Ultrabroad near-infrared photoluminescence from ionic liquids containing subvalent bismuth

We have shown that Lewis-acidic halogenoaluminate ionic liquid (IL) containing subvalent bismuth can be used as a near-IR (NIR) luminescent material. Raman and absorption spectra evidence the coexistence of Bi(5)(3+) and Bi(+) in the liquid. The Bi(5)(3+) and Bi(+) emitters, stabilized by this Lewis-acidic liquid, demonstrate ultrabroad NIR photoluminescence with a lifetime of around 1 μs. We envisage that the bismuth activated ILs would not only enrich the well-established spectrum of soft luminescent materials but also might promote the design of novel photonic materials activated by other p-block elements.     

Polarization-independent refractive index tuning using gold nanoparticle-stabilized blue phase liquid crystals

Polarization-independent refractive index (RI) modulation can be achieved in blue phase (BP) liquid crystals (LCs) by applying an electric field parallel to the direction of light transmission. One of the problems limiting the achievable tuning range is the field-induced phase transition to the cholesteric phase, which is birefringent and chiral. Here we report the RI modulation capabilities of gold nanoparticle-doped BPs I and II, and we show that field-induced BP-cholesteric transition is suppressed in nanoparticle-doped BP II. Because the LC remains optically isotropic even at high applied voltages, a larger RI tuning range can be achieved.     

Surfactant-free solution-dispersible Si nanocrystals surface modification by impurity control

Si nanocrystals (Si-NCs) dispersible in polar liquid without surface functionalization by organic molecules have been realized by simultaneously doping n and p type impurities. We show that the codoped Si-NCs are stable in methanol for more than five months, while intrinsic Si-NCs prepared by the same procedure form large agglomerates. The different behavior of the intrinsic and codoped Si-NCs in solutions suggests that doped impurities exist on the surface of Si-NCs and the surface potential is large enough to prevent the agglomeration. The colloidal solution of codoped Si-NCs exhibits broad photoluminescence with the maximum in the near infrared range (1.1-1.3?eV).     

Regulation of folding and photochromic reactivity of terarylenes through a host-guest interaction

The photochromic reactivity of terarylenes is integrated with molecular folding that is controlled through a host-guest interaction. A thieno[3,2,b]pyridine unit is introduced into a photochromic terarylene structure as an aryl unit to form a guest-interacting site. Thienopyridine-containing terarylenes showed solvent-dependent photochromic reactivity in solution. A terarylene moiety that contains two thienopyridyl units showed significantly high photocoloration reactivity as high as 88% of photocyclization quantum yield in methanol, whereas that value was only 24% in hexane. A temperature-dependent (1)H NMR spectroscopic study in different solvents indicated an interconversion between photochromic-reactive and unreactive conformations. In methanol, the intermolecular interaction between terarylene species and the solvent molecule slows the rate of interconversion and increases the population of the photochromic-active form, whereas the unreactive conformation is dominant in hexane. Crystal-structural studies demonstrated the perfect regulation of molecular folding between a photochromic-active form and an unreactive conformation by changing the solvents for recrystallization. Single crystals prepared from solutions in methanol showed reversible photochromic reactivity, whereas recrystallization from solutions in hexane did not show this reactivity. X-ray crystallographic studies of single crystals from solutions in methanol demonstrated that the photochromic molecules bind a solvent methanol molecule at the guest-interacting site to regulate the molecular conformation into a photochromic-active form in collaboration with specific intramolecular interactions, whereas crystals from solutions in hexane possess the photochromic-unreactive conformation.     

SUSY breaking by nonperturbative dynamics in a matrix model for 2D type IIA superstrings

We explicitly compute nonperturbative effects in a supersymmetric double-well matrix model corresponding to two-dimensional type IIA superstring theory on a nontrivial Ramond–Ramond background. We analytically determine the full one-instanton contribution to the free energy and one-point function, including all perturbative fluctuations around the one-instanton background. The leading order two-instanton contribution is determined as well. We see that supersymmetry is spontaneously broken by instantons, and that the breaking persists after taking a double scaling limit which realizes the type IIA theory from the matrix model. The result implies that spontaneous supersymmetry breaking occurs by nonperturbative dynamics in the target space of the IIA theory. Furthermore, we numerically determine the full nonperturbative effects by recursive evaluation of orthogonal polynomials. The free energy of the matrix model appears well-defined and finite even in the strongly coupled limit of the corresponding type IIA theory. The result might suggest a weakly coupled theory appearing as an S-dual to the two-dimensional type IIA superstring theory.     

Pressure dependence of the electron density in solid iodine by the maximum-entropy method

Abstract

A direct observation of the electron density of solid iodine has been attempted in order to study the electron-density delocalization process due to pressure-induced metallization. A high-accuracy x-ray powder diffraction measurement was carried out with a diamond anvil cell and an imaging plate on a synchrotron-radiation source. The maximum entropy method was employed to analyze the data and to obtain electron-density maps under pressures up to 20 GPa. The electron density between adjacent iodine molecules has been shown to gradually increase with increasing pressure; also, a two-dimensional network is formed at a density level of 0.2 e/ų at around 16 GPa.     

NMR Studies of Silicon Clathrate Compounds

Abstract

NMR spectra of ²⁹Si and ¹³⁷Ba in silicon clathrate compounds, Na_xBa_ySi₄₆, Na_xSi₁₃₆ and Ba₈ T _xSi₄₆ (where T = Au, Ag, and Cu) are reported. We found that the local density of states at the Fermi level increases with rising superconducting transition temperature. The silicon Sl site was suggested to hybridize with Ba-orbital in the superconducting clathrate and has a large local density of states.     

In vivo fate of superparamagnetic iron oxides during sepsis

The enzymatic generation of nitric oxide (NO) in vivo has been reported to be modulated by ions, such as copper and iron. Superparamagnetic iron oxide (SPIO) or ferumoxides is a liver-specific magnetic resonance contrast agent that is taken up by the Kupffer cells, where NO is generated by inducible nitric oxide synthase (iNOS). Thus, it is important to evaluate SPIO in vivo under conditions, such as infectious disease, where significant amounts of NO are generated by iNOS. In this study, we monitored the pharmacokinetics of SPIO in the liver of septic-shock mice and rats. A significant decrease in the ferric iron EPR signal was observed during NO generation in septic-shock mice compared with control mice doped with only SPIO. These results were also confirmed in a model reaction system consisting of SPIO and the NO donor, S-nitroso-N-acetyl DL penicillamine (SNAP). We compared NO generation quantitatively in the liver of the septic-shock rats, either in the presence or absence of SPIO, and found that the presence of SPIO did not affect the NO-generating activity of NOS expressed in the liver. T2-weighted MR images of an agarose gel phantom containing different SPIO to NO donor (SNAP) ratios clearly demonstrated that the contrast enhancement by SPIO decreased with increasing NO at constant SPIO levels. The reduced contrast is most probably due to the reduction of ferric to ferrous irons, resulting in a decrease in paramagnetic relaxation of water protons. These results show that SPIO can be a versatile NO-sensitive indicator, especially employing MRI as a powerful tool to 'visualize' sites of NO generation.     

Level set-based topology optimization for anti-reflection surface

We present a level set-based topology optimization method to model anti-reflection surfaces (ARSs). An objective functional is defined as an integration of scattering intensity of an electric field, and the ARSs are optimally designed by minimizing reflections at the air-dielectric interface. During the topology optimization, geometric constraints are controlled by adjusting a regularization parameter. The performance of the ARSs improves as the value of the regularization parameter becomes small. Level set functions are used to express dielectric structures, and dielectric boundaries are interpreted as lines on the iso-surface of the level set functions.