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Abstract

Photogenerated molecular three-spin systems, composed of a chromophore and a covalently bound stable radical, are promising candidates for applications in the field of molecular spintronics. Through excitation with light, an excited doublet state and a quartet state are generated, whereby their energy difference depends on the exchange interaction J_TR between the chromophore triplet state (T) and the stable radical (R). In order to establish design rules for new materials to be used in molecular spintronics devices, it is of great importance to gain knowledge on the magnitude of J_TR as well as the factors influencing J_TR on a molecular level. Here, we present a robust and reliable computational method to determine excited state exchange couplings in three-electron-three-centre systems based on a CASSCF/QD-NEVPT2 approach. The methodology is benchmarked and then applied to a series of molecules composed of a perylene chromophore covalently linked to various stable radicals. We calculate the phenomenological exchange interaction J_TR between chromophore and radical, which can be compared directly to the experiment, but also illustrate how the individual exchange interactions J_ij can be extracted using an effective Hamiltonian that corresponds to the Heisenberg–Dirac–Van-Vleck Hamiltonian. The latter procedure enables a more detailed analysis of the contributions to the exchange interaction J_TR and yields additional insight that will be invaluable for future design optimisation.