pymdkit 1.1.7

A unified command-line toolkit for atomistic / MD structure workflows.

pymdkit

A single command-line tool that bundles a collection of atomistic / molecular-dynamics structure scripts behind one executable: pymdkit. Instead of copying individual scripts into each working folder and running python some_script.py, you install pymdkit once and call any tool from anywhere as pymdkit <command> [options].

Every command exposes named --flags (no positional guessing), and each underlying script is still runnable on its own.

Install

Create a clean conda environment, activate it, then install pymdkit with pip:

conda create -n pymdkit python=3.10
conda activate pymdkit
pip install pymdkit

This installs the pymdkit command into the active conda environment, together with its dependencies (numpy, scipy, ase, pymatgen, pyxtal, mp_api, gemmi, tqdm).

Verify:

pymdkit --version
pymdkit --help                   # lists every command
pymdkit <command> --help         # shows that command's flags

Commands

Commands that transform structures accept either a single file (-i/-o) or a whole folder (-if/-of); commands that analyse VASP runs scan the current directory for job sub-folders automatically.

Command	What it does
add-groups	Tag atoms with a GPUMD group index by element order
electrostatic-energy	Compute CIF electrostatic energy with pymatgen EwaldSummation
ehull	Auto-detect VASP job folders and compute E_hull vs Materials Project
final-energy	List VASP job final energies from lowest to highest
gather-contcar	Collect CONTCARs from VASP job folders into one folder, renamed <folder>.vasp
msd	Diffusivity & conductivity from GPUMD MSD jobs (auto-scans <structure>/<temp>/)
vasp2xyz	Collect SCF-converged VASP job folders (any name) into one extxyz file
submit-vasp	Submit/resubmit VASP job folders while limiting active queue jobs
rmsd	Compute RMSD between two structure files, or all pairs in a folder
select-candidate	Split a NEP training set into candidate/accurate sets by energy error
stru2xyz	Convert structure file(s) of any format to extxyz
substitute	Randomly substitute or remove selected atoms/sites from a structure
supercell	Build a supercell with cell lengths capped at a maximum (Angstrom); optional per-temperature GPUMD setup
symmetrize	Import space-group symmetry into a structure file (or folder) -> CIF
vasp-relax	Write VASP relaxation inputs for a structure (or folder); INCAR tags overridable
vasp-static	Write VASP static / single-point inputs for a structure (or folder)

Examples

pymdkit add-groups -i opted.cif --elements Li Y Cl -o model.xyz
pymdkit add-groups -if cifs/ --elements Li Y Cl -of cifs-grouped/   # whole folder
pymdkit add-groups --elements Li Y Cl                              # scan subfolders, tag each model.xyz in place
pymdkit stru2xyz -i opted.vasp -o opted.xyz                        # convert one file
pymdkit stru2xyz -if vasp-opted -of xyz-opted                      # convert a whole folder
pymdkit stru2xyz                                                  # scan subfolders, convert structures in place
pymdkit supercell -i opted.vasp -o sc.vasp -max-abc 20            # cell lengths <= 20 A
pymdkit supercell -if vasp-opted -max-abc 20 -individual          # per-structure ./<name>/<name>.<ext>
pymdkit supercell -if extxyz-opted -max-abc 24 -individual -temp 500 600 -md-if input-files -add-groups Li Y Cl
                                                                  # GPUMD: ./<name>/model.xyz (grouped) + ./<name>/<T>/ jobs
pymdkit vasp-relax  -i opted.vasp                                  # relax inputs in current dir
pymdkit vasp-relax  -if optimal_occupancy                          # one ./<name>/ job folder per structure
pymdkit vasp-static -if cifs/ -custom-setting my_incar.txt         # static inputs, custom INCAR
pymdkit vasp-static -it traj.xyz                                    # one ./frame_N/ job per trajectory frame
pymdkit msd                                         # scans <structure>/<temp>/ -> per-job msd/ + msd_summary.txt
pymdkit msd --diffuse_ion Li --ion_charge 1         # choose the mobile ion for conductivity
pymdkit ehull --mp-api-key $MP_API_KEY              # scans ./ for VASP jobs -> ehull.txt
pymdkit final-energy                                # scans ./ for VASP jobs -> final-energy.txt
pymdkit gather-contcar -of vasp-opted               # CONTCARs -> vasp-opted/<folder>.vasp
pymdkit gather-contcar -of vasp-opted -ehull 0.028  # only structures with E_hull < 0.028 eV/atom
pymdkit vasp2xyz                                    # scans ./ for VASP output folders -> scf-converged.xyz
pymdkit vasp2xyz --position-only                    # write positions only, without energy/forces/stress
pymdkit submit-vasp -subscript sub.vasp -queue slurm -max-job-num 30
pymdkit substitute -i Li3YCl6.cif -se Li -sn 3 -we Na -wn 3 -on 100
pymdkit substitute -i Li3YCl6.cif -se Li -sn 3 -we none -on 100
pymdkit substitute -i Li96Ta6La11Cl72.cif -se Li1 Li2 -sn 20 67 -we none -on 100
pymdkit substitute -i Li96Ta6La11Cl72.cif -se Li2 -we none -ref La Ta -d 1.01 1.02
pymdkit substitute -i Li96Ta6La11Cl72.cif -se Li2 -we none -ref La Ta
pymdkit electrostatic-energy -i Li3YCl6.cif
pymdkit electrostatic-energy -if Li3YCl6-all
pymdkit select-candidate                            # RMSE bands: <low all accurate, >high all candidate, else worst 50%
pymdkit select-candidate -r 0.8                     # in the middle band, take worst 80% as candidate.xyz
pymdkit rmsd a.cif b.cif                            # RMSD of two files -> rmsd.txt
pymdkit rmsd vasp-opted/                            # all pairs in a folder -> rmsd.txt
pymdkit symmetrize -i opted.cif --symprec 0.01 --add_oxidation yes -o opted-symm.cif
pymdkit symmetrize -if my_cifs/ --symprec 0.01 --add_oxidation no -of my_cifs-symm

VASP input commands (vasp-relax, vasp-static) always produce individual jobs (one structure per folder): -i writes into the current dir (or -o), -if creates one ./<name>/ folder per structure, and -it creates one ./frame_N/ folder per trajectory frame - all directly in the current path.

They start from sensible default INCAR settings; override them by passing a settings file with -custom-setting FILE. The file may be a Python-dict block or KEY = VALUE lines (a None/blank value clears a tag):

custom_settings = {
    "ENCUT": "600.0",
    "ISIF": "3",
    "MAGMOM": None
}

vasp-static -it traj.xyz (also available on vasp-relax) reads a multi-structure trajectory and writes one job sub-folder per frame (frame_1/, frame_2/, ..., prefix configurable via --frame-prefix). Each folder also keeps a frame_N.xyz, so Config_type survives for a later vasp2xyz.

Each command's full flag list is in pymdkit <command> --help.

substitute -ref removes selected sites near reference sites and writes one <input-stem>_substitute.cif in the current path. If -d is omitted, each cutoff is 0.7 * (selected covalent radius + reference covalent radius) using the covalent radii from Cordero et al., Dalton Trans., 2008, 2832-2838.

VASP-output readers (vasp2xyz, ehull, and other future VASP-output commands) use the global priority vaspout.h5 > vasprun.xml > OUTCAR.

ehull auto-detects every sub-folder of the current path that contains a supported VASP output, groups them by chemical system (elements ordered by electronegativity, e.g. Li-Y-Cl), and builds/reuses one mp_cache_<system>.json per system - so a pure Li-Y-Cl batch yields a single mp_cache_Li-Y-Cl.json, while a mixed Li-Y-Cl + La-O batch yields both mp_cache_Li-Y-Cl.json and mp_cache_La-O.json. (Formation energy is reported alongside E_hull in ehull.txt.)

Layout

pymdkit/
|-- pyproject.toml              # package metadata + the `pymdkit` entry point
|-- README.md
`-- src/pymdkit/
    |-- pymdkit_main.py         # dispatcher: discovers and runs commands
    `-- commands/               # one module per command
        |-- _fileio.py          # shared -i/-o/-if/-of helper (not a command)
        |-- _vaspset.py         # shared VASP input-set helper (not a command)
        |-- add_groups.py
        |-- compute_ehull.py
        |-- compute_rmsd.py
        |-- electrostatic_energy.py
        |-- final_energy.py
        |-- submit_vasp.py
        |-- stru2xyz.py
        |-- substitute.py
        |-- supercell.py
        |-- vasp2xyz.py
        |-- vasp_relax.py
        |-- vasp_static.py
        |-- ...
        `-- symmetrize.py

Modules whose name starts with _ are shared helpers and are skipped by the dispatcher, so they never appear as commands.

Adding a new tool later

Drop a module in src/pymdkit/commands/ that defines four things:

COMMAND = "my-tool"                 # the subcommand name you'll type
HELP = "One-line description."

def add_arguments(parser):          # register flags
    parser.add_argument("--input", required=True)

def run(args):                      # do the work; return an exit code (0 = ok)
    ...
    return 0

if __name__ == "__main__":          # keeps the script runnable on its own
    import argparse
    _p = argparse.ArgumentParser(description=__doc__)
    add_arguments(_p)
    raise SystemExit(run(_p.parse_args()))

It will appear in pymdkit --help automatically - no central registration needed. Put heavy imports (pymatgen, ase, ...) inside run() where practical; the dispatcher reads each command's name and help without importing it, so pymdkit --help stays fast and a missing optional dependency only affects the one command that needs it.

Running a script standalone

Every command module still works directly, which is handy for debugging:

python src/pymdkit/commands/supercell.py -i in.cif -max-abc 20 -o sc.vasp