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Excitonic Hamiltonians for Calculating Optical Absorption Spectra and Optoelectronic Properties of Molecular Aggregates and Solids
Published on: May 27, 2020
Communication: Beyond the gradient expansion approximation: A generalized gradient expansion for exchange
1Department of Chemistry, Department of Physics and Astronomy, CMS-Center for Molecular Simulation, IQST-Institute for Quantum Science and Technology, Quantum Alberta, University of Calgary, 2500 University Drive NW, Calgary, Alberta T2N 1N4, Canada.
Abstract:
The gradient expansion approximation (GEA) exchange in density functional theory is derived from the long-wavelength response of jellium and yields an analytic expansion in even powers of the reduced density gradient s. This structure reflects the perturbative q→0 limit rather than an exact constraint. Relaxing analyticity in s leads naturally to a generalized gradient expansion (GGE) based on a Puiseux series containing both integer and fractional powers. The exchange-hole structure of inhomogeneous jellium indicates that finite-wavevector singularities associated with the Kohn-anomaly at the Fermi surface generate non-analytic contributions, including a leading s3/2 behavior. Non-analytic, non-polynomial, and mixed structures are already intrinsic to widely used generalized gradient approximation (GGA) exchange functionals. With natural extensions to correlation, the GGE provides a minimal and rigorous extension of the GEA, enabling systematic construction of new GGA exchange-correlation functionals.
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