Abstract
Realizing dual charge transfer (CT) based on stable organic radicals in one system is a long-sought goal, however, remains challenging. In this work, a stable mixed-valence radical crystal is designed via a surfactant-assisted method, namely TTF-(TTF(+•) )(2) -RC (where TTF = tetrathiafulvalene), containing dual CT interactions. The solubilization of surfactants enables successful co-crystallization of mixed-valence TTF molecules with different polarity in aqueous solutions. Short intermolecular distances between adjacent TTF moieties within TTF-(TTF(+•) )(2) -RC facilitate both inter-valence CT (IVCT) between neutral TTF and TTF(+•) , and inter-radical CT (IRCT) between two TTF(+•) in radical π-dimer, which are confirmed by single-crystal X-ray diffraction, solid-state absorption, electron spin resonance measurements, and DFT calculations. Moreover, TTF-(TTF(+•) )(2) -RC reveals an open-shell singlet diradical ground state with the antiferromagnetic coupling of 2J = -657 cm(-1) and an unprecedented temperature-dependent magnetic property, manifesting the main monoradical characters of IVCT at 113-203 K while the spin-spin interactions in radical dimers of IRCT are predominant at 263-353 K. Notably, dual CT characters endow TTF-(TTF(+•) )(2) -RC with strong light absorption over the full solar spectrum and outstanding stability. As a result, TTF-(TTF(+•) )(2) -RC exhibits significantly enhanced photothermal property, an increase of 46.6 °C within 180 s upon one-sun illumination.