hamop

One tight-binding Hamiltonian, every observable, strictly consistent. Build a Hamiltonian once, as real-space blocks in an orthogonal or nonorthogonal basis, and compute its band structure, density of states, Kubo-Greenwood optical conductivity and Landauer (NEGF) transmission from the same matrices.

The point of the package is the consistency, not any single solver. When the optics of a model and its spectrum are computed by different codes with different conventions, they drift: a different gauge for the velocity operator, a different treatment of the overlap matrix, a different broadening, and suddenly the absorption edge no longer sits at the band gap. Here every observable diagonalizes the same Bloch matrices through the same canonically orthogonalized solver, and the Kubo velocity operator is built from the exact k-derivative of the same assembly, so spectral, optical and transport statements about one model cannot disagree with each other.

What it does

• TightBindingModel: sites with any number of orbitals, directed hopping blocks with automatic Hermitian completion, optional overlap blocks (LCAO-style nonorthogonal bases), periodic in any dimension or finite. Assembles H(k), S(k) and their exact k-derivatives in the atomic gauge.
• Spectrum (bands, dos, fermi_level, band_edges, k_path): band structures along arbitrary k-lists or interpolated high-symmetry paths, Gaussian-broadened densities of states, chemical potential at a given filling by bisection, band edges and gap about a chemical potential.
• Optics (sigma_optical, drude_weight): Kubo-Greenwood real sheet conductivity in units of e²/(4ℏ) with Gaussian or Lorentzian broadening, plus the intraband (Drude) weight — both built on the nonorthogonal velocity correction v = dH/dk − (eₙ+eₘ)/2 dS/dk that makes them exactly invariant under a shift of the energy zero.
• Topology (berry_phase, berry_curvature, chern_number): Wilson-loop Berry phases and the gauge-invariant lattice field strength of Fukui, Hatsugai and Suzuki (J. Phys. Soc. Jpn. 74, 1674 (2005)), whose Brillouin-zone sum is an exact integer — the Chern number. Orthogonal bases only for now, refused explicitly otherwise.
• Transport (sancho_rubio, transmission, transmission_direct, principal_layers): two-probe Landauer transmission with Sancho-Rubio lead surface Green functions and a recursive Green function sweep, nonorthogonal bases included, plus a dense direct-inversion reference implementation of the same quantity — and automatic partitioning of a finite model into principal layers, which verifies that no coupling skips a layer instead of silently truncating it.
• gen_eigh: generalized eigensolver with canonical orthogonalization (Szabo and Ostlund, Modern Quantum Chemistry, sec. 3.4.5), so mildly overcomplete overlaps cannot blow up the spectrum — the standard remedy used inside electronic-structure codes.

Dependencies: NumPy and SciPy. Nothing else.

Validation against closed forms

Every physical claim in the package is pinned by a test against an exact result, not a stored number:

• the single-orbital chain reproduces E(k) = e₀ + 2t cos ka to machine precision, and its nonorthogonal variant reproduces E(k) = 2t cos ka / (1 + 2s cos ka);
• the chain density of states matches 1/(π√(4t² − E²)) and integrates to the orbital count;
• graphene's nearest-neighbour model gives Dirac-point closure at K exactly, ±3|t| at Γ exactly, and the universal optical sheet conductivity e²/(4ℏ) on the interband plateau (Kuzmenko et al., Phys. Rev. Lett. 100, 117401 (2008)) — which is also the absolute anchor for the package's conductivity unit;
• the two-site molecule absorbs at exactly 2|t| with the hand-derived velocity matrix element |M| = |a t|;
• σ(ω) is invariant to 10⁻¹⁰ under H → H + cS with μ → μ + c, which pins the nonorthogonal velocity term;
• the chain's lead surface Green function matches its closed form (E − i√(4t² − E²))/(2t²); a pristine chain transmits exactly one channel inside the band and nothing outside; two decoupled chains transmit two; an on-site impurity ε reproduces T = (4t² − E²)/((4t² − E²) + ε²);
• the recursive Green function sweep agrees with dense direct inversion to machine precision, disorder and overlap included;
• the Haldane model returns its known phase diagram (Haldane, Phys. Rev. Lett. 61, 2015 (1988)) with the Chern number an exact integer to 10⁻¹²: ±1 inside the topological phase, 0 outside, sign reversal with the flux direction, and zero total over all bands;
• the SSH chain's Zak phase is quantized to 0 or π and the two dimerizations differ by exactly π — the convention-free statement;
• the Drude weight of the half-filled chain reproduces its closed form 8·spin·|t|·a and is exactly invariant under a shift of the energy zero in a nonorthogonal basis;
• the automatic principal-layer partition reproduces hand-built blocks exactly, reproduces the single-impurity closed form end to end, and refuses a layer width smaller than the interaction range.

Run them yourself: pip install -e .[test] then pytest.

Install and use

pip install hamop

import numpy as np
from hamop import graphene, bands, dos, sigma_optical

g = graphene(t=-2.7, a=2.46)          # eV, Angstrom
omega = np.linspace(0.5, 2.0, 60)
sigma = sigma_optical(g, omega, mu=0.0, mesh=120, eta=0.12)
# sigma is ~1.0 on the plateau: the universal e^2/(4 hbar)

Building your own model:

from hamop import TightBindingModel, band_edges

m = TightBindingModel(positions=[[0.0], [0.7]], norb=1, cell=[[2.0]])
m.add_hop(0, 1, (0,), [[-1.0]])       # intra-cell bond
m.add_hop(1, 0, (1,), [[-0.6]])       # inter-cell bond
print(band_edges(m, mu=0.0, mesh=2001))   # the SSH gap, 2|t1 - t2|

Conventions, stated once: energies in eV, positions in Angstrom, k in 1/Angstrom, Cartesian. Each directed hopping block is added once and its Hermitian partner is implied. Optical conductivity is the real sheet conductivity in units of e²/(4ℏ) with spin degeneracy as an explicit factor (default 2). The velocity operator uses the standard atomistic position gauge (position operator diagonal at the sites); the intra-atomic dipole contribution is neglected, the common approximation in tight-binding optics.

Relation to existing tools

Excellent tools cover parts of this space: PythTB and pybinding build tight-binding models and their spectra, and Kwant is the standard for quantum transport. hamop does not replace any of them, and for their core use cases they are more capable. Its niche is the combination they leave open: nonorthogonal (LCAO-style) overlap matrices as first-class citizens across all observables, optics and transport computed from the same Bloch assembly as the spectrum so the three can never disagree, and a deliberately small NumPy/SciPy-only core validated line by line against closed forms -- the shape of engine an LCAO electronic-structure pipeline exports its Hamiltonians into.

Status

v0.2.0 (alpha). Implemented and tested: the model container with exact k-derivatives, canonical-orthogonalization eigensolver, band structures and k-paths, densities of states, filling-resolved chemical potentials, band edges, Kubo-Greenwood optical conductivity (Gaussian or Lorentzian broadening) and the intraband Drude weight for periodic and finite systems, Wilson-loop Berry phases, lattice Berry curvature and Chern numbers, Sancho-Rubio surface Green functions, recursive plus direct-inversion Landauer transmission, and verified automatic principal-layer partitioning.

Not yet implemented, stated plainly: k-space symmetry reduction (grids are full Monkhorst-Pack), Berry phases in nonorthogonal bases (refused with an explicit error), the finite-frequency Hall conductivity σ_xy(ω) (the Chern number is implemented; the full Hall spectrum is not), spin-orbit-coupled blocks as a first-class convention (complex blocks work, but no helper), and interaction self-energies in the transport module. Sparse or very large models are out of scope for now: matrices are dense.

Where it comes from

Methodological basis:

"Learning the quantum Hamiltonian of defective monolayer MoS2 reveals collective vacancy brightness decoupled from defect count"; code for the paper: https://github.com/Tanvir-Mahmud-Mahim/mos2-vacancy-optics

That study computes the optics, the electronic structure and the transport of vacancy-disordered MoS2 supercells from one density-functional Hamiltonian, so that a defect configuration's optical and electronic signatures are strictly consistent — and its conclusions depend on that consistency. This package is the general-purpose engine distilled from that pipeline: the same observables for any Hamiltonian a user supplies, with the material-specific machinery (DFT extraction, machine-learned Hamiltonians, MoS2 structures) left in the paper repository.

Support and governance

The package is written and maintained by Tanvir Mahmud Mahim (Department of Electrical and Electronic Engineering, BRAC University), who reviews every change and takes the final decision on scope and releases. There is no separate governance body; design questions are discussed in the open in issues and pull requests, and the standing rule of CONTRIBUTING.md binds the maintainer exactly as it binds contributors: a change that touches physics arrives with a test, and a constant arrives with its source.

Support runs through the issue tracker at https://github.com/TaN-MM-Org/hamop/issues. Usage questions are welcome there alongside bug reports; a docstring that left a unit or a sign convention unclear is treated as a documentation bug, not as user error. The maintainer aims to respond within a week.

While the version is below 1.0 the API may still move between minor versions; such changes are called out in the release notes. The limitations named under Status are deliberate scope, recorded there precisely so that a user can tell a designed-out feature from an oversight.

License

Apache-2.0 (see LICENSE). Citation metadata is in CITATION.cff; every release is archived on Zenodo under the concept DOI 10.5281/zenodo.22311381, which always resolves to the latest version.