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quantum_package/man/excited_states.1

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.TH "EXCITED_STATES" "1" "Jan 16, 2019" "2.0" "Quantum Package"
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.SH NAME
excited_states \- | Quantum Package >
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It is possible to run excited states calculations with the quantum package. To
do this, set \fBdeterminants n_states\fP to the number of requested states.
The selection criterion will be the maximum of the selection criteria for each
state. If the Davidson diagonalization has difficulties to converge, increase
the \fBdavidson n_states_diag\fP value.
.sp
When computing multiple states, it is good to have the \fBdeterminants
s2_eig\fP flag \fBtrue\fP\&. This will force the Davidson algorithm to choose only
vectors with a value of \ewidehat{S^2} equal to \fBdeterminants expected_s2\fP\&.
Otherwise, different spin states will come out in the diagonalization.
.sp
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The \fIQuantum Package\fP doesnt take account of the symmetry. Due to numerical noise, excited
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states of different symmetries may enter in the calculation. Note that it is
possible to make state\-average calculation of states with different symmetries
and/or different spin multiplicities.
.sp
To include excited state of all possible symmetries, a simple trick is to
run a preliminary multi\-state CIS calculation using the CIS program,
and then running the selected FCI restarting from the CIS states, setting
\fBdeterminants read_wf\fP to \fBtrue\fP\&.
.sp
Usually, it is good practice to use state\-averaged natural MOs so that all
states have MOs of comparable quality. This allows for a faster convergence
of excitation energies.
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.sp
\fBSEE ALSO:\fP
.INDENT 0.0
.INDENT 3.5
The documentation of the \fBscf()\fP, \fBcis()\fP and \fBfci()\fP programs.
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.SH AUTHOR
A. Scemama, E. Giner
.SH COPYRIGHT
2018, A. Scemama, E. Giner
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