Biomedical subjects

Kazunori Takada

Publications and source records attributed to Kazunori Takada.

12 recordsLinked to original sources

PubMed2007

General synthesis and delamination of highly crystalline transition-metal-bearing layered double hydroxides.

In this paper, we describe a general process for the synthesis and delamination of a family of highly crystalline Al-based and transition-metal-bearing layered double hydroxides (LDHs). Large-sized and monodispersed hexagonal platelike particles of binary-component M(II)-Al-CO3 and ternary-component M(II)-M'(II)-Al-CO3 LDHs (M(II) and M'(II) = Fe, Co, Ni, or Zn) were prepared at first by the urea method under optimized conditions. These CO32--LDHs were converted into other monovalent-anion-containing LDHs by means of a salt-acid treatment and subsequent anion-exchange processes. Finally, well-defined LDH nanosheets were obtained by delamination of NO3--LDHs in formamide.

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PubMed2006

Spinel-to-CaFe2O4-type structural transformation in LiMn2O4 under high pressure.

A new form of LiMn2O4 is reported. The structure is the CaFe2O4-type and 6% denser than the spinel. The structure transformation was achieved by heating at 6 GPa. Analysis of the neutron diffraction pattern confirmed an average of the structure; the unit cell was orthorhombic at a = 8.8336(5) angstroms, b = 2.83387(18) angstroms, and c = 10.6535(7) angstroms (Pnma). Electron diffraction patterns indicated an order of superstructure 3a x b x c, which might be initiated by Li vacancies. The exact composition is estimated at Li(0.92)Mn2O4 from the structure analysis and quantity of intercalated Li. The polycrystalline CaFe2O4-type compound showed semiconducting-like characters over the studied range above 5 K. The activation energy was reduced to approximately 0.27 eV from approximately 0.40 eV at the spinel form, suggesting a possible enhancement of hopping mobility. Magnetic and specific-heat data indicated a magnetically glassy transition at approximately 10 K. As the CaFe2O4-type transition was observed for the mineral MgAl2O4, hence the new form of the lithium manganese oxide would provide valuable opportunities to study not only the magnetism of strongly correlated electrons but also the thermodynamics of the phase transition in the mantle.

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PubMed2006

Hollow nanoshell of layered double hydroxide.

Hollow nanoshells of layered double hydroxide (LDH) have been fabricated using exfoliated LDH nanosheets as a shell building block and polystyrene beads as a sacrificial template.

Hydroxides↗

PubMed2006

Thermally stable luminescent composites fabricated by confining rare earth complexes in the two-dimensional gallery of titania nanosheets and their photophysical properties.

Fluorescent composite materials of exfoliated titania nanosheets, Ti(0.91)O(2), and rare earth (RE) complexes, Eu(phen)(2)Cl(3).2H(2)O and Tb(phen)(2)Cl(3).2H(2)O (phen = 1,10-phenanthroline), were synthesized via flocculation between them. X-ray diffraction measurements and transmission electron microscopy observations confirmed a restacked lamellar structure for the composites, and elemental analysis revealed a high RE complex content of 15 wt %. The decomposition temperature of the complexes trapped in the composites was improved to 420 degrees C from 250 degrees C for the free form. The restacked composite composed of Ti(0.91)O(2) nanosheets and Eu(phen)(2) exhibited characteristic red emission from the complex, while the composite with Tb(phen)(2) gave featureless emission originated from the ligand. This phenomenon can be explained by a shift of triplet state level of the ligand after encapsulation in the host titania nanosheets. The quantum yield of europium complex in the composite was enhanced 1.6 times more than that of the pure complex.

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PubMed2006

Tetrahedral Co(II) coordination in alpha-type cobalt hydroxide: Rietveld refinement and X-ray absorption spectroscopy.

We report a Rietveld refinement analysis and X-ray absorption study on a green-color Cl(-)-intercalated alpha-type cobalt hydroxide phase. The refinement clearly demonstrated that one-fifth to one-sixth of the Co(II) at octahedral sites was replaced by pairs of tetrahedrally coordinated Co(II) on each side of the hydroxide plane, represented by a structural formula of [Co(octa)(0.828)Co(tetra)(0.348)(OH)2](0.348+)Cl(0.348).0.456H2O. X-ray absorption spectroscopy also indicated that the divalent cobalt were in local neighboring environments of both octahedral and tetrahedral coordination. Furthermore, UV-vis spectroscopic measurements elucidate the typical green/blue color of an alpha-type cobalt hydroxide.

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PubMed2006

Synthesis, anion exchange, and delamination of Co-Al layered double hydroxide: assembly of the exfoliated nanosheet/polyanion composite films and magneto-optical studies.

This paper describes a systematic study on the synthesis, anion exchange, and delamination of Co-Al layered double hydroxide (LDH), with the aim of achieving fabrication and clarifying the properties of LDH nanosheet/polyanion composite films. Co-Al-CO3 LDH hexagonal platelets of 4 mum in lateral size were synthesized by the urea method under optimized reaction conditions. The as-prepared CO3(2-)-LDH was converted to Cl- -LDH by treating with a NaCl-HCl mixed solution, retaining its high crystallinity and hexagonal platelike morphology. LDHs intercalated with a variety of anions (such as NO3-, ClO4-, acetate, lactate, dodecyl sulfate, and oleate) were further prepared from Cl- -LDH via an anion-exchange process employing corresponding salts. Exchanged products in various anion forms were found to show different delamination behaviors in formamide. Among them, best results were observed for NO3- -LDH in terms of the exfoliating degree and the quality of the exfoliated nanosheets. The delamination gave a pink transparent suspension containing well-defined nanosheets with lateral sizes of up to 2 microm. The resulting nanosheets were assembled layer-by-layer with an anionic polymer, poly(sodium styrene 4-sulfonate) (PSS), onto quartz glass substrates to produce composite films. Magnetic circular dichroism (MCD) measurements revealed that the assembled multilayer films exhibited an interesting magneto-optical response.

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PubMed2006

Photoinduced hydrophilic conversion properties of titania nanosheets.

Photoinduced hydrophilic conversion properties of titania nanosheets were investigated. A highly hydrophilic state was achieved on the monolayer film surface of titania nanosheets, the thickness of which is less than 1 nm. The hydrophilic conversion rate (k) for the monolayer film of titania nanosheets was proportional to the intensity (I) of irradiated light, suggesting that the hydrophilic conversion of the titania nanosheet surface proceeded under light-limited conditions even with a high concentration of photoexcited carriers. As the number of layers of titania nanosheets increased, the dependence behavior changed from k proportional, variant I(1.0) to k proportional, variant I(0.5), indicating that the recombination processes become dominant in the multilayer films of titania nanosheets. In-plane X-ray diffraction (XRD) analyses showed a very small but reproducible structural change of titania nanosheets upon UV irradiation.

Journal Article↗

PubMed2005

Selective and controlled synthesis of alpha- and beta-cobalt hydroxides in highly developed hexagonal platelets.

We report on the controlled synthesis of single-crystal platelets of alpha- and beta-Co(OH)2 via homogeneous precipitation using hexamethylenetetramine as a hydrolysis agent. The alpha- and beta-Co(OH)2 hexagonal platelets of several micrometers in width and about 15 nm in thickness were reproducibly yielded in rather dilute CoCl2 solutions in the presence and absence of NaCl at 90 degrees C, respectively. The phase and size control of the products were achieved by varying both CoCl2 and NaCl concentrations. Polarized optical microscope observations revealed clear liquid crystallinity of colloidal suspensions of these high aspect-ratio platelets. The as-prepared alpha-Co(OH)2 containing interlayer chloride ions was intercalated with various inorganic or organic anions, keeping its high crystallinity and hexagonal platelike morphology.

Cobalt↗

PubMed2005

Photocurrent generation from semiconducting manganese oxide nanosheets in response to visible light.

Unilamellar nanosheet crystallites of manganese oxide generated the anodic photocurrent under visible light irradiation (lambda < 500 nm), while the nanosheets themselves were stable as revealed by in-plane XRD and UV-visible absorption spectra. The band gap energy was estimated to be 2.23 eV on the basis of the photocurrent action spectrum. The molecular thickness of approximately 0.5 nm may facilitate the charge separation of excited electrons and holes, which is generally very difficult for strongly localized d-d transitions. The monolayer film of MnO2 nanosheets exhibited the incident photon-to-electron conversion efficiency of 0.16% in response to the monochromatic light irradiation (lambda = 400 nm), which is comparable to those for sensitization of monolayer dyes adsorbed on a flat single-crystal surface. The efficiency declined with increasing the layer number of MnO2 nanosheets, although the optical absorption was enhanced. The recombination of the excited electron-hole pairs may become dominant when the carriers need to migrate a longer distance than 1 layer through multilayered nanosheets.

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PubMed2004

Electronic band structure of titania semiconductor nanosheets revealed by electrochemical and photoelectrochemical studies.

Electrochemical and photoelectrochemical studies were conducted on self-assembled multilayer films of titania nanosheets on a conductive ITO substrate. Cyclic voltammogram (CV) curves indicated that the titania nanosheet electrode underwent insertion/extraction of Li(+) ions into/from the nanosheet galleries, associated with reduction/oxidation of Ti(4+)/Ti(3+). These processes accompanied reversible changes in UV-vis absorption of the titania nanosheet electrodes. Applying a negative bias of -1.3 V (vs Ag/Ag(+)) and lower brought about absorption reduction where the wavelength is shorter than 323 nm, and vice versa, indicating a flat-band potential of (approximately) -1.3 V and a band gap energy of 3.84 eV. Photocurrents were generated from the titania nanosheet electrodes under a positive bias. The onset potential for photocurrent generation from the titania nanosheet electrodes was around -1.27 V, and the band gap energy estimated from the photocurrent action spectra was 3.82 eV, in excellent agreement with the values obtained from the spectroelectrochemical data. The lack of difference in the band gap energies for titania nanosheet electrodes with different numbers of layers suggests that a nanosheet is electronically isolated in multilayer assemblies without affecting the electronic state of neighboring nanosheets. Similar measurements on the anatase-type TiO(2) electrode revealed that the lower edge of the conduction band for the titania nanosheet is approximately 0.1 V higher than that for anatase, while the upper edge of the valence band is 0.5 V lower.

Journal Article↗

PubMed2004

Ultrathin hollow nanoshells of manganese oxide.

Novel hollow nanoshells of Mn(2)O(3) with controllable ultrathin shell thickness have been fabricated through layer-by-layer assembly of exfoliated MnO(2) nanosheets and polyelectrolytes on polymer bead templates, followed by removal of the polymer cores via calcination.

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PubMed2003

Superconductivity in two-dimensional CoO2 layers.

Since the discovery of high-transition-temperature (high-T(c)) superconductivity in layered copper oxides, many researchers have searched for similar behaviour in other layered metal oxides involving 3d-transition metals, such as cobalt and nickel. Such attempts have so far failed, with the result that the copper oxide layer is thought to be essential for superconductivity. Here we report that Na(x)CoO2*yH2O (x approximately 0.35, y approximately 1.3) is a superconductor with a T(c) of about 5 K. This compound consists of two-dimensional CoO2 layers separated by a thick insulating layer of Na+ ions and H2O molecules. There is a marked resemblance in superconducting properties between the present material and high-T(c) copper oxides, suggesting that the two systems have similar underlying physics.

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