Search results for "electrochemical cell"
showing 10 items of 104 documents
2016
Despite hundreds of cationic bis-cyclometalated iridium(III) complexes having been explored as emitters for light-emitting electrochemical cells (LEECs), uniformly their composition has been in the form of a racemic mixture of Λ and Δ enantiomers. The investigation of LEECs using enantiopure iridium(III) emitters, however, remains unprecedented. Herein, we report the preparation, the crystal structures, and the optoelectronic properties of two families of cyclometalated iridium(III) complexes of the form of [(C^N)2Ir(dtBubpy)]PF6 (where dtBubpy is 4,4′-di-tert-butyl-2,2′-bipyridine) in both their racemic and enantiopure configurations. LEEC devices using Λ and Δ enantiomers as well as the r…
Dynamic doping in bright and stable light emitting electrochemical cells.
2013
By using fast current density and luminance versus voltage (JL-V) analysis the device operation of sandwiched light emitting electrochemical cells (LECs) during their normal voltage driving operation mode is studied. In LECs the application of a voltage results in the movement of ions changing the state of the device, as a result the JL-V scans need to be performed fast and meet certain conditions to be meaningful. Space-charge limited current behavior is observed once the injection barriers are overcome. The increase of the current density after this point imply that the effective thickness of the devices is reduced which indicates the formation of more conductive regions adjacent to the e…
Correlating the Lifetime and Fluorine Content of Iridium(III) Emitters in Green Light-Emitting Electrochemical Cells
2013
In light-emitting electrochemical cells, the lifetime of the device is intrinsically linked to the stability of the phosphorescent emitter. In this study, we present a series of ionic iridium(III) emitters based on cyclometalating phenylpyridine ligands whose fluorine substituents are varied in terms of position and number. Importantly, despite these structural modifications, the emitters exhibit virtually identical electrochemical and spectroscopic properties, which allows for proper comparison in functional devices. Quantum chemical calculations support the properties measured in solution and suggest great similarities regarding the electronic structures of the emitters. In electrolumines…
2017
Two cationic Ir(III) complexes bearing 2-phenylpyridinato cyclometalating ligands and bithiazole-type ancillary ligands have been synthesized and optoelectronically characterised. These emitters exhibit unusually deep red-to-near-infrared emission at room temperature, thereby rendering them as attractive emitters in solution-processed light emitting electrochemical cell (LEEC) electroluminescent devices.
Improving the Turn-On Time of Light-Emitting Electrochemical Cells without Sacrificing their Stability
2010
The luminance, efficiency, and turn-on time of ionic iridium complex-based light-emitting electrochemical cells can be improved by inserting an ionic liquid with high intrinsic conductivity. This results in a device in which the decrease in turn-on time is achieved while maintaining the stability.
Controlling the dynamic behavior of light emitting electrochemical cells
2013
Abstract Light emitting electrochemical cells (LECs) present an attractive route towards cost efficient lighting applications. By utilizing ionic phosphorescent transition metal complexes, efficient electroluminescence can be realized from a single layer device using air stable electrodes. These devices achieve efficient charge carrier injection due to ion accumulation at the interface upon driving, resulting in a dynamic response upon device operation. Here we investigate the device operation by using fast current and luminance versus voltage sweeps during normal fixed bias operating. A universal set of JL–V curves can be identified in which different regimes are observable. The speed and …
Modification of Nanocrystalline WO3 with a Dicationic Perylene Bisimide: Applications to Molecular Level Solar Water Splitting
2015
[(N,N?-Bis(2-(trimethylammonium)ethylene) perylene 3,4,9,10-tetracarboxylic acid bisimide)(PF6)2] (1) was observed to spontaneously adsorb on nanocrystalline WO3 surfaces via aggregation/hydrophobic forces. Under visible irradiation (? > 435 nm), the excited state of 1 underwent oxidative quenching by electron injection (kinj > 108 s-1) to WO3, leaving a strongly positive hole (Eox ? 1.7 V vs SCE), which allows to drive demanding photo-oxidation reactions in photoelectrochemical cells (PECs). The casting of IrO2 nanoparticles (NPs), acting as water oxidation catalysts (WOCs) on the sensitized electrodes, led to a 4-fold enhancement in photoanodic current, consistent with hole transfer from …
Toward large-area targets for “TRAKULA”
2011
Abstract TRAKULA ( Tra nsmutationsrelevante k ernphysikalische U ntersuchungen l anglebiger A ktinide, i.e., nuclear physical investigations of long-lived actinides with relevance to transmutation) is a joint research project of the German Federal Ministry of Science and Education (BMBF) on nuclear physics investigations with modern scientific, technological and numerical methods. Experiments concerning the transmutation of radioactive waste are a central topic of the project. For this, large-area samples (≥40 cm 2 ) of 235,238 U and 239,242 Pu compounds are required for the calibration of fission chambers and for fission yield measurements. Another topic within the project requires large-a…
Host–guest blue light-emitting electrochemical cells
2014
Carbazole, a commonly used hole-transporter for organic electronics, has been modified with an imidazolium cation and a hexafluorophosphate counter-anion to give an ionic hole-transporter. It has been applied as one of the hosts in a host–guest blue light-emitting electrochemical cell (LEC) with the neutral blue emitter FIrPic. We have obtained efficient and bright blue LECs with an electroluminescence maximum at 474 nm and efficacy of 5 cd A−1 at a luminance of 420 cd m−2, thereby demonstrating the potential of the ionic organic charge-transporters and of the host–guest architecture for LECs.
Engineering Charge Injection Interfaces in Hybrid Light-Emitting Electrochemical Cells
2014
Light-emitting electrochemical cells (LECs) consists of a thin film of an ionic organic semiconductor sandwiched between two electrodes. Because of the large density of ions, LECs are often reported to perform independently on the electrodes work function. Here we use metal oxides as charge injection layers and demonstrate that, although electroluminescence is observed independently of the electrodes used, the device performances are strongly dependent on the choice of the interface materials. Relying on metal oxide charge injection layers, such hybrid devices are of interest for real lighting applications and could pave the way for new efficient, stable, low-cost lighting sources.