ABSTRACT
Many methods commonly used to characterize ultrafast laser pulses, such as the frequency-resolved optical gating (FROG) or the dispersion scan (d-scan), face problems when they are used on pulses with a spectrum or phase varying within the laser beam cross section or the acquisition time. The presence of such pulse shape variation leads to discrepancy between the measured FROG trace and its reconstructed counterparts. Nevertheless, it is difficult to reliably discern this shape variation because even the distorted experimental FROG trace can be reasonably reproduced by a realistic pulse shape. In this work, we examine and discern the variation of the pulse shape based on a new method, dispersion-scan FROG (D-FROG), which combines the idea of dispersion scanning with the FROG method. This technique provides a means of careful evaluation of the laser pulse based on a set of FROG traces connected by known dispersion changes. Therefore, this method can disclose seemingly correct pulse retrievals from distorted datasets. The D-FROG method can be used as a simple extension of the FROG technique to provide a consistency check able to identify the shortcomings in the pulse characterization.
ABSTRACT
Semiconducting polymers, particularly of the third generation, including donor-acceptor (D-A) copolymers, are extensively studied due to their huge potential for photonic and electronic applications. Here, we report on two new D-A copolymers, CP1 and CP2, composed of different electron-donor (D) units: 9-(2-ethylhexyl)carbazole or dibenzothiophene-5,5-dioxide, respectively, and of 4,7-bis(4'-(2-octyldodecyl)thiophen-2'-yl)-5,6-difluorobenzo[c][1,2,5]thiadiazole building block with central 5,6-difluorobenzo[c][1,2,5]thiadiazole electron-acceptor (A) units, which were synthesized by Suzuki coupling in the high-boiling solvent xylene and characterized. The copolymers exhibited very good thermal and oxidation stability. A copolymer CP1 with different molecular weights was prepared in order to facilitate a comparison of CP1 with CP2 of comparable molecular weight and to reveal the relationship between molecular weight and properties. The photophysical, electrochemical, and electroluminescence properties were examined. Intense red photoluminescence (PL) with higher PL efficiencies for CP1 than for CP2 was observed in both solutions and films. Red shifts in the PL thin film spectra compared with the PL solution spectra indicated aggregate formation in the solid state. X-ray diffraction measurements revealed differences in the arrangement of molecules in thin films depending on the molecular weight of the copolymers. Light-emitting devices with efficient red emission and low onset voltages were prepared and characterized.
ABSTRACT
Thin films made of formamidinium lead iodide (FAPbI3) perovskites prepared by a two-step sequential deposition method using various solvents for formamidinium iodide (FAI) - isopropanol, n-butanol and tert-butanol, were studied with the aim of finding a correlation between morphology and solvent properties to improve film quality. They were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM) and their photophysical properties were studied by means of absorption and photoluminescence (PL) spectroscopies. XRD patterns, absorption and PL spectra proved α-phase formation for all selected solvents. An excessive amount of PbI2 found in perovskite films prepared with n-butanol indicates incomplete conversion. Thin film morphology, such as grain and crystallite size, depended on the solvent. Using tert-butanol, thin films with a very large grain size of up to several micrometers and with preferred crystallite orientation were fabricated. The grain size increased as follows: 0.2-0.5, 0.2-1 and 2-5 µm for isopropanol, n-butanol and tert-butanol, respectively. A correlation between the grain size and viscosity, electric permittivity and polarizability of the solvent could be considered. Our results, including fabrication of perovskite films with large grains and fewer grain boundaries, are important and of interest for many optoelectronic applications.
ABSTRACT
A targeted shaping of complex femtosecond pulse waveforms and their characterization is essential for many spectroscopic applications. A 4f pulse shaper combined with an advanced pulse characterization technique should, in the idealized case, serve this purpose for an arbitrary pulse shape. This is, however, violated in the real experiment by many imperfections and limitations. Although the complex waveform generation has been studied in-depth, the comparison of the effects of various experimental factors on the actual pulse shape has stayed out of focus so far. In this paper, we present an experimental study on the targeted generation and retrieval of complex pulses by using two commonly-used techniques: spatial-light-modulator (SLM)-based 4f pulse shaper and second-harmonic generation frequency-resolved optical gating (FROG) and cross-correlation FROG (XFROG). By combining FROG and XFROG traces, we analyze the pulses with SLM-adjusted complex random phases ranging from simple to very complex waveforms. We demonstrate that the combination of FROG and XFROG ensures highly consistent pulse retrieval, irrespective of the used retrieval algorithm. This enabled us to evaluate the role of various experimental factors on the agreement between the simulated and actual pulse shape. The factors included the SLM pixelation, SLM pixel crosstalk, finite laser focal spot in the pulse shaper, or interference fringes induced by the SLM. In particular, we observe that including the SLM pixelation and crosstalk effect significantly improved the pulse shaping simulation. We demonstrate that the complete simulation can faithfully reproduce the pulse shape. Nevertheless, even in this case, the intensity of individual peaks differs between the retrieved and simulated pulses, typically by 10-20% of the peak value, with the mean standard deviation of 5-9% of the maximum pulse intensity. We discuss the potential sources of remaining discrepancies between the theoretically expected and experimentally retrieved pulse.
ABSTRACT
The targeted shaping of femtosecond pulses in 4f pulse shapers is complicated by, among other factors, the crosstalk between adjacent pixels of a spatial light modulator (SLM). Current methods for the crosstalk evaluation require setting up a different experiment, which is highly inconvenient. Here, we propose a simple procedure to extract the pixel crosstalk within the standard SLM calibration used in pulse shaping. The calibration is based on an analysis of the contrast of a periodic modulation in the spectra induced via SLM. We demonstrate the calibration procedure on a liquid-crystal-based SLM and show that we attain a constant crosstalk effect represented by a Gaussian function with σ=1.0 pix over a broad operational range of the SLM.
