scholarly journals Conductivity Transitions of La0.7Sr0.3MnO3±δ and La0.6Sr0.4Co0.2Fe0.8O3−δ in Ce0.9Gd0.1O2−δ Matrix for Dual-Phase Oxygen Transport Membranes

Crystals ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 712
Author(s):  
Thuy Linh Pham ◽  
Ji Haeng Yu ◽  
Jong-Sook Lee

Using van der Pauw method, the conductivity of disk samples of La0.7Sr0.3MnO3±δ (LSM) and La0.6Sr0.4Co0.2Fe0.8O3−δ (LSCF) in a Ce0.9Gd0.1O2−δ (GDC) matrix was accurately quasi-continuously measured over 800 °C to −73 °C, and the transition points in Arrhenius behavior were systematically obtained from the extremum points of the second derivatives. While LSM-containing samples showed reproducible conductivity trajectories, the LSCF system exhibited unsystematic changes which may be related to the substantial oxidation/reduction reactions accompanying the ferroelastic–paraelastic transitions with a substantial thermal hysteresis at 650 °C to 750 °C, corresponding to conductivity maxima. A sudden decrease in activation energies on cooling corresponds to the para-to-ferromagnetic, weak insulator–metal transitions and the Curie temperature of LSM appears to gradually decrease in composites to 90 °C, while LSCF composites exhibit blurred transitions at approximately −40 °C. Relatively insulating paramagnetic phases are characterized by activation energy values ~0.2 eV, change to the high temperature phase exhibiting activation energy 0.1 eV for small polaron hopping mechanisms at 300 °C to 500 °C with increasing GDC content in the LSM composites and by two transitions at ∼60 °C and ∼245 °C for the LSCF composites. LSCF single phase shows distinctly lower transition points which appear to match with the singularly large c lattice parameter whereas the composites exhibit decreasing c with LSCF amount together with increasing lattice parameter of GDC. Van der Pauw conductivity is a feasible and sensitive in situ tool for monitoring the status of oxygen transport membranes.

1999 ◽  
Vol 590 ◽  
Author(s):  
Y. Avrahami ◽  
E. Zolotoyabko ◽  
W. Sauer ◽  
T. H. Metzger ◽  
J. Peisl

ABSTRACTTitanium-induced structural modifications in thin waveguide layers of lithium niobate have been investigated by grazing incidence diffraction and complementary thin film techniques. The study was focused on the high-temperature phase transformation in this system and its influence on the lattice parameter changes, depending on the annealing time.


1992 ◽  
Vol 7 (4) ◽  
pp. 226-227 ◽  
Author(s):  
Fu Zhengmin ◽  
Li Wenxiu

AbstractThe crystal structure of the high-temperature phase of Sr2ZnWO6 prepared by air quenching from 1200° C has been determined by means of X-ray powder diffraction. β-Sr2ZnWO6 belongs to the cubic system, with space group Fm3m and a lattice parameter a = 7.9266 Å at room temperature. Its measured density is Dm = 6.93g/cm3, and each unit cell contains four formula weights.


1997 ◽  
Vol 481 ◽  
Author(s):  
Georges DÉnÉ ◽  
M. Cecilia Madamba

ABSTRACTPbF2 is known to exist under two different polymorphic structures. Orthorhombic α-PbF 2 is stable at ambient temperature. It has the PbC12 structure. Cubic β-PbF2 is obtained by heating α-PbF2. It does not transform back to α-PbF2 on cooling, and it seems to be infinitely stable in the metastable state under ambient conditions. β-PbF2 crystallizes in the fluorite (CaF2) type. Owing to the large number of potential interstitial sites, many F- Frenkel defects can be formed, which make β-PbF2 the highest performance fluoride ion conductor among binary fluorides. In this work, both phases of PbF2 have been ball milled. Milling α-PbF2 results in a partial transformation to microcrystalline β-PbF2. The energy required for obtaining the high temperature phase is probably provided in the mechanical form. Milling β-PbF2 leads to partial amorphization and formation of α-PbF2. In this case, milling transforms the high temperature polymorph to the low temperature form, by providing the energy required to overcome the activation energy that keeps PbF2 trapped in the high temperature β-form after cooling.


2000 ◽  
Vol 55 (1-2) ◽  
pp. 117-123 ◽  
Author(s):  
Yasumasa Tomita ◽  
Hiroshi Ohki ◽  
Koji Yamada ◽  
Tsutomu Okuda

NMR, NQR, powder X-ray diffraction, DTA and AC conductivity were measured in RMBr4 (R = Ag, Cu; M = Al, Ga) and RM2Br7 (R = Li, Ag; M = Al, Ga). In RMBr4 , the activation energy of Cu+ diffusion was evaluated from 63Cu NMR and was in good agreement with that from 81Br NQR. In CuAlBr4 , the e2Qq/h value of 63Cu NMR and the η value of 27AI NMR changed linearly with decreasing temperature, although the e2Qq/h value of 27AI NMR did not change so much. These temperature dependences are supposed to be due to Cu+ diffusion and not to a variation of the lattice constants. In RM2Br7 , the activation energy was obtained from the spin-lattice relaxation time T1 of 81Br NQR and is ascribed to a modulation of the cation diffusion. The line width of 7Li NMR in LiAl2Br7 was about 5.9 kHz in the low-temperature phase and 0.4 kHz for the high-temperature phase. The 27AlNMR spectrum was broadened by the quadrupole interaction and unchanged up to 400 K, suggesting that diffusion of Li+ ions occurs in the high-temperature phase.


2017 ◽  
Vol 50 (2) ◽  
pp. 378-384 ◽  
Author(s):  
S. Huband ◽  
A. M. Glazer ◽  
K. Roleder ◽  
A. Majchrowski ◽  
P. A. Thomas

The symmetry of the intermediate high-temperature phase of PbHfO3 has been determined unambiguously to be orthorhombic using a combination of high-resolution X-ray diffraction and birefringence imaging microscopy measurements of crystal plates. While lattice parameter measurements as a function of temperature in the intermediate phase are consistent with either orthorhombic or tetragonal symmetry, domain orientations observed in birefringence imaging microscopy measurements utilizing the Metripol system are only consistent with orthorhombic symmetry with the unit cell in the rhombic orientation of the pseudocubic unit cell.


Author(s):  
J.P.S. Hanjra

Tin mono selenide (SnSe) with an energy gap of about 1 eV is a potential material for photovoltaic applications. Various authors have studied the structure, electronic and photoelectronic properties of thin films of SnSe grown by various deposition techniques. However, for practical photovoltaic junctions the electrical properties of SnSe films need improvement. We have carried out investigations into the properties of flash evaporated SnSe films. In this paper we report our results on the structure, which plays a dominant role on the electrical properties of thin films by TEM, SEM, and electron diffraction (ED).Thin films of SnSe were deposited by flash evaporation of SnSe fine powder prepared from high purity Sn and Se, onto glass, mica and KCl substrates in a vacuum of 2Ø micro Torr. A 15% HF + 2Ø% HNO3 solution was used to detach SnSe film from the glass and mica substrates whereas the film deposited on KCl substrate was floated over an ethanol water mixture by dissolution of KCl. The floating films were picked up on the grids for their EM analysis.


1995 ◽  
Vol 5 (7) ◽  
pp. 763-769 ◽  
Author(s):  
S. Rios ◽  
W. Paulus ◽  
A. Cousson ◽  
M. Quilichini ◽  
G. Heger ◽  
...  

1981 ◽  
Vol 42 (C6) ◽  
pp. C6-599-C6-601 ◽  
Author(s):  
T. Wasiutynski ◽  
I. Natkaniec ◽  
A. I. Belushkin

1989 ◽  
Vol 100 (1) ◽  
pp. 135-141 ◽  
Author(s):  
A. I. Baranov ◽  
V. P. Khiznichenko ◽  
L. A. Shuvalov

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