Correlation function of one-dimensional Ising model with power-law potential

1981 ◽  
Vol 14 (1) ◽  
pp. 227-232 ◽  
Author(s):  
A K Bassiouny
2012 ◽  
Vol 26 (22) ◽  
pp. 1244001 ◽  
Author(s):  
ORION CIFTJA

We describe the relationship between quantum Hall edge states and the one-dimensional Luttinger liquid model. The Luttinger liquid model originated from studies of one-dimensional Fermi systems, however, it results that many ideas inspired by such a model can find applications to phenomena occurring even in higher dimensions. Quantum Hall systems which essentially are correlated two-dimensional electronic systems in a strong perpendicular magnetic field have an edge. It turns out that the quantum Hall edge states can be described by a one-dimensional Luttinger model. In this work, we give a general background of the quantum Hall and Luttinger liquid physics and then point out the relationship between the quantum Hall edge states and its one-dimensional Luttinger liquid representation. Such a description is very useful given that the Luttinger liquid model has the property that it can be bosonized and solved. The fact that we can introduce a simpler model of noninteracting bosons, even if the quantum Hall edge states of electrons are interacting, allows one to calculate exactly various quantities of interest. One such quantity is the correlation function which, in the asymptotic limit, is predicted to have a power law form. The Luttinger liquid model also suggests that such a power law exponent should have a universal value. A large number of experiments have found the quantum Hall edge states to show behavior consistent with a Luttinger liquid description. However, while a power law dependence of the correlation function has been observed, the experimental values of the exponent appear not to be universal. This discrepancy might be due to various correlation effects between electrons that sometimes are not easy to incorporate within a standard Luttinger liquid model.


2017 ◽  
Vol 118 (10) ◽  
pp. 929-934 ◽  
Author(s):  
A. I. Proshkin ◽  
T. Yu. Ponomareva ◽  
I. A. Menshikh ◽  
A. V. Zarubin ◽  
F. A. Kassan-Ogly

1991 ◽  
Vol 56 (2) ◽  
pp. 334-343
Author(s):  
Ondřej Wein

Analytical solutions are given to a class of unsteady one-dimensional convective-diffusion problems assuming power-law velocity profiles close to the transport-active surface.


2012 ◽  
Vol 26 (29) ◽  
pp. 1250146 ◽  
Author(s):  
BHASKAR SEN GUPTA ◽  
SHANKAR P. DAS

The renormalized dynamics described by the equations of nonlinear fluctuating hydrodynamics (NFH) treated at one loop order gives rise to the basic model of the mode coupling theory (MCT). We investigate here by analyzing the density correlation function, a crucial prediction of ideal MCT, namely the validity of the multi step relaxation scenario. The equilibrium density correlation function is calculated here from the direct solutions of NFH equations for a hard sphere system. We make first detailed investigation for the robustness of the correlation functions obtained from the numerical solutions by varying the size of the grid. For an optimum choice of grid size we analyze the decay of the density correlation function to identify the multi-step relaxation process. Weak signatures of two step power law relaxation is seen with exponents which do not match predictions from the one loop MCT. For the final relaxation stretched exponential (KWW) behavior is seen and the relaxation time grows with increase of density. But apparent power law divergences indicate a critical packing fraction much higher than the corresponding MCT predictions for a hard sphere fluid.


The direct correlation function between two points in the gas-liquid surface of the penetrable sphere model is obtained in a mean-field approximation. This function is used to show explicitly that three apparently different ways of calculating the surface tension all lead to the same result. They are (1) from the virial of the intermolecular potential, (2) from the direct correlation function, and (3) from the energy density. The equality of (1) and (2) is shown analytically at all temperatures 0 < T < T c where T c is the critical temperature; the equality of (2) and (3) is shown analytically for T ≈ T c , and by numerical integration at lower temperatures. The equality of (2) and (3) is shown analytically at all temperatures for a one-dimensional potential.


Sign in / Sign up

Export Citation Format

Share Document