اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدturboTDDFT 2.0 - Hybrid functionals and new algorithms within time-dependent density-functional perturbation theory
76
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
We present a new release of the turboTDDFT code featuring an implementation of hybrid functionals, a recently introduced pseudo-Hermitian variant of the Liouville-Lanczos approach to time-dependent density-functional perturbation theory, and a newly developed Davidson-like algorithm to compute selected interior eigenvalues/vectors of the Liouvillian super-operator. Our implementation is thoroughly validated against benchmark calculations performed on the cyanin (C$_{21}$O$_{11}$H$_{21}$) molecule using the Gaussian09 and turboTDDFT 1.0 codes.
قيم البحث
اقرأ أيضاً
Real-time time-dependent density functional theory (rt-TDDFT) with hybrid exchange-correlation functional has wide-ranging applications in chemistry and material science simulations. However, it can be thousands of times more expensive than a convent
ional ground state DFT simulation, hence is limited to small systems. In this paper, we accelerate hybrid functional rt-TDDFT calculations using the parallel transport gauge formalism, and the GPU implementation on Summit. Our implementation can efficiently scale to 786 GPUs for a large system with 1536 silicon atoms, and the wall clock time is only 1.5 hours per femtosecond. This unprecedented speed enables the simulation of large systems with more than 1000 atoms using rt-TDDFT and hybrid functional.
First-principles calculations combining density-functional theory and continuum solvation models enable realistic theoretical modeling and design of electrochemical systems. When a reaction proceeds in such systems, the number of electrons in the por
tion of the system treated quantum mechanically changes continuously, with a balancing charge appearing in the continuum electrolyte. A grand-canonical ensemble of electrons at a chemical potential set by the electrode potential is therefore the ideal description of such systems that directly mimics the experimental condition. We present two distinct algorithms, a self-consistent field method (GC-SCF) and a direct variational free energy minimization method using auxiliary Hamiltonians (GC-AuxH), to solve the Kohn-Sham equations of electronic density-functional theory directly in the grand canonical ensemble at fixed potential. Both methods substantially improve performance compared to a sequence of conventional fixed-number calculations targeting the desired potential, with the GC-AuxH method additionally exhibiting reliable and smooth exponential convergence of the grand free energy. Finally, we apply grand-canonical DFT to the under-potential deposition of copper on platinum from chloride-containing electrolytes and show that chloride desorption, not partial copper monolayer formation, is responsible for the second voltammetric peak.
Imaginary-time time-dependent Density functional theory (it-TDDFT) has been proposed as an alternative method for obtaining the ground state within density functional theory (DFT) which avoids some of the difficulties with convergence encountered by
the self-consistent-field (SCF) iterative method. It-TDDFT was previously applied to clusters of atoms where it was demonstrated to converge in select cases where SCF had difficulty with convergence. In the present work we implement it-TDDFT propagation for {it periodic systems} by modifying the Quantum ESPRESSO package, which uses a plane-wave basis with multiple $boldsymbol{k}$ points, and has the options of non-collinear and DFT+U calculations using ultra-soft or norm-conserving pseudo potentials. We demonstrate that our implementation of it-TDDFT propagation with multiple $boldsymbol{k}$ points is correct for DFT+U non-collinear calculations and for DFT+U calculations with ultra-soft pseudo potentials. Our implementation of it-TDDFT propagation converges to the exact SCF energy (up to the decimal guaranteed by double precision) in all but one case where it converged to a slightly lower value than SCF, suggesting a useful alternative for systems where SCF has difficulty to reach the Kohn-Sham ground state. In addition, we demonstrate that rapid convergence can be achieved if we use adaptive-size imaginary-time-steps for different kinetic-energy plane-waves.
We investigate optical absorption spectra obtained through time-dependent density functional theory (TD-DFT) based on nonempirical hybrid functionals that are designed to correctly reproduce the dielectric function. The comparison with state-of-the-a
rt $GW$ calculations followed by the solution of the Bethe-Sapeter equation (BSE-$GW$) shows close agreement for both the transition energies and the main features of the spectra. We confront TD-DFT with BSE-$GW$ by focusing on the model dielectric function and the local exchange-correlation kernel. The present TD-DFT approach achieves the accuracy of BSE-$GW$ at a fraction of the computational cost.
We present a rigorous framework that combines single-particle Greens function theory with density functional theory based on a separation of electron-electron interactions into short-range and long-range components. Short-range contributions to the t
otal energy and exchange-correlation potential are provided by a density functional approximation, while the long-range contribution is calculated using an explicit many-body Greens function method. Such a hybrid results in a nonlocal, dynamic, and orbital-dependent exchange-correlation functional of a single-particle Greens function. In particular, we present a range-separated hybrid functional called srSVWN5-lrGF2 which combines the local-density approximation and the second-order Greens function theory. We illustrate that similarly to density functional approximations the new functional is weakly basis-set dependent. Furthermore, it offers an improved description of the short-range dynamical correlation. The many-body contribution to the functional allows us to mitigate the many-electron self-interaction error present in most of density functional approximations and provides a better description of molecular properties. Additionally, the new functional can be used to scale down the self-energy and, therefore, introduce an additional sparsity to the self-energy matrix that in the future can be exploited in calculations for large molecules or periodic systems.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
