Microgravity Processing of Biopolymer/Metal Composites for NLO Applications

1998 ◽  
Vol 551 ◽  
Author(s):  
C.M. Cuttle ◽  
M.V. Cattaneo ◽  
J.D. Gresser ◽  
D.L. Wise ◽  
D.O. Frazier ◽  
...  

AbstractThe overall objective of this project is the development of NLO-active materials with optical clarity and mechanical strength. These materials are intended for laser eye protection. By combining χ2 and χ3 optical properties, the intensity of incident laser radiation may be efficiently reduced. Using an in-plane poling technique, aligned films of liquid crystal poly(benzyl-Lglutamate), PBLG, were made which showed higher second harmonic generation (SHG) values compared to quartz. Silver sols in the 10-90 nm diameter size range were complexed with tricyanovinyl aniline, TCVA, resulting in composite PBLG/Ag Sol films with higher than at least an order of magnitude of χ3 values materials such as polydiacetylenes and nitroanilines. These polymeric NLO materials offer definite advantages in terms of easy processability into films for the manufacture of the optical elements necessary for laser eye protection.

Author(s):  
E. Betzig ◽  
A. Harootunian ◽  
M. Isaacson ◽  
A. Lewis

In general, conventional methods of optical imaging are limited in spatial resolution by either the wavelength of the radiation used or by the aberrations of the optical elements. This is true whether one uses a scanning probe or a fixed beam method. The reason for the wavelength limit of resolution is due to the far field methods of producing or detecting the radiation. If one resorts to restricting our probes to the near field optical region, then the possibility exists of obtaining spatial resolutions more than an order of magnitude smaller than the optical wavelength of the radiation used. In this paper, we will describe the principles underlying such "near field" imaging and present some preliminary results from a near field scanning optical microscope (NS0M) that uses visible radiation and is capable of resolutions comparable to an SEM. The advantage of such a technique is the possibility of completely nondestructive imaging in air at spatial resolutions of about 50nm.


2018 ◽  
Vol 9 ◽  
pp. 2306-2314 ◽  
Author(s):  
Valerio F Gili ◽  
Lavinia Ghirardini ◽  
Davide Rocco ◽  
Giuseppe Marino ◽  
Ivan Favero ◽  
...  

Background: Dielectric nanoantennas have recently emerged as an alternative solution to plasmonics for nonlinear light manipulation at the nanoscale, thanks to the magnetic and electric resonances, the strong nonlinearities, and the low ohmic losses characterizing high refractive-index materials in the visible/near-infrared (NIR) region of the spectrum. In this frame, AlGaAs nanoantennas demonstrated to be extremely efficient sources of second harmonic radiation. In particular, the nonlinear polarization of an optical system pumped at the anapole mode can be potentially boosted, due to both the strong dip in the scattering spectrum and the near-field enhancement, which are characteristic of this mode. Plasmonic nanostructures, on the other hand, remain the most promising solution to achieve strong local field confinement, especially in the NIR, where metals such as gold display relatively low losses. Results: We present a nonlinear hybrid antenna based on an AlGaAs nanopillar surrounded by a gold ring, which merges in a single platform the strong field confinement typically produced by plasmonic antennas with the high nonlinearity and low loss characteristics of dielectric nanoantennas. This platform allows enhancing the coupling of light to the nanopillar at coincidence with the anapole mode, hence boosting both second- and third-harmonic generation conversion efficiencies. More than one order of magnitude enhancement factors are measured for both processes with respect to the isolated structure. Conclusion: The present results reveal the possibility to achieve tuneable metamixers and higher resolution in nonlinear sensing and spectroscopy, by means of improved both pump coupling and emission efficiency due to the excitation of the anapole mode enhanced by the plasmonic nanoantenna.


2019 ◽  
Vol 48 (47) ◽  
pp. 17620-17625 ◽  
Author(s):  
Wenhao Xing ◽  
Naizheng Wang ◽  
Yangwu Guo ◽  
Zhuang Li ◽  
Jian Tang ◽  
...  

Two RE-based quaternary metal chalcogenides EuCdGeQ4 (Q = S, Se) are discovered. They possess many attractive properties as preferred IR NLO materials including large band gaps, phase-matched intense SHG and congruent melting behavior.


2019 ◽  
Vol 5 (10) ◽  
pp. eaav8262 ◽  
Author(s):  
Matthew S. Davis ◽  
Wenqi Zhu ◽  
Jay K. Lee ◽  
Henri J. Lezec ◽  
Amit Agrawal

The potential for enhancing the optical activity of natural chiral media using engineered nanophotonic components has been central in the quest toward developing next-generation circular-dichroism spectroscopic techniques. Through confinement and manipulation of optical fields at the nanoscale, ultrathin optical elements have enabled a path toward achieving order-of-magnitude enhancements in the chiroptical response. Here, we develop a model framework to describe the underlying physics governing the origin of the chiroptical response in optical media. The model identifies optical activity to originate from electromagnetic coupling to the hybridized eigenstates of a coupled electron-oscillator system, whereas differential absorption of opposite handedness light, though resulting in a far-field chiroptical response, is shown to have incorrectly been identified as optical activity. We validate the model predictions using experimental measurements and show them to also be consistent with observations in the literature. The work provides a generalized framework for the design and study of chiroptical systems.


1991 ◽  
Vol 224 ◽  
pp. 531-549 ◽  
Author(s):  
Michael S. Longuet-Higgins

In two recent papers (Longuet-Higgins 1989a,b) the author showed that the shape oscillations of bubbles can emit sound like a monopole source, at second order in the distortion parameter ε. In the second paper (LH2) it was predicted that the emission would be amplified when the second harmonic frequency 2σn of the shape oscillation approaches the frequency ω of the breathing mode. This ‘resonance’ would however be drastically limited by damping due to acoustic radiation and thermal diffusion. The predictions were confirmed by further numerical calculations in Longuet-Higgins (1990a).Ffowcs Williams & Guo (1991) have questioned the conclusions of LH2 on the grounds that near resonance there is a slow (secular) transfer of energy between the shape oscillation and the volumetric mode which tends to diminish the amplitude of the shape oscillation and hence falsify the perturbation analysis. They have also argued that the volumetric mode never grows sufficiently to produce sound of the stated order of magnitude. In the present paper we show that these assertions are unfounded. Ffowcs Williams & Guo considered only undamped oscillations. Here we show that when the appropriate damping is included in their analysis the secular transfer of energy becomes completely insignificant. The resulting pressure pulse (figure 5 below) is found to be essentially identical to that calculated in LH2, figure 3. Moreover, in the initial-value problem considered in LH2, the excitation of the volumetric mode takes place not by a secular energy transfer but by a resonance during the first few cycles of the shape oscillation. This accounts for the amplification near resonance found in Longuet-Higgins (1990a). Finally, it is pointed out that the initial energy of the shape oscillations is far greater than is required to produce the O(ε2) volume pulsations that were studied in LH2, and which were used for a comparison with field data. This acoustic radiation was not calculated by Ffowcs Williams & Guo.


2016 ◽  
Vol 23 (4) ◽  
pp. 959-965 ◽  
Author(s):  
Justin A. Newman ◽  
Shijie Zhang ◽  
Shane Z. Sullivan ◽  
Ximeng Y. Dow ◽  
Michael Becker ◽  
...  

Synchronous digitization, in which an optical sensor is probed synchronously with the firing of an ultrafast laser, was integrated into an optical imaging station for macromolecular crystal positioning prior to synchrotron X-ray diffraction. Using the synchronous digitization instrument, second-harmonic generation, two-photon-excited fluorescence and bright field by laser transmittance were all acquired simultaneously with perfect image registry at up to video-rate (15 frames s−1). A simple change in the incident wavelength enabled simultaneous imaging by two-photon-excited ultraviolet fluorescence, one-photon-excited visible fluorescence and laser transmittance. Development of an analytical model for the signal-to-noise enhancement afforded by synchronous digitization suggests a 15.6-fold improvement over previous photon-counting techniques. This improvement in turn allowed acquisition on nearly an order of magnitude more pixels than the preceding generation of instrumentation and reductions of well over an order of magnitude in image acquisition times. These improvements have allowed detection of protein crystals on the order of 1 µm in thickness under cryogenic conditions in the beamline. These capabilities are well suited to support serial crystallography of crystals approaching 1 µm or less in dimension.


e-Polymers ◽  
2010 ◽  
Vol 10 (1) ◽  
Author(s):  
Marański K. ◽  
Kucharski S. ◽  
Ortyl E ◽  
Janik R. ◽  
Nunzi J.-M. ◽  
...  

AbstractThe azo sulfonamide chromophores containing long aliphatic chain were used as active nonlinear optical (NLO) materials in films prepared by spin-coating on glass surfaces. The sulfonamides were: N-{4-[{4-[(pyrimidin-2-ylamino)sulfonyl]phenyl}diazenyl]phenyl} decanamide (Amid P); N-{4-[{4-[(1,3-thiazol-2-ylamino)-sulfonyl]phenyl}diazenyl]phenyl} decanamide (Amid T) and N-{4-[(4-nitrophenyl)-diazenyl]-phenyl}undec-10-enamide (Amid N). The host matrix was a copolymer of methyl and butyl methacrylate. The formation of diffraction grating by the guest-host system was successful only in the case of Amid N. The pitch and amplitude of the grating was 930 nm and ca. 45 nm, respectively. Quantum chemical calculations revealed that the chromophores were moderate NLO-fores showing static β values of ca. 110-130 m4/V. Two procedures were involved to align chromophores to determine first order NLO susceptibility: a) corona poling, and b) all-optical poling. The NLO coefficient d33 determined in corona poled film was 25.2, 28.6 and 93.2 pm/V for Amid P, T and N, respectively.


1998 ◽  
Vol 76 (11) ◽  
pp. 1616-1632
Author(s):  
Bozena Borecka-Bednarz ◽  
Alan V Bree ◽  
Brian O Patrick ◽  
John R Scheffer ◽  
James Trotter

Second-harmonic generation in the solid state is restricted to materials that crystallize in non-centrosymmetric space groups. Unfortunately, the vast majority of solids crystallize in centrosymmetric space groups and are therefore SHG-inactive. The requirement for solid-state asymmetry is addressed in a new series of organic salts. The acid p-nitrophenylglycine, SHG-inactive due to its centrosymmetric (P1) packing, was coupled to six optically pure amines to form salts and (or) complexes that, by virtue of their chiral counterion, crystallized in non-centrosymmetric space groups. The 1064 nm output from a Nd:YAG laser produced 532 nm second-harmonic generation from each of the six salts, with three of the salts producing second-harmonic intensities at least an order of magnitude greater than that of our standard, urea. X-ray crystallographic analysis was carried out on five of the six salts, and an attempt was made to rationalize the second-harmonic intensity of each of these five salts based on the orientation of its molecular charge-transfer axis in the unit cell and on its chromophore density.Key words: second-harmonic generation, nonlinear optics, chiral organic salts, crystal structures.


1994 ◽  
Vol 351 ◽  
Author(s):  
Shlomo Yitzchaik ◽  
Paul M. Lundquist ◽  
Weiping Lin ◽  
David R. Kanis ◽  
Mark A. Ratner ◽  
...  

ABSTRACTAn attractive and challenging approach to the construction of robust, thin film materials with large second-order optical nonlinearities is the covalent self-assembly of aligned arrays of high-β molecular chromophores into multilayer superlattices. In this paper, we describe the dispersion of second harmonic generation (SHG) in a self-assembled (SA) monolayer containing a stilbazolium chromophore. The frequency-dependent measurements were performed on 25 Å thick monolayers on glass using a tunable (0.4–2 μm) light source based on optical parametric amplification (OPA). The SHG spectrum contains a clear two-photon resonance at hω = 1.3eV. The maximum in the second-order susceptibility coincides with a low energy chromophore-centered charge-transfer excitation at 480 nm. The experimental SHG dispersion values compare favorably with theoretical results computed using a sum-over-states (SOS) formalism. However, the measured values exhibit a somewhat broader band response than the theoretical curve, and the origin of this behavior is discussed.


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