Proceedings of Online International Conference on Hybrid and Organic Photovoltaics (OnlineHOPV20)
DOI: https://doi.org/10.29363/nanoge.onlinehopv.2020.012
Publication date: 22nd May 2020
Management of the Coulomb interaction in organic LEDs and solar cells
The physics of organic semiconductors is often controlled by large electron-hole Coulomb interactions and by large spin exchange energies. I will discuss recent strategies that allow these interactions to be harnessed for efficient device operation. For LEDs, 3:1 statistical formation of triplet:singlet excitons through electron-hole recombination limits efficiency if the triplet state is non-emissive, but is recovered for systems with reduced exchange energy and strong spin-orbit coupling in organo-metallic systems or for system where triplet-triplet collisions produce singlet excitons efficiently. We have recently demonstrated that π-conjugated radical materials with doublet ground states can operate with high efficiency in the doublet manifold. For organic PV systems, long-range charge separation from the donor-acceptor heterojunction must overcome a substantial Coulomb barrier, which we find always sets up a measurable optical Stark shift that we measure to be 200 meV or more. Whether this separation is ultrafast (sub-picosecond) or slow (>10 psec) depends on the ‘excess’ energy provided by the photogenerated exciton to the separating electron-hole pair, both for fullerene acceptor systems and those with non-fullerene acceptors. Longer time bimolecular recombination should show similar spin statistics to LED operation, causing significant non-radiative recombination for triplet formation where there is easy access to a low-lying localized triplet states. I will present evidence that though fullerene systems generally show rapid bimolecular triplet formation, this can process can be very strongly reduced in some non-fullerene acceptor systems.