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Nonlocal Orbital-Free Kinetic Energy Functional from the Jellium-with-Gap Model for Finite Systems
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DOI：10.1021/acs.jctc.6c00460.png)
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Abstract
En 中文
The quasi-linear scaling of orbital-free density functional theory (OF-DFT) with system size makes it a computationally efficient alternative to conventional Kohn–Sham density functional theory for many condensed-matter applications. However, its applicability remains limited, particularly for finite systems such as molecular clusters, due to the lack of accurate kinetic energy density functionals. In this context, the development of nonlocal kinetic energy density functionals (NL-KEDFs) has significantly advanced the practical utility of OF-DFT. Here, following an alternative formulation based on the linear-response kernel derived from the jellium-with-gap model (JGM), we develop an NL-KEDF capable of accurately describing the diverse density regimes characteristic of finite systems, including molecular clusters. Benchmark calculations, together with an analysis of the corresponding Pauli potentials, demonstrate that the proposed functional achieves higher accuracy than state-of-the-art orbital-free approaches for finite systems. Furthermore, the optical properties computed using the present method show good agreement with reference results, highlighting its reliability. These results indicate that the proposed NL-KEDF provides a robust and efficient framework for extending OF-DFT to finite systems, with potential implications for nanomaterial design and a deeper understanding of nanoscale phenomena.
Keywords:
Chemical calculations
Cluster chemistry
Density functional theory
Energy density
Kinetics
Journal
IF:
5.5
Papers:
1.1W
Citations:
5.4W