Cleber R. Mendonça

Optical properties of L-threonine crystals

Abstract Second- and third-order optical nonlinearities of L-threonine amino acid crystals grown from aqueous solution are investigated in this work. The absorption spectra indicate a good transparency between 250 and 1500 nm. Refractive indices were measured as a function of temperature and wavelength, allowing the determination of the thermo-optic and Sellmeier equation coefficients. Phase-matching curves for second harmonic generation from radiation at 1.064 μm were obtained. The conversion efficiency was measured along the entire phase-matching loci and its maximum value was found to be comparable to that of KDP. The nonlinear refractive index n 2 , measured through the Z-scan technique with femtosecond pulses, is of the order of 10 −20 m 2 /W.

Z-scan measurements using femtosecond continuum generation

We present a single beam Z-scan technique using an intense, broadband, white-light continuum (WLC) beam for the direct measurement of nonlinear absorption spectra. In order to demonstrate the validity of our technique, we compared the results of tetraaniline and Sudan 3 solutions obtained with WLC and conventional single wavelength light sources. Both approaches lead to the same nonlinear spectrum, indicating that the association of the Z-scan technique and the WLC source results in an useful method for the measurement of nonlinear spectra of both absorbing (saturable absorption or reverse saturable absorption) and transparent (two-photon absorption) samples.

Two-photon absorption in azoaromatic compounds

Abstract We report on the two-photon absorption (2PA) cross-section for eight azoaromatic compounds in dimethyl sulfoxide solutions, using the Z-scan technique with femtosecond laser pulses at 775 nm. The 2PA cross-sections of these molecules are of the order of (1–6)×10 −50 cm 4 s photon −1 . A correlation was established between the molecular structure and the two-photon absorption process, which makes it possible to develop molecular design strategies to create structures with suitable two-photon absorption coefficients.

Characterization of dynamic optical nonlinearities with pulse trains

We report a simple extension of the Z-scan technique where pulse trains characteristic of a Q-switched and mode-locked Nd:YAG laser are employed to investigate the dynamics of third-order optical nonlinearities. The method allows discriminating between fast and accumulative nonlinearities, and was applied to the investigation of liquid samples, namely chloroform, benzene, and a solution of Disperse Red 1 dye.

Femtosecond laser waveguide micromachining of PMMA films with azoaromatic chromophores

We report on the femtosecond-laser micromachining of poly(methyl methacrylate) (PMMA) films doped with nonlinear azoaromatic chromophores: Disperse Red 1, Disperse Red 13 and Disperse Orange 3. We study the conditions for controlling chromophore degradation during the micromachining of PMMA doped with each chromophore. Furthermore, we successfully used fs-micromachining to fabricate optical waveguides within a bulk sample of PMMA doped with these azochromophores.

Three-dimensional fabrication of optically active microstructures containing an electroluminescent polymer

Microfabrication via two-photon absorption polymerization is a technique to design complex microstructures in a simple and fast way. The applications of such structures range from mechanics to photonics to biology, depending on the dopant material and its specific properties. In this paper, we use two-photon absorption polymerization to fabricate optically active microstructures containing the conductive and luminescent polymer poly(2-methoxy-5-(2′-ethylhexyloxy)-1,4-phenylenevinylene) (MEH-PPV). We verify that MEH-PPV retains its optical activity and is distributed throughout the microstructure after fabrication. The microstructures retain the emission characteristics of MEH-PPV and allow waveguiding of locally excited fluorescence when fabricated on top of low refractive index substrates.

Resonant Nonlinear Absorption in Zn-Phthalocyanines

In this work, we investigate the nonlinear absorption dynamics of Zn phthalocyanine in dimethyl sulfoxide (DMSO). We used single pulse and pulse train Z-scan techniques to determine the dynamics and absorption cross-sections of singlet and triplet states at 532 nm. The excited singlet state absorption cross-section was determined to be 3.2 times higher than the ground state one, giving rise to reverse saturable absorption. We also observed that reverse saturable absorption occurs from the triplet state, after its population by intersystem crossing, whose characteristic time was determined to be 8.9 ns. The triplet state absorption cross-section determined is 2.6 times higher than the ground state one. In addition, we used the white light continuum Z-scan to evaluate the singlet excited state spectrum from 450 to 710 nm. The results show two well-defined regions, one above 600 nm, where reverse saturable absorption is predominant. Below 600 nm, we detected a strong saturable absorption. A three-energy-level diagram was used to explain the experimental results, leading to the excited state absorption cross-section determination from 450 nm up to 710 nm.

Optical storage in mixed Langmuir-Blodgett (LB) films of azopolymers and cadmium stearate

Abstract We present a comparative study on the optical storage characteristics of mixed Langmuir–Blodgett (LB) films from azobenzene polymers and cadmium stearate. The amplitude of induced birefringence depends on the azobenzene content in the polymer as well as on the rate of trans – cis – trans isomerization. Structural factors such as main chain rigidity seem to play an important role in the remaining stored information.

Characterization of dynamic optical nonlinearities in ytterbium bis-phthalocyanine solution

Abstract Dynamic optical nonlinearities of ytterbium bis-phthalocyanine (YbPc 2 ) dissolved in chloroform were characterized using the Z-scan technique with pulse trains. Two contributions of opposite signs were observed for the nonlinear refraction: a fast process related to the singlet population, and a slow accumulative contribution arising from the triplet population and thermal lensing. As the fluence increases, the nonlinear absorption first presents a weak saturation, followed by a reverse saturable absorption process. We used a six-energy-level diagram to explain these results and to obtain spectroscopic parameters such as the excited state cross-sections and the intersystem crossing lifetime.

Molecular Structure – Optical Property Relationships for a Series of Non-Centrosymmetric Two-photon Absorbing Push-Pull Triarylamine Molecules

This article reports on a comprehensive study of the two-photon absorption (2PA) properties of six novel push-pull octupolar triarylamine compounds as a function of the nature of the electron-withdrawing groups. These compounds present an octupolar structure consisting of a triarylamine core bearing two 3,3′-bis(trifluoromethyl)phenyl arms and a third group with varying electron-withdrawing strength (H < CN < CHO < NO2 < Cyet < Vin). The 2PA cross-sections, measured by using the femtosecond open-aperture Z-scan technique, showed significant enhancement from 45 up to 125 GM for the lowest energy band and from 95 up to 270 GM for the highest energy band. The results were elucidated based on the large changes in the transition and permanent dipole moments and in terms of (i) EWG strength, (ii) degree of donor-acceptor charge transfer and (iii) electronic coupling between the arms. The 2PA results were eventually supported and confronted with theoretical DFT calculations of the two-photon transition oscillator strengths.