Wide tuning of silicon-on-insulator ring resonators with a liquid crystal cladding

Wide electrical tuning of silicon-on-insulator ring resonators is demonstrated using a top cladding layer of nematic liquid crystals. A tuning range of 31?nm is demonstrated for ring resonators guiding the TM mode, covering nearly the entire C-band of optical communications. Ring resonators guiding the TE mode can be tuned over 4.5?nm. The combination of a liquid crystal director calculation and a fully anisotropic mode solver confirms the interpretation of these experimental results. The realization of broad and low-power tuning in silicon-on-insulator opens up new opportunities in the field of tunable lasers, filters, and detectors.     

Spin-state dynamics of a photochromic iron(II) complex and its immobilization on oxide surfaces via phenol anchors

This work presents a detailed study of the photo-induced spin-state dynamics of the photochromic iron(II) complex 1, where the metal ion is in the field of a tripodal hexa-imine ligand with protolysable phenol groups. The nature of the complex’s ground state has been identified as a spin singlet by ¹H NMR and steady-state UV/vis spectroscopies, and its distorted octahedral structure was analyzed via crystal structure determination. Sub-picosecond and nanosecond time-resolved laser flash photolysis experiments identify the long-lived quintet state of 1 as the selective product of photoexcitation in the UV/vis spectral region. Thermal barriers of spin-state interconversion as a function of solvent and added base are derived from temperature-dependent rates of transient decay. Ground-state recovery is found to be significantly affected by the solvent and is strongly enhanced, in particular, by base-driven solvolysis of the ligand’s phenol groups. Partial spontaneous deprotonation of the phenolic hydroxyl groups of 1 seems to prevail on metal oxide surfaces, i.e. on alumina. Composite materials, like 1 at Al₂O₃, that retain the characteristic spectral features of the parent iron(II) complex can be readily obtained by wet impregnation of hydrous alumina with solutions of 1.     

Polymorphisms in genes involved in innate immunity and susceptibility to benzene-induced hematotoxicity

Benzene, a recognized hematotoxicant and carcinogen, can damage the human immune system. We studied the association between single nucleotide polymorphisms (SNPs) in genes involved in innate immunity and benzene hematotoxicity in a cross-sectional study of workers exposed to benzene (250 workers and 140 controls). A total of 1,236 tag SNPs in 149 gene regions of six pathways were included in the analysis. Six gene regions were significant for their association with white blood cell (WBC) counts (MBP, VCAM1, ALOX5, MPO, RAC2, and CRP) based on gene-region (P<0.05) and SNP analyses (FDR<0.05). VCAM1 rs3176867, ALOX5 rs7099684, and MPO rs2071409 were the three most significant SNPs. They showed similar effects on WBC subtypes, especially granulocytes, lymphocytes, and monocytes. A 3-SNP block in ALOXE3 (rs7215658, rs9892383, and rs3027208) showed a global association (omnibus P = 0.0008) with WBCs even though the three SNPs were not significant individually. Our study suggests that polymorphisms in innate immunity genes may play a role in benzene-induced hematotoxicity; however, independent replication is necessary.     

Ablation of Transparent Materials Using Excimer Lasers for Photonic Applications

For many years, the development of effective ablation or laser machining techniques for making micro-optical components has been the key factor in the birth of new photonic devices and systems. In this article, the ablation characteristics of two types of the most important transparent materials, transparent polymers and glasses, are studied. Simple shaped microcavities are first machined for studying the fundamental ablation parameters, including threshold fluence, effective absorption coefficient, and ablation rate. In studying polymer ablation, five standard grades and five proprietary polymeric compounds are selected. Ablation techniques using these transparent polymers for making arrayed ferrules and curved microlenses are presented. Applications of these ablated microstructures for optical fiber connectors, optical fiber coupling and alignment, and transparent chip encapsulants, are introduced and demonstrated with emphasis on the quality of the ablated profiles and dimensions to satisfy the required performance. In glass ablation, borosilicate glasses are considered and their associated ablation behaviors are studied. The procedures to ablate glass-based arrayed microstructures with flat and curved surfaces are described. The utilizations of these arrayed microstructures for optical waveguide, wave absorber, and beam guider, are specifically discussed. Finally, concluding remakes for future trends are presented.     

Dynamic broadening of the crystal-fluid interface of colloidal hard spheres

We investigate the structure and dynamics of the crystal-fluid interface of colloidal hard spheres in real space by confocal microscopy. Tuning the buoyancy of the particles allows us to study the interface close to and away from equilibrium. We find that the interface broadens from 8-9 particle diameters close to equilibrium to 15 particle diameters away from equilibrium. Furthermore, the interfacial velocity, i.e., the velocity by which the interface moves upwards, increases significantly. The increasing gravitational drive leads to supersaturation of the fluid above the crystal surface. This dramatically affects crystal nucleation and growth, resulting in the observed dynamic broadening of the crystal-fluid interface.     

Location of the Spinel Vacancies in γ‐Al2O3

A non‐spinel model for the structure of γ‐Al₂O₃, with 25 % of the Al³⁺ cations at tetrahedral positions, has been the subject of wide interest. However, ¹⁷O NMR measurements and, more recently, ²⁷Al NMR measurements have shown that there are considerably more Al³⁺ cations at tetrahedral positions. This means that the Al³⁺ vacancies in γ‐Al₂O₃ are not at tetrahedral but at octahedral positions, as in isostructural γ‐Fe₂O₃ and in accordance with density functional theory predictions. This has consequences with regard to the surface structure of γ‐Al₂O₃, and thus, for catalysis.     

Direct Minimization of the least-squares spectral element functional – Part I: Direct solver

This paper describes an equivalent but improved least-squares formulation for the numerical approximation of the solution of partial differential equations. Instead of using variational analysis to impose the conditions for minimizing the residual, the residuals are minimized directly, thus leading to a method we will denote by Direct Minimization (DM). DM circumvents setting up the normal equations which consists of matrix–matrix multiplications. Matrix–matrix multiplications are expensive, may lead to loss of accuracy and destroy the sparsity pattern present in the original system. The condition number of the DM formulation is the square root of the condition number which would be obtained if variational analysis was employed. An element-by-element procedure will be presented which allows for parallelization of DM. A computational comparison between DM and the conventional least-squares formulation based on variational analysis will be presented.