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Hiroaki Tada

Publications and source records attributed to Hiroaki Tada.

At least 19 recordsLinked to original sources
PubMed2006

Dispersion stability of TiO2 nanoparticles covered with SiOx monolayers in water.

The repetition of a two-step route consisting of chemisorption of 1,3,5,7-tetramethylcyclotetrasiloxane (TMCTS) and its subsequent photooxidation has formed SiOx monolayers on the surfaces of TiO2 particles layer by layer (SiOx(n < or = 4)/TiO2, n = repeated number). The trace of these processes using diffuse reflectance FT-IR and solid-state 29Si NMR spectroscopy reveals that TMCTS is chemisorbed on TiO2 through Ti-O-Si bonds followed by growth of Si-O-Si networks via dehydration-condensation of the Si-OH groups generated by TiO2 photocatalytic oxidation of the Si-H and Si-CH3 groups. The point of zero charge of the TiO2 particles decreases from 6.5 to 5.4 at n = 1, reaching 4.9 at n2. As a result of coverage with the SiOx monolayers, the dispersion stability of TiO2 particles in neutral water is significantly improved without changing their optical properties. The dispersion stability further increases with accumulation of SiOx monolayers.

Journal Article↗
PubMed2006

All-solid-state Z-scheme in CdS-Au-TiO2 three-component nanojunction system.

Natural photosynthesis, which achieves efficient solar energy conversion through the combined actions of many types of molecules ingeniously arranged in a nanospace, highlights the importance of a technique for site-selective coupling of different materials to realize artificial high-efficiency devices. In view of increasingly serious energy and environmental problems, semiconductor-based artificial photosynthetic systems consisting of isolated photochemical system 1 (PS1), PS2 and the electron-transfer system have recently been developed. However, the direct coupling of the components is crucial for retarding back reactions to increase the reaction efficiency. Here, we report a simple technique for forming an anisotropic CdS-Au-TiO2 nanojunction, in which PS1(CdS), PS2(TiO2) and the electron-transfer system (Au) are spatially fixed. This three-component system exhibits a high photocatalytic activity, far exceeding those of the single- and two-component systems, as a result of vectorial electron transfer driven by the two-step excitation of TiO2 and CdS.

Journal Article↗
PubMed2006

Ultrafast photosynthetic reduction of elemental sulfur by Au nanoparticle-loaded TiO2.

Nanometer-sized gold particles with varying mean size from 3.2 to 12.2 nm were loaded on the surfaces of TiO2 particles in a highly dispersed state with the loading amount maintained constant (0.46 +/- 0.02 mass %) using the deposition-precipitation method. Light irradiation (lambda(ex) > 300 nm) to a deaerated ethanol TiO2 particle suspension containing elemental sulfur (S8) led to the energetically uphill reduction of S8 to H2S. It has been found that this reaction is dramatically enhanced with such a low level of Au loading on TiO2 and that the zero-order rate constant of reaction increases with decreasing mean size of Au nanoparticles (d). The effects of reaction parameters (substrate concentration, light intensity, temperature) on the rate of reaction were studied to infer the essential reaction mechanism. Further, a kinetic analysis has led to a conclusion that the increase in the rate of reaction with decreasing d results from the improvement of the charge separation efficiency.

Journal Article↗
PubMed2006

Indicators for blood glucose control in diabetics with end-stage chronic renal disease: GHb vs. glycated albumin (GA).

Diabetics with end-stage renal disease (ESRD) exhibit abnormal life span of erythrocytes, and thus, HbAlc is not necessarily a good indicator for blood glucose control. The present study was conducted to reaffirm this point and determine whether glycated albumin (GA) can be used instead of HbAlc. The following three groups of patients with diabetes served as subjects: 49 predialysis patients with ESRD (predialysis group), 37 patients with ESRD on dialysis (dialysis group), and 40 patients without nephropathy (non-dialysis group). The profile set mean blood glucose was calculated by measuring blood glucose levels seven times a day. The relationship of profile set mean blood glucose with HbAlc and GA levels was then investigated. Corrected HbAlc levels were calculated by applying the profile set mean blood glucose of each ESRD patient to the regression formula for the HbAlc of non-dialysis patients. The actual and corrected HbAlc levels for the predialysis patients were 5.4+/-1.1 and 7.9+/-1.1%, respectively, while those for the dialysis patients were 5.6+/-1.0 and 7.5+/-0.9%, respectively (p<0.0001). The changes in GA levels in relation to the blood glucose control in the dialysis patients matched those in non-dialysis patients. HbAlc levels for diabetics with ESRD were lower than indicated by their blood glucose control. When assessing blood glucose control based solely on HbAlc, erroneous results may be obtained. In such cases, GA may be used instead of HbAlc.

Adult↗
PubMed2005

Visible light photocatalytic decomposition of 2-naphthol by anodic-biased alpha-Fe2O3 film.

Transparent alpha-Fe2O3 films with varying film thickness were formed on a SnO2 transparent conducting film-coated glass substrate by metal organic deposition. Under anodic-biased conditions, the alpha-Fe2O3 film showed a high photocatalytic activity for the decomposition of 2-NAP with visible light irradiation. The alpha-Fe2O3 is transformed to inactive hydroxide as the reaction proceeds, while the activity of alpha-Fe2O3 is almost maintained in acetonitrile.

Journal Article↗
PubMed2005

Color properties of gold-silver alternate nanowires electrochemically grown in the pores of aluminum anodic oxidation film.

Repeated electrodeposition of gold and silver on anodized aluminum plate yielded Au-Ag alternate nanowires in the geometrically anisotropic pores of the anodic oxidation films with mean diameter 10 nm and depth 10 mum, respectively. The absorption maximum wavelengths in the visible region resulting from the transverse surface plasmon resonances of Au and Ag nanorods are invariant with their growth. Consequently, the color of the anodized aluminum was simply tuned in a wide range, which is impossible to attain in each monometallic system.

Journal Article↗
PubMed2005

Kinetic and DFT studies on the Ag/TiO2-photocatalyzed selective reduction of nitrobenzene to aniline.

TiO2 particles loaded with silver nanoparticles with a mean diameter of 1.5 nm exhibit a high photocatalytic activity (84 % conversion after 1 h irradiation) for the reduction of nitrobenzene to aniline with 100 % selectivity in the presence of CH3OH (concentration=100 mM). High-resolution transmission electron microscopic studies of Pt-photodeposited Ag/TiO2 demonstrate that the Ag nanoparticles act as reduction sites in the photocatalytic reaction. Both spectroscopic measurements and density functional theory (DFT) calculations reveal that nitrobenzene is selectively adsorbed onto the Ag surfaces of Ag/TiO2 via partial electron transfer from Ag to nitrobenzene, whereas the interaction between aniline and Ag/TiO2 is weak. The kinetic analysis indicates that the recombination between the electrons flowing into the Ag nanoparticle and the holes left in the TiO2 valence band is significantly suppressed, particularly in the presence of CH3OH. The high activity and selectivity in the present Ag/TiO2-photocatalyzed reduction are rationalized in terms of the charge separation efficiency, the selective adsorption of the reactants on the catalyst surfaces, and the restriction of the product readsorption.

Aniline Compounds↗
PubMed2005

Photoinduced dissolution and redeposition of Au nanoparticles supported on TiO2.

Au particles (mean size ca. 3 nm) supported on TiO(2) particles were irradiated by UV light (>300 nm) in aqueous solutions at 278 K. Photo-induced dissolution of Au nanoparticles followed by redeposition occurred in aqueous solutions containing halogen ions. The dissolution of Au nanoparticles yielded a Au(III) complex with a halogen ion; subsequent reduction of the Au(III) complex caused precipitation of larger Au particles on TiO(2).

Letter↗
PubMed2005

Low-temperature synthesis of anatase-brookite composite nanocrystals: the junction effect on photocatalytic activity.

Anatase-brookite composite nanocrystals have successfully been synthesized at 50 degrees C using a simple liquid-phase process. The photocatalytic activity of the sample for the gas-phase oxidation of CH3CHO is 5.4 times greater than that of a single-phase anatase sample with comparable crystallite size and surface area. Electron energy loss spectra suggest that this high activity results from junction between anatase and brookite crystals.

Letter↗
PubMed2004

Photoinduced desorption of sulfur from gold nanoparticles loaded on metal oxide surfaces.

We now report photoinduced sulfur desorption from the surfaces of Au nanoparticles loaded on metal oxides. This reaction occurs in water at ordinary temperature and pressure. Nanometer-sized Au particles have been formed on the surfaces of various metal oxides by deposition-precipitation (Au/oxides). Elemental sulfur (S8) is selectively adsorbed on the Au nanoparticle surfaces of Au/oxides in an atomic state at a coverage of (theta) </= 1/3 and in both atomic and molecular states at theta > 1/3. Irradiation (lambdaex > 300 nm) of the sulfur adsorbed Au/anatase TiO2 in water has led to reductive desorption of the sulfurs at room temperature. Electrochemical measurements using Au/oxides indicate that the driving force for this reaction is the photoinduced upward shift of Fermi energy of the metal oxide-supported Au nanoprticles. This study will open up a novel and wide application of heterogeneous photocatalysis for thermal catalysts.

Journal Article↗
PubMed2004

Drastic enhancement of TiO2-photocatalyzed reduction of nitrobenzene by loading Ag clusters.

Ag clusters (mean diameter = 1.5 nm, standard deviation = 0.37 nm) were photodeposited on TiO(2) particles in a highly dispersed state. The loading of a small amount of the Ag clusters (0.24 wt %) dramatically enhanced both the activity for the TiO(2) photocatalytic reduction of nitrobenzene and the product selectivity of aniline. The essential action mechanism of the Ag clusters is discussed.

Absorption↗
PubMed2004

Deactivation of the TiO2 photocatalyst by coupling with WO3 and the electrochemically assisted high photocatalytic activity of WO3.

Patterned TiO2 stripes were formed on a sol-gel crystalline WO3 film by using a chemically modified sol-gel method (pat-TiO2/WO3), and the coupling effect on the photocatalytic activity was studied. Although the photoinduced electron transfer from TiO2 to WO3 was confirmed by labeling and visualization of the reduction sites with Ag particles, the photocatalytic activities of TiO2 for both the gas-phase oxidation of CH3CHO and the liquid-phase oxidation of 2-naphthol decreased significantly with the coupling. This finding was rationalized in terms of the decrease in the rate of the electron transfer from the semiconductor-(s) to 02 with the coupling, which was estimated from the kinetic analysis of the photopotential relaxation. When the excited electrons were removed by a SnO2 underlayer, the WO3 film exhibited a high photocatalytic activity exceeding that of TiO2 for the oxidation of 2-naphthol.

Journal Article↗
PubMed2003

Photocatalytic activity of rutile-anatase coupled TiO2 particles prepared by a dissolution-reprecipitation method.

Rutile TiO(2) particles were partly dissolved into aqueous solutions of H(2)SO(4), and the Ti(4+) ions were reprecipitated by adding NH(3) aq. Rutile-anatase coupled TiO(2) particles were prepared by heating the solid recovered after centrifugation of the suspension. The content of anatase (c(A), wt%) could be controlled arbitrarily by changing the dissolved amount of rutile. The photocatalytic activity for the gas-phase oxidation of acetaldehyde was evaluated. The first-order rate constant, k, strongly depended on both c(A) and heating temperature (T(c)), increasing with an increase in T(c) at T(c)</=800 degrees C. The sample with c(A)=0.5 wt% prepared at T(c)=800 degrees C exhibited a much higher level of activity (k=0.94 h(-1)m(-2)) than those of pure rutile (k=0.08 h(-1)m(-2)) and anatase (k=0.34 h(-1)m(-2)). This remarkable enhancing effect was explained mainly in terms of photoinduced interfacial electron transfer from anatase to rutile.

Journal Article↗