Abstract
Pyrene and its photophysics have been extensively studied, especially experimentally. Yet to this day there is no conclusive theoretical description of the relaxation from the photo-accessible L-1(a) state to the fluorescent L-1(b) state, which is partly due to the challenge of adequately modeling both states without over-stabilizing one or the other. We first compare several quantum chemical methods to find the best model that offers a good trade-off between a balanced description of both states and computational effort On the basis of the selected electronic structure method, we simulate this relaxation process with two state-of-the-art dynamical techniques. We perform wave packet propagations in reduced dimensions and full-dimensional on-the-fly surface hopping to corroborate our choice of coordinates and obtain a more complete picture of the relaxation mechanism. Our results confirm the important role of a conical intersection between the two excited states that has been postulated in the literature.
Item Type: | Journal article |
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Faculties: | Chemistry and Pharmacy > Department of Chemistry |
Subjects: | 500 Science > 540 Chemistry |
ISSN: | 0301-0104 |
Language: | English |
Item ID: | 67509 |
Date Deposited: | 19. Jul 2019, 12:22 |
Last Modified: | 04. Nov 2020, 13:49 |