pair_style reaxff command¶
Accelerator Variants: reaxff/kk, reaxff/omp
pair_style reaxff cfile keyword value
cfile = NULL or name of a control file
zero or more keyword/value pairs may be appended
keyword = checkqeq or lgvdw or safezone or mincap or minhbonds or tabulate or list/blocking checkqeq value = yes or no = whether or not to require qeq/reaxff or acks2/reaxff fix enobonds value = yes or no = whether or not to tally energy of atoms with no bonds lgvdw value = yes or no = whether or not to use a low gradient vdW correction safezone = factor used for array allocation mincap = minimum size for array allocation minhbonds = minimum size use for storing hydrogen bonds tabulate value = size of interpolation table for Lennard-Jones and Coulomb interactions list/blocking value = yes or no = whether or not to use "blocking" scheme for bond list build
pair_style reaxff NULL pair_style reaxff controlfile checkqeq no pair_style reaxff NULL lgvdw yes pair_style reaxff NULL safezone 1.6 mincap 100 pair_coeff * * ffield.reax C H O N
Style reaxff computes the ReaxFF potential of van Duin, Goddard and co-workers. ReaxFF uses distance-dependent bond-order functions to represent the contributions of chemical bonding to the potential energy. There is more than one version of ReaxFF. The version implemented in LAMMPS uses the functional forms documented in the supplemental information of the following paper: (Chenoweth et al., 2008). The version integrated into LAMMPS matches the version of ReaxFF From Summer 2010. For more technical details about the pair reaxff implementation of ReaxFF, see the (Aktulga) paper. The reaxff style was initially implemented as a stand-alone C code and is now converted to C++ and integrated into LAMMPS as a package.
The reaxff/kk style is a Kokkos version of the ReaxFF potential that is derived from the reaxff style. The Kokkos version can run on GPUs and can also use OpenMP multithreading. For more information about the Kokkos package, see Packages details and Speed kokkos doc pages. One important consideration when using the reaxff/kk style is the choice of either half or full neighbor lists. This setting can be changed using the Kokkos package command.
The reaxff style differs from the (obsolete) “pair_style reax” command in the implementation details. The reax style was a Fortran library, linked to LAMMPS. The reax style has been removed from LAMMPS after the 12 December 2018 version.
LAMMPS provides several different versions of ffield.reax in its potentials dir, each called potentials/ffield.reax.label. These are documented in potentials/README.reax. The default ffield.reax contains parameterizations for the following elements: C, H, O, N.
The format of these files is identical to that used originally by van Duin. We have tested the accuracy of pair_style reaxff potential against the original ReaxFF code for the systems mentioned above. You can use other ffield files for specific chemical systems that may be available elsewhere (but note that their accuracy may not have been tested).
We do not distribute a wide variety of ReaxFF force field files with LAMMPS. Adri van Duin’s group at PSU is the central repository for this kind of data as they are continuously deriving and updating parameterizations for different classes of materials. You can submit a contact request at the Materials Computation Center (MCC) website https://www.mri.psu.edu/materials-computation-center/connect-mcc, describing the material(s) you are interested in modeling with ReaxFF. They can tell you what is currently available or what it would take to create a suitable ReaxFF parameterization.
The cfile setting can be specified as NULL, in which case default settings are used. A control file can be specified which defines values of control variables. Some control variables are global parameters for the ReaxFF potential. Others define certain performance and output settings. Each line in the control file specifies the value for a control variable. The format of the control file is described below.
The LAMMPS default values for the ReaxFF global parameters correspond to those used by Adri van Duin’s stand-alone serial code. If these are changed by setting control variables in the control file, the results from LAMMPS and the serial code will not agree.
Examples using pair_style reaxff are provided in the examples/reax subdirectory.
Use of this pair style requires that a charge be defined for every atom. See the atom_style and read_data commands for details on how to specify charges.
The ReaxFF parameter files provided were created using a charge equilibration (QEq) model for handling the electrostatic interactions. Therefore, by default, LAMMPS requires that either the fix qeq/reaxff or the fix qeq/shielded or fix acks2/reaxff command be used with pair_style reaxff when simulating a ReaxFF model, to equilibrate the charges each timestep.
Using the keyword checkqeq with the value no turns off the check for the QEq fixes, allowing a simulation to be run without charge equilibration. In this case, the static charges you assign to each atom will be used for computing the electrostatic interactions in the system. See the fix qeq/reaxff or fix qeq/shielded or fix acks2/reaxff command documentation for more details.
Using the optional keyword lgvdw with the value yes turns on the low-gradient correction of ReaxFF for long-range London Dispersion, as described in the (Liu) paper. The bundled force field file ffield.reax.lg is designed for this correction, and is trained for several energetic materials (see “Liu”). When using lgvdw yes, the recommended value for parameter thb is 0.01, which can be set in the control file. Note: Force field files are different for the original or lg corrected pair styles, using the wrong ffield file generates an error.
Using the optional keyword enobonds with the value yes, the energy of atoms with no bonds (i.e. isolated atoms) is included in the total potential energy and the per-atom energy of that atom. If the value no is specified then the energy of atoms with no bonds is set to zero. The latter behavior is usual not desired, as it causes discontinuities in the potential energy when the bonding of an atom drops to zero.
Optional keywords safezone, mincap, and minhbonds are used for allocating reaxff arrays. Increasing these values can avoid memory problems, such as segmentation faults and bondchk failed errors, that could occur under certain conditions. These keywords are not used by the Kokkos version, which instead uses a more robust memory allocation scheme that checks if the sizes of the arrays have been exceeded and automatically allocates more memory.
The keyword tabulate controls the size of interpolation table for Lennard-Jones and Coulomb interactions. Tabulation may also be set in the control file (see below). If tabulation is set in both the input script and the control file, the value in the control file will be ignored. A size of 10000 is typically used for the interpolation table. A value of 0 means no tabulation will be used.
The keyword list/blocking is only supported by the Kokkos version of ReaxFF and ignored otherwise. Setting the value to yes enables the “blocking” scheme (dynamically building interaction lists) for the ReaxFF bond neighbor list. This reduces the number of empty interactions and can improve performance in some cases (e.g. large number of atoms/GPU on AMD hardware). It is also enabled by default when running the CPU with Kokkos.
The thermo variable evdwl stores the sum of all the ReaxFF potential energy contributions, with the exception of the Coulombic and charge equilibration contributions which are stored in the thermo variable ecoul. The output of these quantities is controlled by the thermo command.
This pair style tallies a breakdown of the total ReaxFF potential energy into sub-categories, which can be accessed via the compute pair command as a vector of values of length 14. The 14 values correspond to the following sub-categories (the variable names in italics match those used in the original FORTRAN ReaxFF code):
eb = bond energy
ea = atom energy
elp = lone-pair energy
emol = molecule energy (always 0.0)
ev = valence angle energy
epen = double-bond valence angle penalty
ecoa = valence angle conjugation energy
ehb = hydrogen bond energy
et = torsion energy
eco = conjugation energy
ew = van der Waals energy
ep = Coulomb energy
efi = electric field energy (always 0.0)
eqeq = charge equilibration energy
To print these quantities to the log file (with descriptive column headings) the following commands could be included in an input script:
compute reax all pair reaxff variable eb equal c_reax variable ea equal c_reax [...] variable eqeq equal c_reax thermo_style custom step temp epair v_eb v_ea [...] v_eqeq
Only a single pair_coeff command is used with the reaxff style which specifies a ReaxFF potential file with parameters for all needed elements. These are mapped to LAMMPS atom types by specifying N additional arguments after the filename in the pair_coeff command, where N is the number of LAMMPS atom types:
N indices = ReaxFF elements
The filename is the ReaxFF potential file.
In the ReaxFF potential file, near the top, after the general parameters, is the atomic parameters section that contains element names, each with a couple dozen numeric parameters. If there are M elements specified in the ffield file, think of these as numbered 1 to M. Each of the N indices you specify for the N atom types of LAMMPS atoms must be an integer from 1 to M. Atoms with LAMMPS type 1 will be mapped to whatever element you specify as the first index value, etc. If a mapping value is specified as NULL, the mapping is not performed. This can be used when the reaxff style is used as part of the hybrid pair style. The NULL values are placeholders for atom types that will be used with other potentials.
As an example, say your LAMMPS simulation has 4 atom types and the elements are ordered as C, H, O, N in the ffield file. If you want the LAMMPS atom type 1 and 2 to be C, type 3 to be N, and type 4 to be H, you would use the following pair_coeff command:
pair_coeff * * ffield.reax C C N H
The format of a line in the control file is as follows:
and it may be followed by an “!” character and a trailing comment.
If the value of a control variable is not specified, then default values are used. What follows is the list of variables along with a brief description of their use and default values.
Output files produced by pair_style reaxff carry this name + extensions specific to their contents. Partial energies are reported with a “.pot” extension, while the trajectory file has “.trj” extension.
To improve performance, long range interactions can optionally be tabulated (0 means no tabulation). Value of this variable denotes the size of the long range interaction table. The range from 0 to long range cutoff (defined in the ffield file) is divided into tabulate_long_range points. Then at the start of simulation, we fill in the entries of the long range interaction table by computing the energies and forces resulting from van der Waals and Coulomb interactions between every possible atom type pairs present in the input system. During the simulation we consult to the long range interaction table to estimate the energy and forces between a pair of atoms. Linear interpolation is used for estimation. (default value = 0)
Denotes the frequency (in number of steps) of writes into the partial energies file. (default value = 0)
Denotes the near neighbors cutoff (in Angstroms) regarding the bonded interactions. (default value = 5.0)
Denotes the cutoff distance (in Angstroms) for hydrogen bond interactions.(default value = 7.5. A value of 0.0 turns off hydrogen bonds)
is the threshold used in determining what is a physical bond, what is not. Bonds and angles reported in the trajectory file rely on this cutoff. (default value = 0.3)
cutoff value for the strength of bonds to be considered in three body interactions. (default value = 0.001)
cutoff value for the strength of bond order products to be considered in three body interactions. (default value = 0.00001)
Frequency of writes into the trajectory file. (default value = 0)
Title of the trajectory - not the name of the trajectory file.
1 means print only atomic positions + charge (default = 0)
1 adds net forces to atom lines in the trajectory file (default = 0)
1 adds atomic velocities to atoms line (default = 0)
1 prints bonds in the trajectory file (default = 0)
1 prints angles in the trajectory file (default = 0)
Mixing, shift, table, tail correction, restart, rRESPA info¶
This pair style does not support the pair_modify mix, shift, table, and tail options.
This pair style does not write its information to binary restart files, since it is stored in potential files. Thus, you need to re-specify the pair_style and pair_coeff commands in an input script that reads a restart file.
This pair style can only be used via the pair keyword of the run_style respa command. It does not support the inner, middle, outer keywords.
Styles with a gpu, intel, kk, omp, or opt suffix are functionally the same as the corresponding style without the suffix. They have been optimized to run faster, depending on your available hardware, as discussed on the Accelerator packages page. The accelerated styles take the same arguments and should produce the same results, except for round-off and precision issues.
These accelerated styles are part of the GPU, INTEL, KOKKOS, OPENMP, and OPT packages, respectively. They are only enabled if LAMMPS was built with those packages. See the Build package page for more info.
You can specify the accelerated styles explicitly in your input script by including their suffix, or you can use the -suffix command-line switch when you invoke LAMMPS, or you can use the suffix command in your input script.
See the Accelerator packages page for more instructions on how to use the accelerated styles effectively.
This pair style is part of the REAXFF package. It is only enabled if LAMMPS was built with that package. See the Build package page for more info.
The ReaxFF potential files provided with LAMMPS in the potentials directory are parameterized for real units. You can use the ReaxFF pair style with any LAMMPS units, but you would need to create your own potential file with coefficients listed in the appropriate units if your simulation does not use “real” units.
The keyword defaults are checkqeq = yes, enobonds = yes, lgvdw = no, safezone = 1.2, mincap = 50, minhbonds = 25, tabulate = 0, list/blocking = yes on CPU, no on GPU.
(Chenoweth_2008) Chenoweth, van Duin and Goddard, Journal of Physical Chemistry A, 112, 1040-1053 (2008).
(Aktulga) Aktulga, Fogarty, Pandit, Grama, Parallel Computing, 38, 245-259 (2012).
(Liu) L. Liu, Y. Liu, S. V. Zybin, H. Sun and W. A. Goddard, Journal of Physical Chemistry A, 115, 11016-11022 (2011).