The scattering theory of C. Wilcox in elasticity

We extend the abstract time‐dependent scattering theory of C.H. Wilcox to the case of elastic waves. Most of the results are proved with the minimal assumption that the obstacle satisfies the energy local compactness condition (ELC). This holds especially for the existence and unitarity of the wave operators. Copyright © 2002 John Wiley & Sons, Ltd.     

Like a bolt from the blue: phthalocyanines in biomedical optics

The purpose of this review is to compile preclinical and clinical results on phthalocyanines (Pcs) as photosensitizers (PS) for Photodynamic Therapy (PDT) and contrast agents for fluorescence imaging. Indeed, Pcs are excellent candidates in these fields due to their strong absorbance in the NIR region and high chemical and photo-stability. In particular, this is mostly relevant for their in vivo activation in deeper tissular regions. However, most Pcs present two major limitations, i.e., a strong tendency to aggregate and a low water-solubility. In order to overcome these issues, both chemical tuning and pharmaceutical formulation combined with tumor targeting strategies were applied. These aspects will be developed in this review for the most extensively studied Pcs during the last 25 years, i.e., aluminium-, zinc- and silicon-based Pcs.     

Selective aggregation of single-walled carbon nanotubes using the large optical field gradient of a focused laser beam

We demonstrate the selective aggregation of single-walled carbon nanotubes by photon forces, using the large optical field gradient of a laser focused through a high numerical aperture objective lens. The nanotubes, dispersed in an aqueous solution with a surfactant, are detected via Raman scattering from the confocal volume of the optical trap. By using a visible-light laser for both trapping and detection, the dynamics of the radial breathing mode signal taken at short intervals shows an increase of a single breathing mode over time, indicating the increase in the density of only one species of tube in the focal volume. This result represents a significant step toward the development of techniques for the arbitrary manipulation and sorting of nanotubes by optical fields.     

Influence of the polymer structure on the achievement of polar orientation in high glass transition temperature nonlinear optical polyimides by photo-assisted poling

We have used combinations of light, heat, and electrostatic fields to investigate the orientation of nonlinear azo-chromophores chemically incorporated into high glass transition temperature (T_g) polyimides. A number of nonlinear optical polyimides have been synthesized in which the interaction between the nonlinear optical chromophore and the polymer main chain was systematically altered to determine to what extent this steric interaction influences the orientation of the nonlinear chromophore. Chromophores in polymers may be oriented by a number of methods: (a) polarized light at room temperature (i.e., photo-induced orientation or PIO), (b) polarized light and electric fields (i.e., photo-assisted poling or PAP) at temperatures ranging from room temperature to the polymer T_g, and (c) electric fields at T_g (thermal poling). While thermal poling and PIO are usually possible, PAP depends strongly on the molecular structure of the polymer. Previously we have shown that PIO can be accomplished at room temperature in a system where the nonlinear chromophore is embedded into the polyimide main chain via the donor substituent, and this orientation can only be thermally erased at temperatures approaching T_g. In this article we show that, whereas photoisomerization can efficiently depole donor-embedded polyimides in a matter of few minutes at room temperature, PAP does not induce any polar order. This behavior is in marked contrast to a structurally related, side-chain, nonlinear polyimide, in which the azo chromophore is tethered via a flexible linkage to the polymer backbone. In this case some PAP occurs even at room temperature, while no PAP is observed for a donor-embedded system with a similar T_g. We suggest that the orientation during PAP below T_g in the side-chain polyimide is primarily due to the movement of the azo side chains, and there is a very little coupling of this motion to the main chain. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 1669–1677, 1998     

Resolution Enhancement of Plasmonic Sensors by Metal‐Insulator‐Metal Structures

Optical sensors based on surface plasmons have attracted much attention over the past decades owing to the wealth of applications in bio‐ and chemical and gas sensing. In surface plasmon resonance sensors, a single metal layer is commonly used, but its resolution is limited because of broad resonances. In this context, we have developed a sensor chip based on a stack of metals and a dielectric, e.g. a metal‐insulator‐metal structure, consisting of a thick insulator layer sandwiched by metal layers, that exhibits a sharp resonance due to the excitation of surface plasmon polaritons hybrid modes. We have performed both experiments and theoretical simulations to estimate the enhancement of the sensitivity of such a structure. By changing the refractive index of an aqueous solution of glucose on top of the sensor chip, we found that the use of a metal‐insulator‐metal structure improves the figure of merit of the sensor 7.5 times compared to that of a conventional surface plasmon resonance sensor chip.     

The elastic echo problem

We consider a homogeneous isotropic unbounded linear elastic medium Ω??³, having a free boundary Γ. A forcing f (t, x ) creates an incident displacement field u ₀(t, x ). This primary field is scattered by Γ giving rise to a secondary field or echo, for which we determine the asymptotic behaviour in time. These results are obtained via the use of an tension of the time‐dependent scattering theory of C. Wilcox. Copyright © 2003 John Wiley & Sons, Ltd.     

Ordering of azobenzenes by two-photon isomerization

We report on light induced orientation by two-photon isomerization of azobenzenes in films of polymer. The dynamics of isomerization and orientation by one-photon absorption and two-photon absorption (TPA) are similar, and TPA creates a degree of molecular orientation which is comparable to that achieved by single-photon isomerization, in agreement with the theoretical predictions of two-photon isomeric orientation.     

Laser nanofabrication in photoresists and azopolymers

Recent progress in the field of single‐ and two‐photon nanofabrication, both 2‐ and 3‐dimensional, in photopolymerizable resins and in films of photoisomerizable azopolymers are reviewed. The basic processes as well as technological advances and applications of nanofabrication by light are discussed. Recent advances and achievements in polymer photomechanics and light‐activated molecular movement in azopolymers are also reviewed.