RESUMO
The CsPbX3 nanocrystals (NCs) with X = I, Br, Cl, or the mixture of Br:I and Br:Cl in a 1:1 ratio were synthesized and characterized by TEM, DLS, and XRD. Recrystallization of the small luminescent NCs in the metastable cubic phase into bigger orthorhombic nanocrystals was monitored by XRD and identified as the main cause of the nanocolloid coagulation. The recrystallization also leads to a decrease in the photoluminescence quantum yield (QY) of the colloidal solution and shortening of the emission lifetime. The two-photon absorption cross-section σ2 values calculated from femtosecond Z-scan measurements were compared with those obtained based on the two-photon excited emission technique. These two techniques were shown to be equivalent with the cross-section values calculated per molar mass of CsPbX3 perovskite being in the range of 10-200 GM depending on the halide anions X-. The σ2 values recalculated for the mole of the NCs were in the range of 104-105 GM, which is in good agreement with values previously reported elsewhere and the σ2/M parameter was in the range of 0.01 to 0.33. This study shows the perovskite NCs to be a good nonlinear material with the third-order nonlinear optical susceptibility χ(3) of the NCs on the order of 10-11 esu.
RESUMO
Very large molecular two- and three-photon absorption cross-sections are achieved by appending ligated bis(diphosphine)ruthenium units to oligo(p-phenyleneethynylene) (OPE)-based "stars" with arms up to 7â phenyleneethynylene (PE) units in length. Extremely large three- and four-photon absorption cross-sections, through the telecommunications wavelengths range and beyond, are obtained for these complexes upon optimizing OPE length and the ruthenium-coordinated peripheral ligand. Multi-photon absorption (MPA) cross-sections are optimized with stars possessing arms 2â PE units in length. Peripheral ligand variation modifies MPA merit and, in particular, 4-nitrophenylethynyl ligand incorporation enhances maximal MPA values and "switches on" four-photon absorption (4PA) in these low molecular-weight complexes. The 4-nitrophenylethynyl-ligated 2PE-armed star possesses a maximal four-photon absorption cross-section of 1.8×10-108 â cm8 s3 at 1750â nm, and significant MPA activity extending beyond 2000â nm.
RESUMO
New stilbenoid and thiophenic compounds terminally functionalized with donor-donor, acceptor-acceptor, or donor-acceptor moieties and possessing a central [2.2]paracyclophane unit have been prepared, and their properties interpreted in terms of through-bond and through space π-electron delocalization (i.e., π-conjugations). Based on photophysical data, their excited-state properties have been described with a focus on the participation of the central [2.2]paracyclophane in competition with through-bond conjugation in the side arms. To this end, two-photon and one-photon absorption and emission spectroscopy, as a function of temperature, solvent polarity, and pressure in the solid state have been recorded. Furthermore, charge delocalization through the [2.2]paracyclophane in the neutral state and in the oxidized species (radical cations, dications and radical trications) has been investigated, allowing the elucidation of the vibrational Raman fingerprint of through-space charge delocalization. Thus, a complementary approach to both "intermolecular" excitation and charge delocalizations in [2.2]paracyclophane molecules is shown which can serve as models of charge and exciton migration in organic semiconductors.
RESUMO
The nonlinear-optical properties of Prussian Blue nanoparticles have been evaluated with the use of femtosecond Z-scan measurements in the 1350-1750 nm range. This well-known inorganic pigment having interesting magnetic and electrochemical properties was found to be an efficient near-IR three-photon absorber. The maximum of the effective three-photon cross section is as high as 4.5 × 10-78 cm6 s2 at 1375 nm. By a comparison of the three-photon molar-mass-normalized merit factors, σ3/M, we show that this material is a competitive multiphoton absorber, especially in comparison to semiconductor quantum dots.
RESUMO
Three uncharged push-pull oxazol-5(4H)-ones were synthesized and thoroughly characterized. The examined molecules contained electron-donor and electron-acceptor groups interacting via a π-conjugated bridge. Spectral properties of the oxazol-5(4H)-ones were studied in detail in three solvents of different polarities. The results indicate a solvatochromic shift toward lower energy for the charge-transfer state. The compounds are weakly fluorescent in polar solvents, but they have high fluorescence quantum yields in nonpolar solvents. Their two-photon absorption (2PA) properties were characterized by the open- and closed-aperture Z-scan technique, by the pump-probe technique, and by the two-photon excited fluorescence method. The dyes exhibit relatively high effective two-photon absorption cross sections ranging from 490 to 2600 GM at ~100 GW/cm(2), according to the Z-scan results, which are found, however, to contain significant contribution from higher-order absorption processes. In addition, these compounds display good photostability.
RESUMO
Wide wavelength range (550-1600 nm) measurements of nonlinear optical properties of ca. 5 nm CdS quantum dots (QDs) colloidal solution were performed using the Z-scan technique with femtosecond laser pulses at 1 kHz. Parameters characterizing nonlinear absorption and nonlinear refraction were determined. Nonlinear absorption has the character of a two-, three- and four-photon process depending on the wavelength range, with the values of the relevant coefficients peaking at 750 nm, 1200 nm and 1500 nm, respectively. The order of the nonlinear processes was confirmed by measurements of the integral luminescence intensity vs. input excitation intensity. Maxima of the multi-photon absorption bands correspond to the second absorption band of the QDs. The maximum value of the two-photon absorption cross-section σ2 was estimated to be 7.2 × 10(-47) cm(4) s per QD at 750 nm.