Ravi Chandra Raju Nagiri

Room-temperature tilted-target sputtering deposition of highly transparent and low sheet resistance Al doped ZnO electrodes

Target-tilted room temperature sputtering of aluminium doped zinc oxide (AZO) provides transparent conducting electrodes with sheet resistances of <10 Ω □-1 and average transmittance in the visible region of up to 84%. The properties of the AZO electrode are found to be strongly dependent on the target-tilting angle and film thickness. The AZO electrodes showed comparable performance to commercial indium tin oxide (ITO) electrodes in organic photovoltaic (OPV) devices. OPV devices containing a bulk heterojunction active layer comprised of poly(3-n-hexylthiophene) (P3HT):phenyl-C61-butyric acid methyl ester (PCBM) and an AZO transparent conducting electrode had a power conversion efficiency (PCE) of up to 2.5% with those containing ITO giving a PCE of 2.6%. These results demonstrate that AZO films are a good alternative to ITO for transparent conducting electrodes.

Engineering dielectric constants in organic semiconductors

The dielectric properties of three pairs of organic semiconductors that contain increasing numbers of cyclopentadithiophene-co-benzothiadiazole moieties (monomer, dimer and polymer) were studied and compared. The materials in each pair differed in the nature of the ‘solubilizing groups’, which are either alkyl- or glycol-based. At low frequencies (<MHz), dielectric constants of up to ∼9 were obtained for the glycolated materials. In addition, the optical- (high-) frequency dielectric constants for the glycolated dimer and polymer were 4.6 and 4.2 respectively, which are the highest values reported thus far for non-ionic organic semiconductors. The external and internal quantum efficiencies (EQE and IQE) of homojunction (i.e., single component) solar cells comprising the dimer and polymer glycolated materials both showed measurable improvements at wavelengths close to their optical gap when compared with the alkylated equivalents. The improvement is suggestive of an increase in the charge generation efficiency, potentially facilitated by the high optical-frequency dielectric constant.

A Triarylamine-Based Anode Modifier for Efficient Organohalide Perovskite Solar Cells

Organohalide lead perovskite solar cells have emerged as a promising next-generation thin-film photovoltaic technology. It has been clearly recognized that interfacial engineering plays a critical role in cell performance. It has been also proposed that the open-circuit voltage is dependent on the ionization potential of the hole transport layer at the anode. In this communication, we report a simple modification of the anode with a triarylamine-based small molecule (1), which avoids the need to use standard hole transport materials and delivers a relatively high open-circuit voltage of 1.08 V and a power conversion efficiency of 16.5% in a simple planar architecture.

Thiophene dendrimer-based low donor content solar cells

Low donor content solar cells containing polymeric and non-polymeric donors blended with fullerenes have been reported to give rise to efficient devices. In this letter, we report that a dendrimeric donor can also be used in solution-processed low donor content devices when blended with a fullerene. A third generation dendrimer containing 42 thiophene units (42T) was found to give power conversion efficiencies of up to 3.5% when blended with PC70BM in optimized devices. The best efficiency was measured with 10 mole percent (mol. %) of 42T in PC70BM and X-ray reflectometry showed that the blends were uniform. Importantly, while 42T comprised 10 mol. % of the film, it made up 31% of the film by volume. Finally, it was found that solvent annealing was required to achieve the largest open circuit voltage and highest device efficiencies.

An external quantum efficiency of >20% from solution-processed poly(dendrimer) organic light-emitting diodes

Controlling the orientation of the emissive dipole has led to a renaissance of organic light-emitting diode (OLED) research, with external quantum efficiencies (EQEs) of >30% being reported for phosphorescent emitters. These highly efficient OLEDs are generally manufactured using evaporative methods and are comprised of small-molecule heteroleptic phosphorescent iridium(III) complexes blended with a host and additional layers to balance charge injection and transport. Large area OLEDs for lighting and display applications would benefit from low-cost solution processing, provided that high EQEs could be achieved. Here, we show that poly(dendrimer)s consisting of a non-conjugated polymer backbone with iridium(III) complexes forming the cores of first-generation dendrimer side chains can be co-deposited with a host by solution processing to give highly efficient devices. Simple bilayer devices comprising the emissive layer and an electron transport layer gave an EQE of >20% at luminances of up to ≈300 cd/m2, showing that polymer engineering can enable alignment of the emissive dipole of solution-processed phosphorescent materials.Efficient OLEDs from solution: engineering dipole alignment in polymersDipole alignment is achieved in efficient solution-processed organic light-emitting diodes featuring a novel poly(dendrimer). A collaborative team led by Paul Burn from the Centre for Organic Photonics & Electronics, School of Chemistry & Molecular Biosciences at The University of Queensland have developed solution-processed organic light-emitting diodes (OLEDs) based on a phosphorescent poly(dendrimer)-based material with an out-coupling efficiency of around 40% and an external quantum efficiency of above 20%. The key to the enhanced light out-coupling in the devices is the favourable alignment of emissive dipoles in the poly(dendrimer), which consists of dendritic side-chains comprised of hole-transporting carbazole-based dendrons and iridium(III) complex-cores. The poly(dendrimer) is blended with a host material to ensure high efficiency in the device. Ultimately, the intelligent design of the developed poly(dendrimers) allowed the authors to utilise a simple bilayer device structure to demonstrate highly efficient solution-processed organic light-emitting diodes.