Cephalopod coloration model. II. Multiple layer skin effects.

A mathematical model of multiple layer skin coloration in cephalopods, a class of aquatic animals, is presented. The model incorporates diffuse and specular reflection from both pigment and structural photonic components found in the skin of these animals. Specific physical processes of this coloration are identified and modeled utilizing available biological materials data. Several examples of combination spectra are calculated to illustrate multiple layer and incident light effects as well as the potentially rich repertoire of color schemes available to these animals. A detailed understanding of the physical principles underlying cephalopod coloration is expected to yield insights into their possible functions.

Cephalopod coloration model. I. Squid chromatophores and iridophores.

We have developed a mathematical model of skin coloration in cephalopods, a class of aquatic animals. Cephalopods utilize neurological and physiological control of various skin components to achieve active camouflage and communication. Specific physical processes of this coloration are identified and modeled, utilizing available biological materials data, to simulate active spectral changes in pigment-bearing organs and structural iridescent cells. Excellent agreement with in vitro measurements of squid skin is obtained. A detailed understanding of the physical principles underlying cephalopod coloration is expected to yield insights into the behavioral ecology of these animals.

Layer-in-layer hierarchical nanostructures fabricated by combining holographic polymerization and block copolymer self-assembly.

We report the combination of top-down and bottom-up nanomanufacturing techniques to fabricate active, hierarchically structured volume reflection gratings. Holographic polymerization (H-P) formed lamellar structures of approximately 200 nm in thickness, confining a block copolymer (BCP) to approximately 100 nm domains. Subsequently, the BCP self-assembles into nanolayers with a period of approximately 21 nm. We envisage that this approach opens a gateway to fabricating hierarchical nanostructures at different length scales.

Insight into the nonlinear absorbance of two related series of two-photon absorbing chromophores.

A comprehensive photophysical study of the linear and nonlinear absorption properties has been carried out on two series of two-photon absorbing dyes to gain insight into how structure-property relationships influence observed nonlinear absorption. The materials studied consist of an electron accepting benzothiazole group connected to an electron donating diphenylamine via a fluorene bridging group. Two series differ from each other by the addition of one phenyl group and for each series one-arm (dipolar, AF240 and AF270), two-arm (quadrupolar, AF287 and AF295), and three-arm (octupolar, AF350 and AF380) versions were studied. Overall the AF240 series exhibits higher intrinsic two-photon absorption (TPA) cross-sections than the AF270 series as well as enhanced nanosecond nonlinear absorption, with an increase with number of branches. The enhanced nanosecond nonlinearity is understood by taking into account the contribution from the singlet and triplet excited states and was verified by a two-photon assisted excited-state absorption model that satisfactorily predicts the nonlinear absorption of the chromophores.

Determination of large nematic pre-tilt in liquid crystal cells with mechanically rubbed photorefractive Ce:SBN windows.

We report on the determination of liquid crystal pre-tilt inside cells fabricated using single crystal birefringent and dichroic windows of cerium doped strontium barium niobate. We show that the average pre-tilt is significantly affected by the crystalline windows, leading to much larger values than those obtained with glass windows using identical fabrication methods. The same technique can be used to determine pre-tilts as large as 40 degrees, which is significantly larger than normally measurable using the cell rotation method.

Polymer crystallization/melting induced thermal switching in a series of holographically patterned Bragg reflectors.

Holographic photopolymerization (H-P) is a simple, fast and attractive means to fabricate one-, two- and three-dimensional complex structures. Liquid crystals, nanoparticles and silicate nano-plates have been patterned into submicron periodical structures. In this article, we report fabrication of a one-dimensional reflection grating structure by patterning a semicrystalline polymer, polyethylene glycol (PEG), in Norland resin (thiol-ene based UV curable resin) matrix using the H-P technique. Sharp notches observed in the reflection grating of this Norland/PEG system indicate a finite Δ present in the system due to spatial segregation of the PEG and Norland resin. The notch position red shifts upon heating and the diffraction efficiency (ratio between diffraction and incident light intensity, DE) increases from ∼20% to 60% for the Norland 65/PEG 4600 grating. This dynamic behavior of the reflection grating is also fully reversible. The unique thermal switching behavior is attributed to the melting/formation of PEG crystals during heating/cooling. By employing different molecular weight PEGs which have different melting temperatures, a series of switching temperatures have been achieved. Since PEG can be easily coupled with a variety of functional groups, this research might shed light on fabricating multifunctional Bragg gratings using the H-P technique.