Thin-film solid-state electroluminescent devices based on tris(2,2′-bipyridine)ruthenium(II) complexes

The behavior of light-emitting electrochemical cells (LEC) based on solid films (similar to100 nm) of tris(2,2'-bipyridine)ruthenium(II) between an ITO anode and a Ga-In cathode was investigated. The response times were strongly influenced by the nature of the counterion: small anions (BF4- and ClO4-) led to relatively fast transients, while large anions (PF6-, AsF6-) produced a slow time-response. From comparative experiments of cells prepared and tested in a glovebox to those in ambient, mobility of the anions in these films appears to be related to the presence of traces of water from atmospheric moisture. An electrochemical model is proposed to describe the behavior of these LECs. The simulation results agreed well with experimental transients of current and light emission as a function of time and show that the charge injection is asymmetric at the two electrodes. At a small bias, electrons are the major carriers, while for a larger bias the conduction becomes bipolar.