Cubic phase stabilization in nanoparticles of hafnia-zirconia oxides: Particle-size and annealing environment effects

2008 ◽  
Vol 103 (12) ◽  
pp. 124303 ◽  
Author(s):  
Chih-Hsin Lu ◽  
Joan M. Raitano ◽  
Syed Khalid ◽  
Lihua Zhang ◽  
Siu-Wai Chan
Coatings ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 373
Author(s):  
Zheng Yan ◽  
Haoran Peng ◽  
Kang Yuan ◽  
Xin Zhang

Yb2O3-Gd2O3-Y2O3 co-doped ZrO2 (YGYZ) is considered to be a promising material in thermal barrier coating (TBC) applications. In this study, 2Yb2O3–2Gd2O3–6Y2O3–90ZrO2 (mol.%) (10YGYZ) feedstock candidates for air plasma spraying (APS) were prepared by calcination of agglomerated powders at 1100, 1200, 1300, 1400, and 1500 °C for 3 h, respectively. Incomplete solid solution was observed in calcined powders at 1100, 1200 and 1300 °C, and the 1500 °C calcined powder exhibited poor flowability due to intense sintering effect. The 1400 °C calcined powders were eventually determined to be the optimized feedstock for proper phase structure (cubic phase), great flowability, suitable apparent density and particle size distribution, etc. 10YGYZ TBCs with the optimized feedstock were prepared by APS, exhibiting pure c phase and good chemical uniformity. Controllable preparation of coatings with different porosity (i.e., 7%–9% and 12%–14%) was realized by stand-off distance adjustment.


1991 ◽  
Vol 6 (6) ◽  
pp. 1287-1292 ◽  
Author(s):  
Ram Srinivasan ◽  
Robert J. De Angelis ◽  
Gene Ice ◽  
Burtron H. Davis

X-ray diffraction from a synchrotron source was employed in an attempt to identify the crystal structures in zirconia ceramics produced by the sol-gel method. The particles of chemically precipitated zirconia, after calcination below 600 °C, are very fine, and have a diffracting particle size in the range of 7–15 nm. As the tetragonal and cubic structures of zirconia have similar lattice parameters, it is difficult to distinguish between the two. The tetragonal structure can be identified only by the characteristic splittings of the Bragg profiles from the “c” index planes. However, these split Bragg peaks from the tetragonal phase in zirconia overlap with one another due to particle size broadening. In order to distinguish between the tetragonal and cubic structures of zirconia, three samples were studied using synchrotron radiation source. The results indicated that a sample containing 13 mol% yttria-stabilized zirconia possessed the cubic structure with a0 = 0.51420 ± 0.00012 nm. A sample containing 6.5 mol% yttria stabilized zirconia was found to consist of a cubic phase with a0 = 0.51430 ± 0.00008 nm. Finally, a sample which was precipitated from a pH 13.5 solution was observed to have the tetragonal structure with a0 = 0.51441 ± 0.00085 nm and c0 = 0.51902 ± 0.00086.


2017 ◽  
Vol 139 (9) ◽  
pp. 3320-3323 ◽  
Author(s):  
Li-Qiang Xie ◽  
Liang Chen ◽  
Zi-Ang Nan ◽  
Hai-Xin Lin ◽  
Tan Wang ◽  
...  

2021 ◽  
Author(s):  
A.E. Sukharev ◽  

Phase transformations of pyrolytic boron nitride were studied under thermobaric conditions, providing direct transformation of a hexagonal structure into a cubic one. If only the martensitic mechanism of the cooperative rearrangement of atoms is realized, diamond-like aggregates with an equiaxed highly dispersed structure and submicron grain sizes are formed. The presence of a solvent-catalyst (RC) in the system leads to an increase in the particle size of the cubic phase due to recrystallization by the diffusion mechanism, and the high catalytic activity of RC causes the appearance of zones of directional crystal growth in the synthesized samples.


1994 ◽  
Vol 346 ◽  
Author(s):  
Akihiko Yamaji ◽  
Takao Ishii ◽  
Masami Kanzaki

ABSTRACTThe oxygen-ion conductor 0.88ZrO2-0.12Sc2O3 has a discontinuous change in ion conductivity at about 660°C. This change accompanies the structural transition from rhombohedral to cubic phase. Since the high temperature cubic phase shows large ion conductivity, it is of interest to examine whether or not the cubic phase stabilizes in the low temperature region by another dopant . By adding only 0.005 mole % La2O3, the cubic phase is stabilized below about 500 °C without any loss of conductivity compared with 0.88ZrO2-0.12Sc2O3. The ion conductivity of cubic stabilized ZrO2-Sc2O3-La2O3 system is around 1×10-1 S/cm at 800°C. Cubic phase stabilization using second dopant in a ZrO2-Sc2O3 system led to the finding of a fast oxygen-ion conductor in the ZrO2-Sc2O3-La2O3 system.


1996 ◽  
Vol 11 (5) ◽  
pp. 1199-1209 ◽  
Author(s):  
J. M. McHale ◽  
P. C. McIntyre ◽  
K. E. Sickafus ◽  
N. V. Coppa

An aqueous, all nitrate, solution-based preparation of BaTiO3 is reported here. Rapid freezing of a barium and titanyl nitrate solution, followed by low temperature sublimitation of the solvent, yielded a freeze-dried nitrate precursor which was thermally processed to produce BaTiO3. XRD revealed that 10 min at temperatures ≧600 °C resulted in the formation of phase pure nanocrystalline BaTiO3. TEM revealed that the material was uniform and nanocrystalline (10–15 nm). The high surface to volume ratio inherent in these small particles stabilized the cubic phase of BaTiO3 at room temperature. It was also found that the average particle size of the BaTiO3 produced was highly dependent upon calcination temperature and only slightly dependent upon annealing time. This result suggests a means of selection of particle size of the product through judicious choice of calcination temperature. The experimental details of the freeze-dried precursor preparation, thermal processing of the precursor, product formation, and product morphology are discussed.


Materials ◽  
2020 ◽  
Vol 13 (3) ◽  
pp. 560 ◽  
Author(s):  
Yan Ji ◽  
Cankai Zhou ◽  
Feng Lin ◽  
Bingjing Li ◽  
Feifan Yang ◽  
...  

The garnet Li7La3Zr2O12 (LLZO) has been widely investigated because of its high conductivity, wide electrochemical window, and chemical stability with regards to lithium metal. However, the usual preparation process of LLZO requires high-temperature sintering for a long time and a lot of mother powder to compensate for lithium evaporation. In this study submicron Li6.6La3Zr1.6Nb0.4O12 (LLZNO) powder―which has a stable cubic phase and high sintering activity―was prepared using the conventional solid-state reaction and the attrition milling process, and Li stoichiometric LLZNO ceramics were obtained by sintering this powder―which is difficult to control under high sintering temperatures and when sintered for a long time―at a relatively low temperature or for a short amount of time. The particle-size distribution, phase structure, microstructure, distribution of elements, total ionic conductivity, relative density, and activation energy of the submicron LLZNO powder and the LLZNO ceramics were tested and analyzed using laser diffraction particle-size analyzer (LD), X-Ray Diffraction (XRD), Scanning Electron Microscope (SEM), Electrochemical Impedance Spectroscopy (EIS), and the Archimedean method. The total ionic conductivity of samples sintered at 1200 °C for 30 min was 5.09 × 10−4 S·cm−1, the activation energy was 0.311 eV, and the relative density was 87.3%. When the samples were sintered at 1150 °C for 60 min the total ionic conductivity was 3.49 × 10−4 S·cm−1, the activation energy was 0.316 eV, and the relative density was 90.4%. At the same time, quasi-solid-state batteries were assembled with LiMn2O4 as the positive electrode and submicron LLZNO powder as the solid-state electrolyte. After 50 cycles, the discharge specific capacity was 105.5 mAh/g and the columbic efficiency was above 95%.


2001 ◽  
Vol 189-191 ◽  
pp. 181-185 ◽  
Author(s):  
D. Freitas ◽  
Maria do Carmo de Andrade Nono ◽  
Carlos Kuranaga ◽  
A.J.S. Machado ◽  
Sergio Luiz Mineiro

2010 ◽  
Vol 638-642 ◽  
pp. 1708-1713
Author(s):  
Tae Suk Jang ◽  
J.H. Yu ◽  
D.W. Lee ◽  
B.K. Kim

FePt binary alloy nanopowder has been synthesized by a chemical vapor condensation process using a mixture of iron acetylacetonate and platinum acetylacetonate. Particle size of the synthesized powder was less than 10 nm and the powder had very narrow size distribution with relatively high dispersivity. FePt nanopowder possessing L10 ordered phase was synthesized at the condition of well controlled precursor mixing ratio and reaction temperature with some disordered cubic phase.


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