Nonlinear Absorption and Refraction of Picosecond and Femtosecond Pulses in HgTe Quantum Dot Films.

We report measurements of the saturated intensities, saturable absorption, and nonlinear refraction in 70-nm thick films containing 4 nm HgTe quantum dots. We demonstrate strong nonlinear refraction and saturable absorption in the thin films using tunable picosecond and femtosecond pulses. Studies were carried out using tunable laser pulses in the range of 400-1100 nm. A significant variation of the nonlinear refraction along this spectral range was demonstrated. The maximal values of the nonlinear absorption coefficients and nonlinear refractive indices determined within the studied wavelength range were -2.4 × 10-5 cm2 W-1 (in the case of 28 ps, 700 nm probe pulses) and -3 × 10-9 cm2 W-1 (in the case of 28 ps, 400 nm probe pulses), respectively. Our studies show that HgTe quantum dots can be used in different fields e.g., as efficient emitters of high-order harmonics of ultrashort laser pulses or as laser mode-lockers.

Oxidative C-H/C-H Coupling of Dipyrromethanes with Azines by TiO2-Based Photocatalytic System. Synthesis of New BODIPY Dyes and Their Photophysical and Electrochemical Properties.

Oxidative C-H/C-H coupling reactions of dipyrromethanes with azines in the presence of a heterophase oxidative photocatalytic system (O2/TiO2/visible light irradiation) were carried out. As a result of cyclization of obtained compounds with boron trifluoride etherate, new hetaryl-containing derivatives of 4,4-difluoro-4-boron-3a,4a-diaza-s-indacene were synthesized. For the obtained compounds, absorption and luminescence spectra, quantum yields of luminescence as well as cyclic volt-amperograms were measured.

Nonlinear Optical Characterization of InP@ZnS Core-Shell Colloidal Quantum Dots Using 532 nm, 10 ns Pulses.

InP@ZnS core-shell colloidal quantum dots (CQDs) were synthesized and characterized using the z-scan technique. The nonlinear refraction and nonlinear absorption coefficients (γ = -2 × 10-12 cm2 W-1, ß = 4 × 10-8 cm W-1) of these CQDs were determined using 10 ns, 532 nm pulses. The saturable absorption (ß = -1.4 × 10-9 cm W-1, Isat = 3.7 × 108 W cm-2) in the 3.5 nm CQDs dominated at small intensities of the probe pulses (I ≤ 7 × 107 W cm-2) followed by reverse saturable absorption at higher laser intensities. We report the optical limiting studies using these CQDs showing the suppression of propagated nanosecond radiation in the intensity range of 8 × 107-2 × 109 W cm-2. The role of nonlinear scattering is considered using off-axis z-scan scheme, which demonstrated the insignificant role of this process along the whole range of used intensities of 532 nm pulses. We discuss the thermal nature of the negative nonlinear refraction in the studied species.

Synthesis and low-order optical nonlinearities of colloidal HgSe quantum dots in the visible and near infrared ranges.

We synthesize colloidal HgSe quantum dots and characterize their nonlinear refraction and nonlinear absorption using a Nd:YAG laser and its second harmonic. The 7.5 nm quantum dots were synthesized using the hot-injection method. The nonlinear absorption (ß = 9×10-7 cm W-1) and negative nonlinear refraction (γ = -5×10-12 cm2 W-1) coefficients of colloidal quantum dots were determined using the 10 ns, 532 nm laser radiation. The joint influence of above processes was realized at a higher intensity of probe pulses. In the case of 10 ns, 1064 nm radiation, only negative nonlinear refraction dominated during z-scans of these quantum dots. The studies of optical limiting using two laser sources demonstrated the effectiveness of this process at 532 nm. The role of nonlinear scattering is analyzed. We discuss the mechanisms responsible for the nonlinear refraction processes in colloidal HgSe quantum dots.

Studying the size-selective precipitation of colloidal quantum dots by decomposing the excitation-emission matrix.

The exciton peak in the excitation-emission matrix (EEM) of colloidal quantum dots implicitly contains information about inhomogeneous broadening and the photoluminescence (PL) and photoluminescence excitation (PLE) spectra of individual particles in the vicinity of the absorption onset. A numerical procedure for extracting this information has been developed and applied to the EEMs of polydisperse InP/ZnS core/shell colloidal quantum dots and their supernatant solutions obtained by partial precipitation with a non-solvent. The inhomogeneous broadenings obtained in this way have been converted by the sizing curve into particle-size distributions. These distributions have been found to be in agreement with the size-selective precipitation theory proposed recently. The homogeneous PL and PLE line shapes obtained by analyzing the EEMs were found to satisfy the Kennard-Stepanov relation, which is the first more or less direct evidence of its validity for colloidal quantum dots.

Towards understanding the behavior of indigo thin films in organic field-effect transistors: a template effect of the aliphatic hydrocarbon dielectric on the crystal structure and electrical performance of the semiconductor.

Here we report a systematic investigation of indigo thin films grown on different dielectric underlayers. It has been revealed that aliphatic hydrocarbon chains serve as templates inducing the formation of a new crystal modification of indigo which possesses advanced charge transport properties and affords a dramatic improvement in the electrical performance of organic field-effect transistors.

Influence of surfactant polydispersity on the structure of polyoxyethylene (5) nonylphenyl ether/cyclohexane/water reverse microemulsions.

The distribution of the number of oxyethylene groups in molecules of polyoxyethylene (5) nonylphenyl ether (NP5) is shown to significantly affect the structure of NP5/cyclohexane/water reverse microemulsions. The effect is caused by the difference in solubility of NP5 components. This difference leads to fractionation: surfactant molecules dissolved in the intermicellar nonpolar medium have, on average, shorter polyoxyethylene chains than surfactant molecules forming reverse micelles. A model is proposed which takes into account the influence of this fractionation on reverse micelle size and free surfactant concentration. The validity of this model for NP5/cyclohexane/water reverse microemulsions is experimentally confirmed by dynamic light scattering. It is found that changing the degree of surfactant fractionation in the above mentioned microemulsions can result in the formation of non-spherical reverse micelles.

Material structure-composite morphology-photovoltaic performance relationship for organic bulk heterojunction solar cells.

Conjugated PPV-PPE copolymer has been investigated in organic solar cells in combination with twelve different fullerene derivatives. It was shown that the length of solubilizing alkyl chains in the fullerene derivative structures correlates well with the performance of photovoltaic cells.

Indigo--a natural pigment for high performance ambipolar organic field effect transistors and circuits.

Millenniums-old natural dye indigo--a "new" ambipolar organic semiconductor. Indigo shows balanced electron and hole mobilities of 1 × 10(-2) cm(2) V(-1) s(-1) and good stability against degradation in air. Inverters with gains of 105 in the first and 110 in the third quadrant are demonstrated. Fabricated entirely from natural and biodegradable compounds, these devices show the large potential of such materials for green organic electronics.

[70]fullerene-based materials for organic solar cells.

The synthesis, characterization and photovoltaic study of two novel derivatives of [70]fullerene, phenyl-C71-propionic acid propyl ester ([70]PCPP) and phenyl-C71-propionic acid butyl ester ([70]PCPB), are reported. [70]PCPP and [70]PCPB outperform the conventional material (6,6)-phenyl-C71-butyric acid methyl ester ([70]PCBM) in solar cells based on poly(2-methoxy-5-{3',7'-dimethyloctyloxy}-p-phenylene vinylene) (MDMO-PPV) as a donor polymer using chlorobenzene (CB) or dichlorobenzene (DCB) as solvents. AFM data suggest that improvement of the device efficiency should be attributed to the increased phase compatibility between the novel C70 derivatives and the polymer matrix. [70]PCPP and [70]PCBM showed more or less equally high performances in solar cells comprising poly(3-hexylthiophene) (P3HT) as a donor polymer. Optical modeling revealed that the application of [70]fullerene derivatives as acceptor materials in P3HT-based bulk heterojunction solar cells might give approximately 10 % higher short circuit current densities than using C60-based materials such as [60]PCBM. The high solubility of [70]PCPP and [70]PCPB and their good compatibility with the donor polymers suggest these fullerene derivatives as promising electron acceptor materials for use in efficient bulk heterojunction organic solar cells.

On the composition fluctuations of reverse micelles.

The polydispersity of the reverse micelles is determined mainly by the fluctuations of their composition. The composition of the reverse micelle is a two-dimensional random variable whose components are the numbers of water (i) and surfactant (j) molecules. In this study the fluctuations of the composition of the reverse micelles are considered in the Gaussian approximation. It is shown that the standard deviation of the quantity w=i/j may be calculated from the dependence of the water vapor pressure above the microemulsion on the molar ratio W=[water]/[surfactant]. The estimation based on the literature data for microemulsion system sodium bis(2-ethylhexyl)sulfosuccinate/water/isooctane at 37°C in the range W=0-18 has shown that the relative standard deviation of the quantity w is about 10%. It is shown that the value of the composition fluctuations is related to the dependence of average composition on the concentration of reverse micelles at constant parameter W.

Self-assembly of thiophene- and furan-appended methanofullerenes with poly(3-hexylthiophene) in organic solar cells.

Novel fullerene derivatives bearing thiophene and furan residues were synthesized and studied as electron acceptor materials in bulk heterojunction organic solar cells, together with poly(3-hexylthiophene) (P3HT) as the donor polymer. Some compounds showed large nanomorphological inhomogenities in blends with P3HT; in particular, clusters with dimensions in the range of 100-1000 nm were formed. However, some blends that showed such large clusters yielded at the same time high power conversion efficiencies in photovoltaic devices, approaching 3.7 %. This is in sharp contrast with previously studied systems, in which a substantial phase separation always resulted in a poor photovoltaic performance. We assume that the attachment of thienyl or furyl groups to the fullerene cage results in a certain ordering of the designed fullerene derivatives I-IX with P3HT in photoactive blends. Both the fullerene derivative and P3HT might assemble via pi-pi stacking of the thiophene units to form the nanostructures observed in the films by optical and atomic force microscopy. The presence of ordered donor and acceptor counterparts in these nanostructures results in superior photovoltaic device operation.

Organic solar cells with semitransparent metal back contacts for power window applications.

To provide truly transparent solar cells for power window applications, both semiconductor and electrode materials have to have a very low absorption over as much of the visible spectrum as possible. We present some promising visible transparent semiconductor combinations, namely zinc-phthalocyanine or zinc-naphthalocyanine together with soluble fullerenes in conjunction with a method for obtaining highly transparent thin metal films by tuning the interference patterns in the multilayer organic solar cells structure. In an optimal combination, solar cells with an efficiency of about 0.5 % and a peak transparency of more than 60 % in the visible part of the spectrum were fabricated.

Growth kinetics for AgI nanoparticles in AOT reverse micelles: effect of molecular length of hydrocarbon solvents.

The growth kinetics for AgI nanoparticles formed in the solutions of water/AOT reverse micelles in n-hexane, n-octane, n-decane, and n-dodecane were investigated. In small micelles, the rate of nanoparticles growth was found to be independent of the type of solvent, while in large micelles the growth rate grew with increasing length of solvent molecules. The effect was explained by a different amount of free water in the micelle pools of the same size.