Excitations in time-dependent density-functional theory.
نویسندگان
چکیده
An approximate solution to the time-dependent density-functional theory response equations for finite systems is developed, yielding corrections to the single-pole approximation. These explain why allowed Kohn-Sham transition frequencies and oscillator strengths are usually good approximations to the true values, and why sometimes they are not. The approximation yields simple expressions for Görling-Levy perturbation theory results, and a method for estimating expectation values of the unknown exchange-correlation kernel.
منابع مشابه
Charge transfer, double and bond-breaking excitations with time-dependent density matrix functional theory.
Time-dependent density functional theory (TDDFT) in its current adiabatic implementations exhibits three remarkable failures: (a) completely wrong behavior of the excited state surface along a bond-breaking coordinate; (b) lack of doubly excited configurations; (c) much too low charge transfer excitation energies. These TDDFT failure cases are all strikingly exhibited by prototype two-electron ...
متن کاملTransverse dynamical magnetic susceptibilities from regular static density functional theory: Evaluation of damping and g shifts of spin excitations
The dynamical transverse magnetic Kohn-Sham susceptibility calculated within time-dependent density functional theory shows a fairly linear behavior for a finite energy window. This observation is used to propose a scheme where the computation of this quantity is greatly simplified. Regular simulations based on static density functional theory can be used to extract the dynamical behavior of th...
متن کاملHartree-Fock exchange in time dependent density functional theory: application to charge transfer excitations in solvated molecular systems
The performance of time dependent density functional theory methods for the computation of electronic absorption spectra of molecular solutions is investigated using aqueous acetone as model system. Solute and solvent are treated at the same level of theory. Whereas transition energy and intensity for the intra-molecular (1)A(2)n-->pi{*} transition are described to good accuracy by a convention...
متن کاملDiscontinuities of the exchange-correlation kernel and charge-transfer excitations in time-dependent density-functional theory
We identify the key property that the exchange-correlation (XC) kernel of time-dependent density-functional theory must have in order to describe long-range charge-transfer excitations. We show that the discontinuity of the XC potential as a function of particle number induces a spaceand frequency-dependent discontinuity of the XC kernel that diverges as r → ∞. In a combined donor-acceptor syst...
متن کاملDensity functional approximations for charge transfer excitations with intermediate spatial overlapw
Density functional theory is now the method of choice for calculating the electronic structure of complex systems, and time-dependent density functional theory (TDDFT) is now the preferred method for calculating spectroscopic properties of large molecules. The validity of the theory depends mainly on the quality of the approximation to the unknown exchange–correlation energy. In the present pap...
متن کاملApplication of time-dependent density functional theory to electron-vibration coupling in benzene
Optical properties of symmetry-forbidden π-π transitions in benzene are calculated with the time-dependent density functional theory (TDDFT), using an adiabatic LDA functional. Quantities calculated are the envelopes of the Franck-Condon factors of the vibrationally promoted transitions and the associated oscillator strengths. The strengths, which span three orders of magnitude, are reproduced ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Physical review letters
دوره 90 4 شماره
صفحات -
تاریخ انتشار 2003