Third-order nonlinear optical measurement

The nonlinear optical (NLO) susceptibilities of bioengineered aromatic polymers synthesized by enzyme-catalyzed reactions are given in Tables 2, 3, and 4. Homopolymers and copolymers are synthesized by enzyme-catalyzed reactions from aromatic monomers such as phenols and aromatic amines and their alkyl-substituted derivatives. The third-order nonlinear optical measurements are carried out in solutions at a concentration of 1 mg/mL of the solvent. Unless otherwise indicated, most of the polymers are solubilized in a solvent mixture of dimethyl formamide and methanol (DMF-MeOH) or dimethyl sulfoxide and methanol (DMSO-MeOH), both in a 4 1 ratio. These solvent mixtures are selected on the basis of their optical properties at 532 nm (where all the NLO measurements reported here are carried out), such as low noise and optical absorption, and solubility of the bioengineered polymers in the solvent system selected. To reduce light scattering, the polymer solutions are filtered to remove undissolved materials, the polymer concentrations are corrected for the final x calculations, and x values are extrapolated to the pure sample based on the concentrations of NLO materials in the solvent used. Other details of the experimental setup and calculations used to determine third-order nonlinear susceptibilities were given earlier and described in earlier publications [5,6,9,17-19]. 

There have been very few measurements made on the physical properties of Tg derivatives, their relative greater difficulty of preparation when compared with the Tg analogs has meant little interest in their properties. However, TglOSiMeslg has been found to show photoluminescence in the blue region of the spectrum, third-order nonlinear optical properties for TgMeg have been modeled, and electronic properties for and TgMeg have been calculated. 

Fig. 8. Examples of some of the donor-acceptor substituted TEEs prepared for the exploration of structure-property relationships in the second- and third-order nonlinear optical effects of fully two-dimensionally-conjugated chromophores. For all compounds, the second hyperpolarizability y [10 esu], measured by third harmonic generation experiments in CHCI3 solution at a laser frequency of either A = 1.9 or 2.1 (second value if shown) pm is given in parentheses. n.o. not obtained...

Measurement Techniques for Third-Order Nonlinear Optical Effects... 

In a recent communication we reported that the third order nonlinear optical susceptibility of Pt, Pb, and H2 tetrakis(cumylphenoxy)phthalocyanines was large and varied substantially with the metal substituent. (1) The structure of these compounds is shown in Fig. 1. The susceptibility was measured by degenerate four-wave mixing at 1.064 pm, a wavelength far from the main absorption bands of phthalocyanines near 650 nm. The nonlinear susceptibility of the Pt phthalocyanine was about a factor of 9 larger than that of the Pb phthalocyanine and a factor of 45 larger than the metal free compound. 

On the route to all-optical signal processing the development of materials with large third-order nonlinear optical effects is of decisive importance. For the material characterization and the assessment of its usefulness for applications the absolute value of the third-order nonlinear optical susceptibility y has to be known. Since most measurements are performed relative to a reference material, the establishment of a well accepted value for a standard material is important. 

The most widely employed material characterization techniques in third-order nonlinear optics are third-harmonic generation (THG) [21], degenerate four wave-mixing (DFWM) [22], Z-scan [6], and optical limiting by direct two-photon absorption (TPA) and fluorescence spectroscopy induced by TPA [23]. All of them will be discussed in the following. Further measurement techniques such as electric-field induced second-harmonic generation (EFISH) [24], optical Kerr... 

The first common method for molecular first hyperpolarizability determination is the electric field-induced second harmonic generation (EFISH) technique in solution [6-10]. This technique can be applied only to dipolar molecules. Under an applied external electric field, molecules in solution orient approximately in the direction of the field giving rise to second harmonic generation. The measured third-order nonlinear optical susceptibility is given by the following expression ... 

The third-order nonlinear optical susceptibility x was obtained by comparing the measured signals for the sample with that of carbon disulfide as reference under the same experimental condition. The measured x value is 6.2 x 10 esu for the subphthalocyanine at a concentration 1.25 x 10 M. Considering an isotropic media under the Lorenz-Lorentz approximation, the second hyperpolarizability value was found to be 3.0 x 10 esu. Furthermore, A pirc corresponding to the pure subphthalocyanine 17 was calculated to be 6.9 x 10 esu, about four times higher... 

Coherent Anti-Stokes Raman Scattering (CARS) Thermometry is a technique for temperature measurement in high temperature environments using a third-order nonlinear optical process involving a pump and a Stokes frequency laser beam that interacts with the sample and generates a coherent anti-Stokes frequency beam. 

Sinclair and coworkersmeasured the third-order nonlinear optical susceptibility of rm 5 -polyacetylene. The measured susceptibility was 5 x 10 esu, which is comparable to the magnitude of the large nonlinear susceptibilities measured in the polydiacetylenes. 

The temporal response of the third-order nonlinear optical susceptibility in poly(PTS) crystal was determined by time-resolved degenerate four-wave mixing (DFWM) by Carter and coworkers. The excited lifetime T ws measured to be 1.8 0.5 ps at 652 nm in the resonant region. The values of phase relxation time T2 measures by Hattori and Kobayashi for a cast film of poly(3BCMU) were 30 and 90 fs for the respective incident... 

We measured third order nonlinear optical susceptibility for all the compounds in... 

In conclusion we measured the real and imaginary components of the third-order nonlinear optical susceptibility for polybenzidine solutions from the results we obtained for intensity dependent transmission experiments the dominantmechanism causing the nonlinearity appears to be two-photon absorption. 

The third order nonlinear optical properties of monomers, polymers and copolymers were measured by DFWM in solution. The solutions of these materials were prepared in a solvent mixture of dimethyl formamide and methanol in the ratio 4 1 (v/v) at a concentration of 0.1% (w/v). The solvent mixture DMF MeOH (4 1) was used as a control. Measurements under identical conditions were made with carbon disulfide as the reference standard and this compound has a reported x value of 6.8 x 10 i3 esu (19). The schematic of the experimental setup is shown in Figure 2. 

As with phthalocyanines, the third-order nonlinear optical susceptibility, of porphyrins can be manipulated by chemical substitution. The third-order NLO properties of several tetraphenylporphyrin compounds were first reported by Meloney et The was measured by the degenerate four-wave mixing (DFWM) technique from... 

Table 7. Third-Order Nonlinear Optical Susceptibility Data of Metalloporphyrins Compounds Measured by Different Techniques...

Abstract The anisotropic third-order nonlinear optical susceptibility of monodomain samples of nematic solutions of poly[l,4-phenylene-2,6-benzobisthiazole], PBT, a rodlike polymer, have been studied by third harmonic generation. Corresponding measurements have also been made for isotropic solutions of PBT. A substantial off-diagonal component of X( H-3co o),co,co) is measured, resulting in the generation of an elliptically polarized third harmonic signal for a fundamental linearly polarized along the director. 

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