Abstract
We present an approximate approach for the simulation of UV/vis spectra using conventional [non-time-dependent (non-TD)] DFT computations. It uses Kohn-Sham orbitals and orbital energies to estimate both the excitation energies and the associated oscillator strengths. For a wide range of systems from small molecules to large molecular dyes used in electrochromic and solar-cell applications, reasonable UV/vis spectra are generated, each with just two conventional DFT computations. The accuracy is generally comparable to what one would expect from TD-DFT calculations. In comparison to TD-DFT, the protocol of the present study provides an intuitive and notably more rapid means for simulating electronic absorption properties. It enables efficient screening of materials for a wide range of relevant applications.
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