# Pushing the limits#

VeloxChem has the stated goal to be *science-enabling*. Behind this term there are a multitude of software requirements that we find important and strive against, including:

coverage of dense 3D system of sizes up to and beyond 500 atoms in the quantum region

accurate description of electronically excited states that show a more diffuse character than the ground state

stable and reliable convergence of iterative equation solvers also with use of diffuse basis functions

time-efficient prototyping of novel scientific approaches

transparent exposure of data structures to enable in-depth analyses for standard users

flexible ways to interact with other components of the simulation (such as molecular dynamics, parameterizing the embedding, and data visualization)

a fast return of results so as to remain in synchronicity with experimental project partners

For the most parts, VeloxChem implements few schemes to improve the formal scaling of the calculation but rather focus to implement the general and stable algorithms efficiently for HPC cluster computing.

Basically, the only underlying approximation made is the adoption of Cauchy–Schwarz screening in the evaluation of electron-repulsion integrals, but also this is done with rigor using a small screening threshold per default.

## Polarizabilities and C6 dispersion coefficients#

With a highly efficient implementation of the linear complex polarization propagator in VeloxChem, Hartree–Fock and Kohn–Sham density-functional theory calculations were performed of the frequency-dependent polarizabilities for fullerenes consisting of up to 540 carbon atoms. Results for the static polarizabilities and C6 coefficients show scalings of \(N^{1.2}\) and \(N^{2.2}\), respectively, thereby deviating significantly from the previously reported values obtained with use of semi-classical/empirical methods. See Ref. [BAL+21] for further details.