In this example, we show how to perform molecular dynamics of bulk water using the popular interatomic TIP3P potential (W. L. Jorgensen et. al.) and LAMMPS.

In [1]:

```
import numpy as np
%matplotlib inline
import matplotlib.pylab as plt
from pyiron.project import Project
import ase.units as units
import pandas
```

In [2]:

```
pr = Project("tip3p_water")
```

We will setup a cubic simulation box consisting of 27 water molecules density density is 1 g/cm$^3$. The target density is achieved by determining the required size of the simulation cell and repeating it in all three spatial dimensions

In [3]:

```
density = 1.0e-24 # g/A^3
n_mols = 27
mol_mass_water = 18.015 # g/mol
# Determining the supercell size size
mass = mol_mass_water * n_mols / units.mol # g
vol_h2o = mass / density # in A^3
a = vol_h2o ** (1./3.) # A
# Constructing the unitcell
n = int(round(n_mols ** (1. / 3.)))
dx = 0.7
r_O = [0, 0, 0]
r_H1 = [dx, dx, 0]
r_H2 = [-dx, dx, 0]
unit_cell = (a / n) * np.eye(3)
water = pr.create_atoms(elements=['H', 'H', 'O'],
positions=[r_H1, r_H2, r_O],
cell=unit_cell)
water.set_repeat([n, n, n])
water.plot3d()
```

In [4]:

```
water.get_chemical_formula()
```

Out[4]:

The initial water structure is obviously a poor starting point and requires equilibration (Due to the highly artificial structure a MD simulation with a standard time step of 1fs shows poor convergence). Molecular dynamics using a time step that is two orders of magnitude smaller allows us to generate an equilibrated water structure. We use the NVT ensemble for this calculation:

In [5]:

```
water_potential = pandas.DataFrame({
'Name': ['H2O_tip3p'],
'Filename': [[]],
'Model': ["TIP3P"],
'Species': [['H', 'O']],
'Config': [['# @potential_species H_O ### species in potential\n', '# W.L. Jorgensen et.al., The Journal of Chemical Physics 79, 926 (1983); https://doi.org/10.1063/1.445869\n', '#\n', '\n', 'units real\n', 'dimension 3\n', 'atom_style full\n', '\n', '# create groups ###\n', 'group O type 2\n', 'group H type 1\n', '\n', '## set charges - beside manually ###\n', 'set group O charge -0.830\n', 'set group H charge 0.415\n', '\n', '### TIP3P Potential Parameters ###\n', 'pair_style lj/cut/coul/long 10.0\n', 'pair_coeff * * 0.0 0.0 \n', 'pair_coeff 2 2 0.102 3.188 \n', 'bond_style harmonic\n', 'bond_coeff 1 450 0.9572\n', 'angle_style harmonic\n', 'angle_coeff 1 55 104.52\n', 'kspace_style pppm 1.0e-5\n', '\n']]
})
```

In [6]:

```
job_name = "water_slow"
ham = pr.create_job("Lammps", job_name)
ham.structure = water
ham.potential = water_potential
```

In [7]:

```
ham.calc_md(temperature=300,
n_ionic_steps=1e4,
time_step=0.01)
ham.run()
```

In [8]:

```
view = ham.animate_structure()
view
```

At the end of this simulation, we have obtained a structure that approximately resembles water. Now we increase the time step to get a reasonably equilibrated structure

In [9]:

```
# Get the final structure from the previous simulation
struct = ham.get_structure(iteration_step=-1)
job_name = "water_fast"
ham_eq = pr.create_job("Lammps", job_name)
ham_eq.structure = struct
ham_eq.potential = water_potential
ham_eq.calc_md(temperature=300,
n_ionic_steps=1e4,
n_print=10,
time_step=1)
ham_eq.run()
```

In [10]:

```
view = ham_eq.animate_structure()
view
```

We can now plot the trajectories

In [11]:

```
plt.plot(ham_eq["output/generic/energy_pot"])
plt.xlabel("Steps")
plt.ylabel("Potential energy [eV]");
```

In [12]:

```
plt.plot(ham_eq["output/generic/temperature"])
plt.xlabel("Steps")
plt.ylabel("Temperature [K]");
```

We will now use the `get_neighbors()`

function to determine structural properties from the computed trajectories. We take advantage of the fact that the TIP3P water model is a rigid water model which means the neighbors of each molecule never change. Therefore they need to be indexed only once

In [13]:

```
final_struct = ham_eq.get_structure(iteration_step=-1)
# Get the indices based on species
O_indices = final_struct.select_index("O")
H_indices = final_struct.select_index("H")
# Getting only the first two neighbors
neighbors = final_struct.get_neighbors(num_neighbors=2)
```

Every O atom has two H atoms as immediate neighbors. The distribution of this bond length is obtained by:

In [14]:

```
bins = np.linspace(0.5, 1.5, 100)
plt.hist(neighbors.distances[O_indices].flatten(), bins=bins)
plt.xlim(0.5, 1.5)
plt.xlabel(r"d$_{OH}$ [$\AA$]")
plt.ylabel("Count");
```

We need to extend the analysis to go beyond nearest neighbors. We do this by controlling the cutoff distance

In [15]:

```
neighbors = final_struct.get_neighbors(cutoff_radius=8)
```

In [16]:

```
neigh_indices = np.hstack(neighbors.indices[O_indices])
neigh_distances = np.hstack(neighbors.distances[O_indices])
```

One is often intended in an element specific pair correlation function. To obtain for example, the O-O coordination function, we do the following:

In [17]:

```
# Getting the neighboring Oxyhen indices
O_neigh_indices = np.in1d(neigh_indices, O_indices)
O_neigh_distances = neigh_distances[O_neigh_indices]
```

In [18]:

```
bins = np.linspace(1, 5, 100)
count = plt.hist(O_neigh_distances, bins=bins)
plt.xlim(2, 4)
plt.title("O-O pair correlation")
plt.xlabel(r"d$_{OO}$ [$\AA$]")
plt.ylabel("Count");
```

In [ ]:

```
```