To design efficient sensitizers for dye-sensitized solar cells (DSSCs), a series of porphyrin sensitizers with different electron-donating and withdrawing substituents are investigated using the density functional theory (DFT) and time-dependent DFT approach. We found that the designed dyes have smaller highest occupied molecular orbital to lowest unoccupied molecular orbital (HOMO-LUMO) energy gap values, and the absorption bands are broadened and shifted to longer wavelengths compared to the so far best sensitizer (YD2-o-C8). Importantly, our designed dyes have larger contributions of the anchoring group to the LUMOs, which enhance the electron injection process. Our calculation results indicated that the new systems should have better performance than the existing efficient dyes due to their improved optical properties.
The polarized molecular orbital (PMO) method, a neglect-of-diatomic-differential-overlap (NDDO) semiempirical molecular orbital method previously parameterized for systems composed of O and H, is here extended to carbon. We modified the formalism and optimized all the parameters in the PMO Hamiltonian by using a genetic algorithm and a database containing both electrostatic and energetic properties; the new parameter set is called PMO2. The quality of the resulting predictions is compared to results obtained by previous NDDO semiempirical molecular orbital methods, both including and excluding dispersion terms. We also compare the PMO2 properties to SCC-DFTB calculations. Within the class of semiempirical molecular orbital methods, the PMO2 method is found to be especially accurate for polarizabilities, atomization energies, proton transfer energies, noncovalent complexation energies, and chemical reaction barrier heights and to have good across-the-board accuracy for a range of other properties, including dipole moments, partial atomic charges, and molecular geometries.
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