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Michael E. Fisher

Publications and source records attributed to Michael E. Fisher.

At least 37 records · Page 2Linked to original sources

Fluid Coexistence close to Criticality: Scaling Algorithms for Precise Simulation

A novel algorithm is presented that yields precise estimates of coexisting liquid and gas densities, $ρ^{\pm}(T)$, from grand canonical Monte Carlo simulations of model fluids near criticality. The algorithm utilizes data for the isothermal minima of the moment ratio $Q_{L}(T;<ρ>_{L})$ $\equiv< m^{2}>_{L}^{2}/< m^{4}>_{L}$ in $L$$ \times$$ ...$$ \times$$ L$ boxes, where $m=ρ-<ρ>_{L}$. When $L$$ \to$$ \infty$ the minima, $Q_{\scriptsize m}^{\pm}(T;L)$, tend to zero while their locations, $ρ_{\scriptsize m}^{\pm}(T;L)$, approach $ρ^{+}(T)$ and $ρ^{-}(T)$. Finite-size scaling relates the ratio {\boldmath $\mathcal Y$}$ = $$(ρ_{\scriptsize m}^{+}-ρ_{\scriptsize m}^{-})/Δρ_{\infty}(T)$ {\em universally} to ${1/2}(Q_{\scriptsize m}^{+}+Q_{\scriptsize m}^{-})$, where $Δρ_{\infty}$$ = $$ρ^{+}(T)-ρ^{-}(T)$ is the desired width of the coexistence curve. Utilizing the exact limiting $(L$$ \to $$\infty)$ form, the corresponding scaling function can be generated in recursive steps by fitting overlapping data for three or more box sizes, $L_{1}$, $L_{2}$, $...$, $L_{n}$. Starting at a $T_{0}$ sufficiently far below $T_{\scriptsize c}$ and suitably choosing intervals $ΔT_{j}$$ = $$T_{j+1}-T_{j}$$ > $0 yields $Δρ_{\infty}(T_{j})$ and precisely locates $T_{\scriptsize c}$.

cond-mat.stat-mech↗

Scaling for Interfacial Tensions near Critical Endpoints

Parametric scaling representations are obtained and studied for the asymptotic behavior of interfacial tensions in the \textit{full} neighborhood of a fluid (or Ising-type) critical endpoint, i.e., as a function \textit{both} of temperature \textit{and} of density/order parameter \textit{or} chemical potential/ordering field. Accurate \textit{nonclassical critical exponents} and reliable estimates for the \textit{universal amplitude ratios} are included naturally on the basis of the ``extended de Gennes-Fisher'' local-functional theory. Serious defects in previous scaling treatments are rectified and complete wetting behavior is represented; however, quantitatively small, but unphysical residual nonanalyticities on the wetting side of the critical isotherm are smoothed out ``manually.'' Comparisons with the limited available observations are presented elsewhere but the theory invites new, searching experiments and simulations, e.g., for the vapor-liquid interfacial tension on the two sides of the critical endpoint isotherm for which an amplitude ratio $-3.25 \pm 0.05$ is predicted.

cond-mat.stat-mech↗

Discretization Dependence of Criticality in Model Fluids: a Hard-core Electrolyte

Grand canonical simulations at various levels, $ζ=5$-20, of fine- lattice discretization are reported for the near-critical 1:1 hard-core electrolyte or RPM. With the aid of finite-size scaling analyses it is shown convincingly that, contrary to recent suggestions, the universal critical behavior is independent of $ζ$ $(\grtsim 4)$; thus the continuum $(ζ\to\infty)$ RPM exhibits Ising-type (as against classical, SAW, XY, etc.) criticality. A general consideration of lattice discretization provides effective extrapolation of the {\em intrinsically} erratic $ζ$-dependence, yielding $(\Tc^ {\ast},\rhoc^{\ast})\simeq (0.0493_{3},0.075)$ for the $ζ=\infty$ RPM.

cond-mat.stat-mech↗

Ionic criticality : an exactly soluble model

Gas-liquid criticality in ionic fluids is studied in exactly soluble spherical models that use interlaced sublattices to represent hard-core \textit{multi}component systems. Short range attractions in the uncharged fluid drive criticality but charged ions do not alter the universality class. Debye screening remains exponential \textit{at} criticality in charge-symmetric 1:1 models. However, \textit{asymmetry} couples charge and density fluctuations in a direct manner: the charge correlation length then diverges precisely as the density correlation length and the Stillinger-Lovett rule is violated \textit{at} criticality.

cond-mat.stat-mech↗

Fluid Critical Points from Simulations: the Bruce-Wilding method and Yang-Yang anomalies

A critique is presented of the frequently used Bruce-Wilding (BW) mixed-field scaling method for estimating the critical points of nonsymmetric model fluids from grand canonical simulation data. An explicit, systematic technique for implementing this method is set out thereby revealing clearly a fortunate, close cancelation of contributions from the leading correction- to-scaling and thermal scaling functions that makes the method effective for Ising-type systems but which lacks a general theoretical basis. Pressure mixing is considered in this work which modifies the leading behavior of the critical density estimator while the critical temperature estimator maintains the leading behavior asserted by BW.

cond-mat.stat-mech↗

Precise Simulation of Near-critical Fluid Coexistence

We present a novel method to derive liquid-gas coexisting densities, $ρ^{\pm}(T)$, from grand canonical simulations (without knowledge of $\Tc$ or criticality class). The minima of $ Q_{L}\equiv< m^{2} >_{L}^{2}/< m^{4}>_{L}$ in an $L$$\times$$L \times$$L$ box with $m = ρ- <ρ>_{L}$ are used to generate recursively an unbiased universal finite-size scaling function. Monte Carlo data for a hard-core square-well fluid and for the restricted primitive model electrolyte yield $ρ^{\pm}$ to $\pm 1$-2% of $\rhoc$ down to 1 part in $10^4$-$10^3$ of $\Tc$ (and confirm well Ising character). Pressure mixing in the scaling fields is unequivocally revealed and indicates Yang-Yang ratios $R_μ = -0.04_{4}$ and $0.2_{6}$ for the two models, respectively.

cond-mat.stat-mech↗

Asymmetric Fluid Criticality II: Finite-Size Scaling for Simulations

The vapor-liquid critical behavior of intrinsically asymmetric fluids is studied in finite systems of linear dimensions, $L$, focusing on periodic boundary conditions, as appropriate for simulations. The recently propounded ``complete'' thermodynamic $(L\to\infty)$ scaling theory incorporating pressure mixing in the scaling fields as well as corrections to scaling ${[arXiv:cond-mat/0212145]}$, is extended to finite $L$, initially in a grand canonical representation. The theory allows for a Yang-Yang anomaly in which, when $L\to\infty$, the second temperature derivative, $(d^{2}μ_σ/dT^{2})$, of the chemical potential along the phase boundary, $μ_σ(T)$, diverges when $T\to\Tc -$. The finite-size behavior of various special {\em critical loci} in the temperature-density or $(T,ρ)$ plane, in particular, the $k$-inflection susceptibility loci and the $Q$-maximal loci -- derived from $Q_{L}(T,<ρ>_{L}) \equiv < m^{2}>^{2}_{L}/< m^{4}>_{L}$ where $m \equiv ρ- <ρ>_{L}$ -- is carefully elucidated and shown to be of value in estimating $\Tc$ and $\rhoc$. Concrete illustrations are presented for the hard-core square-well fluid and for the restricted primitive model electrolyte including an estimate of the correlation exponent $ν$ that confirms Ising-type character. The treatment is extended to the canonical representation where further complications appear.

cond-mat.stat-mech↗

A Simple Kinetic Model Describes the Processivity of Myosin-V

Myosin-V is a motor protein responsible for organelle and vesicle transport in cells. Recent single-molecule experiments have shown that it is an efficient processive motor that walks along actin filaments taking steps of mean size close to 36 nm. A theoretical study of myosin-V motility is presented following an approach used successfully to analyze the dynamics of conventional kinesin but also taking some account of step-size variations. Much of the present experimental data for myosin-V can be well described by a two-state chemical kinetic model with three load-dependent rates. In addition, the analysis predicts the variation of the mean velocity and of the randomness -- a quantitative measure of the stochastic deviations from uniform, constant-speed motion -- with ATP concentration under both resisting and assisting loads, and indicates a {\it sub}step of size $d_{0} \simeq$ 13-14 nm (from the ATP-binding site) that appears to accord with independent observations.

cond-mat.stat-mech↗

Asymmetric Fluid Criticality I: Scaling with Pressure Mixing

The thermodynamic behavior of a fluid near a vapor-liquid and, hence, asymmetric critical point is discussed within a general ``complete'' scaling theory incorporating pressure mixing in the nonlinear scaling fields as well as corrections to scaling. This theory allows for a Yang-Yang anomaly in which μ_σ^{\prime\prime}(T), the second temperature derivative of the chemical potential along the phase boundary, diverges like the specific heat when T\to T_{\scriptsize c}; it also generates a leading singular term, |t|^{2β}, in the coexistence curve diameter, where t\equiv (T-T_{\scriptsize c}) /T_{\scriptsize c}. The behavior of various special loci, such as the critical isochore, the critical isotherm, the k-inflection loci, on which χ^{(k)}\equiv χ(ρ,T)/ρ^{k} (with χ= ρ^{2} k_{\scriptsize B}TK_{T}) and C_{V}^{(k)}\equiv C_{V}(ρ,T)/ρ^{k} are maximal at fixed T, is carefully elucidated. These results are useful for analyzing simulations and experiments, since particular, nonuniversal values of k specify loci that approach the critical density most rapidly and reflect the pressure-mixing coefficient. Concrete illustrations are presented for the hard-core square-well fluid and for the restricted primitive model electrolyte. For comparison, a discussion of the classical (or Landau) theory is presented briefly and various interesting loci are determined explicitly and illustrated quantitatively for a van der Waals fluid.

cond-mat.stat-mech↗

Universality class of criticality in the restricted primitive model electrolyte

The 1:1 equisized hard-sphere electrolyte or restricted primitive model has been simulated via grand-canonical fine-discretization Monte Carlo. Newly devised unbiased finite-size extrapolation methods using temperature-density, (T, rho), loci of inflections, Q = ^2/ maxima, canonical and C_V criticality, yield estimates of (T_c, rho_c) to +- (0.04, 3)%. Extrapolated exponents and Q-ratio are (gamma, nu, Q_c) = [1.24(3), 0.63(3); 0.624(2)] which support Ising (n = 1) behavior with (1.23_9, 0.630_3; 0.623_6), but exclude classical, XY (n = 2), SAW (n = 0), and n = 1 criticality with potentials phi(r)>Phi/r^{4.9} when r \to \infty.

cond-mat.stat-mech↗

Lattice Models of Ionic Systems

A theoretical analysis of Coulomb systems on lattices in general dimensions is presented. The thermodynamics is developed using Debye-Huckel theory with ion-pairing and dipole-ion solvation, specific calculations being performed for 3D lattices. As for continuum electrolytes, low-density results for sc, bcc and fcc lattices indicate the existence of gas-liquid phase separation. The predicted critical densities have values comparable to those of continuum ionic systems, while the critical temperatures are 60-70% higher. However, when the possibility of sublattice ordering as well as Debye screening is taken into account systematically, order-disorder transitions and a tricritical point are found on sc and bcc lattices, and gas-liquid coexistence is suppressed. Our results agree with recent Monte Carlo simulations of lattice electrolytes.

cond-mat.stat-mech↗

Asymmetric Primitive-Model Electrolytes: Debye-Huckel Theory, Criticality and Energy Bounds

Debye-Huckel (DH) theory is extended to treat two-component size- and charge-asymmetric primitive models, focussing primarily on the 1:1 additive hard-sphere electrolyte with, say, negative ion diameters, a--, larger than the positive ion diameters, a++. The treatment highlights the crucial importance of the charge-unbalanced ``border zones'' around each ion into which other ions of only one species may penetrate. Extensions of the DH approach which describe the border zones in a physically reasonable way are exact at high $T$ and low density, $ρ$, and, furthermore, are also in substantial agreement with recent simulation predictions for \emph{trends} in the critical parameters, $T_c$ and $ρ_c$, with increasing size asymmetry. Conversely, the simplest linear asymmetric DH description, which fails to account for physically expected behavior in the border zones at low $T$, can violate a new lower bound on the energy (which applies generally to models asymmetric in both charge and size). Other recent theories, including those based on the mean spherical approximation, have predicted trends in the critical parameters quite opposite to those established by the simulations.

cond-mat.stat-mech↗

The Isothermal Binodal Curves Near a Critical Endpoint

Thermodynamics in the vicinity of a critical endpoint with nonclassical exponents $α$, $β$, $γ$, $δ$, $...$ is analyzed in terms of density variables (mole fractions, magnetizations, etc.). The shapes of the isothermal binodals or two-phase coexistence curves are found at andnear the endpoint for symmetric and nonsymmetric situations. The spectator- (or noncritical)-phase binodal at $T=T_{e}$ is characterized by an exponent $(δ+1)/δ$ $(\simeq 1.21)$ with leading corrections of relative order $1/δ$ $(\simeq 0.21)$, $θ_{4}/βδ$ $(\simeq 0.34)$ and $1 -(βδ)^{-1}$$(\simeq 0.36)$; in contrast to classical (van der Waals, mean field, $...$) theory, the critical endpoint binodal is singular with leading exponent $(1-α)/β$ $(\simeq 2.73)$ and corrections which are elucidated; the remaining, $λ$-line binodals also display the `renormalized exponent,' $(1-α)/β$ butwith more singular corrections. (The numerical values quoted here pertain to $(d=3)$-dimensional-fluid or Ising-type systems.)

cond-mat↗

The heat capacity of the restricted primitive model electrolyte

The constant-volume heat capacity, C_V(T, rho), of the restricted primitive model (RPM) electrolyte is considered in the vicinity of its critical point. It is demonstrated that, despite claims, recent simulations for finite systems do not convincingly indicate the absence of a divergence in C_V(T, rho)--which would point to non-Ising-type criticality. The strong qualitative difference between C_V for the RPM and for a Lennard-Jones fluid is shown to result from the low critical density of the former. If one considers the theoretically preferable configurational heat-capacity density, C_V/V, the finite-size results for the two systems display qualitatively similar behavior on near-critical isotherms.

cond-mat.soft↗

Extended Kinetic Models with Waiting-Time Distributions: Exact Results

Inspired by the need for effective stochastic models to describe the complex behavior of biological motor proteins that move on linear tracks exact results are derived for the velocity and dispersion of simple linear sequential models (or one-dimensional random walks) with general waiting-time distributions. The concept of ``mechanicity'' is introduced in order to conveniently quantify departures from simple ``chemical,'' kinetic rate processes, and its significance is briefly indicated. The results are extended to more elaborate models that have finite side-branches and include death processes (to represent the detachment of a motor from the track).

cond-mat.stat-mech↗

Identity of the universal repulsive-core singularity with Yang-Lee edge criticality

Lattice and continuum fluid models with repulsive-core interactions typically display a dominant, critical-type singularity on the real, negative activity axis. Lai and Fisher recently suggested, mainly on numerical grounds, that this repulsive-core singularity is universal and in the same class as the Yang-Lee edge singularities, which arise above criticality at complex activities with positive real part. A general analytic demonstration of this identification is presented here using a field-theory approach with separate representation of the repulsive and attractive parts of the pair interactions.

cond-mat.stat-mech↗

The Force Exerted by a Molecular Motor

The stochastic driving force exerted by a single molecular motor (e.g., a kinesin, or myosin) moving on a periodic molecular track (microtubule, actin filament, etc.) is discussed from a general viewpoint open to experimental test. An elementary "barometric" relation for the driving force is introduced that (i) applies to a range of kinetic and stochastic models, (ii) is consistent with more elaborate expressions entailing explicit representations of externally applied loads and, (iii) sufficiently close to thermal equilibrium, satisfies an Einstein-type relation in terms of the velocity and diffusion coefficient of the (load-free) motor. Even in the simplest two-state models, the velocity-vs.-load plots exhibit a variety of contrasting shapes (including nonmonotonic behavior). Previously suggested bounds on the driving force are shown to be inapplicable in general by analyzing discrete jump models with waiting time distributions.

cond-mat.stat-mech↗

Chemical Association via Exact Thermodynamic Formulations

It can be fruitful to view two-component physical systems of attractive monomers, A and B, ``chemically'' in terms of a reaction A + B <-> C, where C = AB is an associated pair or complex. We show how to construct free energies in the three-component or chemical picture which, under mass-action equilibration, exactly reproduce any given two-component or ``physical'' thermodynamics. Order-by-order matching conditions and closed-form chemical representations reveal the freedom available to modify the A-C, B-C, and C-C interactions and to adjust the association constant. The theory (in the simpler one-component, i.e., A = B, case) is illustrated by treating a van der Waals fluid.

physics.chem-ph↗