Paul E. Shaw

Low-threshold organic laser based on an oligofluorene truxene with low optical losses

A blue-emitting distributed feedback laser based on a star-shaped oligofluorene truxene molecule is presented. The gain, loss, refractive index, and (lack of) anisotropy are measured by amplified spontaneous emission and variable-angle ellipsometry. The waveguide losses are very low for an organic semiconductor gain medium, particularly for a neat film. The results suggest that truxenes are promising for reducing loss, a key parameter in the operation of organic semiconductor lasers. Distributed feedback lasers fabricated from solution by spin-coating show a low lasing threshold of 270 W/cm2 and broad tunability across 25 nm in the blue part of the spectrum.

Spectral Dependence of the Internal Quantum Efficiency of Organic Solar Cells: Effect of Charge Generation Pathways

The conventional picture of photocurrent generation in organic solar cells involves photoexcitation of the electron donor, followed by electron transfer to the acceptor via an interfacial charge-transfer state (Channel I). It has been shown that the mirror-image process of acceptor photoexcitation leading to hole transfer to the donor is also an efficient means to generate photocurrent (Channel II). The donor and acceptor components may have overlapping or distinct absorption characteristics. Hence, different excitation wavelengths may preferentially activate one channel or the other, or indeed both. As such, the internal quantum efficiency (IQE) of the solar cell may likewise depend on the excitation wavelength. We show that several model high-efficiency organic solar cell blends, notably PCDTBT:PC70BM and PCPDTBT:PC60/70BM, exhibit flat IQEs across the visible spectrum, suggesting that charge generation is occurring either via a dominant single channel or via both channels but with comparable efficiencies. In contrast, blends of the narrow optical gap copolymer DPP-DTT with PC70BM show two distinct spectrally flat regions in their IQEs, consistent with the two channels operating at different efficiencies. The observed energy dependence of the IQE can be successfully modeled as two parallel photodiodes, each with its own energetics and exciton dynamics but both having the same extraction efficiency. Hence, an excitation-energy dependence of the IQE in this case can be explained as the interplay between two photocurrent-generating channels, without recourse to hot excitons or other exotic processes.

Unambiguous detection of nitrated explosive vapours by fluorescence quenching of dendrimer films

Unambiguous and selective standoff (non-contact) infield detection of nitro-containing explosives and taggants is an important goal but difficult to achieve with standard analytical techniques. Oxidative fluorescence quenching is emerging as a high sensitivity method for detecting such materials but is prone to false positives—everyday items such as perfumes elicit similar responses. Here we report thin films of light-emitting dendrimers that detect vapours of explosives and taggants selectively—fluorescence quenching is not observed for a range of common interferents. Using a combination of neutron reflectometry, quartz crystal microbalance and photophysical measurements we show that the origin of the selectivity is primarily electronic and not the diffusion kinetics of the analyte or its distribution in the film. The results are a major advance in the development of sensing materials for the standoff detection of nitro-based explosive vapours, and deliver significant insights into the physical processes that govern the sensing efficacy.

Probing the nanoscale phase separation in binary photovoltaic blends of poly(3-hexylthiophene) and methanofullerene by energy transfer

The generation of charge carriers in organic photovoltaic devices requires exciton diffusion to an interface of electron donor and acceptor materials, where charge separation occurs. We report a time resolved study of fluorescence quenching in films of poly(3-hexylthiophene) containing a range of fractions of the electron acceptor [6,6]-phenyl-C61-butyric acid methyl ester (PCBM). We show that energy transfer from P3HT to PCBM helps to bring excitons to the interface, where they dissociate into charge carriers. Fluorescence quenching in blends with < or = 50 wt% of PCBM is controlled by exciton diffusion in P3HT. This allows us to estimate the average size of PCBM domains to be about 9 nm in the 1:1 blend. The implications for polymer solar cells are discussed.

High‐Performance, Fullerene‐Free Organic Photodiodes Based on a Solution‐Processable Indigo

A solution-processable dibromoindigo with an alkyoxyphenyl solubilizing group is developed and used as a new electron acceptor in organic photodiodes. The solution-processed fullerene-free organic photodiodes show an almost spectrally flat response with a high responsivity (0.4 A W(-1)) and a high detectivity (1 × 10(12) Jones). These values are comparable to silicon-based photodiodes.

The binding and fluorescence quenching efficiency of nitroaromatic (explosive) vapors in fluorescent carbazole dendrimer thin films

We present a study on three generations of fluorescent carbazole dendrimers that exhibit strong binding with nitroaromatic compounds accompanied by photoluminescence (PL) quenching, making them attractive sensing materials for the detection of explosives such as 2,4,6-trinitrotoluene (TNT). The absorption and release of vapors of the (deuterated) TNT analogue 4-nitrotoluene (pNT) from thin films of the dendrimers were studied with a combination of time-correlated neutron reflectometry and PL spectroscopy. When saturated with pNT the PL of the films was fully quenched and could not be recovered with flowing nitrogen at room temperature but only upon heating to 40-80 °C. Although the majority of the absorbed pNT could be removed with this method the recovered films were found to still contain a residual pNT concentration of ~0.1 molecules per cubic nanometer. However, the proportion of the PL recovered increased with generation with the third generation dendrimer exhibiting close to full recovery despite the presence of residual pNT. This result is attributed to a combination of two effects. First, the dendrimer films present a range of binding sites for nitroaromatic molecules with the stronger binding sites surviving the thermal recovery process. Second, there is a large decrease of the exciton diffusion coefficient with dendrimer generation, preventing migration of the excitation to the remaining bound pNT.

Photophysics of Delocalized Excitons in Carbazole Dendrimers

The photophysical properties in solution of three generations of carbazole-based dendrons and dendrimers with fluorenyl surface groups were studied using steady-state, time-resolved femtosecond transient absorption and anisotropy, and coherent two-dimensional ultraviolet spectroscopy. It was found that increasing the generation caused a switch in the nature of the emissive state between the first-generation compounds and the second- and third-generation dendrimers. Time-resolved anisotropy measurements revealed low initial anisotropies that decreased with increasing dendrimer generation consistent with increasing intradendrimer interchromophore coupling. Two-dimensional UV spectroscopy showed that the signal from the second- and third-generation dendrimers is the product of multiple chromophores interacting. The maximum number of interacting chromophores is reached by the second generation.

Design protocols in triarylamine cored dendrimer-based explosive sensors

The preparation, photophysical characterisation and explosive sensing of two first-generation triarylamine-based dendrimers are reported. The dendrimers are constructed of a triphenylamine core, dendrons comprised of a phenyl branching unit with thiophene (Dendrimer 1) or bithiophene (Dendrimer 2) moieties, and dodecyl surface groups. By simply changing the number of thiophene units within the dendrons, it was found that the emissive chromophore could be switched from the centre (Dendrimer 1) to the dendrons (Dendrimer 2). Both Dendrimer 1 and 2 detected nitro-aromatic and -aliphatic analytes by fluorescence quenching, with the former showing a much greater response. In particular, Dendrimer 1 showed a particularly high affinity for the difficult-to-detect nitroaliphatic taggant 2,3-dinitro-2,3-dimethylbutane (DMNB). A combination of steady-state and time-resolved Stern–Volmer measurements revealed that the high affinity for DMNB was due to a combination of long luminescence lifetime and dominant static quenching.

Singlet energy transfer and singlet-singlet annihilation in light-emitting blends of organic semiconductors

Excitation energy transfer from host to guest is studied in spin-cast blends of 4,4′-bis(N-carbazolyl)biphenyl (CBP) and a phosphorescent fac-tris(2-phenylpyridyl)iridium(III)-cored dendrimer using time resolved fluorescence. The kinetics of energy transfer are consistent with homogeneous dispersion of the dendrimers in the CBP host. Diffusion-controlled singlet-singlet exciton annihilation is observed in the CBP host at moderate excitation densities, similar to those encountered in high brightness light-emitting devices and organic lasers. The results are important for organic lighting and the understanding of exciton diffusion in guest-host systems for electrophosphorescence.

Tuning the Optoelectronic Properties of Nonfullerene Electron Acceptors

Broad spectral coverage over the solar spectrum is necessary for photovoltaic technologies and is a focus for organic solar cells. We report a series of small-molecule, nonfullerene electron acceptors containing the [(benzo[c][1,2,5]thiadiazol-4-yl)methylene]malononitrile unit as a high electron affinity component. The optoelectronic properties of these molecules were fine-tuned with the objective of attaining strong absorption at longer wavelengths by changing the low-ionization-potential moiety. The electron-accepting function of these materials was investigated with poly(3-n-hexylthiophene) (P3HT) as a standard electron donor. Significant photocurrent generation in the near infrared region, with an external quantum yield reaching as high as 22 % at 700 nm and an onset >800 nm was achieved. The results support efficient hole transfer to P3HT taking place after light absorption by the acceptor molecules. A Channel II-dominated power conversion efficiency of up to 1.5 % was, thus, achieved.