This lesson aims at showing how to get the following physical properties, for finite systems :
This lesson should take about 30 minutes.
In order to do Time-Dependent Density Functional Theory calculations (TDDFT) of electronic excitations
and oscillator strengths, in the Casida's approach, you should first have some theoretical background.
TDDFT was first developed in the eighties, but the direct calculation of electronic excitations was introduced much later, by Casida and co-workers. A comprehensive description of the underlying formalism is given in
"Time-Dependent Density Functional Response Theory of Molecular Systems: Theory, Computational Methods, and Functionals" M. E. Casida in Recent Development and Applications of Modern Density Functional Theory, edited by J.M. Seminario (Elsevier, Amsterdam, 1996), p. 391. http://dx.doi.org/10.1016/S1380-7323(96)80093-8However this reference might be hard to get, that is why we have based the tutorial instead on the following (also early) papers :
"Molecular excitation energies to high-lying bound states from time-dependent density-functional response theory: Characterization and correction of the time-dependent local density approximation ionization threshold" Mark E. Casida, Christine Jamorski, Kim C. Casida, and Dennis R. Salahub J. Chem. Phys. 108, 4439 (1998) http://dx.doi.org/10.1063/1.475855
"Excited-state potential energy curves from time-dependent density-functional theory: A cross section of formaldehyde's 1A1 manifold" Mark E. Casida, Kim C. Casida, Dennis R. Salahub International Journal of Quantum Chemistry Volume 70, Issue 4-5, pages 933-941, 1998 http://dx.doi.org/10.1002/(SICI)1097-461X(1998)70:4/5<933::AID-QUA39>3.0.CO;2-Z
"Ab initio Excitation Spectra and Collective Electronic Response in Atoms and Clusters" I. Vasiliev, S. Ogut, and J. R. Chelikowsky Phys. Rev. Lett. 82, 1919-1922 (1999) http://dx.doi.org/10.1103/PhysRevLett.82.1919The first of these papers, CasidaJCP1998, will be used as main reference for our tutorial.
From these papers, you will learn that a TDDFT calculation of electronic excitation energies start first from a usual ground-state calculation, with a chosen XC functional. Such a calculation produces a spectrum of Kohn-Sham electronic energies. It is widely known that differences between occupied and unoccupied Kohn-Sham electronic energies resemble excitation energies (the difference in energy between an excited state and the ground state), although there is no real theoretical justification for this similarity.
These differences between Kohn-Sham electronic energies are the starting point of Casida's approach : in the framework of TDDFT, their square give the main contribution to the diagonal part of a matrix, whose eigenvalues will be the square of the seeked excitation energies. One has to add to the diagonal matrix made from the squares of Kohn-Sham energy differences, a coupling matrix, whose elements are four-wavefunction integrals of the Coulomb and Exchange-Correlation kernel. The exchange-correlation kernel contribution will differ in the spin-singlet and in the spin-triplet states, this being the only difference between spin-singlet and spin-triplet states. See Eqs.(1.3) and (1.4) of CasidaIJQC1998, and Eqs.(1-2) of Vasiliev1999
The construction of the coupling matrix can be done on the basis of an exchange-correlation kernel that is derived from the exchange-correlation functional used for the ground-state, but this is not a requirement of the theory, since such a correspondance only holds for the exact functional. In practice, the approximation to the XC potential and the one to the XC kernel are often different. See section III of CasidaJCP1998.
A big drawback of the currently known XC potentials and XC kernels is observed when the system is infinite in at least one direction (e.g. polymers, slabs, or solids). In this case, the addition of the coupling matrix is unable to shift the edges of the Kohn-Sham band structure (each four-wavefunction integral becomes too small). There is only a redistribution of the oscillator strengths. In particular, the DFT band gap problem is NOT solved by TDDFT. Also, the Casida's approach relies on the discreteness of the Kohn-Sham spectrum.
Thus, the TDDFT approach to electronic excitation energies in ABINIT is ONLY valid for finite systems (atoms, molecules, clusters). Actually, only one k-point can be used, and a "box center" must be defined, close to the center of gravity of the system.
The Casida formalism also gives access to the oscillator strengths, needed to obtain the frequency-dependent polarizability, and corresponding optical spectrum. In the ABINIT implementation, the oscillators strengths are given as a second-rank tensor, in cartesian coordinates, as well as the average over all directions usually used for molecules and clusters. It is left to the user to generate the polarisability spectrum, according to e.g. Eq.(1.2) of CasidaIJQC1998.
One can also combine the ground state total energy with the electronic excitation energies to obtain Born-Oppenheimer potential energy curves for excited states. This is illustrated for formaldehyde in CasidaIJQC1998.
Given its simplicity, and the relatively modest CPU cost of this type of calculation, Casida's approach enjoys a wide popularity. There has been hundreds of papers published on the basis of methodology. Still, its accuracy might be below the expectations, as you will see. As often, test this method to see if it suits your needs, and read the recent litterature ...
We will now compute and analyse the excitation energies of the diatomic molecule N2. This is a rather simple system, with cylindrical symmetry, allowing interesting understanding. Although we will suppose that you are familiarized with quantum numbers for diatomic molecules, this should not play an important role in the understanding of the way to use Abinit's implementation of Casida's formalism.
Before beginning, you might consider to work in a different subdirectory as for the other lessons. Why not "Work_tddft" ?
Now, you are ready to run ABINIT and prepare the needed file.
Copy the files ttddft_x.files and ttddft_1.in in "Work_tddft" :
So, issue now :
The computation is quite fast : about 15 secs on a 2.8 GHz PC.
Let's examine the input file ttddft_1.in.
There are two datasets : the first one corresponds to a typical ground-state calculation, with only occupied bands. The density and wavefunctions are written, for use in the second data set. The second dataset is the one where the TDDFT calculation is done. Moreover, the non-self-consistent calculation of the occupied eigenfunctions and corresponding eigenenergies is also accomplished. This is obtained by setting iscf to -1. Please, take now some time to read the information about this value of iscf, and the few input variables that acquire some meaning in this context (namely, boxcenter, td_mexcit, and td_maxene). Actually, this is most of the information that should be known to use the TDDFT in ABINIT !
You will note that we have 5 occupied bands (defined for dataset 1), and that we add 7 unoccupied bands in the dataset 2, to obtain a total of 12 bands. The box is not very large (6x5x5 Angstrom), the cutoff is quite reasonable, 25 Hartree), and as requested for the Casida's formalism, only one k point is used. We have chosen the Perdew-Wang 92 LDA functional for both the self-consistent and non-self-consistent calculations (ixc=7).
We can now examine the output file ttddft_1.out.
One can jump to the second dataset section, and skip a few non-interesting information, in order to reach the following information :
*** TDDFT : computation of excited states *** Splitting of 12 bands in 5 occupied bands, and 7 unoccupied bands, giving 35 excitations.The matrix that is diagonalized, in the Casida's formalism, is thus a 35x35 matrix. It will give 35 excitation energies.
Transition (Ha) and (eV) Tot. Ene. (Ha) Aver XX YY ZZ 5-> 6 3.10888E-01 8.45969E+00 -1.92741E+01 0.0000E+00 0.00E+00 0.00E+00 0.00E+00 5-> 7 3.10888E-01 8.45969E+00 -1.92741E+01 0.0000E+00 0.00E+00 0.00E+00 0.00E+00 5-> 8 3.44036E-01 9.36171E+00 -1.92409E+01 0.0000E+00 0.00E+00 0.00E+00 0.00E+00 4-> 6 3.64203E-01 9.91046E+00 -1.92207E+01 1.4460E-01 4.34E-01 0.00E+00 0.00E+00 3-> 6 3.64203E-01 9.91046E+00 -1.92207E+01 4.2302E-01 1.27E+00 0.00E+00 0.00E+00 4-> 7 3.64203E-01 9.91046E+00 -1.92207E+01 4.2302E-01 1.27E+00 0.00E+00 0.00E+00 3-> 7 3.64203E-01 9.91046E+00 -1.92207E+01 1.4460E-01 4.34E-01 0.00E+00 0.00E+00 4-> 8 3.97351E-01 1.08125E+01 -1.91876E+01 4.0028E-02 0.00E+00 1.20E-01 0.00E+00 3-> 8 3.97351E-01 1.08125E+01 -1.91876E+01 4.0028E-02 0.00E+00 0.00E+00 1.20E-01Without the coupling matrix, these would be the excitation energies, for both the spin-singlet and spin-triplet states. The coupling matrix modifies the eigenenergies, by mixing different electronic excitations, and also lift some degeneracies, e.g. the quadruplet formed by the combination of the degenerate states 3-4 and 6-7 that gives the excitation energies with 3.64203E-01 Ha in the above table.
Indeed, concerning the spin-singlet, the following excitation energies are obtained (see the next section of the output file):
TDDFT singlet excitation energies (at most 20 of them are printed), and corresponding total energies. Excit# (Ha) and (eV) total energy (Ha) major contributions 1 3.47952E-01 9.46826E+00 -1.923699E+01 0.83( 5-> 6) 0.17( 5-> 7) 2 3.48006E-01 9.46971E+00 -1.923693E+01 0.83( 5-> 7) 0.17( 5-> 6) 3 3.62425E-01 9.86208E+00 -1.922251E+01 0.99( 5-> 8) 0.00( 2-> 10) 4 3.64202E-01 9.91044E+00 -1.922074E+01 0.37( 3-> 7) 0.37( 4-> 6) 5 3.84223E-01 1.04553E+01 -1.920072E+01 0.37( 4-> 6) 0.37( 3-> 7) 6 3.84236E-01 1.04556E+01 -1.920070E+01 0.37( 4-> 7) 0.37( 3-> 6) 7 3.96699E-01 1.07947E+01 -1.918824E+01 0.99( 3-> 8) 0.01( 4-> 8) 8 3.96723E-01 1.07954E+01 -1.918822E+01 0.99( 4-> 8) 0.01( 3-> 8) 9 4.54145E-01 1.23579E+01 -1.913079E+01 1.00( 5-> 9) 0.00( 3-> 12) ...The excitation energies are numbered according to increasing energies, in Ha as well as in eV. The total energy is also given (adding excitation energy to the the ground-state energy), and finally, the two major contributions to each of these excitations are mentioned (size of the contribution then identification).
It is seen that the first and second excitations are degenerate
(numerical inaccuracies accounts for the meV difference), and mainly comes from
the first and second Kohn-Sham energy differences (between occupied state 5
and inoccupied states 6 and 7). This is also true for the third
excitation, that comes from the third Kohn-Sham energy difference (between occupied
state 5 and unoccupied state 8).
The quadruplet of Kohn-Sham energy differences, that was observed at 3.64203E-01 Ha,
has been split into one doublet and two singlets, with numbers 4 (the lowest singlet), 5-6
(the doublet) while the last singlet is not present in the 20 lowest excitations.
The list of oscillator strength is then provided.
Oscillator strengths : (elements smaller than 1.e-6 are set to zero) Excit# (Ha) Average XX YY ZZ XY XZ YZ 1 3.47952E-01 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.00E+00 0.00E+00 0.00E+00 2 3.48006E-01 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.00E+00 0.00E+00 0.00E+00 3 3.62425E-01 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.00E+00 0.00E+00 0.00E+00 4 3.64202E-01 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.00E+00 0.00E+00 0.00E+00 5 3.84223E-01 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.00E+00 0.00E+00 0.00E+00 6 3.84236E-01 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.00E+00 0.00E+00 0.00E+00 7 3.96699E-01 5.759E-02 0.000E+00 1.928E-03 1.709E-01 0.00E+00 0.00E+00 -1.81E-02 8 3.96723E-01 5.544E-02 0.000E+00 1.645E-01 1.855E-03 0.00E+00 0.00E+00 1.75E-02 9 4.54145E-01 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.00E+00 0.00E+00 0.00E+00 10 4.60223E-01 9.496E-02 2.849E-01 0.000E+00 0.000E+00 0.00E+00 0.00E+00 0.00E+00 ...The first six transitions are forbidden, with zero oscillator strength. The seventh and eighth transitions are allowed, with sizeable YY, YZ and ZZ components.
Next, one finds the excitation energies for the spin-triplet states :
TDDFT triplet excitation energies (at most 20 of them are printed), and corresponding total energies. Excit# (Ha) and (eV) total energy (Ha) major contributions 1 2.88423E-01 7.84838E+00 -1.929652E+01 0.82( 5-> 6) 0.18( 5-> 7) 2 2.88424E-01 7.84842E+00 -1.929652E+01 0.82( 5-> 7) 0.18( 5-> 6) 3 2.99762E-01 8.15693E+00 -1.928518E+01 0.37( 3-> 6) 0.37( 4-> 7) 4 3.33749E-01 9.08177E+00 -1.925119E+01 0.37( 4-> 6) 0.37( 3-> 7) 5 3.33809E-01 9.08339E+00 -1.925113E+01 0.37( 4-> 7) 0.37( 3-> 6) 6 3.36922E-01 9.16812E+00 -1.924802E+01 1.00( 5-> 8) 0.00( 2-> 10) 7 3.64202E-01 9.91045E+00 -1.922074E+01 0.37( 3-> 7) 0.37( 4-> 6) 8 3.90779E-01 1.06336E+01 -1.919416E+01 0.67( 3-> 8) 0.27( 2-> 6) 9 3.90834E-01 1.06351E+01 -1.919411E+01 0.67( 4-> 8) 0.27( 2-> 7) ...Spin-triplet energies are markedly lower than the corresponding spin-singlet energies. Also, the highest singlet derived from the Kohn-Sham quadruplet is now the excitation number 7. The oscillator strengths also follow. At this stage, we are in position to compare with experimental data, and try to improve the quality of our calculation.
To summarize our results, we obtain the following five lowest-lying spin-singlet excitation energies, with corresponding quantum numbers (that we derive from the knowledge of the Kohn-Sham states quantum numbers):
9.47 eV m=+1,-1 even parity (Pi_g state) 9.86 eV m=0 even parity (Sigma_g state) 9.91 eV m=0 odd parity (Sigma_u state) 10.46 eV m=+2,-2 odd parity (Delta_u state) 10.79 eV m=+1,-1 odd parity (Pi_u state)and the following five lowest-lying spin-triplet excitations energies, with corresponding quantum numbers :
7.85 eV m=+1,-1 even parity (Pi_g state) 8.16 eV m=0 odd parity (Sigma_u state) 9.08 eV m=+2,-2 odd parity (Delta_u state) 9.16 eV m=0 even parity (Sigma_g state) 9.91 eV m=0 odd parity (Sigma_u state)The quantum number related to the effect of a mirror plane, needed for Sigma states, could not be attributed on the sole basis of the knowledge of Kohn-Sham orbitals quantum numbers.
The lowest-lying experimental spin-singlet excitation energies, see table III of CasidaJCP1998, are as follows :
9.31 eV m=+1,-1 even parity (Pi_g state) 9.92 eV m=0 odd parity (Sigma_u- state) 10.27 eV m=+2,-2 odd parity (Delta_u state)and the lowest-lying experimental spin-triplet excitations energies are :
7.75 eV m=0 odd parity (Sigma_u+ state) 8.04 eV m=+1,-1 even parity (Pi_g state) 8.88 eV m=+2,-2 odd parity (Delta_u state) 9.67 eV m=0 odd parity (Sigma_u- state)In several cases, the agreement is quite satisfactory, on the order of 0.1-0.2 eV. However, there are also noticeable discrepancies. Indeed, we have to understand, in our simulation :
Still, the agreement between these TDDFT values and the experimental values is much better than anything that can be done on the sole basis of Kohn-Sham energy differences, that are (for spin-singlet and -triplet) :
8.46 eV m=+1,-1 even parity (Pi_g state) 9.36 eV m=0 odd parity (Sigma_u state) 9.91 eV m=0(twice),+2,-2 odd parity (Sigma_u and Delta_u states) 10.81 eV m=+1,-1 odd parity (Pi_u state)
We will start with the number of unoccupied states. The only input parameter to be changed in the input file is the value of nband2. The following results are obtained, for nband2 = 12, 30, 60, 100 and 150 (Energies given in eV):
Singlet 1 : 9.47 9.44 9.39 9.36 9.35 Singlet 2 : 9.86 9.74 9.68 9.66 9.66 Singlet 3 : 9.91 9.91 9.91 9.91 9.91 Singlet 4 : 10.46 10.45 10.44 10.44 10.43 Singlet 5 : 10.79 10.79 10.79 10.79 10.79 Triplet 1 : 7.85 7.84 7.83 7.82 7.82 Triplet 2 : 8.16 8.08 8.03 8.00 8.00 Triplet 3 : 9.08 9.07 9.05 9.05 9.04 Triplet 4 : 9.16 9.16 9.15 9.15 9.15 Triplet 5 : 9.91 9.91 9.91 9.91 9.91You might try to obtain one of these ... The computation with nband2=100 takes about 7 minutes on a 2.8 GHz PC, and gives a result likely converged within 0.01 eV. Let's have a look at these data. Unfortunately, none of the above-mentioned discrepancies with experimental data is resolved, although the difference between the first and second spin-triplet states decreases significantly. Although we see that at least 60 bands are needed to obtain results converged within 0.05 eV, we will continue to rely on 12 bands to try to understand the most important discrepancies, while keeping the CPU time to a low level.
We next try to increase the cut-off energy. Again, this is fairly easy. One can e.g. set up a double dataset loop. The following results are obtained, for ecut = 25, 35, 45, 55, 65, and 75 Ha :
Singlet 1 : 9.47 9.41 9.39 9.36 9.36 Singlet 2 : 9.86 9.83 9.78 9.76 9.76 Singlet 3 : 9.91 9.97 10.01 10.02 10.03 Singlet 4 : 10.46 10.37 10.32 10.30 10.29 Singlet 5 : 10.79 10.87 10.90 10.91 10.92 Triplet 1 : 7.85 7.79 7.76 7.74 7.73 Triplet 2 : 8.16 8.02 7.94 7.92 7.91 Triplet 3 : 9.08 8.98 8.92 8.90 8.89 Triplet 4 : 9.16 9.28 9.33 9.34 9.34 Triplet 5 : 9.91 9.83 9.78 9.77 9.76You might try to obtain one of these ... The computation with ecut=75 takes about 90 secs on a 2.8 GHz PC, and gives a result likely converged within 0.01 eV. Let us have a look at these data. Concerning the discrepancies with the experimental results, we see that the position of the second spin-singlet state has even worsened, the difference between the first and second spin-triplet states decreases, so that, together with an increase of nband, their order might become the correct one, and the fourth spin-triplet state energy has increased, but not enough.
We finally examine the effect of the cell size. Again, this is fairly easy. One can e.g. set up a double dataset loop. The following results are obtained, for acell = (6 5 5), (7 6 6), (8 7 7), (9 8 8), (10 9 9) and (12 11 11) :
Singlet 1 : 9.47 9.37 9.33 9.33 9.33 9.33 Singlet 2 : 9.86 9.78 9.84 9.91 9.96 10.03 Singlet 3 : 9.91 9.88 9.85 9.85 9.85 9.85 Singlet 4 : 10.46 10.41 10.38 10.37 10.37 10.37 Singlet 5 : 10.79 10.98 11.14 11.27 11.19 11.04 Triplet 1 : 7.85 7.75 7.72 7.71 7.72 7.72 Triplet 2 : 8.16 8.18 8.18 8.18 8.19 8.20 Triplet 3 : 9.08 9.07 9.06 9.06 9.06 9.06 Triplet 4 : 9.16 9.36 9.55 9.68 9.78 9.90 Triplet 5 : 9.91 9.88 9.85 9.85 9.85 9.85Obviously, the cell size plays an important role in the spurious appearance of the states, that was remarked when comparing against experimental data. Indeed, the singlet 2 and triplet 4 states energy increases strongly with the cell size, while all other states quickly stabilize (except the still higher singlet 5 state).
There is one lesson to be learned from that convergence study : the convergence of different states can be quite different. Usually, converging the lower excited states do not require too much effort, while it is quite difficult, especially concerning the supercell size, to converge higher states.
At this stage, we will simply stop this convergence study, and give the results of an ABINIT calculation using ecut 45 Hartree, acell 12 11 11, and 30 bands (not fully converged, though !), then compare the results with other LDA/TDLDA results (from CasidaJCP1998) and experimental results :
present Casida experimental Singlet Pi_g : 9.25 9.05 9.31 Singlet Sigma_u- : 9.72 9.63 9.92 Singlet Delta_u : 10.22 10.22 10.27 Triplet Sigma_u+ : 7.95 7.85 7.75 Triplet Pi_g : 7.64 7.54 8.04 Triplet Delta_u : 8.89 8.82 8.88 Triplet Sigma_u- : 9.72 9.63 9.67Our calculation is based on pseudopotentials, while Casida's calculation is an all-electron one. This fact might account for the 0.1-0.2 eV discrepancy between both calculations (it is of course the user's responsability to test the influence of different pseudopotentials on his/her calculations). The agreement with experimental data is on the order of 0.2 eV, with the exception of the Triplet Pi_g state (0.4 eV). In particular, we note that LDA/TDLDA is not able to get the correct ordering of the lower two triplet states ... One of our problems was intrinsic to the LDA/TDLDA approximation ...
In order to activate this procedure, set the value of ixc in dataset 1 to the SCF functional, and the value of ixc in dataset 2 to the XC functional to be used for the kernel. Use pseudopotentials that agree with the SCF functional.