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Organic light-emitting diodes (OLEDs) using the red phosphorescent emitter iridium(III)bis(2methyldibenzo[f,h]quinoxaline) (acetylacetonate) [Ir(MDQ) 2 (acac)] are studied by time-resolved electroluminescence measurements. A transient overshoot after voltage turn-off is found, which is attributed to electron accumulation on Ir(MDQ) 2 (acac) molecules. The mechanism is verified via impedance spectroscopy and by application of positive and negative off-voltages. We calculate the density of accumulated electrons and find that it scales linearly with the doping concentration of the emitter. Using thin quenching layers, we locate the position of the emission zone during normal OLED operation and after voltage turn-off. In addition, the transient overshoot is also observed in three-color white-emitting OLEDs. By time-and spectrally resolved measurements using a streak camera, we directly attribute the overshoot to electron accumulation on Ir(MDQ) 2 (acac). We propose that similar processes are present in many state-of-the-art OLEDs and believe that the quantification of charge carrier storage will help to improve the efficiency of OLEDs.

During the last decade interest in dye-sensitized solar cells (DSC) has grown enormously. Electrical impedance spectroscopy (EIS) is an electrochemical technique commonly used for investigation of charge carrier dynamics in these photovoltaic devices. We used EIS for characterization of our DSC; moreover, symmetric cells with counter-counter or photo-photo electrodes were realized and measured in order to simplify impedance cell analysis by separating the contribution of counter and photoelectrode, respectively. In particular, we provided very accurate illumination of the photoelectrode symmetric cell, aiming to approach the experimental conditions of a complete cell. By fitting of experimental data, we obtained values for the charge transfer resistance at the counter-electrode and the electron percolation time at the photoelectrode. Moreover, the simulation of a whole cell, combining the data from the fitting procedures above, was in good agreement with experimental data

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Dye solar cells with Co(III)/Co(II) redox mediators have been prepared. To obtain higher conversion efficiencies, the recombination between photoinjected electrons and Co(III) species was minimized by deposition of a thin Al2O3 blocking layer over the mesoporous TiO2 surface. Measurements of current-voltage characteristic curves, both under illumination and in dark conditions, together with electrochemical impedance spectroscopy demonstrate the great effectiveness of the addition of a blocking layer in cells containing cobalt based electrolyte, by substantially reducing the recombination current. The consequent power conversion efficiency increase is more than double, passing from 0.94% to 2.48% under 300 W m−2 AM 1.5 illumination.

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Losses of charge carriers, due to the interfacial charge recombination processes, in small molecule organic solar cells (SMOSCs) have been investigated under operating conditions. The devices consist of zinc phthalocyanine (ZnPc) as electron donor material and C60 as electron acceptor. The results obtained by using time-resolved techniques such as charge extraction (CE) and photoinduced transient photovoltage (TPV) have been compared to the measurements carried out with impedance spectroscopy (IS) and show good agreement. Significantly, much difference is observed in either the charge density distribution versus the device voltage or the charge carriers lifetime when comparing bulk heterojunction versus bilayer-type ZnPc:C60 devices. The implications of the faster charge carrier recombination with the device fill factor (FF) and the open circuit voltage (V OC) are discussed.