SF TDDFT Examples - Open-Quantum-Platform/openqp GitHub Wiki
[input]
system=
8 0.000000000 0.000000000 -0.041061554
1 -0.533194329 0.533194329 -0.614469223
1 0.533194329 -0.533194329 -0.614469223
charge=0
runtype=energy
basis=6-31gs
functional=bhhlyp
method=tdhf
[guess]
type=huckel
[scf]
multiplicity=3
type=rohf
[tdhf]
type=sf
nstate=3
[input] Section
- system: This is the coordination of your system, your system's coordination can be achieved through two primary methods for OQP. The first method employs the Standard Cartesian format, as illustrated in the provided example. The second method utilizes the .XYZ format. To leverage the .XYZ format, save your coordination details in this format within your input folder, for instance, as H2O.xyz. Subsequently, it can be easily applied by specifying system=H2O.xyz in your input file. Here is an example of .XYZ format:
3
symmetry c1
O 0.000000000 0.000000000 -0.041061554
H -0.533194329 0.533194329 -0.614469223
H 0.533194329 -0.533194329 -0.614469223
-
charge: The total charge of the system. A value of 0 indicates that the molecule is neutral, with no net charge.
-
runtype: Specifies the type of calculation. energy means that the computation aims to determine the electronic energy of the molecule without performing geometry optimization or calculating properties like gradients or Hessians.
-
basis: The basis set used for the calculation, 6-31gs in this case. The 6-31gs is a split-valence basis set with polarization functions on heavy atoms, designed to provide a good balance between accuracy and computational cost. You can find all of the basis-sets supported by OQP within the basis_set folder.
Just for your information, you can see the 6-31g* basis set provided for Hydrogen and Oxygen atom within the GAMESS US format
#----------------------------------------------------------------------
# Basis Set Exchange
# Version v0.9.1
# https://www.basissetexchange.org
#----------------------------------------------------------------------
# Basis set: 6-31+G*
# Description: 6-31G + diffuse and polarization functions on heavy
# atoms
# Role: orbital
# Version: 1 (Data from Gaussian 09/GAMESS)
#----------------------------------------------------------------------
# HYDROGEN
S H
0.3349460434E-01 0.1873113696E+02
0.2347269535E+00 0.2825394365E+01
0.8137573261E+00 0.6401216923E+00
S H
1.0000000 0.1612777588E+00
# OXYGEN
S O
0.1831074430E-02 0.5484671660E+04
0.1395017220E-01 0.8252349460E+03
0.6844507810E-01 0.1880469580E+03
0.2327143360E+00 0.5296450000E+02
0.4701928980E+00 0.1689757040E+02
0.3585208530E+00 0.5799635340E+01
L O
-0.1107775495E+00 0.1553961625E+02 0.7087426823E-01
-0.1480262627E+00 0.3599933586E+01 0.3397528391E+00
0.1130767015E+01 0.1013761750E+01 0.7271585773E+00
L O
0.1000000000E+01 0.2700058226E+00 0.1000000000E+01
L O
0.1000000000E+01 0.8450000000E-01 0.1000000000E+01
D O
1.0000000 0.8000000000E+00
- functional: Specifies the DFT functional to be used. bhhlyp is a hybrid functional that combines Hartree-Fock exchange with B88 exchange and LYP correlation. It's known for its good performance in a variety of systems.
Just for your information, here are some more explanation on BHHLYP
The BHHLYP functional is unique in its approach to mixing exact exchange with DFT exchange-correlation terms. Specifically, it combines:
-
50% of exact exchange from Hartree-Fock theory, - 50% of exchange from the B88 functional (developed by Becke in 1988),
-
and correlation from the LYP functional (developed by Lee, Yang, and Parr).
This particular combination is designed to balance the need for accurate exchange energy representation with the computational efficiency and additional electron correlation effects provided by DFT.
- method: Indicates the computational method, tdhf for time-dependent Hartree-Fock.
[guess] Section
- type: The initial guess for the molecular orbitals. huckel suggests using a simple Hückel molecular orbital (HMO) theory-based guess, which is particularly useful for π-conjugated systems but can serve as a starting point for various molecular systems.
[scf] Section
-
multiplicity: The multiplicity of the system, given by 2S+1 where S is the total spin angular momentum. A multiplicity of 3 suggests a triplet state (S=1), indicating unpaired electrons and a potentially open-shell configuration.
-
type: The SCF calculation type, rohf for Restricted Open-Shell Hartree-Fock. ROHF methods are used for molecules with open-shell electronic configurations, providing a way to handle both closed-shell (paired electrons) and open-shell (unpaired electrons) components of the wavefunction.
[tdhf] Section
-
type: The sf (spin-flip) type denotes a focus on spin-flip transitions, where an electron changes its spin state from up to down or vice versa. This approach is particularly valuable for studying systems with open-shell character and for exploring excited states that are accessible through such spin transitions.
-
nstate: The number of states for which the energy will be calculated, including the ground state. A value of 3 means the calculation will cover the ground state and two excited states, providing insight into the low-lying electronic excitations of the molecule.
[input]
system=
8 0.000000000 0.000000000 -0.041061554
1 -0.533194329 0.533194329 -0.614469223
1 0.533194329 -0.533194329 -0.614469223
charge=0
runtype=grad
basis=6-31gs
functional=bhhlyp
method=tdhf
[guess]
type=huckel
[scf]
multiplicity=3
type=rohf
[tdhf]
type=sf
nstate=3
[properties]
grad=3
[input] Section
- runtype: Specifies the type of calculation, grad in this case. This means the calculation aims to compute the gradients of the energy with respect to the atomic positions, which are essential for understanding the forces experienced by the atoms and for subsequent molecular dynamics simulations or geometry optimizations.
[properties] Section
- grad: Specifies that the gradient calculation will be performed for the third state, likely referring to one of the excited states.
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