves exhibit a sizeable tail (with respect to the mean-field curves) which is clearly associated with the transient onset of first-neighbor correlations in the system, due to the effect of short-range interactions. The case of negative short-range interaction is briefly discussed in terms of two-step properties. Received 29 October 1999 and Received in final form 30 December 1999     

Phase transitions induced by thermal fluctuations

The present study generalizes the model of extended stochastic systems with a field-dependent kinetic coefficient [M. Ibanes, J. Garcia-Ojalvo, R. Toral, J.M. Sancho, Phys. Rev. Lett. 87, 020601 (2001)] to systems with symmetric and asymmetric bistable potentials. It is found that in systems with a relaxational flow and a symmetric local potential, reentrant phase transitions can be observed. In the case of an asymmetric local potential, a hysteresis-like behaviour in the order parameter appears. It is shown that such phase transitions can be controlled by the constant that governs relaxation flow, noise intensity and spatial coupling intensity.     

Spontaneous-search method and short-time dynamics: applications to the Domany-Kinzel cellular automaton

The one-dimensional Domany-Kinzel cellular automaton is investigated by two numerical approaches: (i) the spontaneous-search method, which is a method appropriated for a search of criticality; (ii) short-time dynamics. Both critical frontiers of the system are investigated, namely, the one separating the frozen and active phases, as well as the critical line determined by damage spreading between two cellular automata, that splits the active phase into the nonchaotic and chaotic phases. The efficiency of the spontaneous-search method is established herein through a precise estimate of both critical frontiers, and in addition to that, it is shown that this method may also be used in the determination of the critical exponent ν_⊥. Using the critical frontiers obtained, other exponents are estimated through short-time dynamics. It is verified that the critical exponents of both critical frontiers fall in the universality class of directed percolation.     

Application of large deviation theory to the mean-field $\boldsymbol{\varphi}^\mathsf{4}$-model

A large deviation technique is used to calculate the microcanonical entropy function s(v,m) of the mean-field ϕ⁴-model as a function of the potential energy v and the magnetization m. As in the canonical ensemble, a continuous phase transition is found. An analytical expression is obtained for the critical energy v_c(J) as a function of the coupling parameter J.     

Phase transitions in a cluster molecular field approximation

Cluster molecular field approximations represent a substantial progress over the simple Weiss theory where only one spin is considered in the molecular field resulting from all the other spins. In this work we discuss a systematic way of improving the molecular field approximation by inserting spin clusters of variable sizes into a homogeneously magnetised background. The density of states of these spin clusters is then computed exactly. We show that the true non-classical critical exponents can be extracted from spin clusters treated in such a manner. For this purpose a molecular field finite size scaling theory is discussed and effective critical exponents are analysed. Reliable values of critical quantities of various Ising and Potts models are extracted from very small system sizes. Received 30 September 2002 / Received in final form 25 November 2002 Published online 27 January 2003 RID="a" ID="a"e-mail: pleim@theorie1.physik.uni-erlangen.de     

Structural stability and structural imitation of (M = Mn,Mo, Nb,Ti, V,Al, Cr,Ni and Si)

The structural stability of La₂Co_17-xM_x (M = Mn, Mo, Nb, Ti, V, Al, Cr, Ni and Si) based on the interatomic potential has been studied. The calculated site preference of the third element M is found to be the 6c site, which is in agreement with the experiments. In the calculations, if the crystal cohesive energy of La₂Co₁₆Mn is taken as the highest one in the crystallization of La₂Co_17-xM_x, the lowest content x of the third element M (M = Mn, Mo, Nb, Ti and V) required to stabilize La₂Co_17-xM_x, is near that found in the experiments. The differences of the cell parameters between the calculated and the experimental values are less than 0.4%. The differences of the atomic parameters for Co (or M) between the calculated and the experimental values are about or even smaller than 1%, and that of La is about 3%. Because the energies of La(Co_1-xAl_x)₁₃ are lower than those of La₂(Co_1-xAl_x)₁₇, La₂(Co_1-xAl_x)₁₇ could not be formed in the experiments. In the calculations, with either a range of deformation of the structure or the reconstruction of the initial structure La₂Co₁₇ from LaCo₅, the same results including the cohesive energy curves and the crystallographic parameters can be retrieved after the action of the interatomic potentials. Received 1st November 2002 / Received in final form 17 February 2003 Published online 23 May 2003 RID="a" ID="a"e-mail: hchang@aphy.iphy.ac.cn     

Domain wall delocalization,dynamics and fluctuations in an exclusion process with two internal states

We investigate the delocalization transition appearing in an exclusion process with two internal states, respectively on two parallel lanes. At the transition, delocalized domain walls form in the density profiles of both internal states, in agreement with a mean-field approach. Remarkably, the topology of the system’s phase diagram allows for the delocalization of a (localized) domain wall when approaching the transition. We quantify the domain wall’s delocalization close to the transition by analytic results obtained within the framework of the domain wall picture. Power law dependences of the domain wall width on the distance to the delocalization transition as well as on the system size are uncovered, they agree with numerical results.