共查询到20条相似文献,搜索用时 31 毫秒
1.
Kazumi Kato Can Zheng Jeffrey M. Finder Sandwip K. Dey Yasuyoshi Torii 《Journal of the American Ceramic Society》1998,81(7):1869-1875
Precursors for layer-structured perovskite thin films of SrBi2 Ta2 O9 (SBT) and SrBi2 Nb2 O9 (SBN) were prepared by the reactions of a strontium-bismuth double methoxyethoxide and tantalum or niobium methoxyethoxide in methoxyethanol, followed by partial hydrolysis. Several spectroscopic techniques, such as 1 H-, 13 C-, and 93 Nb-NMR (nuclear magnetic resonance), and Fourier-transform infrared spectroscopy were used to analyze the arrangement of the metals and oxygen in the precursor molecules. The precursors contained Sr-O-M (where M is Ta or Nb) bonds (i.e., a strontium is connected to two MO6 octahedra) and Sr-O-Bi bonds with a bismuth atom bonded to the oxygens of the MO6 octahedron. The arrangement of metals and oxygens was considered to be similar to the layer-structured perovskite crystal sublattice. As a result, the sol-gel-derived SBT thin films crystallized, by rapid thermal annealing in an oxygen atmosphere below 550°C, and they exhibited preferred (115) orientation. The crystallinity improved and the crystallite size increased with temperature up to 700°C. In the case of SBN thin films, a low heating rate (2°C/min) was necessary for the control of the crystallographic (115) orientation, whereas a rate of 200°C/s (rapid thermal annealing) produced films that exhibited c -axis orientation. The (115) SBT thin film, heated to 700°C, exhibited improved ferroelectric properties. 相似文献
2.
Bo-Yun Jang Young-Hun Jeong Suk-Jin Lee Kyong-Jae Lee Sahn Nahm Ho-Jung Sun Hwack-Joo Lee 《Journal of the American Ceramic Society》2005,88(5):1209-1212
BaTi4 O9 thin films were grown on a Pt/Ti/SiO2 /Si substrate using rf magnetron sputtering and the structure of the thin films were then investigated. For the films grown at low temperature (≤350°C), an amorphous phase was formed during the deposition, which then changed to the BaTi5 O11 phase when the annealing was conducted below 950°C. However, when the annealing temperature was higher than 950°C, a BaTi4 O9 phase was formed. On the contrary, for the films grown at high temperature (>450°C), small BaTi4 O9 grains were formed during the deposition, which grew during the annealing. The homogeneous BaTi4 O9 thin films were successfully grown on Pt/Ti/SiO2 /Si substrate when they were deposited at 550°C and subsequently rapid thermal annealed at 900°C for 3 min. 相似文献
3.
Lili Jiao Zongming Liu Guangda Hu Shougang Cui Zhijie Jin Qi Wang Weibing Wu Changhong Yang 《Journal of the American Ceramic Society》2009,92(7):1556-1559
Bi3.7 Nd0.3 Ti3 O12 (BNT0.3) films were fabricated on indium tin oxide/glass substrates using a metal organic decomposition method at temperatures ranging from 500° to 650°C. A predominantly (100)-oriented BNT0.3 film can be obtained even at 550°C. The growth mode of the predominantly (100)-oriented BNT0.3 films fabricated by the sequential layer annealing method was discussed based on the structure evolution with the annealing temperature and the film thickness. The largest values of the remanent polarization and piezoresponse are observed in the BNT0.3 film annealed at 650°C, which can be ascribed to the grain growth and the release of the in-plane residue tension stress. 相似文献
4.
Joanna McKittrick Carlos F. Bacalski G. A. Hirata Kevin M. Hubbard S. G. Pattillo Kenneth V. Salazar M. Trkula 《Journal of the American Ceramic Society》2000,83(5):1241-1246
The purpose of this study was to identify and correlate the microstructural and luminescence properties of europium-doped Y2 O3 (Y1– x Eu x )2 O3 thin films deposited by metallorganic chemical vapor deposition (MOCVD), as a function of deposition time and temperature. The influence of deposition parameters on the crystallite size and microstructural morphology were examined, as well as the influence of these parameters on the photoluminescence emission spectra. (Y1– x Eu x )2 O3 thin films were deposited onto (111) silicon and (001) sapphire substrates by MOCVD. The films were grown by reacting yttrium and europium tris(2,2,6,6-tetramethyl–3,5-heptanedionate) precursors with an oxygen atmosphere at low pressures (5 torr (1.7 × 103 Pa)) and low substrate temperatures (500°–700°C). The films deposited at 500°C were smooth and composed of nanocrystalline regions of cubic Y2 O3 , grown in a textured [100] or [110] orientation to the substrate surface. Films deposited at 600°C developed, with increasing deposition time, from a flat, nanocrystalline morphology into a platelike growth morphology with [111] orientation. Monoclinic (Y1– x Eu x )2 O3 was observed in the photoluminescence emission spectra for all deposition temperatures. The increase in photoluminescence emission intensity with increasing postdeposition annealing temperature was attributed to the surface/grain boundary area-reduction effect. 相似文献
5.
J. J. COMER N. C. TOMBS J. F. FITZGERALD 《Journal of the American Ceramic Society》1966,49(5):237-240
Single-crystal and polycrystalline films of Mg-Al2 O4 and MgFe2 O4 were formed by two methods on cleavage surfaces of MgO single crystals. In one procedure, aluminum was deposited on MgO by vacuum evaporation. Subsequent heating in air at about 510°C formed a polycrystalline γ-Al2 O8 film. Above 540°C, the γ-Al2 O, and MgO reacted to form a single-crystal MgAl2 O4 film with {001} MgAl2 O4 ‖{001} MgO. Above 590°C, an additional layer of MgAl2 O4 , which is polycrystalline, formed between the γ-Al2 O3 and the single-crystal spinel. Polycrystalline Mg-Al2 O4 formed only when diffusion of Mg2+ ions proceeded into the polycrystalline γ-Al2 O3 region. Corresponding results were obtained for Mg-Fe2 O4 . MgAl2 O4 films were also formed on cleaved MgO single-crystal substrates by direct evaporation, using an Al2 O3 crucible as a source. Very slow deposition rates were used with source temperatures of ∼1350°C and substrate temperatures of ∼800°C. Departures from single-crystal character in the films may arise through temperature gradients in the substrate. 相似文献
6.
The mechanism of parahydrogen conversion was studied on Gd2 O3 and Y2 O3 powders and on Gd and Y evaporated metal films at low and high temperatures (77° to 90°K and 298° to 418°K). Absolute rates of conversion are compared to theoretical values for 3 possible reaction mechanisms, and it is concluded that a paramagnetic vibrational mechanism is operative on Gd2 O3 , Gd, and Y. On Y2 O3 the reaction rate is enhanced by additional surface paramagnetic sites. The portion of the surface which is active is ∼1 for the metals and ∼0.01 for the oxides. 相似文献
7.
Dmitry D. Zaitsev Ekaterina A. Gravchikova Pavel E. Kazin Yury D. Tretyakov Martin Jansen 《International Journal of Applied Ceramic Technology》2006,3(4):279-283
Glass samples with nominal compositions SrFe12 O19 +(12− n )SrB2 O4 +nSrSiO3 , n =3, 6, 9 were prepared by rapid quenching of the melt. Processes of glass devitrification were studied. The samples were annealed at temperatures of 600–900°C, and the resulting glass–ceramics was characterized by XRD, SEM, EDX, and magnetic measurements. SrFe12 O19 crystallizes above 700°C and forms nano- and submicron platelet particles with the aspect ratio depending on the thermal treatment conditions. The glass–ceramic samples annealed at 900°C show coercive force values in the range of 422–455 kA/m. 相似文献
8.
Rong-ping Wang rei Rode Duk-Yong Choi Barry Luther-Davies 《Journal of the American Ceramic Society》2008,91(7):2371-2373
Ge33 As12 Se33 films deposited by ultrafast pulse laser deposition were annealed at various temperatures and pressures, and the dependence of the surface oxidation on the processing conditions was investigated by X-ray photoelectron spectroscopy (XPS). We found that even as-grown film contains a thin oxidized surface and the oxygen distribution exponentially decays along the normal direction of the films regardless of different processing conditions. The critical thicknesses of the oxidized layers were 6.5, 11, 48, and 98 nm, respectively, for the as-grown, 250°C annealing sample for 4 h under 1 × 10−6 Torr, and 150° and 250°C annealing samples for 15 h under 20 mTorr. 相似文献
9.
Elena R. Andrievskaya Lidia M. Lopato Vasily P. Smirnov 《Journal of the American Ceramic Society》1996,79(3):714-720
A mathematical model of the liquidus surface based on a reduced polynomial method was proposed for the system HfO2 -Y2 O3 -Er2 O3 . The results of calculations according to this model agree fairly well with the experimental data. Phase equilibria in the system HfO2 -Y2 O3 -Er2 O3 were studied on melted (as-cast) and annealed samples using X-ray diffraction (at room and high temperatures) and micro-structural and petrographic analyses. The crystallization paths in the system HfO2 -Y2 O3 -Er2 O3 were established. The system HfO2 -Y2 O3 -Er2 O3 is characterized by the formation of extended solid solutions based on the fluorite-type (F) form of HfO2 and cubic (C) and hexagonal (H) forms of Y2 O3 and Er2 O3 . The boundary curves of these solid solutions have the minima at 2370°C (15. 5 mol% HfO2 , 49. 5 mol% Y2 O3 ) and 2360°C (10. 5 mol% HfO2 , 45. 5 mol% Y2 O3 ). No compounds were found to exist in the system investigated. 相似文献
10.
Naonori Sakamoto Masahito Hori Yuki Matsuyama Naoki Wakiya Hisao Suzuki 《Journal of the American Ceramic Society》2009,92(S1):S189-S191
12CaO·7Al2 O3 (C12A7) composed of nanosize cage structure can clathrate oxygen radicals (O− ) and has a high potential to application of strong oxidizing catalysis. In the present report, we demonstrate a fabrication route to C12A7 fine powders by Chemical Solution Deposition method in order to enhance the catalytic reactivity. Aluminum sec-butoxide, calcium nitrate tetrahydrate, acetylacetone, 2-methoxyethanol, and nitric acid were used as raw materials. Precursor solution was dried and annealed at 800°–900°C in air or O2 atmosphere. Crystalline C12A7 powders were obtained by annealing at 900°C in O2 atmosphere. Scanning electron microscope and transmission electron microscope images of the obtained powders revealed C12A7 particles were sintered and formed several micrometer particles with many pores. BET specific surface area of the powders was 4.2 m2 /g. Possibility for synthesizing C12A7 powder with higher specific surface area by the solution process was indicated. 相似文献
11.
Monika Agarwal Mark R. de Guire Arthur H. Heuer 《Journal of the American Ceramic Society》1997,80(12):2967-2981
Undoped or Y2 O3 -doped ZrO2 thin films were deposited on self-assembled monolayers (SAMs) with either sulfonate or methyl terminal functionalities on single-crystal silicon substrates. The undoped films were formed by enhanced hydrolysis of zirconium sulfate (Zr(SO4 )·4H4 O) solutions in the presence of HCl at 70°C. Typically, these films were a mixture of two phases: nanocrystalline tetragonal- ( t -) ZrO2 and an amorphous basic zirconium sulfate. However, films with little or no amorphous material could be produced. The mechanism of film formation and the growth kinetics have been explained through a coagulation model involving homogeneous nucleation, particle adhesion, and aggregation onto the substrate. Annealing of these films at 500°C led to complete crystallization to t -ZrO2 . Amorphous Y2 O3 -containing ZrO2 films were prepared from a precursor solution containing zirconium sulfate, yttrium sulfate (Y2 (SO4 )3 8·H2 O), and urea (NH2 CONH2 ) at pH 2.2–3.0 at 80°C. These films also were fully crystalline after annealing at 500°C. 相似文献
12.
Y. Xu A. Goyal J. Lian N. A. Rutter D. Shi S. Sathyamurthy M. Paranthaman L. Wang P. M. Martin D. M. Kroeger 《Journal of the American Ceramic Society》2004,87(9):1669-1676
YBa2 Cu3 O7−δ (YBCO) films were fabricated via a fluorine-free metal organic deposition (MOD) method followed by high-temperature, low oxygen partial pressure annealing. Trimethyl acetate salts of copper, yttrium, and barium hydroxide were used as the precursors, which were dissolved in proponic acid- and amine-based solvents. After spin-coating and burnout, samples were annealed at 740°C in 180 ppm oxygen partial pressure and exposed to humid atmosphere for different times. A critical transition temperature, T c ( R =0) of 90.2 K and a transport critical current density ( J c ) of 0.55 MA/cm2 (77 K and self-field) were obtained for 0.2 μm YBCO films on CeO2 -buffered yttria-stabilized zirconia (YSZ) substrates. X-ray studies shows that the YBCO films have sharp in-plane and out-of-plane texture for all samples; however, the porosity of the YBCO film varies with the time of exposure to the humid atmosphere. A reaction between YBCO and CeO2 during the high-temperature anneals and formation of the reaction product BaCeO3 was confirmed by X-ray diffraction (XRD) studies. The XRD and transmission electron microscopy analysis indicated that the epitaxial relations in the film were YBCO (00 l )//CeO2 (00 l )//YSZ (00 l ) and YBCO [100]//CeO2 [110]//YSZ [110]. 相似文献
13.
Michel W. Barsoum Alexander Elkind Fadel A. Selim 《Journal of the American Ceramic Society》1996,79(4):962-966
Diffusion of molten Bi2 O3 into the grain boundaries of sintered, alumina-doped (0.23 and 0.7 mol%) ZnO pellets resulted in varistors with breakdown voltages in the 3–5 V range and nonlinearity coefficients of 10–24. The varistors were fabricated by spreading a thin layer of Bi2 O3 powder on the surface of ZnO pellets and heating the combination to various temperatures (860–1155°C) and different times. The highest nonlinearity coefficients (20–24) and lowest breakdown voltages (3–5 V) were recorded in samples annealed at 860°C for 35 min. Longer annealing times and/or higher temperatures resulted in progressively higher breakdown voltages. Eventually the devices became insulating, which was attributed to the formation of an insulating Bi2 O3 layer between the grains. Separate wetting experiments have shown that the penetration of Bi2 O3 into ZnO grain boundaries was a strong function of alumina doping —the penetration rate was decreased by a factor of 5–7 as the ZnO was doped with as little as 0.2 mol% alumina. It is this slowing down of the penetration of the ZnO grain boundaries that is believed to be critical in the development of the low breakdown voltages observed. 相似文献
14.
Stephan Senz reas Graff Werner Blum Dietrich Hesse Hans-Peter Abicht 《Journal of the American Ceramic Society》1998,81(5):1317-1321
Fresnoite grows at 700° and 800°C, and Ba6 Ti7 O40 grows at 1200°C with definite orientations, which are determined by X-ray diffraction pole figure analysis. Partially textured fresnoite is formed at higher temperatures. The SiO2 films react with the BaTiO3 crystals, forming the phases Ba2 TiSi2 O8 (fresnoite) and Ba6 Ti17 O40 . At 700° and 800°C, both phases grow with definite orientations, which are determined by X-ray diffraction pole figure analysis. Partially textured polycrystalline phases are formed at higher temperatures. 相似文献
15.
Hyunjung Shin Monika Agarwal Mark R. De Guire Arthur H. Heuer 《Journal of the American Ceramic Society》1996,79(7):1975-1978
Thin films of crystalline TiO2 were deposited on self-assembled organic monolayers from aqueous TiCl4 solutions at 80°C; partially crystalline ZrO2 films were deposited on top of the TiO2 layers from Zr(SO4 )2 solutions at 70°C. In the absence of a ZrO2 film, the TiO2 films had the anatase structure and underwent grain coarsening on annealing at temperatures up to 800°C; in the absence of a TiO2 film, the ZrO2 films crystallized to the tetragonal polymorph at 500°C. However, the TiO2 and ZrO2 bilayers underwent solid-state diffusive amorphization at 500°C, and ZrTiO4 crystallization could be observed only at temperatures of 550°C or higher. This result implies that metastable amorphous ZrTiO4 is energetically favorable compared to two-phase mixtures of crystalline TiO2 and ZrO2 , but that crystallization of ZrTiO4 involves a high activation barrier. 相似文献
16.
Sintering YBa2 Cu3 O7- x bulk forms at 1050°C followed by annealing at 980°C causes the development of a thick oriented surface layer (Lotgering factor = 0.7). The thickness of the layer depends on the thermal treatment, which is a two-step sintering process. Firing at 1050°C for 2.5 h followed by 30 h at 980°C leads to the development of a 0.1-mm-thick surface layer, with clear indication that longer annealing would result in a thicker film. Some orientation develops during un-axial compaction of the powders. Lotgering orientation factor calculation from X-ray diffraction analysis. SEM, and TEM were used to characterize the microstructure of these samples. T c was similar to that of conventionally processed high-density samples, between 83 and 87 K. Some thermal treatments resulted in samples that displayed high resistivity above T c , possibly caused by segregation of Cu to the grain boundaries. 相似文献
17.
Pb(Mg1/3 Ta2/3 )0.7 Ti0.3 O3 thin films of single perovskite phase were successfully synthesized by using the RF sputtering deposition technique, followed by post-thermal annealing. While the perovskite structure of Pb(Mg1/3 Ta2/3 )0.7 Ti0.3 O3 is rather unstable, phase evolution in the thin films was manipulated by controlling both working pressure during the sputtering process and post-thermal annealing temperature. The desirable perovskite phase was promoted by increasing the working pressure in the range of 10–25 mTorr, followed by thermal annealing at 600°C. The ferroelectric, dielectric, and polarization behaviors of Pb(Mg1/3 Ta2/3 )0.7 Ti0.3 O3 films were characterized over a wide range of frequencies. They are strongly affected by the film thickness, where the relative permittivity and remanent polarization increase, while the coercive field decreases with increasing film thickness in the range of 115–360 nm. 相似文献
18.
Anita Fossdal Mari-Ann Einarsrud Tor Grande 《Journal of the American Ceramic Society》2005,88(7):1988-1991
The phase relations in the pseudo-ternary system La2 O3 –SrO–Fe2 O3 have been investigated in air. Isothermal sections at 1100° and 1300°C are presented based on X-ray diffraction and thermal analysis of annealed samples. Extended solid solubility was observed for the compounds Sr n +1− v La v Fe n O3 n +1−δ ( n =1, 2, 3, and ∞) and Sr1− x La x Fe12 O19 , while only limited solubility of La in Sr4− z La z Fe6 O13±δ was observed. At high Fe2 O3 content, a liquid with low La2 O3 content was stable at 1300°C. 相似文献
19.
David H. Chmielewski Kenneth H. Sandhage 《Journal of the American Ceramic Society》1995,78(9):2504-2512
Bi2 Sr2 Ca2 Cu2 O8±δ -type compound thick films were exposed to oxygen-argon-gas mixtures (1% to 20% oxygen gas) at elevated pressures (up to 207 MPa) and temperatures (500° to 940°C) for times ranging from 5 to 96 h. At a sufficiently high oxygen fugacity and temperature, Bi2 Sr2 Ca1 Cu2 O8±δ decomposed via a solid-state reaction. Room-temperature X-ray diffractometry and electron probe microanalysis of decomposed films revealed the presence of Bi2 (Sr,Ca)2 -Cu1 O6±θ ro-type compound, Bi2 Sr2 ,Ca1 O8±δ -type compound, and CuO. Bi2 Sr2 Ca1 Cu2 O8±δ decomposition was accompanied by a modest weight gain, which was consistent with an oxidation reaction. The solid-state decomposition reaction could be reversed by heat treatment of decomposed films at 860°C in pure, flowing oxygen at ambient pressure. 相似文献
20.
An intercalation compound of WOP2 O7 /phenanthroline and a mixture of WOP2 O7 /carbon black were prepared to have equal carbon contents. Both samples were heated below 1400°C under a nitrogen atmosphere and their thermal degradation behaviors compared, with the following results: (1) CO gas evolved through carbothermal reduction at a temperature 150°C lower in the intercalation compound than in the WOP2 O7 /carbon black mixture. (2) Both WP and W formed at temperatures approximately 100°C lower in the intercalation compound than in the mixture. (3) Thermal degradation occurred homogeneously throughout the intercalation compound particles, and the particle morphology remained favorable after thermal degradation. 相似文献