اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدDirect Minimization for Ensemble Electronic Structure Calculations
117
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
We consider a direct optimization approach for ensemble density functional theory electronic structure calculations. The update operator for the electronic orbitals takes the structure of the Stiefel manifold into account and we present an optimization scheme for the occupation numbers that ensures that the constraints remain satisfied. We also compare sequential and simultaneous quasi-Newton and nonlinear conjugate gradient optimization procedures, and demonstrate that simultaneous optimization of the electronic orbitals and occupation numbers improve performance compared to the sequential approach.
قيم البحث
اقرأ أيضاً
We consider a minimization scheme based on the Householder transport operator for the Grassman manifold, where a point on the manifold is represented by a m x n matrix with orthonormal columns. In particular, we consider the case where m >> n and pre
sent a method with asymptotic complexity mn^2. To avoid explicit parametrization of the manifold we use Householder transforms to move on the manifold, and present a formulation for simultaneous Householder reflections for S-orthonormal columns. We compare a quasi-Newton and nonlinear conjugate gradient implementation adapted to the manifold with a projected nonlinear conjugate gradient method, and demonstrate that the convergence rate is significantly improved if the manifold is taken into account when designing the optimization procedure.
We present an implicit solvent model for ab initio electronic structure calculations which is fully self-consistent and is based on direct solution of the nonhomogeneous Poisson equation. The solute cavity is naturally defined in terms of an isosurfa
ce of the electronic density according to the formula of Fattebert and Gygi (J. Comp. Chem. 23, 6 (2002)). While this model depends on only two parameters, we demonstrate that by using appropriate boundary conditions and dispersion-repulsion contributions, solvation energies obtained for an extensive test set including neutral and charged molecules show dramatic improvement compared to existing models. Our approach is implemented in, but not restricted to, a linear-scaling density functional theory (DFT) framework, opening the path for self-consistent implicit solvent DFT calculations on systems of unprecedented size, which we demonstrate with calculations on a 2615-atom protein-ligand complex.
We propose an adaptive planewave method for eigenvalue problems in electronic structure calculations. The method combines a priori convergence rates and accurate a posteriori error estimates into an effective way of updating the energy cut-off for pl
anewave discretizations, for both linear and nonlinear eigenvalue problems. The method is error controllable for linear eigenvalue problems in the sense that for a given required accuracy, an energy cut-off for which the solution matches the target accuracy can be reached efficiently. Further, the method is particularly promising for nonlinear eigenvalue problems in electronic structure calculations as it shall reduce the cost of early iterations in self-consistent algorithms. We present some numerical experiments for both linear and nonlinear eigenvalue problems. In particular, we provide electronic structure calculations for some insulator and metallic systems simulated with Kohn--Sham density functional theory (DFT) and the projector augmented wave (PAW) method, illustrating the efficiency and potential of the algorithm.
We outline a generic, flexible, modular, yet efficient framework to the computation of energies and states for general nanoscopic systems with a focus on semiconductor quantum dots. The approach utilizes the configuration interaction method, in princ
ipal obtaining all many-body correlations in the system. The approach exploits the powerful abstracting mechanisms of C++s template facility to produce efficient yet general code. The primary utility of the present approach is not in the resulting raw computational speed, but rather in minimizing the time from initial idea to final results.
Motivated by the recently proposed parallel orbital-updating approach in real space method, we propose a parallel orbital-updating based plane-wave basis method for electronic structure calculations, for solving the corresponding eigenvalue problems.
In addition, we propose two new modified parallel orbital-updating methods. Compared to the traditional plane-wave methods, our methods allow for two-level parallelization, which is particularly interesting for large scale parallelization. Numerical experiments show that these new methods are more reliable and efficient for large scale calculations on modern supercomputers
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
