pair_style smtbq command


pair_style smtbq


pair_style smtbq
pair_coeff * * ffield.smtbq.Al2O3 O Al


This pair stylecomputes a variable charge SMTB-Q (Second-Moment tight-Binding QEq) potential as described in SMTB-Q_1 and SMTB-Q_2. Briefly, the energy of metallic-oxygen systems is given by three contributions:


where E<sub>tot</sub> is the total potential energy of the system, E<sub>ES</sub> is the electrostatic part of the total energy, E<sub>OO</sub> is the interaction between oxygens and E<sub>MO</sub> is a short-range interaction between metal and oxygen atoms. This interactions depend on interatomic distance r<sub>ij</sub> and/or the charge Q<sub>i</sub> of atoms i. Cut-off function enables smooth convergence to zero interaction.

The parameters appearing in the upper expressions are set in the ffield.SMTBQ.Syst file where Syst corresponds to the selected system (e.g. field.SMTBQ.Al2O3). Examples for TiO<sub>2</sub>, Al<sub>2</sub>O<sub>3</sub> are provided. A single pair_coeff command is used with the SMTBQ styles which provides the path to the potential file with parameters for needed elements. These are mapped to LAMMPS atom types by specifying additional arguments after the potential filename in the pair_coeff command. Note that atom type 1 must always correspond to oxygen atoms. As an example, to simulate a TiO2 system, atom type 1 has to be oxygen and atom type 2 Ti. The following pair_coeff command should then be used:

pair_coeff * * PathToLammps/potentials/ffield.smtbq.TiO2 O Ti

The electrostatic part of the energy consists of two components

self-energy of atom i in the form of a second order charge dependent polynomial and a long-range Coulombic electrostatic interaction. The latter uses the wolf summation method described in Wolf, spherically truncated at a longer cutoff, R<sub>coul</sub>. The charge of each ion is modeled by an orbital Slater which depends on the principal quantum number (n) of the outer orbital shared by the ion.

Interaction between oxygen, E<sub>OO</sub>, consists of two parts, an attractive and a repulsive part. The attractive part is effective only at short range (< r<sub>2</sub><sup>OO</sup>). The attractive contribution was optimized to study surfaces reconstruction (e.g. SMTB-Q_2 in TiO<sub>2</sub>) and is not necessary for oxide bulk modeling. The repulsive part is the Pauli interaction between the electron clouds of oxygen. The Pauli repulsion and the coulombic electrostatic interaction have same cut off value. In the ffield.SMTBQ.Syst, the keyword ‘buck’ allows to consider only the repulsive O-O interactions. The keyword ‘buckPlusAttr’ allows to consider the repulsive and the attractive O-O interactions.

The short-range interaction between metal-oxygen, E<sub>MO</sub> is based on the second moment approximation of the density of states with a N-body potential for the band energy term, E<sup>i</sup><sub>cov</sub>, and a Born-Mayer type repulsive terms as indicated by the keyword ‘second_moment’ in the ffield.SMTBQ.Syst. The energy band term is given by:


where &#951<sub>i</sub> is the stoichiometry of atom i, &#948Q<sub>i</sub> is the charge delocalization of atom i, compared to its formal charge Q<sup>F</sup><sub>i</sub>. n<sub>0</sub>, the number of hybridized orbitals, is calculated with to the atomic orbitals shared d<sub>i</sub> and the stoichiometry &#951<sub>i</sub>. r<sub>c1</sub> and r<sub>c2</sub> are the two cutoff radius around the fourth neighbors in the cutoff function.

In the formalism used here, &#958<sup>0</sup> is the energy parameter. &#958<sup>0</sup> is in tight-binding approximation the hopping integral between the hybridized orbitals of the cation and the anion. In the literature we find many ways to write the hopping integral depending on whether one takes the point of view of the anion or cation. These are equivalent vision. The correspondence between the two visions is explained in appendix A of the article in the SrTiO<sub>3</sub> SMTB-Q_3 (parameter &#946 shown in this article is in fact the &#946<sub>O</sub>). To summarize the relationship between the hopping integral &#958<sup>0</sup> and the others, we have in an oxide C<sub>n</sub>O<sub>m</sub> the following relationship:


Thus parameter &#956, indicated above, is given by : &#956 = (&#8730n + &#8730m) &#8260 2

The potential offers the possibility to consider the polarizability of the electron clouds of oxygen by changing the slater radius of the charge density around the oxygens through the parameters rBB, rB and rS in the ffield.SMTBQ.Syst. This change in radius is performed according to the method developed by E. Maras SMTB-Q_2. This method needs to determine the number of nearest neighbors around the oxygen. This calculation is based on first (r<sub>1n</sub>) and second (r<sub>2n</sub>) distances neighbors.

The SMTB-Q potential is a variable charge potential. The equilibrium charge on each atom is calculated by the electronegativity equalization (QEq) method. See Rick for further detail. One can adjust the frequency, the maximum number of iterative loop and the convergence of the equilibrium charge calculation. To obtain the energy conservation in NVE thermodynamic ensemble, we recommend to use a convergence parameter in the interval 10<sup>-5</sup> - 10<sup>-6</sup> eV.

The ffield.SMTBQ.Syst files are provided for few systems. They consist of nine parts and the lines beginning with ‘#’ are comments (note that the number of comment lines matter). The first sections are on the potential parameters and others are on the simulation options and might be modified. Keywords are character type and must be enclosed in quotation marks (‘’).

  1. Number of different element in the oxide:
  • N<sub>elem</sub>= 2 or 3
  • Divided line
  1. Atomic parameters

For the anion (oxygen)

  • Name of element (char) and stoichiometry in oxide
  • Formal charge and mass of element
  • Principal quantic number of outer orbital (n), electronegativity (&#967<sup>0</sup><sub>i</simulationub>) and hardness (J<sup>0</sup><sub>i</sub>)
  • Ionic radius parameters : max coordination number (coordBB = 6 by default), bulk coordination number (coordB), surface coordination number (coordS) and rBB, rB and rS the slater radius for each coordination number. (<b>note : If you don’t want to change the slater radius, use three identical radius values</b>)
  • Number of orbital shared by the element in the oxide (d<sub>i</sub>)
  • Divided line

For each cations (metal):

  • Name of element (char) and stoichiometry in oxide
  • Formal charge and mass of element
  • Number of electron in outer orbital (ne), electronegativity (&#967<sup>0</sup><sub>i</simulationub>), hardness (J<sup>0</sup><sub>i</sub>) and r<sub>Salter</sub> the slater radius for the cation.
  • Number of orbitals shared by the elements in the oxide (d<sub>i</sub>)
  • Divided line
  1. Potential parameters:
  • Keyword for element1, element2 and interaction potential (‘second_moment’ or ‘buck’ or ‘buckPlusAttr’) between element 1 and 2. If the potential is ‘second_moment’, specify ‘oxide’ or ‘metal’ for metal-oxygen or metal-metal interactions respectively.
  • Potential parameter: <pre><br/> If type of potential is ‘second_moment’ : A (eV), p, &#958<sup>0</sup> (eV) and q <br/> r<sub>c1</sub> (&#197), r<sub>c2</sub> (&#197) and r<sub>0</sub> (&#197) <br/> If type of potential is ‘buck’ : C (eV) and &#961 (&#197) <br/> If type of potential is ‘buckPlusAttr’ : C (eV) and &#961 (&#197) <br/> D (eV), B (&#197<sup>-1</sup>), r<sub>1</sub><sup>OO</sup> (&#197) and r<sub>2</sub><sup>OO</sup> (&#197) </pre>
  • Divided line
  1. Tables parameters:
  • Cutoff radius for the Coulomb interaction (R<sub>coul</sub>)
  • Starting radius (r<sub>min</sub> = 1,18845 &#197) and increments (dr = 0,001 &#197) for creating the potential table.
  • Divided line
  1. Rick model parameter:
  • Nevery : parameter to set the frequency (1/Nevery) of the charge resolution. The charges are evaluated each Nevery time steps.
  • Max number of iterative loop (loopmax) and precision criterion (prec) in eV of the charge resolution
  • Divided line
  1. Coordination parameter:
  • First (r<sub>1n</sub>) and second (r<sub>2n</sub>) neighbor distances in &#197
  • Divided line
  1. Charge initialization mode:
  • Keyword (QInitMode) and initial oxygen charge (Q<sub>init</sub>). If keyword = ‘true’, all oxygen charges are initially set equal to Q<sub>init</sub>. The charges on the cations are initially set in order to respect the neutrality of the box. If keyword = ‘false’, all atom charges are initially set equal to 0 if you use “create_atom”#create_atom command or the charge specified in the file structure using read_data command.
  • Divided line
  1. Mode for the electronegativity equalization (Qeq)
  • Keyword mode: <pre> <br/> QEqAll (one QEq group) | no parameters <br/> QEqAllParallel (several QEq groups) | no parameters <br/> Surface | zlim (QEq only for z>zlim) </pre>
  • Parameter if necessary
  • Divided line
  1. Verbose
  • If you want the code to work in verbose mode or not : ‘true’ or ‘false’
  • If you want to print or not in file ‘Energy_component.txt’ the three main contributions to the energy of the system according to the description presented above : ‘true’ or ‘false’ and N<sub>Energy</sub>. This option writes in file every N<sub>Energy</sub> time step. If the value is ‘false’ then N<sub>Energy</sub> = 0. The file take into account the possibility to have several QEq group g then it writes: time step, number of atoms in group g, electrostatic part of energy, E<sub>ES</sub>, the interaction between oxygen, E<sub>OO</sub>, and short range metal-oxygen interaction, E<sub>MO</sub>.
  • If you want to print in file ‘Electroneg_component.txt’ the electronegativity component (&#8706E<sub>tot</sub> &#8260&#8706Q<sub>i</sub>) or not: ‘true’ or ‘false’ and N<sub>Electroneg</sub>.This option writes in file every N<sub>Electroneg</sub> time step. If the value is ‘false’ then N<sub>Electroneg</sub> = 0. The file consist in atom number i, atom type (1 for oxygen and # higher than 1 for metal), atom position: x, y and z, atomic charge of atom i, electrostatic part of atom i electronegativity, covalent part of atom i electronegativity, the hopping integral of atom i (Z&#946<sup>2</sup>)<sub>i<sub> and box electronegativity.


This last option slows down the calculation dramatically. Use only with a single processor simulation.

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 needs 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.


This pair style is part of the USER-SMTBQ package and is only enabled if LAMMPS is built with that package. See the Making LAMMPS section for more info.

This potential requires using atom type 1 for oxygen and atom type higher than 1 for metal atoms.

This pair style requires the newton setting to be “on” for pair interactions.

The SMTB-Q potential files provided with LAMMPS (see the potentials directory) are parameterized for metal units.

Citing this work:

Please cite related publication: N. Salles, O. Politano, E. Amzallag and R. Tetot, Comput. Mater. Sci. 111 (2016) 181-189

(SMTB-Q_1) N. Salles, O. Politano, E. Amzallag, R. Tetot, Comput. Mater. Sci. 111 (2016) 181-189

(SMTB-Q_2) E. Maras, N. Salles, R. Tetot, T. Ala-Nissila, H. Jonsson, J. Phys. Chem. C 2015, 119, 10391-10399

(SMTB-Q_3) R. Tetot, N. Salles, S. Landron, E. Amzallag, Surface Science 616, 19-8722 28 (2013)

(Wolf) D. Wolf, P. Keblinski, S. R. Phillpot, J. Eggebrecht, J Chem Phys, 110, 8254 (1999).

(Rick) S. W. Rick, S. J. Stuart, B. J. Berne, J Chem Phys 101, 6141 (1994).