Authorship：Corresponding author   Language：English   Publishing type：Research paper (scientific journal)  

DOI： 10.1021/acs.inorgchem.3c03789

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DOI： 10.35848/1882-0786/ad13ce

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DOI： 10.1021/acsnano.3c07861

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DOI： 10.1021/acsnano.3c00815

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DOI： 10.1021/acs.nanolett.3c00079

Authorship：Lead author,　Corresponding author   Language：English   Publishing type：Research paper (scientific journal)  

DOI： 10.1246/cl.230136

Authorship：Corresponding author   Language：English   Publishing type：Research paper (scientific journal)  

DOI： 10.1246/cl.230073

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DOI： 10.2109/jcersj2.22150

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DOI： 10.1021/acsami.3c02250

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DOI： 10.1002/smll.202300022

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DOI： 10.1002/aelm.202201239

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DOI： 10.1038/s41598-023-29281-w

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DOI： 10.1246/cl.220466

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DOI： 10.1039/D2NR01807A

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DOI： 10.1039/D2SE00065B

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DOI： 10.2109/jcersj2.21127

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DOI： 10.1021/acs.inorgchem.0c01175

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Publishing type：Research paper (scientific journal)   Publisher：Elsevier BV  

DOI： 10.1016/j.apcatb.2019.04.009

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：AMER CHEMICAL SOC  

Control over TiO2 rutile crystal growth and morphology using additives is essential for the development of functional materials. Computer simulation studies on the thermodynamically stable conformations of additives at the surfaces of rutile crystals contribute to understanding the mechanisms underlying this control. In this study, a metadynamics method was combined with molecular dynamics simulations to investigate the thermodynamically stable conformations of glycolate, lactate, and 2-hydroxybutyrate ions at the {001} and {110} planes of rutile crystals. Two simple atom-atom distances were selected as collective variables for the metadynamics method. At the {001} plane, a conformation in which the COO- group was oriented toward the surface was found to be the most stable for the lactate and 2-hydroxybutyrate ions, whereas a conformation in which the COO- group was oriented toward water was the most stable for the glycolate ion. At the {110} plane, a conformation in which the COO- group was oriented toward the surface was the most stable for all three hydroxylate ions, and a second most stable conformation was also observed for the lactate ion at positions close to the {110} plane. For all three hydroxylate ions (α-hydroxycarboxylate ions), the stability of the most stable conformation was higher for the {110} plane than for the {001} plane. At both planes, the stability of the most stable conformation was highest for the 2-hydroxybutyrate ion and lowest for the glycolate ion. Supposing that all three hydroxylate ions serve to decrease the surface free energy at the rutile surface and that a more stable conformation at the rutile surface leads to a greater decrease in the surface free energy, the present results partially explain experimentally observed differences in the changes in growth rate and morphology of rutile crystals in the presence of glycolic, lactic, and 2-hydroxybutyric acids.

DOI： 10.1021/acsomega.9b01100

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Tantalum/nitrogen codoped titanium dioxide (TiO2:Ta,N) having a rutile structure has recently been reported to be a good photocatalyst for visible-light water oxidation. In this work, three different polymorphs of TiO2:Ta,N (anatase, brookite and rutile) were synthesized by a hydrothermal method using water-soluble titanium/tantalum complexes as precursors, followed by thermal nitridation with dry ammonia gas. Effects of the physicochemical properties on photocatalytic activity for O-2 evolution from an aqueous silver nitrate solution under visible light (lambda > 400 nm) were investigated. Experimental results indicated that defect formation during the nitridation procedure was the dominant factor for photocatalytic activity. Anatase TiO2:Ta,N was the most active for O-2 evolution among the three polymorphs, and also served as an O-2 evolution photocatalyst in Z-scheme overall water splitting in combination with Rh-doped strontium titanate (SrTiO3:Rh) and an Fe3+/Fe2+ redox-shuttle mediator.

DOI： 10.1246/bcsj.20190037

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Authorship：Corresponding author   Language：English   Publishing type：Research paper (scientific journal)  

DOI： 10.1016/j.jssc.2019.05.012

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Authorship：Lead author,　Corresponding author   Language：English   Publishing type：Research paper (scientific journal)   Publisher：INT UNION CRYSTALLOGRAPHY  

Single crystals of the solid solution series Ca(4+x)Y(3-x)Si(7)O(15+x)N(5-x )were obtained by a solid-state reaction method using a flux for x = 0, 0.5 and 1, resulting in Ca4Y3Si7O15N5 (tetracalcium triyttrium heptasilicon oxynitride), Ca-4.5 Y-2.5 Si7O15.5N4.5 and Ca5Y2Si7O16N4 (pentacalcium diyttrium heptasilicon oxynitride). Single-crystal X-ray analysis revealed that the three compounds are isotypic and belong to space-group type P6(3)/m. Ca2+ and Y3+ cations are distributed over two crystallographic sites (site symmetry (3) over bar.. and 1) in a disordered manner. The corresponding (Ca,Y)-centred polyhedra are connected by edge-sharing, resulting in the formation of a layer structure extending parallel to (001). Three [Si(O,N)](4) tetrahedra (two with point group symmetry m one with 3.. and half-occupancy) are condensed into an isolated [Si-7(O,N)(19)] unit, in which an [Si(O,N)](4) tetrahedron is located at the center of a 12-membered oxynitride ring with composition [Si6O15N3]. The present compounds are the first to have such an [Si-7(O,N)(1)(9)] unit in their structures.

DOI： 10.1107/S2056989019001257

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DOI： 10.3390/ceramics2010005

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：ROYAL SOC CHEMISTRY  

A mixed valence compound, sodium titanium oxide bronze (NaxTiO2-B), combines intriguing properties of high electric conductivity and good chemical stability together with a unique one-dimensional tunnel crystal structure available for cation storage. However, this compound has not been studied for a long period because of the strongly reductive condition at high temperature required for its preparation, which limits the morphological control such as the preparation of nanocrystals. For the first time in this paper, the topotactic synthesis of nano-sized NaxTiO2-B with high specific surface area (>130 m(2) g(-1)) from TiO2(B) nanoparticles has been demonstrated. The reaction of metastable TiO2(B) with NaBH4 allows carrier electrons to be doped simultaneously with incorporation of Na+ ions into the interstitial sites of the host Ti-O lattice at relatively low temperature. An electrochemical investigation of Li+- and Na+-ion storage behaviors suggests that the incorporated Na+ ions are mainly placed in the 6-fold coordination sites of bronze. In addition, optical measurements including time-resolved transient spectroscopy revealed that the doped electrons in the NaxTiO2-B nanoparticles are predominantly in the Ti3+ state and behave as a small polaron. The pelletized NaxTiO2-B nanoparticles shows a good electronic conductivity of 1.4 x 10(-2) S cm(-1) at 30 degrees C with an activation energy of 0.17 eV, which is attributable to the thermal barrier for the polaron hopping.

DOI： 10.1039/c8nr08372j

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：TECHNICAL ASSOC PHOTOPOLYMERS,JAPAN  

B-site-ordered double-perovskite oxide up-conversion phosphors La2ZnTiO6, La2MgTiO6, and Ba2LaTaO6 doped with Yb and Ho, Er, or Tm were synthesized by a citric acid complex gelation method and a polymerizable complex method. Under 980-nm excitation, the double-perovskite oxide phosphors doped with luminescent ions at the A-site (La2ZnTiO6 and La2MgTiO6) showed stronger up-conversion emission than the phosphor doped with luminescent ions at the B-site (Ba2LaTaO6). La2ZnTiO6 and La2MgTiO6, in which dopants occupied the A-site, showed different up-conversion emission behaviors because of structural distortion resulting from the substitution of B-site cations.

DOI： 10.2494/photopolymer.32.593

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Ce4+-based charge transfer phosphor is not common and has been reported mainly in Sr2CeO4 with an excitation band peaking at ∼290 nm, mismatching with the near-ultraviolet light emitting diodes. Herein, we report a new series of Ce4+-based compounds Sr4.4Ce2.6REZnO12 (RE = Y, La, and Eu) capable of photoluminescence induced by O2--Ce4+ charge transfer excitation under near-ultraviolet-visible light. The crystal structure of Sr4.4Ce2.6EuZnO12 was determined by single crystal X-ray diffraction. The RE = La and Y samples were confirmed to be iso-structure compounds of the RE = Eu sample by powder X-ray diffraction. By introducing highly covalent Zn2+-O2- bonds into the framework, the Ce4+-O2- bonds are lengthened due to the effect of the Ce4+-O2--Zn2+ stretch. The lengthened Ce4+-O2- bond weakens the repulsion of the electrons between Ce4+ and O2-, thereby lowering the charge transfer energy to the visible light region. Incorporation of Eu3+ into the present compounds realized red emission under near-ultraviolet-visible excitation by the O2--Ce4+ charge transfer followed by energy transfer to Eu3+.

DOI： 10.1021/acs.inorgchem.8b01900

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DOI： 10.1039/C8RA07830K

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DOI： 10.3389/fchem.2018.00467

Authorship：Lead author   Language：English   Publishing type：Research paper (scientific journal)  

DOI： 10.1246/cl.180620

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DOI： 10.1246/cl.180605

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DOI： 10.1016/j.snb.2018.08.021

Authorship：Lead author   Language：Japanese  

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Powders of REMO4 (RE: rare earth, M: Nb and Ta) were synthesized by a coprecipitation method employing water-soluble peroxo Nb/Ta complexes. This peroxo-based method is an aqueous solution route free from organics and halides. REMO4 was directly crystallized by annealing the precursor under moderate conditions. It has been revealed that the precursors are also useful for synthesis of oxynitrides under mild nitriding conditions.

DOI： 10.1246/cl.170652

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：Elsevier B.V.  

Control of crystal growth leads to highly functional materials with desired morphologies. In this study, the relationship between select additives and the crystal growth of rutile-type titania under hydrothermal conditions using α-hydroxy acids, carboxylic acids, or alcohols as additives was systematically investigated. Without additives, rod-like rutile crystals with average dimensions of 295 nm × 67 nm were formed. Acceleration of the crystal growth was observed and the aspect ratios of the resulting rod-like crystals were found to increase in the presence of the additives. Alcohols promoted crystal growth along the c-axis, but not in the direction to perpendicular to [001]. Carboxylic acids accelerated the overall crystal growth and this increase was more enhanced along the c-axis than that along others. Both effects were observed using α-hydroxy acids. In addition, the present results implied that the size of the hydrocarbon groups in alcohols and α-hydroxy acids appeared to be related to the acceleration of crystal growth along the c-axis. Hydroxy groups may reduce the surface energy of the crystal facets perpendicular to the c-axis by their adsorption on those facets, resulting in the formation of rod-like crystals with high aspect ratio.

DOI： 10.1016/j.jascer.2017.06.006

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：ROYAL SOC CHEMISTRY  

Crystalline mesoporous materials with oriented configurations are promising for high-performance energy storage and conversion devices. In this work, hierarchical microspheres constructed from radially oriented single-crystalline TiO2 nanorods have been fabricated by a facile hydrothermal approach using oxalic acid as a chelating and structure-directing agent. The obtained mesoporous TiO2 microspheres have been characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy and Brunauer-Emmett-Teller specific surface area measurement to reveal their unique properties. The growth and assembly process of the nanorod-based microspheres were elucidated in view of chelation-assisted assembly. It was found that oxalic acid played a crucial role in the oriented assembly of nanorods into well-defined microspheres.

DOI： 10.1039/c7ce01158j

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：AMER CHEMICAL SOC  

Tetravalent manganese is known as one of the candidate luminous centers to obtain red emission. There are still unclear factors in Mn4+-activated oxide phosphors to achieve intense emission. In this paper, we studied the photoluminescence properties of double perovskite-type tantalates AE(2)LaTaO(6) (AE = Ca, Sr, and Ba) activated with Mn4+. All AE(2)LaTaO(6):Mn exhibited Mn4+-emission in the deep red region under excitation by near ultraviolet-green light (300-570 nm) at room temperature. Co-substitution of Mg2+, Al3+, and Ti4+ compensates unbalanced charge caused by oxygen defects, resulting in the enhancement of Mn4(+-)emission. The present cosubstitution effect is different from the usual cosubstitution, such as the replacement of two Al3+ by Mn4+ and Mg2+, taking into consideration the charge balance between cations. Theoretical calculation of band structures based on density functional theory suggests the presence of two kinds of quenching schemes in AE(2)LaTaO(6):Mn, photoionization and electron transfer from valence band to t(2g) orbitals of Mn.

DOI： 10.1021/acs.jpcc.7b06280

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Authorship：Lead author   Language：Japanese  

Language：English   Publishing type：Research paper (scientific journal)   Publisher：ELSEVIER SCIENCE BV  

Synthesis of a series of oxynitride Ba3-chi La chi Ta5O14-chi N1+x (x= 0-1.5) with a tetragonal tungsten bronze (TTB) structure was examined using moist-NH3 and 5% NH3-N-2 as nitriding atmosphere. The samples with x=0-1 were successfully obtained as phase pure TTB oxynitride whereas the x= 1.5 samples gave a mixture of TTB oxynitride, Ta3N5, and LaTaO4. Absorption of TTB oxynitrides in visible region was enhanced as increasing the content of nitrogen. TTB oxynitrides exhibited both of H-2 and O-2 evolution under visible light in the presence of methanol and silver ions, respectively, as sacrificial reagents. Nitrogen poor surface in the samples synthesized under moist-NH3 atmosphere was modified by annealing treatment using 5% NH3, resulting in improvement of photocatalytic activity for H2 evolution. Evaluation using monochromatic light revealed that the apparent quantum efficiency of Ba2LaTa5O13N2 was higher than that of Ba3Ta5O14N. (C) 2017 Elsevier B.V. All rights reserved.

DOI： 10.1016/j.apcatb.2017.01.057

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A novel oxynitride, BaYSi2O5N, has been synthesized by a solid-state reaction method. Its crystal structure was determined by single-crystal X-ray analysis. Eu2+- and Ce3+-doped BaYSi2O5N exhibit broad blue emission with peaks around 459 and 412 nm under excitation at 250-450 and 250-370 nm, respectively. This is the first report on the synthesis of oxynitrides in the BaO-Y2O3-SiO2-Si3N4 system.

DOI： 10.1246/cl.170144

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In this work, novel single-phase white emitting Ca(3)Ln(AlO)(3)(BO3)(4): Ce3+, Tb3+, Mn2+ (Ln = Y and Gd) phosphors were synthesized by a conventional solid-state reaction method. The crystal structure and photoluminescence properties were investigated for the first time. The structure of Ca(3)Ln(AlO) (3)(BO3)(4) was formed by AlO6 octahedral chains interconnected by BO3 triangles. Along the [001] direction, the Ca/Ln cations fill in the trigonal and hexagonal tunnels. For Ca(3)Ln(AlO)(3)(BO3)(4): Ce3+ and Ca(3)Ln(AlO)(3)(BO3)(4): Mn2+, large Ce3+ preferred to occupy the smaller coordination site, while small Mn2+ occupied the larger coordination site, which was explained by the space hindrance. Due to the cation disorder, the local environment of Ce3+ was complicated and the emission band was extremely broad. In Ca(3)Ln(AlO) (3)(BO3)(4), the emission color can be tuned from blue to green or red by tuning the Ce3+-Tb3+ or Ce3+-Mn2+ concentration based on energy transfer. Thus, the combination of blue, green and red emitting Ce3+, Tb3+ and Mn2+ generated white emission.

DOI： 10.1039/c7tc00941k

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：TECHNICAL ASSOC PHOTOPOLYMERS,JAPAN  

Er3+/Yb3+ co-doped calcium tantalate up-conversion (UC) phosphors were synthesized via a parallel synthesis scheme using the gelable citrate complex method. Samples with various Ca/Ta atomic ratios were prepared, and their UC emission properties were compared. Under 980-nm near-infrared laser excitation, alpha-CazTa(2)O(7) : Er3+, Yb3+ showed an extremely weak UC emission intensity and CaTa4O11 : Er3+, Yb3+ demonstrated an excellent UC emission intensity. In addition, the local symmetry around the rare-earth dopant ions affected the UC luminescence properties.

DOI： 10.2494/photopolymer.30.507

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Authorship：Lead author   Language：English  

DOI： 10.2109/jcersj2.16117

Language：English   Publishing type：Research paper (scientific journal)   Publisher：CHEMICAL SOC JAPAN  

Upconversion (UC) phosphors comprising Er3+/Yb3+ co-doped rare-earth complex oxides, RExTayOz and RExNbyOz (RE = Y, La, or Gd), were synthesized via the gelable citrate complex method, and their UC emission properties were compared. This led to the discovery of an intense green-emitting UC phosphor, YTa7O19:Er3+/Yb3+, which is the first example of a YTa7O19 UC phosphor host material. Green UC emission obtained using optimum Er3+ and Yb3+ content was 20 times stronger than that obtained using a Y2O3 host.

DOI： 10.1246/cl.160413

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Phosphors with sufficient red emission component are necessary for warm white light-emitting diodes. In this work on (Sr,Ba)2(1-x)Eu2xSiO4 phosphors, (Sr,Ba)1.5Eu0.5SiO4 achieved 75% of an internal quantum efficiency under excitation by blue light. Surprisingly, the (Sr,Ba)1.5Eu0.5SiO4 exhibited orange emission, against the well-known traditional green-yellow emission of (Sr,Ba)2SiO4:Eu(2+). Moreover, the concentration quenching of Eu(2+) in (Sr,Ba)2SiO4 was abnormally unobvious. With the help of calculations based on the density functional theory, it was discovered that the distinct local environment of luminescence centers rather than usual explanation such as self-absorption or intensified crystal field splitting, is responsible to the interesting red shifts in excitation and emission spectra. The refinement analysis based on X-ray diffraction revealed that the unequal distribution of Eu(2+) to two crystallographic sites caused low concentration of Eu(2+) at the 9-coordination site, inhibiting the concentration quenching. The (Sr,Ba)1.5Eu0.5SiO4 phosphor has warmer emission than the commercial Y3Al5O12:Ce(3+). This study also promotes research on the effect of site occupancy and the local environment of luminescence centers.

DOI： 10.1021/acsami.6b02237

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：AMER CHEMICAL SOC  

A molecular dynamics simulation was conducted to elucidate the conformation and dynamics of a glycolate ion (CH2(OH)COO-) at the surface of a TiO2 rutile crystal. The simulation was performed for the {001} and {110} planes of the crystal. The results indicate that, for both planes, the conformation and dynamics of the ion are strongly dominated by a layered structure of water on the surface. The simulation suggests that the ion binds to the surface more stably on the {110} plane than on the {001} plane, and that the stable conformation of the ion at the surface differs between the planes: on the {110} plane the carboxyl group of the ion is preferentially oriented toward the surface, whereas on the {001} plane it is oriented toward liquid water. These simulation results are compared with the growth shapes of rutile crystals synthesized in the presence of glycolic acid, and the role of glycolate ions in controlling the morphology of rutile crystals is discussed.

DOI： 10.1021/acs.jpcc.5b11087

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Calcium silicate cosubstituted with Sr2+ and Eu2+ was studied in order to examine the relationship between emission characteristics and Eu2+ occupancy at two types of Ca sites (Ca(1n) and Ca(2n)). The results clearly indicate that red emission of the Ca2SiO4:Eu2+ phosphor is caused by Eu2+ substitution at the Ca(2n) site. In addition, red shift in emission of Eu(2n) occurs when large amounts of Eu were substituted.

DOI： 10.1246/cl.151145

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：CAMBRIDGE UNIV PRESS  

Although there are numerous reports on the synthesis of spherical materials, the development of new approaches remains important for theory construction to realize tailor-made synthesis of spherical materials. Herein, we report the synthesis of polydispersed spherical particles of H2Ti2O5 intercalated with a polyethyleneamine, such as an ethylenediamine, on the basis of a solvothermal treatment using concentrated polyethyleneamine aqueous solutions. The diameter of the micrometer-sized spheres enlarged with increasing amine concentration in the reaction solution. It was speculated that high ionic strength caused the self-assembly of polyethyleneamine-intercalated H2Ti2O5, resulting in the formation of spherical agglomerates. The spheres had a specific a surface area of 200 m(2) g(-1) and approximately 5 nm pores, and these values were controlled by amine concentration and treatment time. Conversion to single phase anatase and rutile without changes in spherical morphology was achieved by heat treatment. The present approach may assist with the design morphology of agglomerates.

DOI： 10.1557/jmr.2016.67

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Language：Japanese   Publishing type：Research paper (scientific journal)  

Control of crystal growth is rather important in the field of materials, because the shape directly affects their functional abilities. Our research group engages in hydrothermal synthesis of titanium dioxide, which is regarded as one of the representative ceramics, using water-soluble titanium complexes. The high chemical stability and peculiar molecule structures of these titanium complexes allowed us to use various compounds which play a role in control of crystal growth, resulting in the selective synthesis of four titanium dioxide polymorphs, that is, rutile, anatase, brookite and TiO_2(B), with a controlled shape. This paper summarizes our past study and reported researches on synthesis of titania polymorph crystals by classification of zero-, one-, two-, and three-dimensional structures.

DOI： 10.19009/jjacg.42.4_283

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：PERGAMON-ELSEVIER SCIENCE LTD  

Graphene/MxWO3 (M = Na, K) nanocomposites with different weight ratios were successfully synthesized using MBH4 as a reducing agent in aqueous solution, followed by crystallization of amorphous precursors under calcination in H-2 (5 vol.%)/N-2 atmosphere at 600 degrees C. The coupled samples showed good shielding properties in NIR wavelength range together with certain visible lights transparency. The as-prepared tungsten bronze nanoparticles are homogeneously anchored on graphene sheets, and the graphene/tungsten bronze nanocomposite showed an enhanced electrical conductivity with good shielding properties in the NIR range together with certain visible lights transparency. With the increment of graphene amount in the composites, the contact between the graphene sheets was enhanced, and the MxWO3 might enhance the charge transport properties of graphene by generating the short conductive path for electrons over the remained oxygenated functional groups. The synergistic effects could be observed in the composites. When 5 wt.% or more graphene were composed into MxWO3, the hybrid composite showed the higher electrical conductivity than those of uncoupled graphene and tungsten bronze alone. (C) 2015 Elsevier Ltd. All rights reserved.

DOI： 10.1016/j.carbon.2015.06.072

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It has been found that Mn4+-activated La2MTiO6 (M = Mg and Zn) functions as novel Eu-free phosphors for red emission in this work. La2MTiO6:Mn4+ exhibited emission with a peak at 710 nm under excitation by ultraviolet to blue light (300 550 nm). La2MgTiO6:Mn4+ exhibited stronger emission than La2ZnTiO6:Mn4+. The internal quantum yield of La2MgTiO6: Mn4+ was 58.7% under the excitation at 330 nm.

DOI： 10.1246/cl.150748

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DOI： 10.4236/opj.2015.511031

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Reduced graphene oxide (rGO)/rod-shaped potassium tungsten bronze nanocomposites with the different ratio were successfully synthesized by solvothermal reaction and followed by the reduction in H2(5 vol.%)/N2 atmosphere at 550 degrees C. The coupled samples showed excellent shielding ability of NIR light as well as certain visible lights transparency. The synergistic effects could be observed in the composites, i.e., when 15 wt% and 20 wt% of rGO which was fabricated by chemical reduction of graphene oxide, were composed into K(x)WO3, the composite showed the higher electrical conductivity than those of rGO and potassium tungsten bronze.

DOI： 10.1166/jnn.2015.10579

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：CERAMIC SOC JAPAN-NIPPON SERAMIKKUSU KYOKAI  

A novel picolinate-iron(III) compound, Fe(C6H4NO2)(2)(OH) (1), was synthesized from an aqueous solution of a picolinate-iron(II) complex. Compound 1 was obtained by a thermal treatment of the picolinate-iron complex aqueous solution, whose pH was adjusted to 3-7, containing more than twice molar picolinic acid (Hpa) to Fe at 353K for 72 h. When the iron aqueous solution in the presence of more than six times molar Hpa to Fe at pH 2-5 was heated, Fe(C6H4NO2)(3)center dot H2O (2) appeared. Millimeter-sized yellow-green single crystals of 2 could be obtained by the heat treatment of the picolinate-iron aqueous solution, whose pH was adjusted to 3, with Fe2+:Hpa = 1: 10 at 373K for 72 h. Formation mechanism of 1 and 2 was also discussed through investigations of relationship between synthesis conditions and products. Our approach opens a promising new route for preparation of precursors for synthesis of high functional ceramics and development of new organic-inorganic hybrids. (C) 2015 The Ceramic Society of Japan. All rights reserved.

DOI： 10.2109/jcersj2.123.751

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Two novel pyrazine-2-carboxylate titanium complexes were synthesized from an aqueous solution (1) and 1 in N,N-dimethylformamide (DMF) (2). The structure of 2 was determined to be [Ti6O8(C4H3N2COO)(8)(C3H7NO)(4)]center dot 4C(3)H(7)NO center dot H2O by single-crystal X-ray analysis. Both complexes exhibited solvent adsorption desorption accompanying reversible structural change. 1 and 2 were compatible, and 1 was vital for the synthesis of 2. The degassed 1 showed gate adsorption property for water vapor.

DOI： 10.1246/cl.150393

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Novel delafossite-type compounds Cu(Li1/3Ti2/3)O-2 with 3R- and 2H-type structures have been discovered through the reaction between Li4Ti5O12 and Cu2O. Cu(Li1/3Ti2/3)O-2 is the first Cu(I)-titanate containing no d(n) (n = 1-9) metal ions. It has been found that Cu(Li1/3Ti2/3)O-2 with a band gap of 2.1 eV functions as a photocatalyst for H-2 evolution under visible light irradiation.

DOI： 10.1246/cl.150341

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：ELSEVIER SCIENCE BV  

Recently, shape-controlled synthesis of crystals exposing high-index facets has attracted much research interest due to their importance for both fundamental studies and technological applications. Herein, crystals of rutile-type TiO2 with hierarchical structures exposing high-index facets have been synthesized by a facile hydrothermal method using water-soluble titanium complex as a precursor and picolinic acid as structure-directing and shape-controlling agents. The synthesized particles were composed of several branches of pyramidal crystals with relatively smooth surface. On the basis of investigation results, it was speculated that the mutual pi-stacking and selective adsorption of picolinic acid on specific {111} facets resulted in the formation of rutile crystals bound by high-index surfaces such as {331}. (C) 2015 Elsevier B.V. All rights reserved.

DOI： 10.1016/j.jcrysgro.2015.02.056

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Language：Japanese   Publishing type：Research paper (scientific journal)   Publisher：Journal of the Japan Society of Powder and Powder Metallurgy  

In this paper, we demonstrated the synthesis of silicate-based phosphors by solution techniques using glycolmodified silane (GMS) as a Si source. GMS is a water-dispersible inorganic Si cluster, which is vitally involatile and nonflammable compounds, compared to volatile and flammable Si-alkoxides such as tetraethoxysilane (TEOS). Therefore, GMS has allowed the silicon containing compounds to be synthesized through various solution processes for ceramic compounds such as polymerizable complex (PC) and amorphous metal complex (AMC) methods. This paper provides examples of synthesis of new silicate-based phosphors such as NaAlSiO4:Eu2+, BaZrSi3O9:Eu2+, and CaSrSiO4:Eu2+. In addition, other examples of improvement of emission for conventional silicate-based phosphors, Y2SiO5:Ce3+-Tb3+ and Zn2SiO4:Mn2+, prepared by the above solution techniques including homogeneous precipitation using GMS are also given in this paper.

DOI： 10.2497/jjspm.62.127

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：NATURE PUBLISHING GROUP  

Nature produces materials with excellent physical and chemical properties using water as a medium under ambient temperature and pressure. The current need for more highly functional and compact materials makes the mimicking of natural processes to produce these materials a very interesting approach, not only to obtain highly functionalized materials but also to reduce the environmental impact. Our research group is engaged in the development of new stable water-soluble compounds that follow natural processes for the synthesis of materials using water as a medium. This paper summarizes a hydrothermal synthesis of rutile-type titanium oxide using water-soluble titanium complexes, controlling the crystal morphology by utilizing organic molecules as shape-control agents as well as their speculative formation mechanism and superior dielectric properties of unusually shaped titanium oxide crystals. By recapitulating our results, we indicate that control of the nano-and macro-structures and functional improvement are accomplished through the development of new precursor compounds.

DOI： 10.1038/pj.2014.89

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NaBa(1-x)Ca(x)PO4:Eu(2+) were synthesized using polymerizable complex method. New phases were observed at x = 1/3 and 0.5, which were identified by single-crystal XRD analysis as Na3Ba2Ca(PO4)3 and NaBa0.5Ca0.5PO4 with a trigonal system. Though both phases pretend to be solid solutions between NaBaPO4 and NaCaPO4, they have different coordination environments and PO4 orderings. 1 mol% Eu(2+)-activated NaBaPO4, Na3Ba2Ca(PO4)3, and NaBa0.5Ca0.5PO4 exhibited an emission maximum at 435 nm, 458 nm, and 460 nm, respectively. The shift of the emission maximum might be due to a change in the Eu-O bond length.

DOI： 10.1039/c4dt03024a

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：ROYAL SOC CHEMISTRY  

Controlled/living radical polymerization was examined with the use of magnetic iron oxide (Fe3O4) prepared through various processes, including hydrothermal synthesis, a bioinspired process, and magnetotactic bacteria. Prior to the use of various types of Fe3O4, commercially available Fe3O4 was employed as a heterogeneous catalyst for styrene polymerization in conjunction with an alkyl halide as an initiator. Under appropriately optimized conditions, with the addition of Ph3P in a solvent mixture of toluene and DMF, the polymerization proceeded in a well-controlled manner. In addition, solid Fe3O4 was recovered using a magnetic approach and was reused for a polymerization reaction. The effects of stirring on the polymerization rate suggest that the surface of Fe3O4 is responsible for the catalysis in polymerization. Fe3O4 samples prepared through various processes were then used for styrene polymerization and showed different activities depending on the preparation process. In particular, Fe3O4 prepared through hydrothermal synthesis exhibited a much higher activity compared with commercial Fe3O4.

DOI： 10.1039/c5ra09149g

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：ROYAL SOC CHEMISTRY  

Single phase Zn1-2x(CuGa)(x)Ga2S4 was successfully synthesized by a two-step route: synthesis of an oxide precursor by a polymerizable complex (PC) method followed by sulfurization under a H2S-Ar flow. The samples thus obtained were porous aggregates consisting of fine crystals with 50 nm size. Among the examined compositions, Zn-0.4(CuGa)(0.3)Ga2S4 (x = 0.3) showed the highest activity for H-2 evolution from an aqueous solution containing S2- and SO32- as electron donors under visible light irradiation. The apparent quantum yield of the optimized sample with deposition of 2 wt% of Rh was 19% at 420 nm. This value is higher than that of the sample synthesized by a solid state reaction (15%). Therefore, improvement of the photocatalytic performance of Zn-0.4(CuGa)(0.3)Ga2S4 for H-2 evolution has been achieved by using the two-step synthesis method including the preparation of an oxide precursor by the PC method.

DOI： 10.1039/c5ta02114f

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Language：English   Publishing type：Research paper (scientific journal)  

DOI： 10.1039/c5ta02482j

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：Royal Society of Chemistry  

A carbon modified NaTaO&lt
inf&gt
3&lt
/inf&gt
mesocrystal nanoparticle (ca. 20 nm) was successfully synthesized by a one-pot solvothermal method, employing TaCl&lt
inf&gt
5&lt
/inf&gt
and NaOH as the starting materials and distilled water/EG mixed solution as a reaction solvent in the presence of appropriate amounts of glucose. The mesocrystal sample presented a high specific surface area 90.8 m&lt
sup&gt
2&lt
/sup&gt
g&lt
sup&gt
-1&lt
/sup&gt
with large amounts of well-dispersed mesopores in the particle, owing to the co-effect of EG and glucose during the reaction process. A non-classic mechanism of formation was proposed for the growth of the NaTaO&lt
inf&gt
3&lt
/inf&gt
mesocrystal. Furthermore, the NaTaO&lt
inf&gt
3&lt
/inf&gt
mesocrystal exhibited considerably improved visible light absorption in addition to the intrinsic UV light absorption as a result of carbon modification originated from glucose. On the basis of the large specific surface area, high crystallinity and optical property, the carbon modified NaTaO&lt
inf&gt
3&lt
/inf&gt
mesocrystal demonstrated excellent efficiency for continuous NO gas destruction under irradiation of UV, short wavelength visible lights (&gt
400 m) and even long wavelength visible light (&gt
510 nm), considerably superior to those of the unmodified NaTaO&lt
inf&gt
3&lt
/inf&gt
specimen and commercial titania, P25. The carbon modified NaTaO&lt
inf&gt
3&lt
/inf&gt
mesocrystal nanoparticles prepared in this work would probably have potential utilization in environmental purification and energy conversion.

DOI： 10.1039/c4ta04132a

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：ELSEVIER SCIENCE BV  

Two novel Eu2+-activated phosphors in the Na-Sc-Si-O system were developed in this study, NaScSi2O6:Eu and Na3ScSi3O9:Eu. NaScSi2O6:Eu2+ showed yellow emission with a peak at 555 nm under excitation at 220-430 nm. When flux-treatment was performed for NaScSi2O6:Eu2+, we found the existence of a new phase. We then succeeded in synthesis of a high-purity sample of this new compound by a parallel solution synthesis method. It was revealed that the new phase was Na3ScSi3O9 with isostructure to Na3YSi3O9, and Eu2+-activated Na3ScSi3O9 exhibited photoluminescence. Na3ScSi3O9:Eu showed green emission with a peak at 530 nm and a corresponding broad excitation band up to 500 nm. However, photoluminescence of Eu2+ was negligible for Na3YSi3O9:Eu because of the stabilization of Eu3+ at the Y3+ site. (C) 2014 Elsevier B.V. All rights reserved.

DOI： 10.1016/j.jlumin.2014.05.006

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：CERAMIC SOC JAPAN-NIPPON SERAMIKKUSU KYOKAI  

The synthesis of oxyfluoride solid solutions with the composition (Ca1-xSrx)(4)Si2O7F2 is reported in this study. (Ca1-xSrx)(4)Si2O7F2 is found to form a solid solution within the entire composition range. Synthesis of Sr4Si2O7F2, which is the first compound in the Sr-Si-O-F system, can be regarded as one of the interesting results of this study. The Eu2+-activated (Ca1-xSrx)(4)Si2O7F2 solid solutions, except for Sr4Si2O7F2 exhibited photoluminescence under excitation at 300-450nm at room temperature. The samples with x = 0.25-0.75 showed a broad red emission band with a peak around 630 nm, whereas the Ca4Si2O7F2:Eu2+ (x = 0) showed blue emission with a peak at 470 nm. Thus, the substitution of Sr for Ca in Ca4SiO7F2:Eu2+ changed the photoluminescence properties remarkably. (C) 2014 The Ceramic Society of Japan. All rights reserved.

DOI： 10.2109/jcersj2.122.630

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：CERAMIC SOC JAPAN-NIPPON SERAMIKKUSU KYOKAI  

The stability and reactivity of phosphate raw materials, including two water-soluble phosphates, ethylene glycol-conjugated phosphate (EG-P), and polyethylene glycol-conjugated phosphate (PEG-P) developed by our group, were examined with the aim of synthesizing phosphates with high functionalities. EG-P was found to gradually hydrolyze in an aqueous solution, resulting in the formation of H3PO4, while PEG-P was stable for more than two months. EG-P and PEG-P did not form insoluble materials in aqueous solution in the presence of many other cations, while precipitates were often observed using conventional phosphate raw materials. In particular, there were no precipitates in an aqueous solution of PEG-P in the presence of Ca2+ and Li+ ions, which easily formed insoluble phosphates in a given aqueous condition. Consequently, single-phase LiCaPO4 with high luminescence properties could be obtained by a polymerizable complex method employing PEG-P, while impurity phases were formed using other P sources, and KSrPO4 was formed as a single phase using EG-P and PEG-P. (C) 2014 The Ceramic Society of Japan. All rights reserved.

DOI： 10.2109/jcersj2.122.626

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Language：English   Publishing type：Research paper (scientific journal)  

We report a new dicalcium silicate phosphor, Ca(2-x)Eu(x)SiO4, which emits red light in response to blue-light excitation. When excited at 450 nm, deep-red emission at 650 nm was clearly observed in Ca1.2Eu0.8SiO4, the external and internal quantum efficiencies of which were 44 % and 50 %, respectively. The red emission from Ca(2-x)Eu(x)SiO4 was strongly related to the peculiar coordination environments of Eu(2+) in two types of Ca sites. The red-emitting Ca2SiO4:Eu(2+) phosphors are promising materials for next-generation, white-light-emitting diode applications.

DOI： 10.1002/anie.201402520

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Language：Japanese   Publishing type：Research paper (conference, symposium, etc.)  

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：CAMBRIDGE UNIV PRESS  

Novel water-soluble titanium complexes coordinated by hydroxycarboxylic acids or amines were developed, and the hydrothermal treatment of the new complexes was carried out to elucidate the formation mechanism of the titania polymorphs including rutile, anatase, and brookite. An empirical relationship among the crystal structure of TiO2, the ligand, and the complex structure was found. Anatase, rutile, or a mixture of both was obtained by the hydrothermal treatment of the complexes coordinated by hydroxycarboxylic acids. The structure of complexes prepared using hydroxycarboxylic acids, which have one hydroxyl and one carboxylic groups, seems to be preferable for the formation of rutile. It was also found that the hydrothermal treatment of titanium complexes coordinated by amine with NAc2 structure resulted in the formation of brookite. Thus, the effect of ligand and complex structure on the crystal structure of TiO2 synthesized by the hydrothermal treatment of the complexes was proposed.

DOI： 10.1557/jmr.2013.229

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：Elsevier B.V.  

Hydrothermal synthesis of Fe3O4 (magnetite) particles was carried out using organic compounds as morphology control agents to obtain magnetite crystals with uncommon facets. It was established that the morphology of Fe3O4 crystals obtained by hydrothermal treatment of an aqueous solution containing Fe2+ and organic compounds depended on the organic compound used. The shape of the Fe3O4 particles obtained when no additives were used was quasi-octahedral. In contrast, the addition of picolinic acid, citric acid or pyridine resulted in the formation of polyhedral crystals, indicating the presence of not only {111}, {100} and {110} facets but also high-index facets including at least {311} and {331}. When citric acid was used as an additive, octahedral crystals with {111} facets also appeared, and their size decreased as the amount of citric acid was increased. Thus, control of Fe3O4 particle morphology was achieved by a simple hydrothermal treatment using additives. © 2014 The Ceramic Society of Japan and the Korean Ceramic Society.

DOI： 10.1016/j.jascer.2014.05.008

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7678

DOI： 10.4236/opj.2013.36A003

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7679

DOI： 10.4236/opj.2013.36A004

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7677

DOI： 10.4236/opj.2013.36A002

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7680

DOI： 10.4236/opj.2013.36A006

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7621

DOI： 10.2109/jcersj2.121.593

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：CHEMICAL SOC JAPAN  

It has been found that cocatalyst-loaded LaTa7O19 with a band gap of 4.1 eV functions as a photocatalyst for water splitting under ultraviolet irradiation. The activity of Rh0.5Cr1.5O3-loaded LaTa7O19 prepared by a polymerizable complex method exhibited double of that prepared by a solid-state reaction. An apparent quantum yield of Rh0.5Cr1.5O3-loaded LaTa7O19 was determined to be 9.0% at 254 nm.

DOI： 10.1246/cl.130216

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：SPRINGER  

SrTiO3 nanoparticles modified with a carboxyl group were successfully prepared by microwave-assisted solvothermal reaction of SrCl2 center dot 6H(2)O and Ti(OC3H7)(4) in methanol-organic acid solution. The as-prepared products were characterized using X-ray diffraction (XRD), diffuse reflectance spectroscopy, and Fourier-transform infrared (FTIR) spectroscopy. The photocatalytic activity was determined by DeNO (x) ability using a mercury arc with filters to control irradiation wavelengths to > 290, > 400, and > 510 nm. Nanoparticles of perovskite-type SrTiO3 were successfully synthesized above pH 12. The photocatalytic activity of SrTiO3 under visible-light (> 510 nm) irradiation could be promoted by surface modification of SrTiO3 with the carboxyl group (-COO), especially from oleic acid.

DOI： 10.1007/s11164-012-0894-1

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：ROYAL SOC CHEMISTRY  

A series of oxynitride solid solutions, NaxLa1-xTaO1+2xN2-2x with x 0.1, 0.2, 0.25, 0.3, 0.5, 0.75 and 0.85, was successfully synthesized by nitridation of amorphous oxide precursors under an NH3 stream at 1273 K. The band gaps of the solid solutions increased with the Na content. Photoelectrochemical analysis was conducted to obtain information on the band potentials of the solid solutions. The valence band maxima of the solid solutions were at more positive potentials than that of LaTaON2 (x = 0). Solid solutions of NaxLa1-xTaO1+2xN2-2x with x = 0.20-0.85 exhibited photocatalytic activity for both H-2 and O-2 evolution under visible light irradiation in the presence of sacrificial reagents, while LaTaON2 had no activity for O-2 evolution. The achievement of O-2 evolution with these solid solutions is due to control of the valence band potential; therefore, control of the photocatalytic properties of LaTaON2 was achieved by the formation of solid solutions.

DOI： 10.1039/c3ta10257b

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：ROYAL SOC CHEMISTRY  

A novel phosphate raw material having an oligomeric structure with desirable stability and solubility under aqueous conditions was prepared via an esterification reaction between H3PO4 and ethylene glycol under reflux. A blue emitting KSrPO4:Eu2+ phosphor with high luminescence was subsequently synthesized using a polymerizable complex (PC) method with the prepared phosphate oligomers as a source of P. KSrPO4:Eu2+ thus prepared exhibited higher emission intensity than samples prepared using a solid state reaction method or the PC method using H3PO4. This high luminescence was attributed to the excellent homogeneity of the constituents in the sample. It was found that KSrPO4 doped with more than 3 mol% of Eu2+ showed a new low-energy emission band at approximately 480 nm, in addition to the known emission band at 428 nm. This new feature was speculated to be derived from disordering of K and Sr ions caused by the high homogeneity of the constituents. Moreover, it was confirmed that thermal quenching of emission at 428 nm above 423 K was recovered in samples doped with more than 7% of Eu.

DOI： 10.1039/c3tc31121j

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：ROYAL SOC CHEMISTRY  

Development of new visible-light-driven oxide photocatalysts for H2 evolution was conducted with a concept of formation of solid solutions containing Cu(I) ions. Band gaps of Cu3xLa1-xTa7O19 solid solutions were 2.57-2.71 eV being remarkably narrower than that of LaTa7O19 (x = 0, 4.14 eV). The remarkable narrowing of the band gaps was due to the contribution of Cu 3d orbitals to valence bands. The solid solutions were capable of photocatalytic H-2 evolution under visible light irradiation in the presence of methanol as an electron donor. Interestingly, the solid solutions with x = 0.2-0.8 showed higher activities than that of a native Cu(I)-tantalate, Cu3Ta7O19 (x = 0). Among the solid solutions, the x = 0.6 sample, Cu1.8La0.4Ta7O19, exhibited the highest activity. The apparent quantum yield of the optimized photocatalyst was 0.48% at 420 nm. Moreover, the good stability of Cu(I) ions in the solid solutions was proven through the investigation of photocatalytic properties and the XPS analysis. Thus, new visible-light-driven oxide photocatalysts capable of H-2 evolution were developed by the formation of the Cu(3x)La(1-x)Ta(7)O19 solid solutions.

DOI： 10.1039/c3cy00557g

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Solid solutions of (Ba1-XSrX)4Al 2S7 (X = 0.2 to 0.6) novel thioaluminate compound were synthesized, whose crystal structure was determined. The crystal structure of the (Ba1-XSrX)4Al2S7 solid solution is related to that of monoclinic Ba4Ga 2S7 consisting of isolated Ga2S7 units. However, the local structures around Ba/Sr in (Ba1-XSr X)4Al2S7, such as coordination number and one unusually long bond (d(Ba,Sr)-S 4 Å) in 7- and 8-coordinated (Ba,Sr)-S, are different from those in Ba4Ga 2S7. Eu2+-activated (Ba1-XSr X)4Al2S7 exhibited orange emission with a peak maximum at 594 nm and a corresponding excitation band at 300 to 550 nm. This is the first report of an orange phosphor in the thioaluminate system. The thermal quenching of luminescence in the (Ba1-XSr X)4Al2S7:Eu2+ phosphor was comparable to that in a conventional Y3Al5O 12:Ce3+ phosphor. © 2012 The Electrochemical Society.

DOI： 10.1149/2.019302jss

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：ROYAL SOC CHEMISTRY  

Flux treatment using various molten salts was performed for SrTiO3 powders. Morphology of SrTiO3 crystals obtained by the flux treatment strongly depended on the kinds of molten salts used. Large cubic crystals exposing {100} facets with a size of 5-6 mm were obtained by the flux treatment with LiCl whereas truncated cubes exposing {100} and {110} facets with a size of 200-400 nm were obtained when NaCl or SrCl2 was used as a flux reagent. In contrast, the flux treatment with KCl gave characteristic shaped crystals with a size of 300 nm. Electron microscope observation and electron diffraction analysis revealed that the crystals treated with the KCl flux expose {100}, {120}, and {121} facets. SrTiO3 treated with the KCl flux exhibited higher activity by 20 times than the non-flux-treated sample. Thus, a remarkable improvement of activity has been achieved by the fabrication of SrTiO3 crystals exposing high-index facets, {120} and {121}, using the KCl flux.

DOI： 10.1039/c3cy00014a

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：CERAMIC SOC JAPAN-NIPPON SERAMIKKUSU KYOKAI  

Morphological control as well as formation of nanoparticles of anatase-type titanium dioxide has been achieved by a solvothermal treatment of a water-soluble citratoperoxotitanium (CPT) complex using ethylenediamine (EDA) as a key solvent in the presence of a given amount of water. When the EDA concentration in the whole solvent (EDA + H2O) remained low less than 12 M, the powder obtained after the solvothermal treatment consisted of spindle-like anatase particles. With an increase of the EDA concentration in the solvent, the shape of the obtained particles changed from spindle to square bipyramid. When another water-soluble oxoglycolatoperoxotitanate complex or TiCl4 was used as a starting source of Ti, similar shaped anatase particles could be obtained by a careful choice of synthetic conditions. Using a mixed solvent of EDA and water, sheet-like titanic acid was produced as an intermediate phase, regardless of the EDA concentration. Therefore, the formation of anatase in the current system may take place through dissolution-recrystallization of titanic acid. The formation of square bipyramidal anatase particle achieved in the present study is not agreement with a reported theoretical calculation of equilibrium phase, because the calculation reveals that truncated square bipyramid-like anatase is obtained under an acidic condition and spindle-like anatase was formed under a basic condition. An adsorption of EDA on particle surface and the pH of the solvent may contribute to the achievement of morphological control. (C)2012 The Ceramic Society of Japan All rights reserved.

DOI： 10.2109/jcersj2.120.494

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：WILEY-V C H VERLAG GMBH  

A facile approach, based on the polyelectrolyte-mediated electrostatic adsorption of a water-soluble titanium complex on colloid templates and hydrothermal treatment, is presented for the formation of hollow TiO2 spheres of the desired polymorphs. The coreshell particles were formed by the alternate deposition of titaniumglycolate complex 1 and positively charged polyelectrolyte, poly(allylamine hydrochloride) (PAH) on spherical polystyrene (PS) templates by utilizing electrostatic interactions for shell formation. Hollow spheres formed with the polyionic complex of 1 and PAH were obtained by removal of the PS templates. Formation of the polyionic complex affected the crystallization of TiO2 from 1 by hydrothermal treatment. Hollow spheres of brookite and anatase were obtained by hydrothermal treatment at pH 4 and 10, respectively. The approach presented here can be exploited for the fabrication of novel advanced titania-based materials with desired structures and polymorphs.

DOI： 10.1002/ejic.201200421

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The morphology-controlled synthesis and near-infrared (NIR) absorption properties of W(18)O(49) were systematically investigated for the application of innovative energy-saving windows. Various morphologies of W(18)O(49), such as nanorods, nanofibers, nanograins, nanoassembles, nanoplates, and nanoparticles, with various sizes were successfully synthesized by solvothermal reactions using organic alcohols as reaction media and WCl(6), W(EtO)(6), and WO(3) solids as the tungsten source. W(18)O(49) nanorods of less than 50 nm in length showed the best optical performance as an effective solar filter, which realized high transmittance in the visible region as well as excellent shielding properties of NIR light. Meanwhile, the W(18)O(49) nanorods also exhibited strong absorption of NIR light and instantaneous conversion of the absorbed photoenergy to the local heat.

DOI： 10.1021/ic300049j

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Hydrothermal synthesis of brookite-type titanium dioxide was performed with excellent reproducibility using an aqueous NH3 solution of a water-soluble citratoperoxotitanate (CPT) complex. X-ray diffraction confirmed that the brookite phase was formed by hydrothermal treatment of the CPT complex in NH3 solution with a concentration of more than 6.5 wt%, whereas single phase anatase was obtained when distilled water without any additives was applied as the solvent. The aspect ratios of the obtained rod-like brookite particles increased from 5 up to 20 with an increase of the NH3 concentration. Transmission electron microscopy and selected area electron diffraction measurements provided evidence that the growth of the brookite particles is along the c-axis. Hydrothermal treatment of the CPT complex at high NH3 concentrations resulted in the formation of agglomerated brookite particles with unusual shapes, where many rod-like particles were branched around a somewhat longer central particle, and the side view of the agglomerated particles revealed two-dimensional crystal growth within a given restricted plane. The multi-needle agglomerate of particles was snowflake shaped. The reason for the formation of brookite with this unique morphology may be attributed to an intrinsic character of the CPT complex itself, although the mechanism is yet to be clarified. © 2011 Elsevier B.V. All rights reserved.

DOI： 10.1016/j.jcrysgro.2011.09.046

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：Ceramic Society of Japan  

Phase- and morphology-control of TiO2 was performed by a facile hydrothermal method using a novel water-soluble titaniumpicolinato complex as a precursor. Single-phase rutile or brookite type titania can be obtained by tailoring the pH of the complex solution. Rutile with a hierarchical microstructure was synthesized using an excess amount of ligand as an additive and the final product consisted of microspheres with mesopores formed by a self-assembly of nanorods. The anisotropic growth of nanorods with a high aspect ratio was explained by a capping mechanism. © 2011 The Ceramic Society of Japan.

DOI： 10.2109/jcersj2.119.513

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：CHEMICAL SOC JAPAN  

The growing significance of nanocrystalline inorganic functional materials in the fields of catalysis, electronics, and energy conversion together with the increasing demand of the society for safer, softer, and "greener" technologies has drawn considerable attention of the researchers toward water-based solution processes for synthesis of such materials. In this respect complex oxides, containing d(0)-transition metals, such as Ti, Nb, Ta, or Si represent an outstanding challenge. for materials chemists due to the extremely narrow range or almost complete absence of suitable precursor compounds compatible with aqueous systems. In the recent 10 years, a remarkable progress has been achieved in the development of new water-soluble complexes of titanium and considerable experience was accumulated in the application of these compounds for synthesis of nanocrystalline titanium-containing materials. The essential knowledge of coordination chemistry of such water-soluble titanium complexes is reviewed in this work, which succeeded to identify the key structural features responsible for stability of the compounds against hydrolysis and to provide guidelines for synthesis of these complexes. Finally, an extensive overview of highly selective aqueous solution based synthesis of TiO2 polymorphs as well as complex oxide materials with the help of the novel water-soluble titanium complexes is provided.

DOI： 10.1246/bcsj.20100103

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Language：Japanese   Publishing type：Research paper (scientific journal)  

A panel of new stable and water soluble complexes of titanium (IV) with natural hydroxy-carboxylic acids such as citric, tartaric, lactic or glycolic acid as ligands was developed. A typical structure of these complex ions includes a peroxo-group, and a hydroxy-carboxylic acid molecule attached to the metal ion by carboxylic and hydroxylic groups to form stable species. The tight coordination and negative charge of complex ions are responsible for stability of these new compounds in water solutions in a wide range of temperatures and pH. Use of natural non-toxic ligands and ammonium as counterions make such titanium compounds convenient reagents for "green" synthesis of titanium containing materials by aqueous solution methods.<BR>The architecture of titanium complexes includes structural motifs of different polymorphic forms of TiO<SUB>2</SUB>, which allows for application of these compounds as building blocks (tecton) for synthesis of titania with different crystal structures by a simple hydrothermal processes. In this way anatase, rutile, TiO<SUB>2</SUB>(B) and brookite were prepared in a reproducible and highly selective way. For the first time TiO<SUB>2</SUB>(B) and brookite were synthesized as single phase nano-crystals by a "one-pot" hydrothermal process, and their outstanding photo-catalytic activities were revealed.

DOI： 10.2497/jjspm.56.188

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：CERAMIC SOC JAPAN-NIPPON SERAMIKKUSU KYOKAI  

Nanocrystalline brookite titanium oxide was prepared by hydrothermal treatment of a water-soluble titanium complex with ethylenediaminetetraacetic acid (EDTA). In this work, we examined the effect of synthesis conditions such as reaction time, titanium concentration and solution pH on the brookite phase formation and its photocatalyitic performance. It was found that hydrothermal treatment of the titanium complex may yield anatase and brookite phases, and their ratio can be varied depending on titanium concentration. Single phase brookite could be prepared when titanium concentration in the starting solution was higher than 0.25 mol/dm(3), while lower concentration favors formation of anatase. Remarkably, brookite could be synthesized from the Ti-EDTA complex in the wide range of pH including both acidic and basic media. The samples prepared from Ti-EDTA complex demonstrated higher photocatalytic activity in terms of NO gas decomposition than the brookite powders synthesized from Ti-glycolate complex or commercial TiO2 photocatalyst P25. Higher photocatalytic activity of powders obtained from Ti-EDTA complex aqueous solution is explained by higher surface area of smaller but well-crystallized brookite particles that can be achieved when this new titanium complex is employed. (C) 2009 The Ceramic Society of Japan. All rights reserved.

DOI： 10.2109/jcersj2.117.320

Web of Science

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：CERAMIC SOC JAPAN-NIPPON SERAMIKKUSU KYOKAI  

The metastable phase of TiO2(B), one of the polymorphs of titanium dioxide (TiO2), was prepared by a hydrothermal treatment of a titanium glycolate complex ([Ti-4(C2H2O3)(4)(C2H3O3)(2)(O-2)(4)O-2](6-)) at 473 K for 1-72 h in the presence of H2SO4. Characterization by X-ray diffraction (XRD) and transmission electron microscopy (TEM) revealed that the obtained samples were composed of single phase TiO2(B) and the particles had plate-like morphology. After post-synthetic hydrothermal crystal growth (PHCG) applied to the as-prepared sample, thicker plate-like shaped particles were obtained. The photocatalytic activities of the samples obtained by the hydrothermal treatment and after the subsequent PHCG were evaluated in terms of methanol decomposition. (C) 2009 The Ceramic Society of Japan. All rights reserved.

DOI： 10.2109/jcersj2.117.347

Web of Science

Scopus

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Authorship：Lead author   Language：Japanese  

Language：English   Publishing type：Research paper (scientific journal)   Publisher：WILEY-BLACKWELL PUBLISHING, INC  

Nanowhiskers of rutile-type titanium dioxide (TiO(2)) were synthesized by a simple hydrothermal treatment of a water-soluble titanium-glycolate complex at 473 K. The aspect ratio of the obtained rutile particles could be controlled by changing the concentration of the glycolic acid additive in the starting aqueous solution of the titanium complex. According to high-resolution transmission electron microscopy, whisker-like nanoparticles grow along the c-axis of rutile, the side facets of which are (110), (-110), (1-10), and (-1-10). Glycolic acid controls promotion of the rutile particles in the specified direction due to its preferred adsorption on the titanium-rich facets. Evaluation of the photocatalytic activity of the synthesized TiO(2) was performed in terms of decomposition of oxalic acid in an aqueous system under ultraviolet irradiation. It turned out that this particular whisker-like shape is responsible for the tremendous enhancement of rutile photocatalytic activity, and even rutile samples with low surface area demonstrated photocatalytic performance comparable with one of the best nanosized anatase photocatalytic materials. Therefore, it can be concluded that the (110) rutile facet plays an important role in the photocatalytic oxidation reaction, and that it exhibits higher photocatalytic activity than the (001) facet in the decomposition of oxalic acid.

DOI： 10.1111/j.1551-2916.2008.02641.x

Web of Science

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：ELSEVIER SCIENCE BV  

Titanium dioxide (TiO2(B), one of metastable polymorphs of TiO2 was prepared by hydrothermal reaction of glycolato peroxotitanium complex ([Ti-4(C2H2O3)(4)(C2H3O3)(2)(O-2)(2)](6) in the presence of H2SO4 as an additive. Characterization by X-ray diffraction (XRD), Raman spectroscopy, and transmission electron microscopy (TEM) revealed that the obtained powders were single-phase TiO2(B) with rod-like shape, Particle size and aspect ratio of TiO2(B) can be controlled by post-synthetic hydrothermal crystal growth (PHCG) of the as-prepared powder sample. (C) 2008 Elsevier B.V. All rights reserved.

DOI： 10.1016/j.jcrysgro.2008.09.041

Web of Science

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Language：English  

Language：English   Publishing type：Research paper (scientific journal)   Publisher：SPRINGER  

It was demonstrated that brookite-type titanium oxide can be directly synthesized by the hydrothermal treatment of novel water-soluble titanium complexes under basic conditions in the presence of an additive. In particular, single-phase brookite was synthesized from the titanium-glycolate complex at a pH of about 10 in the presence of excess NH(3) aqueous solution or ethylenediamine, and powder thus obtained consisted of rod-like nanosized particles. It was suggested that the structures of titanium complexes are important for the formation of brookite.

DOI： 10.1007/s10853-007-1912-3

Web of Science

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Language：English   Publishing type：Research paper (international conference proceedings)  

Hydrothermal treatment of a series of water-soluble titanium complexes resulted in the formation of TiO2. Rutile, anatase or a mixture of both can be synthesized by varying the ligands. The titania obtained was composed of nano-sized particles with large specific surface areas. These TiO2 powders exhibited high photocatalytic activity for NO x decomposition. In particular, they demonstrated higher activity than P25 (Degussa) under visible-light irradiation. © 2007 Springer Science+Business Media, LLC.

DOI： 10.1007/s10853-007-2113-9

Scopus

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：CERAMIC SOC JAPAN-NIPPON SERAMIKKUSU KYOKAI  

We prepared two new water-soluble complexes of titanium with L-serine and L(-)-threonine amino acids. It was demonstrated that these compounds can be outstanding precursors for a hydrothermal synthesis of nanocrystalline TiO2. The obtained powders were composed of anatase or a mixture of anatase and brookite. Particles diameters were -10 nm and BET surface areas were -120 m(2)/g. The powder composed of anallase and brookite synthesized by hydrothermal treatment of the titanium-threonine complex aqueous solution at 200 degrees C for 24 h exhibited higher photocatalytic activity for oxalic acid oxidation than the commercial anatase-type TiO2 photocatalyst (ST-01, Ishihara Sangyo Kaisya, average diameter: 7 nm, specific surface area: 257.5 m(2)/g). (c) 2008 The Ceramic Society of Japan. All rights reserved.

DOI： 10.2109/jcersj2.116.578

Web of Science

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Language：English   Publishing type：Research paper (other academic)   Publisher：AMER CHEMICAL SOC  

Web of Science

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：CERAMIC SOC JAPAN-NIPPON SERAMIKKUSU KYOKAI  

Nanoparticles of brookite titanium oxide were prepared by microwave-assisted hydrothermal (MH) method at 200 degrees C (heating time 5 min) for 0-60 minutes starting from the titanium peroxo glycolate complex in basic solution. The effect of microwave heating on the morphology of the brookite particles was examined. The samples were characterized by X-ray diffraction (XRD), Raman spectroscopy and transmission electron microscopy (TEM). It was found that all powders were composed of single phase brookite and contained two different types of particles. The activity in photodecomposition of oxalic acid by the samples prepared using MH method was higher than activities of brookite nanoparticles synthesized by the conventional hydrothermal method.

DOI： 10.2109/jcersj2.115.826

Web of Science

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Language：English   Publishing type：Research paper (scientific journal)   Publisher：CERAMIC SOC JAPAN-NIPPON SERAMIKKUSU KYOKAI  

Single phase rutile was synthesized by a simple hydrothermal treatment of an aqueous titanium glycolate complex solution at 200 degrees C for 24 h. The obtained sample was composed of 50 x 150 nm rod-like nanoparticles. The aspect ratio of the prepared particles could be controlled by adding glycolic acid or lactic acid to reaction solution. Up to 30 x 2000 nm whisker-like particles could be obtained. The hydroxycarboxylic acids favor development of specific crystal facets and allow to control the aspect ratio of the rutile nanoparticles. We also proposed a model, which explains formation of anatase and rutile, and disappearance of anatase particles during rutile crystals development.

DOI： 10.2109/jcersj2.115.835

Web of Science

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Language：English   Publishing type：Research paper (scientific journal)  

DOI： 10.1021/cm071370q

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Language：Japanese  

Language：English   Publishing type：Research paper (other academic)  

DOI： 10.4028/www.scientific.net/SSP.124-126.723

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Language：English   Publishing type：Research paper (scientific journal)  

DOI： 10.1002/anie.200503565

PubMed

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Authorship：Lead author   Language：Japanese  

Language：Japanese  

Total pages：416   Responsible for pages：217-226   Language：Japanese Book type：Scholarly book

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Responsible for pages：71-92   Language：English Book type：Scholarly book

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Responsible for pages：1-27   Language：English Book type：Scholarly book

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Responsible for pages：1-40   Language：English Book type：Scholarly book

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Total pages：262   Responsible for pages：15-27   Language：Japanese Book type：Scholarly book

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Total pages：262   Language：Japanese Book type：Scholarly book

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Venue：オンライン   Country：Japan  

Event date： 2021.9

Language：Japanese   Presentation type：Oral presentation (general)  

Venue：オンライン   Country：Japan  

Event date： 2021.9

Language：Japanese   Presentation type：Oral presentation (general)  

Venue：オンライン   Country：Japan  

Event date： 2021.7

Language：Japanese   Presentation type：Poster presentation  

Venue：オンライン   Country：Japan  

Event date： 2021.3

Language：Japanese   Presentation type：Oral presentation (invited, special)  

Venue：オンライン  

Event date： 2021.3

Language：Japanese   Presentation type：Oral presentation (general)  

Venue：オンライン  

Event date： 2021.3

Language：Japanese   Presentation type：Oral presentation (general)  

Venue：オンライン  

Event date： 2021.3

Language：Japanese   Presentation type：Oral presentation (general)  

Venue：オンライン  

Event date： 2021.3

Language：Japanese   Presentation type：Oral presentation (general)  

Venue：オンライン  

Event date： 2021.3

Language：Japanese   Presentation type：Oral presentation (general)  

Venue：オンライン  

Event date： 2021.3

Language：Japanese   Presentation type：Oral presentation (general)  

Venue：オンライン  

Event date： 2021.3

Language：Japanese   Presentation type：Oral presentation (general)  

Venue：オンライン  

Event date： 2021.3

Language：Japanese   Presentation type：Oral presentation (general)  

Venue：オンライン  

Event date： 2021.3

Language：Japanese   Presentation type：Oral presentation (general)  

Venue：オンライン  

Event date： 2020.12

Language：Japanese   Presentation type：Oral presentation (general)  

Venue：オンライン  

Event date： 2020.12

Language：Japanese   Presentation type：Oral presentation (general)  

Venue：オンライン  

Event date： 2020.12

Language：Japanese   Presentation type：Oral presentation (general)  

Venue：オンライン  

Event date： 2020.12

Language：Japanese   Presentation type：Oral presentation (general)  

Venue：オンライン  

Event date： 2020.11

Language：Japanese   Presentation type：Oral presentation (general)  

Venue：オンライン  

Event date： 2020.11

Language：Japanese   Presentation type：Oral presentation (general)  

Venue：オンライン  

Event date： 2020.11

Language：Japanese   Presentation type：Oral presentation (general)  

Venue：オンライン  

Event date： 2020.11

Language：Japanese   Presentation type：Oral presentation (general)  

Venue：オンライン  

Event date： 2020.11

Language：Japanese   Presentation type：Oral presentation (general)  

Venue：オンライン  

Event date： 2020.11

Language：Japanese   Presentation type：Oral presentation (general)  

Venue：オンライン  

Event date： 2020.11

Language：Japanese   Presentation type：Oral presentation (general)  

Venue：オンライン  

Event date： 2020.11

Language：Japanese   Presentation type：Oral presentation (general)  

Venue：オンライン  

Event date： 2020.10

Language：Japanese   Presentation type：Poster presentation  

Venue：オンライン  

Event date： 2020.10

Language：Japanese   Presentation type：Poster presentation  

Venue：オンライン  

Event date： 2020.10

Language：Japanese   Presentation type：Poster presentation  

Venue：オンライン  

Event date： 2020.10

Language：Japanese   Presentation type：Poster presentation  

Venue：オンライン  

Event date： 2020.10

Language：Japanese   Presentation type：Poster presentation  

Venue：オンライン  

Event date： 2020.10

Language：Japanese   Presentation type：Poster presentation  

Venue：オンライン  

Event date： 2020.9

Language：Japanese   Presentation type：Oral presentation (general)  

Venue：オンライン  

Event date： 2020.7

Language：Japanese   Presentation type：Oral presentation (invited, special)  

Venue：オンライン  

Event date： 2019.1 - 2019.2

Language：English   Presentation type：Oral presentation (invited, special)  

Venue：Daytona Beach, FL United States   Country：United States  

Event date： 2018.9

Language：Japanese   Presentation type：Oral presentation (invited, special)  

Country：Japan  

Event date： 2017.11

Language：Japanese   Presentation type：Oral presentation (invited, special)  

Venue：静岡大学 浜松キャンパス   Country：Japan  

Event date： 2017.10

Language：Japanese   Presentation type：Oral presentation (invited, special)  

Venue：タワーホール船堀   Country：Japan  

Event date： 2017.8 - 2017.9

Language：English   Presentation type：Oral presentation (invited, special)  

Venue：Kyoto University   Country：Japan  

Event date： 2017.8

Language：Japanese   Presentation type：Oral presentation (invited, special)  

Venue：東京工業大学 すずかけ台キャンパス   Country：Japan  

Event date： 2017.3

Language：Japanese   Presentation type：Oral presentation (invited, special)