Fabrication of dielectric nanocubes in ordered structure by capillary force assisted self-assembly method and their piezoresponse properties

Ordered structures of barium titanate (BT) nanocubes, strontium titanate (ST) nanocubes and BT/ST nanocubes mixture were directly fabricated on Si and Pt-coated Si substrates using a capillary force assisted assembly method. The morphology of self-assembled structures was observed using field emission scanning electron microscopy (FE-SEM) and scanning probe microscopy (SPM). It was revealed that nanocubes were arranged with various degrees of ordering to develop multilayer and monolayer regions at the surface of substrates. The elemental mapping of the structure consisting of the nanocubes mixture was also investigated by transmission electron microscopy (TEM) with an energy dispersive X-ray spectroscopy (EDX). It was revealed that BT and ST nanocubes coexisted homogeneously in the structure and had possibility to be arranged in order to each other. The piezoresponse properties obtained by scanning probe microscopy (SPM) indicated that the hetero-interface between BT and ST nanocubes would introduce anomaly in piezoelectric properties.     

Waves in a rotating elastic solid

Wave propagation in a uniformly rotating elastic solid is discussed based on displacement equations in a moving frame. The time-harmonic Green’s dyadic for a point body force is obtained in closed form. It is reconfirmed that two quasi dilatational and shear waves are coupled to each other, and the deformation decomposition into the dilatation and rotation is not possible for the rotating solid. Further, it is also confirmed that the velocity of the Rayleigh surface wave depends not only on the rotational velocity but also on its direction and that the Rayleigh wave vanishes when the rotational velocity approaches the Rayleigh wave velocity of the immovable solid.     

On approximate solutions for the deformation of plane anisotropic beams

Plane deformation of anisotropic beams with narrow rectangular cross sections exhibits coupling of stretching, bending and transverse shearing. For anisotropic cantilever beams with a stiff end-cap under end forces and an end couple, assessments were made for approximate solutions by comparing these with numerically exact finite element (FE) solutions. Specific attention is given to point-wise or approximate satisfaction of the end-fixity conditions. As approximate methodologies, (i) the elementary polynomial form of Airy's stress function for the plane stress problem in a rectangular region, (ii) a Timoshenko-type beam theory, and (iii) the Bernoulli-Euler beam theory were selected. Among these, only the polynomial form of Airy's stress function violates the point-wise end-fixity conditions. Both the polynomial Airy stress function and the Timoshenko-type beam theory successfully model the effects of transverse shear deformation and the coupling of stretching and transverse deflection. Analytical solutions demonstrate that the normal shear coupling effect increases linearly with the thickness-to-span ratios in axial normal stress and axial displacement, while the coupling manifests quadratically in transverse displacement. The comparison of end displacements with the numerically exact FE solutions indicates that the polynomial form of Airy's stress function is no better than the Timoshenko-type beam theory. Similar conclusions were reached for the problem of uniformly loaded cantilever beams. It has been found that the accurate prediction of the deformation of thick anisotropic beams with significant normal-shear coupling requires the use of higher order theories.     

Manipulating the chemical affinity and kinetics of 3D silica particle network via the phase-separation technique

We developed a simple and versatile technique for a particle’s self-organizing-network based on a non-solvent induced micro-phase separation (NIPS). When a good solvent vaporizes from a particle dispersion in a ternary solution including the polymer, good solvent and non-solvent, the suspension is separated into the polymer network and non-solvent phase. If the affinity between the particles and polymer is sufficient enough, the particles are entrapped in the polymer network and particle network can be achieved. To expand this technique to particles with various physical properties, the surface of the particles was identified using the Hansen dispersibility parameter (HDP). From a comparison of the HDP of the unmodified and modified silica, an NH₂ group is suitable for entrapment of the silica by cellulose acetate as the polymer. However, with an increase in number of the silica particles, entrapment of the silica in the polymer was prevented. Control of the phase separation rate by the lowering temperature leaded to entrapment of silica particles in the polymer network. The proposed technique is effective not only for spherical oxide particles, but also for non-oxides, various shapes and structures. Depending on particle characteristics, functional films and bulk materials for thermal insulation, light diffusion, and electro conductivity can be obtained.     

Fabrication of ferromagnetic nanoconstriction using atomic force microscopy nanoscratching

Nanolithography used in conjunction with atomic force microscopy (AFM) has attracted considerable attention as a technique for fabricating nanoscale structures. To obtain nanostructures and devices, AFM nanoscratching was performed on a photoresist and on NiFe at various values of the applied force, scan speed, and number of scan cycles. The scratching process was carried out using a diamond-coated tip on NiFe and a Si tip on the photoresist. By conducting scratching processes on NiFe and on the photoresist, we investigated the dependence of the size of the scratched part on the scratching parameters. These results show that the width and depth of the scratched part increase as the applied force and number of scan cycles increase, but not as the scan speed increases. This means that it is possible to control the size of the scratched parts by adjusting the applied force and number of scan cycles. AFM nanoscratching was then used to directly fabricate a nanoconstricted area with a width of 139 nm and a cross-sectional area of less than 300 nm2 was fabricated.     

Fusion and molecular aspects of liposomal nanocarriers incorporated with isoprenoids

The present study was conducted to investigate whether typical isoprenyl compounds (TICs) can control liposomal fusion reactions through changes in the physical properties of membranes. The fusion capabilities of TIC-incorporated liposomes were characterized by measuring the 13C spin-lattice relaxation times (13CT1) and the gel permeation chromatogram (GPC) patterns. The 13CT1 relaxivities of some of these TIC-liposomes were remarkably enhanced at 27 degrees C. The highest 13CT1 value obtained was for the beta-carotene-liposome, which ruptured, and was attributed to the highest membrane fusion reactivity. The other TIC-liposomes incorporated with alpha-tocopherol, canthaxanthin, or coenzyme Q10 also induced significant fusion and did not rupture in comparison with the beta-carotene-liposome. These results show that the incorporations of TICs into lipid bilayers are useful to control liposomal nanocarriers for suitable membrane packing and advantageous phase separation, which could affect membrane-related processes.     

Synthesis and antihypertensive activity of 4-(diazabicyclo[4.1.0]-heptenyloxy)benzopyran derivatives and their analogues

A series of 3,4-dihydro-3-hydroxy-4-[(5-oxo-3,4-diazabicyclo[4.1.0]hept- 2-en-2-yl)oxy]-2H-1-benzopyrans and their analogues were synthesized and evaluated on potassium channel opening and hypotensive activities. Compound (-)-13B with a (4-methyl-5-oxo-3,4-diazabicyclo[4.1.0]hept-2-en-2-yl)oxy group for the 4-position of the benzopyran ring was 3 times as potent as EMD 57283 (II), the lead compound, in hypotensive activity. The results would demonstrate that 5-oxo-3,4-diazabicyclo[4.1.0]hept-2-en-2-yloxy moieties are effective as the substituents at the 4-position of benzopyran-type potassium channel openers.     

Wide-gap layered oxychalcogenide semiconductors: Materials, electronic structures and optoelectronic properties

Applying the concept of materials design for transparent conductive oxides to layered oxychalcogenides, several p-type and n-type layered oxychalcogenides were proposed as wide-gap semiconductors and their basic optical and electrical properties were examined. The layered oxychalcogenides are composed of ionic oxide layers and covalent chalcogenide layers, which bring wide-gap and conductive properties to these materials, respectively. The electronic structures of the materials were examined by normal/inverse photoemission spectroscopy and energy band calculations. The results of the examinations suggested that these materials possess unique features more than simple wide-gap semiconductors. Namely, the layered oxychalcogenides are considered to be extremely thin quantum wells composed of the oxide and chalcogenide layers or 2D chalcogenide crystals/molecules embedded in an oxide matrix. Observation of step-like absorption edges, large band gap energy and large exciton binding energy demonstrated these features originating from 2D density of states and quantum size effects in these layered materials.