Abstract
We characterize the dynamic nature of the lowest excited state in a pentacene/C60 complex on the femtosecond time scale, via a combination of ab initio molecular dynamics and time-dependent density functional theory. We analyze the correlations between the molecular vibrations of the complex and the oscillations in the electron-transfer character of its lowest excited state, which point to vibration-induced coherences between the (pentacene-based) local-excitation (LE) state and the complex charge-transfer (CT) state. We discuss the implications of our results on this model system for the exciton-dissociation process in organic solar cells.
Original language | English (US) |
---|---|
Pages (from-to) | 5171-5176 |
Number of pages | 6 |
Journal | The Journal of Physical Chemistry Letters |
Volume | 8 |
Issue number | 20 |
DOIs | |
State | Published - Oct 9 2017 |