DFT and TD-DFT study on structures, related energies, frontier molecular orbitals and UV-Vis spectra of [M(Tp)(PPh3)(Cl)(L)] (M = Ru and Fe; L = C3H4N2 and C13H11N)

doi:10.1016/j.poly.2015.09.046

CNU IR > College of Sustainable Environment and Recreation > Dept. of Environmental Engineering and Science (including master's program) > Periodical Articles > Item 310902800/29703

Please use this identifier to cite or link to this item: https://ir.cnu.edu.tw/handle/310902800/29703

Title:	DFT and TD-DFT study on structures, related energies, frontier molecular orbitals and UV-Vis spectra of [M(Tp)(PPh3)(Cl)(L)] (M = Ru and Fe;L = C3H4N2 and C13H11N)
Authors:	Wang, Tsang-Hsiu Hsiao, Ching-Hsiang Chen, Shih-Hsiung Cheng, Yi-Tung Chen, Li-Yun
Contributors:	環境工程與科學系職業安全衛生系(含防災所)
Keywords:	Photo-sensitizer DFT TD-DFT DSSC UV
Date:	2015-12
Issue Date:	2016-04-19 19:05:13 (UTC+8)
Publisher:	Pergamon-Elsevier Science Ltd
Abstract:	Density functional theory (DFT) and time-dependent density functional theory (TD-DFT) with the DZVP/DZVP2 all-electron mixed basis sets are used to study the related energies, structures, frontier molecular orbitals and UV-Vis spectra for [M(Tp)(PPh3)(Cl)(L)](M = Ru and Fe; L = C3H4N2 and Cl3H11N). The related energies between the singlet state (low-spin) and nonet state (high-spin) for these complexes are reported. Because of the low related energies, these complexes are expected to be in the singlet state (low-spin). The calculated structural parameters for complexes 1 and 3 (Ru-based) are in very good agreement with the experimental values, and the geometries of complexes 2 and 4 (Fe-based) have been studied as well. The metal-ligand bond distances for the Fe-based complexes are predicted to be slightly shorter than those of the Ru-based complexes due to the small spatial extent of the 3d wave functions of the Fe atom. These complexes display a HOMO of metal d and pi(Cl) orbitals in character, and the LUMO is contributed by metal d and pi(PPh3) or pi(C13H11N) orbitals. The HOMO-LUMO energy gap (Delta EL-H) can be reduced by a pi-electron rich ligand (such as C13H11N) and a low electronegativity metal atom (such as Fe). A pi-electron rich ligand (such as C13H11N) can increase the electron accepting ability, which leads to more electrons being pumped into the pi(PPh3) and pi(C13H11N) orbitals and results in a red-shift and intensity-enhanced absorption in the UV-Vis spectrum. The UV-Vis absorption intensity can be enhanced by solvent (such as CH3OH) as well as resulting in a blue-shift, which suggests that it is due to the polarizability and dielectric strength of the solvent. Owing to the low electronegativity of the Fe atom, a red-shift occurs in the UV-Vis spectra for complexes 2 and 4. The primary absorption features for complexes 1 and 3 are attributed to MLCT/LLCT transitions; on the other hand, a MLCT transition results in the primary absorption features for complexes 2 and 4. Our results show that Ru can be replaced by the inexpensive Fe as the photo-sensitizer. In addition, these Ru- and Fe-based complexes are good candidates for photo-sensitizers in DSSCs due to rich absorption bands and strong absorption intensities in the visible region.
Relation:	Polyhedron, v.102, pp.216-223
Appears in Collections:	[Dept. of Occupational Safety] Periodical Articles [Dept. of Environmental Engineering and Science (including master's program)] Periodical Articles

Files in This Item:

File	Description	Size	Format
index.html		0Kb	HTML	1852	View/Open

Loading...