Intensity noise in difference frequency generation-based tunable femtosecond MIR sources.

We characterize the intensity noise of two mid-infrared (MIR) ultrafast tunable (3.5-11 µm) sources based on difference frequency generation (DFG). While both sources are pumped by a high repetition rate Yb-doped amplifier delivering 200 µJ 300 fs at a central wavelength of 1030 nm, the first is based on intrapulse DFG (intraDFG), and the second on DFG at the output of an optical parametric amplifier (OPA). The noise properties are assessed through measurement of the relative intensity noise (RIN) power spectral density and pulse-to-pulse stability. The noise transfer mechanisms from the pump to the MIR beam is empirically demonstrated. As an example, improving the pump laser noise performance allows reduction of the integrated RIN (IRIN) of one of the MIR source from 2.7% RMS down to 0.4% RMS. The intensity noise is also measured at various stages and in several wavelength ranges in both laser system architectures, allowing us to identify the physical origin of their variation. This study presents numerical values for the pulse to pulse stability, and analyze the frequency content of the RINs of particular importance for the design of low-noise high repetition rate tunable MIR sources and future high performance time-resolved molecular spectroscopy experiments.

Inline amplification of mid-infrared intrapulse difference frequency generation.

We demonstrate an ultrafast mid-infrared source architecture that implements both intrapulse difference frequency generation (iDFG) and further optical parametric amplification (OPA), in an all-inline configuration. The source is driven by a nonlinearly compressed high-energy Yb-doped-fiber amplifier delivering 7.4 fs pulses at a central wavelength of 1030 nm, at a repetition rate of 250 kHz. It delivers 1 µJ, 73 fs pulses at a central wavelength of 8 µm, tunable over more than one octave. By enrolling all the pump photons in the iDFG process and recycling the long wavelength pump photons amplified in the iDFG in the subsequent OPA, we obtain an unprecedented overall optical efficiency of 2%. These performances, combining high energy and repetition rate in a very simple all-inline setup, make this technique ideally suited for a growing number of applications, such as high harmonic generation in solids or two-dimensional infrared spectroscopy experiments.

Enhanced intrapulse difference frequency generation in the mid-infrared by a spectrally dependent polarization state.

We present a technique to optimize the intrapulse difference frequency generation efficiency for mid-infrared generation. The approach employs a multi-order wave plate that is designed to selectively rotate the polarization state of the incoming spectral components on the relevant orthogonal axes for subsequent nonlinear interaction. We demonstrate a significant increase of the mid-infrared average power generated, of a factor ≥2.5 compared with the conventional scheme, owing to an optimally distributed number of photons enrolled in the difference frequency generation process.

CEP-stable high-energy ytterbium-doped fiber amplifier.

We report on the carrier-envelope phase (CEP) stabilization of a Yb-doped fiber amplifier system delivering 30 µJ pulses at 100 kHz repetition rate. A single-shot, every-shot measurement of the CEP stability based on a simple f-2f interferometer is performed, yielding a CEP standard deviation of 320 mrad rms over 1 s. Long-term stability is also assessed, with 380 mrad measured over 1 h. This level of performance is allowed by a hybrid architecture, including a passively CEP-stabilized front-end based on difference frequency generation and an active CEP stabilization loop for the fiber amplifier system, acting on a telecom-grade integrated LiNbO3 phase modulator. Together with recent demonstrations of temporal compression down to the few-cycle regime, the presented results demonstrate the relevance of the Yb-doped high repetition rate laser for attoscience.

High-power two-cycle ultrafast source based on hybrid nonlinear compression.

We demonstrate a hybrid dual-stage nonlinear compression scheme, which allows the temporal compression of 330 fs-pulses down to 6.8 fs-pulses, with an overall transmission of 61%. This high transmission is obtained by using a first compression stage based on a gas-filled multipass cell, and a second stage based on a large-core gas-filled capillary. The source output is fully characterized in terms of spectral, temporal, spatial, and short- and long-term stability properties. The system's compactness, stability, and high average power makes it ideally suited to drive high photon flux XUV sources through high harmonic generation.

Nonlinear pulse compression based on a gas-filled multipass cell.

We demonstrate nonlinear temporal compression of a high-energy Yb-doped fiber laser source in a multipass cell filled with argon. The 160 µJ 275 fs input pulses are compressed down to 135 µJ 33 fs at the output, corresponding to an overall transmission of 85%. We also analyze the output beam, revealing essentially no space-time couplings. We believe this technique can be scalable to higher pulse energies and shorter pulse durations, enabling access to a wider parameter range for a large variety of ultrafast laser sources.

Original Ti:Sa 10 kHz front-end design delivering 17 fs, 170 mrad CEP stabilized pulses up to 5 W.

We present a compact 10 kHz Ti:Sa front end relying on an original double-crystal regenerative amplifier design. This new configuration optimizes the thermal heat load management, allowing the production of a 110 nm large spectrum and maintaining a good beam profile quality. The front end delivers up to 5 W after compression, 17 fs pulses with a 170 mrad shot-to-shot residual carrier-envelope phase noise.

High-energy few-cycle Yb-doped fiber amplifier source based on a single nonlinear compression stage.

A simple, compact, and efficient few-cycle laser source at a central wavelength of 1 µm is presented. The system is based on a high-energy femtosecond ytterbium-doped fiber amplifier delivering 130 fs, 250 µJ pulses at 200 kHz, corresponding to 1.5 GW of peak power and an average power of 50 W. The unprecedented short pulse duration at the output of this system is obtained by use of spectral intensity and phase shaping, allowing for both gain narrowing mitigation and the compensation of the nonlinear accumulated spectral phase. This laser source is followed by a single-stage of nonlinear compression in a xenon-filled capillary, allowing for the generation of 14 fs, 120 µJ pulses at 200 kHz resulting in 24 W of average power. High-harmonic generation driven by this type of source will trigger numerous new applications in the XUV range and attosecond science.

ZnO@SnO2 engineered composite photoanodes for dye sensitized solar cells.

Layered multi-oxide concept was applied for fabrication of photoanodes for dye-sensitized solar cells based on ZnO and SnO2, capitalizing on the beneficial properties of each oxide. The effect of different combinations of ZnO@SnO2 layers was investigated, aimed at exploiting the high carrier mobility provided by the ZnO and the higher stability under UV irradiation pledged by SnO2. Bi-oxide photoanodes performed much better in terms of photoconversion efficiency (PCE) (4.96%) compared to bare SnO2 (1.20%) and ZnO (1.03%). Synergistic cooperation is effective for both open circuit voltage and photocurrent density: enhanced values were indeed recorded for the layered photoanode as compared with bare oxides (Voc enhanced from 0.39 V in case of bare SnO2 to 0.60 V and Jsc improved from 2.58 mA/cm(2) pertaining to single ZnO to 14.8 mA/cm(2)). Improved functional performances of the layered network were ascribable to the optimization of both high chemical capacitance (provided by the SnO2) and low recombination resistance (guaranteed by ZnO) and inhibition of back electron transfer from the SnO2 conduction band to the oxidized species of the electrolyte. Compared with previously reported results, this study testifies how a simple electrode design is powerful in enhancing the functional performances of the final device.

Controlling photoinduced electron transfer from PbS@CdS core@shell quantum dots to metal oxide nanostructured thin films.

N-type metal oxide solar cells sensitized by infrared absorbing PbS quantum dots (QDs) represent a promising alternative to traditional photovoltaic devices. However, colloidal PbS QDs capped with pure organic ligand shells suffer from surface oxidation that affects the long term stability of the cells. Application of a passivating CdS shell guarantees the increased long term stability of PbS QDs, but can negatively affect photoinduced charge transfer from the QD to the oxide and the resulting photoconversion efficiency (PCE). For this reason, the characterization of electron injection rates in these systems is very important, yet has never been reported. Here we investigate the photoelectron transfer rate from PbS@CdS core@shell QDs to wide bandgap semiconducting mesoporous films using photoluminescence (PL) lifetime spectroscopy. The different electron affinity of the oxides (SiO2, TiO2 and SnO2), the core size and the shell thickness allow us to fine tune the electron injection rate by determining the width and height of the energy barrier for tunneling from the core to the oxide. Theoretical modeling using the semi-classical approximation provides an estimate for the escape time of an electron from the QD 1S state, in good agreement with experiments. The results demonstrate the possibility of obtaining fast charge injection in near infrared (NIR) QDs stabilized by an external shell (injection rates in the range of 110-250 ns for TiO2 films and in the range of 100-170 ns for SnO2 films for PbS cores with diameters in the 3-4.2 nm range and shell thickness around 0.3 nm), with the aim of providing viable solutions to the stability issues typical of NIR QDs capped with pure organic ligand shells.

Highly crystalline strontium ferrites SrFeO(3-δ): an easy and effective wet-chemistry synthesis.

The synthesis of strontium ferrite SrFeO(3-δ) has been explored through wet-chemistry methods in order to optimize a quick, easy and reproducible method to obtain the perovskite in pure crystalline form with a high yield. Among the three investigated synthetic paths, (i) coprecipitation of hydroxides, (ii) coprecipitation of oxalates and (iii) polyol-assisted coprecipitation, only the second one was effective in obtaining the desired perovskite modification as a single phase. The products were analyzed by means of powder X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS), to determine the crystalline structure and the chemical composition of the sample surface, respectively, and to optimise the synthetic process. Pure samples were further characterised by means of inductively coupled plasma (ICP-AES) analysis, nitrogen adsorption, elemental analysis, temperature programmed reduction (TPR) and Mössbauer spectroscopy.

CdSe spherical quantum dots stabilised by thiomalic acid: biphasic wet synthesis and characterisation.

CdSe quantum dots stabilised by thiomalic acid have been synthesised by an aqueous biphasic ligand exchange reaction in air. The materials are completely water-soluble and were found to be stable over a long time. X-ray diffraction and transmission electron microscopy reveal the formation of CdSe nanocrystals with cubic structure (a=0.6077 nm; spatial group: F-43m). The average particle size is about 5 nm. Energy dispersive X-ray analysis shows that the nanocrystals are nonstoichiometric, with a Cd/Se ratio varying between 60/40 and 70/30, and indicates the presence of Cd(2+) ions at the nanocrystal surface. Diffuse reflectance infrared Fourier transform measurements suggest that thiomalic acid chelates CdSe through the thiol group and one carboxylic function, while the second COOH group is semi-free. A complex-like structure is proposed, in which thiomalic acid forms a five-membered chelate ring with the Cd(2+) ions present on the nanocrystal surface. Chelate effect accounts for the easiness of ligand exchange and is expected to additionally stabilise the nanosystem.

[Phytoterapy: a glimmer of hope in the prevention of recurrent respiratory tract infections in children]. / Fitoterapia: un barlume di speranza per la prevenzione delle infezioni respiratorie ricorrenti nel bambino.

Evidence on the efficacy of standardised phytoterapic extracts for the prevention of recurrent respiratory tract infections (RRTIs) in children is reviewed. Echinacea extracts are widely used in European countries and in the United States as immune-stimulating agents. However, further prospective, appropriately powered clinical studies are required to confirm their benefits in reducing duration and severity of RRTIs.

Soy-based formulas and phyto-oestrogens: a safety profile.

Phyto-oestrogens are non-steroidal plant-derived compounds that possess oestrogenic activity and act as selective oestrogen receptor modulators (SERMs). Among the dietary oestrogens, the isoflavone class enjoy a wide-spread distribution in most of the members of the Leguminosae family, including such prominent high-content representatives as soybean. Phyto-oestrogen research has grown rapidly in recent years owing to epidemiological studies suggesting that diets rich in soy may be associated with potential health benefits. There is a paucity of data on endocrine effects of soy phytochemicals during infancy, the most sensitive period of life for the induction of toxicity. The safety of isoflavones in infant formulas has been questioned recently owing to reports of possible hormonal effects. Infants fed soy formula receive high levels of phyto-oestrogens in the form of isoflavones (genistein, daidzein and their glycosides). To date, no adverse effects of short- or long-term use of soy proteins have been observed in humans and exposure to soy-based infant formulas does not appear to lead to different reproductive outcomes than exposure to cow milk formulas. Soy formula seems to be a safe feeding option for most infants. Nevertheless, much closer studies in experimental animals and human populations exposed to phyto-oestrogen-containing products, and particularly soy-based infant formulas, are necessary.