Whereas the FF procedure described in Section 10.12.2 is a
straightforward, finite-difference implementation of the derivatives suggested
in Eq. (10.106), in the Romberg procedure
279
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one
combines energy values obtained for a succession of external electric
fields with amplitudes that form a geometric progression:
| (10.107) |
The FF expressions are obtained by combining truncated Taylor expansions of the energy with different amplitudes and/or external field directions. For example, in the case of the diagonal -tensor components the Romberg FF expression is
| (10.108) |
The field index refers to the possible field directions, i.e., , or . Truncation of the Taylor expansions means that the results are contaminated by higher-order hyperpolarizabilities, and to remove this contamination, successive “Romberg iterations” are performed using a recursive expression. For a component of a (hyper)polarizability tensor , the recursive expression is
| (10.109) |
This expression leads to a triangular Romberg table enabling monitoring of the
convergence of the numerical derivative.
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As with any finite-difference procedure, the FF method for computing (hyper)polarizabilities is sensitive to the details of numerical differentiation. The Romberg procedure allows one to find a field window, defined by its upper and lower bounds, where the finite-difference procedure is stable. Energy values for field amplitudes below that window suffer from too-large round-off errors, which are proportional to the energy convergence threshold. The upper bound is imposed by the critical field amplitude corresponding to the intersection between the ground and excited-state energies. In the Romberg procedure, this stability window defines a sub-triangle, determination of which is the primary goal in analyzing Romberg tables.
The automatic procedure based on the analysis of field amplitude errors is implemented in scripts provided with Q-Chem’s distribution. The field amplitude error is defined as the difference between -values obtained for consecutive field amplitudes at the same Romberg iteration:
| (10.110) |
By virtue of Romberg’s recursive expression, the field error is expected to decrease with each iteration. Convergence of the Romberg procedure can be probed using the iteration (order) error, defined as
| (10.111) |
Automatic analysis of these quantities is described in detail in
Ref.
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.
Note: • The automatic procedure can fail if the field window is not chosen wisely. • The Romberg procedure can be performed either for one specific diagonal direction or for all Cartesian components. In the case of the second hyperpolarizability, only the , components are available.
To perform Romberg calculations of (hyper)polarizabilities, the following utilities are in the $QC/bin/tools/Romberg directory:
input-Q-Chem-t-rex.sh
parse-t-rex.sh
input-Q-Chem-t-rex-3.0
romberg_tddft_read
romberg_eom_read
T-REX-3.0.3
and this directory must be manually added to the $PATH environment variable depending on the shell being used:
# bash syntax for ~/.bashrc: export PATH="$QC/bin/tools/Romberg:$PATH" # csh/tcsh syntax for ~/.cshrc: set path=($QC/bin/tools/Romberg $path)
To run the calculation, create an input called input that specifies your molecule, an electronic structure method, and several additional $rem variables that
turn off symmetry (INTEGRAL_SYMMETRY and CC_SYMMETRY for CC/EOM calculations),
request higher-precision printing (CC_PRINT_PREC), and
set up very tight convergence (SCF_CONVERGENCE, CC_CONVERGENCE, EOM_DAVIDSON_CONVERGENCE, etc.).
An example of an input file is given below.
Example 10.50 Input for Romberg calculations of the ethylene molecule using B3LYP.
$molecule 0 1 C 0.00000000 0.00000000 -0.66880000 H 0.94859916 0.00000000 -1.19917145 H -0.94859916 0.00000000 -1.19917145 C -0.00000000 0.00000000 0.66880000 H -0.54409413 0.77704694 1.19917145 H 0.54409413 -0.77704694 1.19917145 $end $rem BASIS = sto-3g EXCHANGE = B3lyp SCF_CONVERGENCE = 13 Need tight convergence for finite field calculations SCF_MAX_CYCLES = 200 integral_symmetry = false All symmetries need to be turned off CC_PRINT_PREC = 16 16 decimal points of total energies will be printed $end
Run the script input-Q-Chem-t-rex.sh and answer the questions regarding the parameters of the geometrical progression of field amplitudes (see example below). The script will create multiple input files for the FF calculations based on the input file template that you provided. The file name that is requested serves as a prefix to each automatically-generated FF input file. For example, if you specify the filename as water, input files named water001.inp, water002.inp, … will be generated. These must be run independently of the Romberg procedure, such as on a computing cluster, or locally with GNU parallel or xargs. For example, with GNU parallel, to run 6 Q-Chem jobs at a time, each with 4 threads,
ls hello*.inp | parallel -j6 ’qchem -nt 4 {.}.inp {.}.out’
After running the calculations, parse the output files using the script parse-t-rex.sh. Then run the T-REX program. Answer the the questions to compute the dipole moment and (hyper)polarizabilities (see example below).
Romberg differentiation is only available for methods where printing the total energy to high precision has been enabled. In the current version of Q-Chem, CC_PRINT_PREC is implemented for the following methods: HF, DFT, MP2, RI-MP2, MP3, CCD, CCSD, CCSD(T), QCISD, QCISD(T), TDDFT, and EOM-CCSD.
Note: When using excited-state methods such as TDDFT, CIS, and EOM-CC, state ordering may switch when the external field is large.
With the T-REX program, you can compute the static dipole moment, polarizability, and first and second hyperpolarizabilities for one specific diagonal direction or for all Cartesian components, except that second hyperpolarizabilities are limited to and components. When computing all the components, you can obtain the norm of the dipole moment and polarizability, the Hyper-Rayleigh scattering first hyperpolarizability, the mean of the second hyperpolarizability, and other information
Put the sample input file (given above) for a DFT calculation in the new directory; the name of the input file should be input. Run the input-Q-Chem-t-rex.sh script. The following questions are asked:
Components: x=1 y=2 z=3 all_beta=4 all_alpha=5 4 File name eth- Number of field amplitudes 5 Smallest field amplitude F_0 0.0004 a (F_k=a^k F_0) 2.0 Number of files created 101
In this example, the answers correspond to FF calculations for and for a geometric progression () of external field amplitudes. The calculation is set up for all the components, with the input files eth-001.inp, eth-002.inp, eth-003.inp, …, generated, where the exact number of inputs generated depends on the chosen geometric progression.
After the individual FF calculations (i.e., after executing Q-Chem jobs for all generated inputs), parse the outputs using the parse-t-rex.sh script. The energies are written in a file called prelogfile.
Run the T-REX program and answer the questions:
Components: x=1 y=2 z=3 all_beta=4 4 Number of methods 1 Number of field amplitudes k_max+1 5 Smallest field amplitude F_0 0.0004 Step-size a 2.0
The energies are ordered in a file called logfile and the results are printed in the results file.