Pomarico, E.Silatani, M.Messina, F.Braem, O.Cannizzo, A.Barranoff, E.Klein, J. H.Lambert, C.Chergui, M.2016-10-182016-10-182016-10-18201610.1021/acs.jpcc.6b04896https://infoscience.epfl.ch/handle/20.500.14299/130370WOS:000381236100021Femtosecond broadband photoluminescence studies are presented for Ir(ppy)(3) (Ir1), Ir(ppy)(2)(pic) (Ir2), Ir(ppy)(2)(bpy)(PF6) (Ir3), Ir(ppz)(3) (Ir4), and Ir(ppz)(2)dipy (Ir5) (where ppy = 2-phenylpyridine, pic = picolinate, bpy = 2,2'-bipyridine, ppz = 1-phenylpyrazole, and dipy = 5-phenyldipyrrinato) in solution. Upon 400-nm excitation of Ir1-Ir3, we observed a prompt population of the lowest MLCT states. The higher states decay on an ultrafast time scale (<100 fs), whereas the lowest (MLCT)-M-3 state undergoes further vibrational relaxation on a 1-ps time scale. In Ir3, this relaxation is accompanied by an interligand decay from the ppy to the bpy ligand in similar to 1.5 ps. For the ppy-containing complexes (Ir1 and Ir2), we found that, at 100 ps, the luminescence is red-shifted with respect to the steady-state emission. This is explained in terms of a time-delayed dual luminescence, which we attribute to a double-well minimum configuration of the lowest emitting triplet states involving the ppy moiety. Ir4 shows a prompt population of the lowest excited state, which then undergoes vibrational relaxation in similar to 0.5 ps. Finally, at short times, Ir5 exhibits fluorescence from the lowest (LC)-L-1 state, which decays in similar to 100 fs to the manifold of (LC)-L-3 states. Overall, this study shows that, although the ultrafast relaxation to the lowest electronic states is quite similar to that of other transition-metal complexes, most of the differences occur at the lowest emissive states, with effects such as time-delayed dual fluorescence, interligand decay, and nonradiative relaxation to the ground or lower-lying metal-centered states. Understanding these effects is crucial for obtaining optimal performances of iridium complexes, calling for further iterations between chemical synthesis and photophysical studies to optimize these complexes.text::journal::journal article::research article