Theoretical Rationalization of the Dual Photophysical Behavior of C60+

Jordi Soler (1) , Rudraditya Sarkar (1) , Martial Boggio-Pasqua (1)

1 PTC - Photochimie théorique et computationnelle (LCPQ)

Interest in fullerenes has been renewed recently in astrophysics as a consequence of their detection in circumstellar environments. In particular, C60 + was detected in the diffuse interstellar medium and its presence has been related to some diffuse interstellar bands (DIBs) whose origin was previously unknown. A single recent laboratory experiment (J. Phys. Chem. A 2017, 121, 7356-7361) shows that upon laser excitation at 785 nm, C60 + in neon matrices exhibits a radiative decay at 965 nm, while UV photoexcitation does not lead to any significant luminescence. To rationalize this original dual photophysical behavior, we have performed time-dependent density functional theory (TD-DFT) calculations on C60 + to investigate the potential energy surfaces of the relevant electronic states, completed by the simulations of vibrationally-resolved absorption and emission spectra. The proposed photophysical pathways shed light on the experimental measurements: The near-IR laser excitation populates the eleventh doublet excited state (D11) that decays to the lowest first bright excited state D5, from which photoluminescence is predicted. Indeed, D5 is largely separated from the lower electronic states (D0-D4). Thus, D5 behaves effectively as the first excited state, while the D0-D4 set of states act as the electronic ground state. In addition, there are no low-lying conical intersections between D5 and lower excited states energetically accessible upon near-IR excitation that can provide efficient nonradiative decay channels for this state, leaving radiative decay as the most likely deactivation pathway. However, a sloped conical intersection between D5 and D4 was located around 2.9 eV above D0. While it is too high in energy to be accessible upon near-IR excitation, it provides a funnel for efficient nonradiative decay down to the ground state (D0) accessible upon UV light excitation. Thus, the photophysics of C60+ is controlled by the ability to access this funnel: Upon near-IR excitation, the system fluoresces because the funnel for nonradiative decay cannot be reached, while UV irradiation provides a different route by opening up a radiationless decay channel via this funnel accounting for the absence of fluorescence.

Domaines: Chimie théorique et/ou physique

Jordi Soler, Rudraditya Sarkar, Martial Boggio-Pasqua. Theoretical Rationalization of the Dual Photophysical Behavior of C60+. Journal of Physical Chemistry A, 2019, 123 (9), pp.1824-1829. ⟨10.1021/acs.jpca.8b11761⟩. ⟨hal-02127513⟩