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The essential challenge in orbital-free density functional theory (OF-DFT) is to construct accurate kinetic energy density functionals (KEDFs) with general applicability (i.e., transferability). During the last decade, several linear-response (LR)-based KEDFs have been proposed. Among them, the Wang-Govind-Carter (WGC) KEDF, containing a density-dependent response kernel, is one of the most accurate that still affords a linear scaling algorithm. For nearly-free-electron-like metals such as Al and its alloys, OF-DFT employing the WGC KEDF produces bulk properties in good agreement with orbital-based Kohn-Sham (KS) DFT predictions. However, when OF-DFT, using the WGC KEDF combined with a recently proposed bulk-derived local pseudopotential (BLPS), was applied to semiconducting and metallic phases of Si, problems arose with convergence of the self-consistent density and energy, leading to poor results. Here we provide evidence that the convergence problem is very likely caused by the use of a truncated Taylor series expansion of the WGC response kernel. Moreover, we show that a defect in the ansatz for the first-order reduced density matrix underlying the LR KEDFs limits the accuracy of these KEDFs. By optimizing the two free parameters involved in the WGC KEDF, the two-body Fermi wave vector mixing parameter gamma and the reference density rho* used in the Taylor expansion, OF-DFT calculations with the BLPS can achieve semiquantitative results for nine phases of bulk silicon. These new parameters are recommended whenever the WGC KEDF is used to study nonmetallic systems.

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The accuracy of Time-Dependent Density Functional Theory in predicting the vertical absorption wavelength of 50 widely-used fused-ring electron acceptors (FREAs) has been investigated by considering the solvent effects.