اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدAccurate sampling using Langevin dynamics
106
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
We show how to derive a simple integrator for the Langevin equation and illustrate how it is possible to check the accuracy of the obtained distribution on the fly, using the concept of effective energy introduced in a recent paper [J. Chem. Phys. 126, 014101 (2007)]. Our integrator leads to correct sampling also in the difficult high-friction limit. We also show how these ideas can be applied in practical simulations, using a Lennard-Jones crystal as a paradigmatic case.
قيم البحث
اقرأ أيضاً
We expand on the previously published Gr{o}nbech-Jensen Farago (GJF) thermostat, which is a thermodynamically sound variation on the St{o}rmer-Verlet algorithm for simulating discrete-time Langevin equations. The GJF method has been demonstrated to g
ive robust and accurate configurational sampling of the phase space, and its applications to, e.g., Molecular Dynamics is well established. A new definition of the discrete-time velocity variable is proposed based on analytical calculations of the kinetic response of a harmonic oscillator subjected to friction and noise. The new companion velocity to the GJF method is demonstrated to yield correct and time-step-independent kinetic responses for, e.g., kinetic energy, its fluctuations, and Green-Kubo diffusion based on velocity autocorrelations. This observation allows for a new and convenient Leap-Frog algorithm, which efficiently and precisely represents statistical measures of both kinetic and configurational properties at any time step within the stability limit for the harmonic oscillator. We outline the simplicity of the algorithm and demonstrate its attractive time-step-independent features for nonlinear and complex systems through applications to a one-dimensional nonlinear oscillator and three-dimensional Molecular Dynamics.
The computational study of conformational transitions in RNA and proteins with atomistic molecular dynamics often requires suitable enhanced sampling techniques. We here introduce a novel method where concurrent metadynamics are integrated in a Hamil
tonian replica-exchange scheme. The ladder of replicas is built with different strength of the bias potential exploiting the tunability of well-tempered metadynamics. Using this method, free-energy barriers of individual collective variables are significantly reduced compared with simple force-field scaling. The introduced methodology is flexible and allows adaptive bias potentials to be self-consistently constructed for a large number of simple collective variables, such as distances and dihedral angles. The method is tested on alanine dipeptide and applied to the difficult problem of conformational sampling in a tetranucleotide.
We study the exponential convergence to the stationary state for nonequilibrium Langevin dynamics, by a perturbative approach based on hypocoercive techniques developed for equilibrium Langevin dynamics. The Hamiltonian and overdamped limits (corresp
onding respectively to frictions going to zero or infinity) are carefully investigated. In particular, the maximal magnitude of admissible perturbations are quantified as a function of the friction. Numerical results based on a Galerkin discretization of the generator of the dynamics confirm the theoretical lower bounds on the spectral gap.
Kinetic energy equipartition is a premise for many deterministic and stochastic molecular dynamics methods that aim at sampling a canonical ensemble. While this is expected for real systems, discretization errors introduced by the numerical integrati
on may distort such assumption. Fortunately, backward error analysis allows us to identify the quantity that is actually subject to equipartition. This is related to a shadow Hamiltonian, which coincides with the specified Hamiltonian only when the time-step size approaches zero. This paper deals with discretization effects in a straightforward way. With a small computational overhead, we obtain refine
In light of the recently published complete set of statistically correct GJ methods for discrete-time thermodynamics, we revise the differential operator splitting method for the Langevin equation in order to comply with the basic GJ thermodynamic sa
mpling features, namely the Boltzmann distribution and Einstein diffusion, in linear systems. This revision, which is based on the introduction of time scaling along with flexibility of a discrete-time velocity attenuation parameter, provides a direct link between the ABO splitting formalism and the GJ methods. This link brings about the conclusion that any GJ method has at least weak second order accuracy in the applied time step. It further helps identify a novel half-step velocity, which simultaneously produces both correct kinetic statistics and correct transport measures for any of the statistically sound GJ methods. Explicit algorithmic expressions are given for the integration of the new half-step velocity into the GJ set of methods. Numerical simulations, including quantum-based molecular dynamics (QMD) using the QMD suite LATTE, highlight the discussed properties of the algorithms as well as exhibit the direct application of robust, time step independent stochastic integrators to quantum-based molecular dynamics.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
