Influence of oxygen partial pressure on the kinetics of YBa2Cu3O7−x formation

1994 ◽  
Vol 9 (2) ◽  
pp. 275-285 ◽  
Author(s):  
V. Milonopoulou ◽  
K.M. Forster ◽  
J.P. Formica ◽  
J. Kulik ◽  
J.T. Richardson ◽  
...  

The YBa2Cu3O7−x formation kinetics from a spray-roasted precursor powder containing Y2O3, BaCO3, and CuO was followed via in situ, time-resolved x-ray diffraction as a function of gas atmosphere and temperature. In inert atmospheres, BaCO3 and CuO form BaCu2O2 which subsequently reacts with Y2O3 to form YBa2Cu3O6. However, YBa2Cu3O6 decomposes at temperatures exceeding 725 °C with Y2BaCuO5 being one of the decomposition products. In oxidizing atmospheres, YBa2Cu3O7−x formation involves the BaCuO2. At high temperatures (800–840 °C), oxygen increases the yield of YBa2Cu3O6. A nuclei growth model assuming two-dimensional, diffusion-controlled growth with second-order nucleation rate fits the experimental data.

2016 ◽  
Vol 88 (11) ◽  
pp. 1684-1692 ◽  
Author(s):  
Lukas C. Buelens ◽  
Vladimir V. Galvita ◽  
Hilde Poelman ◽  
Christophe Detavernier ◽  
Guy B. Marin

2007 ◽  
Vol 558-559 ◽  
pp. 943-947 ◽  
Author(s):  
E. Otterstein ◽  
R. Nicula ◽  
J. Bednarčík ◽  
M. Stir ◽  
E. Burkel

Quasicrystals are aperiodic long-range ordered solids with a high potential for many modern applications. Interest is nowadays paid to the development of economically viable large-scale synthesis procedures of quasicrystalline materials involving solid-state transformations. The kinetics of the high-temperature phase transition from the complex ω-phase to the icosahedral quasicrystalline (iQC) ψ-phase in AlCuFe nanopowders was here examined by in-situ time-resolved X-ray diffraction experiments using synchrotron radiation. In-situ XRD experiments will allow insight on the influence of uniaxial applied pressure on the kinetics of phase transitions leading to the formation of single-phase QC nanopowders and further contribute to the optimization of sintering procedures for nano-quasicrystalline AlCuFe alloy powders.


2007 ◽  
Vol 515 (15) ◽  
pp. 5837-5842 ◽  
Author(s):  
W.K. Kim ◽  
E.A. Payzant ◽  
T.J. Anderson ◽  
O.D. Crisalle

CrystEngComm ◽  
2015 ◽  
Vol 17 (36) ◽  
pp. 6940-6946 ◽  
Author(s):  
Anders C. S. Jensen ◽  
Mogens Hinge ◽  
Henrik Birkedal

Nanocrystalline calcite is formed under the influence of block copolymers containing thermoresponsive PNIPAM and a mineralization controlling block of poly(acrylic acid) and the nanocrystal formation kinetics studied by in situ X-ray diffraction.


1993 ◽  
Vol 311 ◽  
Author(s):  
J. Sariel ◽  
Haydn Chen ◽  
J. F. Jongste ◽  
S. Radelaar

ABSTRACTAmorphous Si/Ti multilayers transform at high temperatures (above 700°C) to TiSi2-C54. This phase is important for microelectronics applications because of its low resistivity, stability up to 900°C, and compatibility with silicon processing. However, an unfavorable metastable TiSi2-C49 phase is usually formed at lower temperatures. Thus, an understanding of the C49 phase formation kinetics is useful to the device processing strategy. The kinetics of the transformation of TiSi2-C49 phase can be characterized as a process of nucleation and growth, using the well known Johnson Mehl Avrami (JMA) equation. In the present work the formation kinetics of the C49 phase has been studied by an in situ x-ray diffraction technique. Isothermal annealing in vacuum was done at four temperatures, in the range of 275"C to 310°C. A position sensitive detector (PSD) was used to simultaneously collect the diffracted beams of (131) and (150) peaks of the C49 phase. From the data, the Avrami exponent, n, was determined to be 2.0±0.1. The reaction rate constant k follows a familiar Arrhenius-type equation with a measured activation energy of 2.5eV. Comparison of our x-ray results with kinetic data obtained by other means will be discussed.


2008 ◽  
Vol 1072 ◽  
Author(s):  
Riccardo De Bastiani ◽  
Alberto Maria Piro ◽  
Maria Grazia Grimaldi ◽  
Emanuele Rimini ◽  
Giuseppe Baratta ◽  
...  

ABSTRACTThe crystallization kinetics of as-deposited amorphous Ge2Sb2Te5 thin films has been measured by in situ time resolved reflectivity. X-ray diffraction and Raman scattering analyses of partially transformed samples allowed to correlate the evolution of the transition to the structural modification in the long and short range configuration. The experimental results evidenced that during the early stages of crystallization there is a reduction of Ge-Te tetrahedral bonds, characteristics of the Ge coordination in amorphous Ge2Sb2Te5 films.


2006 ◽  
Vol 31 (14) ◽  
pp. 2052-2062 ◽  
Author(s):  
T JENSEN ◽  
A ANDREASEN ◽  
T VEGGE ◽  
J ANDREASEN ◽  
K STAHL ◽  
...  

2000 ◽  
Vol 10 (10) ◽  
pp. 2355-2357 ◽  
Author(s):  
Andrew M. Fogg ◽  
Stephen J. Price ◽  
Robin J. Francis ◽  
Stephen O'Brien ◽  
Dermot O'Hare

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