RESUMEN
We present a comprehensive tensorial characterization of second-harmonic generation from silicon nitride films with varying compositions. The samples were fabricated using plasma-enhanced chemical vapor deposition, and the material composition was varied by the reactive gas mixture in the process. We found a six-fold enhancement between the lowest and highest second-order susceptibility, with the highest value of approximately 5 pm/V from the most silicon-rich sample. Moreover, the optical losses were found to be sufficiently small (below 6 dB/cm) for applications. The tensorial results show that all samples retain in-plane isotropy independent of the silicon content, highlighting the controllability of the fabrication process.
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Chirality is one of the most fundamental and essential structural properties of biological molecules. Many important biological molecules including amino acids and polysaccharides are intrinsically chiral. Conventionally, chiral species can be distinguished by interaction with circularly polarized light, and circular dichroism is one of the best-known approaches for chirality detection. As a linear optical process, circular dichroism suffers from very low signal contrast and lack of spatial resolution in the axial direction. It has been demonstrated that by incorporating nonlinear interaction with circularly polarized excitation, second-harmonic generation circular dichroism can provide much higher signal contrast. However, previous circular dichroism and second-harmonic generation circular dichroism studies are mostly limited to probe chiralities at surfaces and interfaces. It is known that second-harmonic generation, as a second-order nonlinear optical effect, provides excellent optical sectioning capability when combined with a laser-scanning microscope. In this work, we combine the axial resolving power of second-harmonic generation and chiral sensitivity of second-harmonic generation circular dichroism to realize three-dimensional chiral detection in biological tissues. Within the point spread function of a tight focus, second-harmonic generation circular dichroism could arise from the macroscopic supramolecular packing as well as the microscopic intramolecular chirality, so our aim is to clarify the origins of second-harmonic generation circular dichroism response in complicated three-dimensional biological systems. The sample we use is starch granules whose second-harmonic generation-active molecules are amylopectin with both microscopic chirality due to its helical structure and macroscopic chirality due to its crystallized packing. We found that in a starch granule, the second-harmonic generation for right-handed circularly polarized excitation is significantly different from second-harmonic generation for left-handed one, offering excellent second-harmonic generation circular dichroism contrast that approaches 100%. In addition, three-dimensional visualization of second-harmonic generation circular dichroism distribution with sub-micrometer spatial resolution is realized. We observed second-harmonic generation circular dichroism sign change across the starch granules, and the result suggests that in thick biological tissue, second-harmonic generation circular dichroism arises from macroscopic molecular packing. Our result provides a new method to visualize the organization of three-dimensional structures of starch granules. The second-harmonic generation circular dichroism imaging method expands the horizon of nonlinear chiroptical studies from simplified surface/solution environments to complicated biological tissues.
Asunto(s)
Dicroismo Circular/métodos , Imagenología Tridimensional/métodos , Almidón/química , Solanum tuberosum/químicaRESUMEN
We demonstrate a purely dielectric resonant waveguide structure that enhances the efficiency of second-harmonic generation by a factor of at least 5500 compared to a flat reference surface in the same geometry. We also show that the structure emits second-harmonic radiation in four different directions when the sample is illuminated with fundamental radiation incident at the resonant angle of the sample.
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Voltage-activated and spontaneous chloride-channel activity was studied in melanoma cell-line A2058 by patch-clamp technique. Whole-cell and inside-out patch recordings carried out with leak subtraction show voltage-activated chloride-conductance. In addition, a large leak-type conductance typical of epithelial cells was found in whole-cell experiments. This current was carried mostly by chloride-ions but also a leak-type potassium conductance was found showing KCl fluxes to be possible. Cell-attached and inside-out patch recordings showed at least two types of spontaneous chloride-channel activity. Bursting, flickering-type channels were found only in cell-attached recordings. That led to the conclusion that some intracellular factors are needed for that kind of activity. A second spontaneous, 30 pS chloride-channel with slow kinetics was found both in cell-attached and inside-out patch configuration. A voltage-activated chloride-channel found had a conductance of approximately 25 pS. In our experiments these channels did not need external calcium for activation. Voltage ramp recordings in cell-attached configuration gives the intracellular chloride concentration of 163 mM on the basis of chloride reversal potential (extracellular 146 mM in our experiments). Intracellular chloride concentration thus seems to be maintained slightly higher than the extracellular one.
Asunto(s)
Canales de Cloruro/fisiología , Cloruros/fisiología , Membrana Celular/fisiología , Conductividad Eléctrica , Humanos , Activación del Canal Iónico , Potenciales de la Membrana , Técnicas de Placa-Clamp , Potasio/fisiología , Células Tumorales CultivadasRESUMEN
The second-order nonlinear optical coefficients associated with chirality differ in sign for the two mirror-image forms (enantiomers) of a chiral material. Structures comprised of alternating stacks of the enantiomers can therefore be used for quasi-phase-matched frequency conversion, as we demonstrate here by second-harmonic generation from Langmuir-Blodgett films of a helicenebisquinone. Such structures could lead to new types of frequency converters in which both the second-order nonlinear response and quasi-phase-matching arise from the chirality of a material rather than its polar order.
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We provide evidence that the chirality of collagen can give rise to strong second-harmonic generation circular dichroism (SHG-CD) responses in nonlinear microscopy. Although chirality is an intrinsic structural property of collagen, most of the previous studies ignore that property. We demonstrate chiral imaging of individual collagen fibers by using a laser scanning microscope and type-I collagen from pig ligaments. 100% contrast level of SHG-CD is achieved with sub-micrometer spatial resolution. As a new contrast mechanism for imaging chiral structures in bio-tissues, this technique provides information about collagen morphology and three-dimensional orientation of collagen molecules.
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We have used a phase-conjugate interferometer to determine the real and imaginary parts of the third-order hyperpolarizability of 3,3'-diethyloxadicarbocyanine iodide (DODCI) and 4-methoxy-4'-nitrostilbene (MONS) at 1064 nm. For DODCI the values are enhanced by a two-photon resonance, and the two-photon extinction coefficient is determined. However, the nonlinear loss of DODCI is dominated by linear absorption from the two-photon excited state. We could not observe linear or nonlinear absorption for the MONS solutions, and we have determined the nonresonant third-order hyperpolarizability for this molecule.
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Behavior of the conjugate and specular reflections from a phase-conjugate resonator is studied in the presence of phase-conjugate mirror noise. Phase and amplitude fluctuations are described by a sudden-jump model. Analytical results show that the system is partially self-compensating for the phase noise. Numerical simulations of amplitude fluctuations reveal strong deviations from the coherent case when amplitude correlation time is long and the resonator is close to instability threshold.
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We describe a conical emission process that occurs when two beams of near-resonant light intersect as they pass through sodium vapor. The light is emitted on the surface of a circular cone that is centered on the bisector of the two applied beams and has an angular extent equal to the crossing angle of the two applied beams. We ascribe the origin of this effect to a perfectly phase-matched four-wave mixing process.
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The spatial effects of cross-phase modulation on a weak probe beam as it copropagates with an intense pump beam through a self-defocusing medium are investigated. Experimental results are presented that demonstrate induced focusing, beam deflection, and the spatial analog of optical wave breaking. The experimental results are in good qualitative agreement with theoretical predictions.
RESUMEN
A new approach to second-order nonlinear optical (NLO) materials is reported, in which chirality and supramolecular organization play key roles. Langmuir-Blodgett films of a chiral helicene are composed of supramolecular arrays of the molecules. The chiral supramolecular organization makes the second-order NLO susceptibility about 30 times larger for the nonracemic material than for the racemic material with the same chemical structure. The susceptibility of the nonracemic films is a respectable 50 picometers per volt, even though the helicene structure lacks features commonly associated with high nonlinearity. Susceptibility components that are allowed only by chirality dominate the second-order NLO response.