## Abstract

Linear scaling density functional theory (DFT) approaches to the electronic structure of materials are often based on the tendency of electrons to localize in large atomic and molecular systems. However, in many cases of actual interest, such as semiconductor nanocrystals, system sizes can reach a substantial extension before significant electron localization sets in, causing a considerable deviation from linear scaling. Herein, we address this class of systems by developing a massively parallel DFT approach which does not rely on electron localization and is formally quadratic scaling yet enables highly efficient linear wall-time complexity in the weak scalability regime. The method extends from the stochastic DFT approach described in Fabian et al. (WIRES: Comp. Mol. Sci. 2019, e1412) but is entirely deterministic. It uses standard quantum chemical atom-centered Gaussian basis sets to represent the electronic wave functions combined with Cartesian real-space grids for some operators and enables a fast solver for the Poisson equation. Our main conclusion is that when a processor-abundant high-performance computing (HPC) infrastructure is available, this type of approach has the potential to allow the study of large systems in regimes where quantum confinement or electron delocalization prevents linear scaling.

Original language | American English |
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Pages (from-to) | 2162-2170 |

Number of pages | 9 |

Journal | Journal of Chemical Theory and Computation |

Volume | 18 |

Issue number | 4 |

DOIs | |

State | Published - 12 Apr 2022 |

### Bibliographical note

Funding Information:We gratefully acknowledge support from the Israel Science Foundation grant 800/19. M.D.F. expresses special thanks to Roie Dann for helpful discussions. a

Publisher Copyright:

© 2022 American Chemical Society. All rights reserved.