Aggregates of diketopyrrolopyrrole dimers in solution

Dimers based on diketopyrrolopyrrole (DPP) chromophores have gained tremendous interest as an excellent material building block for organic solar cells and photodiodes. However, a counterintuitive blue-shift in their solution absorption spectra occurs with an increasing number of thiophene units bridging the DPP moieties. We allocate this to aggregates in solution, which might hinder adequate mixing in blends, leading to poor film forming quality and reduced charge generation in solution processed devices. Hence, identification of such aggregates is crucial in order to find measures for device optimisation. In this study, we present synthesis and characterisation of three pyridyl end-capped DPP dimers of different conjugation length using thiophene linkers and compare their parent monomer to evidence the behaviours of aggregates in solution. We employ conventional and temperature dependent UV–Vis spectroscopy, fluorescence and excitation-emission spectroscopy as well as TD-DFT calculations to show that such DPP dimers predominantly form aggregates in solution even at low concentrations. By disentangling the spectroscopic behaviour of both aggregated and non-aggregated species, we refute literature's explanation that the apparent blue shift in absorption arises from a reduced conjugation length due to more molecular flexibility. Instead, absorption and emission signals of non-aggregated dimers are mostly masked by their aggregated species. This work provides a tool set using common laboratory spectroscopic equipment to identify and characterise solution aggregates—information particularly important towards optimisation of organic electronics processed from solution

Nano-Alignment in Semiconducting Polymer Films: A Path to Achieve High Current Density and Brightness in Organic Light Emitting Transistors

Organic light emitting field effect transistors (LEFETs) integrate light emission of a diode with logic functions of a transistor into a single device architecture. This integration has the potential to provide simplified displays at low costs and access to injection lasing. However, the charge carrier mobility in LEFETs is a limiting factor in realizing high current densities along with a trade-off between brightness and efficiency. Herein, we present a technique controlling the nanoscale morphology of semiconducting polymers using nanoscale grooved substrates and dip-coating deposition to achieve high current density. We then applied this approach to heterostructure LEFETs and demonstrated brightness exceeding 29000 cd m–2 at an EQE of 0.4% for a yellow emitter and 9600 cd m–2 at an EQE of 0.7% for a blue emitter. These results represent a significant advancement in organic optoelectronics and are an important milestone toward the realization of new applications in displays and electrically pumped lasing

High mobility solution-processed hybrid light emitting transistors

We report the design, fabrication, and characterization of high-performance, solution-processed hybrid (inorganic-organic) light emitting transistors (HLETs). The devices employ a high-mobility, solution-processed cadmium sulfide layer as the switching and transport layer, with a conjugated polymer Super Yellow as an emissive material in non-planar source/drain transistor geometry. We demonstrate HLETs with electron mobilities of up to 19.5 cm2/V s, current on/off ratios of >107, and external quantum efficiency of 10-2% at 2100 cd/m2. These combined optical and electrical performance exceed those reported to date for HLETs. Furthermore, we provide full analysis of charge injection, charge transport, and recombination mechanism of the HLETs. The high brightness coupled with a high on/off ratio and low-cost solution processing makes this type of hybrid device attractive from a manufacturing perspective.open0

Triplet exciton diffusion in fac-tris(2-phenylpyridine) iridium(III)-cored electroluminescent dendrimers

We have studied triplet-triplet annihilation in neat films of electrophosphorescent fac-tris(2-phenylpyridine) iridium(III) [Ir(ppy)(3)]-cored dendrimers containing phenylene- and carbazole-based dendrons with 2-ethylhexyloxy surface groups using time-resolved photoluminescence. From measured annihilation rates, the limiting current densities above which annihilation would dominate in dendrimer light-emitting devices are found to be > 1 A/cm(2). The triplet exciton diffusion length varies in the range of 2-10 nm depending on the dendron size. The distance dependence of the nearest-neighbor hopping rate shows that energy transfer is dominated by the exchange mechanism. (C) 2005 American Institute of Physics

Tuning of emission color for blue dendrimer blend light-emitting diodes

Published versio

Low-threshold room temperature polariton lasing from fluorene-based oligomers

The authors are grateful to the Australian Research Council (ARC DP160100700 and DP200103036), Australian Department of Industry, Innovation and Science (AISRF53765), the UK Engineering and Physical Sciences Research Council (Grants EP/M025330/1 and EP/L017008/1), China Scholarship Council and the Rank Prize Funds for financial support.Organic semiconductors possessing tightly bound Frenkel excitons are known to be attractive candidates for demonstrating polariton lasing at room temperature. As polariton lasing can occur without inversion, it is a potential route to very low threshold coherent light sources. However, so far, the thresholds of organic polariton lasers have generally been much higher than those of organic photon lasers. Here this problem has been addressed by investigating two new organic molecules with a structure combining fluorene and carbazole groups. The materials are readily deposited from solution and exhibit high photoluminescence quantum yields, high absorption coefficients, and large radiative decay rates in neat films. Room temperature polariton lasing is realized in both materials with incident thresholds of 13.5 and 9.7 µJ cm−2, corresponding to absorbed thresholds of 3.3 and 2.2 µJ cm−2, respectively. These are the lowest values reported to date for polariton lasing in organic semiconductor materials, and approach typical values for organic photon lasers. The step-like power dependent blue-shift of polariton modes indicates an interplay between different depletion channels of the exciton reservoir. This work brings practical room temperature polaritonic devices and future realization of electrically driven polariton lasers a step closer.Publisher PDFPeer reviewe

Highly efficient single-layer dendrimer light-emitting diodes with balanced charge transport

Published versio

Conjugated dendrimers: A modular approach to materials for full colour displays

Conjugated dendrimers provide an excellent molecular architecture for tuning material properties for organic light emitting diodes. Here we demonstrate a modular approach allowing highly efficient fluorescent and phosphorescent emissive chromophores to be used to make red, green and blue solution-processed light emitting diodes. The choice of a common dendritic architecture ensures good solubility and film forming properties irrespective of the choice of core unit. In addition, this architecture allows blending of dendrimers with different cores without phase separation. We show that blending provides a simple but powerful way of tuning the colour of dendrimer LEDs from deep blue to blue-green, and from green to red with little impact on the device properties