Exciton Regeneration at Polymeric Semiconductor Heterojunctions

Control of the band-edge offsets at heterojunctions between organic semiconductors allows efficient operation of either photovoltaic or light-emitting diodes. We investigate systems where the exciton is marginally stable against charge separation, and show via E-field-dependent time-resolved photoluminescence spectroscopy that excitons that have undergone charge separation at a heterojunction can be efficiently regenerated. This is because the charge transfer produces a geminate electron-hole pair (separation 2.2-3.1nm) which may collapse into an exciplex and then endothermically (E=100-200meV) back-transfer towards the exciton.Comment: 10 pages, 4 figures. Manuscript in press in Phys. Rev. Let

Verrucae vulgaris (warts)

This issue of eMedRef provides information to clinicians on the pathophysiology, diagnosis, and therapeutics of verrucae vulgaris

Efficient Energy Transport in an Organic Semiconductor Mediated by Transient Exciton Delocalization

Efficient energy transport is highly desirable for organic semiconductor (OSC) devices such as photovoltaics, photodetectors, and photocatalytic systems. However, photo-generated excitons in OSC films mostly occupy highly localized states over their lifetime. Energy transport is hence thought to be mainly mediated by the site-to-site hopping of localized excitons, limiting exciton diffusion coefficients to below ~10-2 cm2/s with corresponding diffusion lengths below ~50 nm. Here, using ultrafast optical microscopy combined with non-adiabatic molecular dynamics simulations, we present evidence for a new highly-efficient energy transport regime: transient exciton delocalization, where energy exchange with vibrational modes allows excitons to temporarily re-access spatially extended states under equilibrium conditions. In films of highly-ordered poly(3-hexylthiophene) nanofibers, prepared using living crystallization-driven self-assembly, we show that this enables exciton diffusion constants up to 1.1±0.1 cm2/s and diffusion lengths of 300±50 nm. Our results reveal the dynamic interplay between localized and delocalized exciton configurations at equilibrium conditions, calling for a re-evaluation of the basic picture of exciton dynamics. This establishes new design rules to engineer efficient energy transport in OSC films, which will enable new devices architectures not based on restrictive bulk heterojunctions

Tuning the wavelength of lasing emission in organic semiconducting laser by the orientation of liquid crystalline conjugated polymer

We report the optical pumping of one-dimensional distributed feedback (DFB) conjugated polymer devices using a uniaxially aligned liquid crystalline polymer, poly(9,9-dioctylfluorene). We can independently select the alignment direction (via a rubbed polyimide layer) and the DFB structure (via nanoimprinting). In comparison with unaligned film, we show that lasing threshold is substantially reduced when absorption is parallel to the aligned direction (similar to 20.0 mu J cm(-2) pulse(-1)). This is mainly due to the higher absorption coefficient estimated in the table by calculating the exciton densities at each threshold value. We also report the control of lasing wavelength through independent selection of alignment direction and DFB orientation, which is achieved through the control of the effective refractive index of waveguide (n(eff)).open171

Morphology, structure and optical properties of low bandgap organic-inorganic halide perovskite based on CH₃NH₃SnxPb₁₋ₓI₃

Herein, we investigate morphology, structure and optical properties of low band gap organic-inorganic halide perovskite based on a mixture of lead and tin as the divalent cation in ABX3 structure. A significant change in morphology of CH3NH3SnxPb1−xI3 perovskite with x as well as an alteration in crystal structure from I4cm (β-phase) to pseudocubic P4mm (α-phase) space groups is observed when Sn is the dominant divalent cation (x ≥ 0.5). Photo thermal defection optical absorption spectroscopy (PDS) and photoluminescence (PL) of CH3NH3SnxPb1−xI3 show the non-linear change in the band edge of perovskite. The bandgap as low as 1.17 eV and the most red-shifted PL at 1035nm is achieved for perovskite with x=0.8. In addition, higher electronic disorder is measured for CH3NH3SnxPb1−xI3 compounds with higher x

The role of intermolecular coupling in the photophysics of disordered organic semiconductors: Aggregate emission in regioregular polythiophene

We address the role of excitonic coulping on the nature of photoexcitations in the conjugated polymer regioregular poly(3-hexylthiophene). By means of temperature-dependent absorption and photoluminescence spectroscopy, we show that optical emission is overwhelmingly dominated by weakly coupled H-aggregates. The relative absorbance of the 0-0 and 0-1 vibronic peaks provides a powerfully simple means to extract the magnitude of the intermolecular coupling energy, approximately 5 and 30 meV for films spun from isodurene and chloroform solutions respectively.Comment: 10 pages, 4 figures, published in Phys. Rev. Let