Size distribution and magnetic behavior of lead inclusions in silicon single crystals

1997 ◽  
Vol 81 (5) ◽  
pp. 2148-2152 ◽  
Author(s):  
K. Milants ◽  
J. Verheyden ◽  
T. Barancira ◽  
W. Deweerd ◽  
H. Pattyn ◽  
...  
2015 ◽  
Vol 233-234 ◽  
pp. 133-136 ◽  
Author(s):  
Leonard Bezmaternykh ◽  
Evgeniya Moshkina ◽  
Evgeniy Eremin ◽  
Maxim Molokeev ◽  
Nikita Volkov ◽  
...  

Temperature-field and orientational magnetization dependences of single crystals were measured. Both samples demonstrate significant field-depending temperature hysteresis and low-temperature counter field magnetization. The correlation of orientational dependences of these effects and magnetic anisotropy is analyzed; the role of spin-lattice interactions is discussed.


2007 ◽  
Vol 22 (8) ◽  
pp. 2116-2124 ◽  
Author(s):  
Li Feng ◽  
Haiyan Guo ◽  
Zuo-Guang Ye

Single crystals of the perovskite solid solution (1 − x)Pb(Fe2/3W1/3)O3–xPbTiO3, with x = 0, 0.07, 0.27, and 0.75, have been synthesized by the high-temperature solution growth using PbO as flux and characterized by x-ray diffraction and dielectric and magnetic measurements. The crystal structure at room temperature changes from a pseudocubic to a tetragonal phase with the PbTiO3 (PT) content increasing to x ⩾ 0.27. As the amount of PT increases, the relaxor ferroelectric behavior of Pb(Fe2/3W1/3)O3 (PFW) is transformed toward a normal ferroelectric state with sharp and nondispersive peaks of dielectric permittivity at TC. Two types of magnetic orderings are observed on the temperature dependence of the magnetization in the crystals with x ⩽ 0.27. This behavior is explained based on the relationships among the magnetic ordering, perovskite structure, composition, and relaxor ferroelectric properties. Furthermore, the macroscopic magnetization of the system was measured under the application of a magnetic field, which demonstrates different magnetic behavior associated with the weakly ferromagnetic, antiferromagnetic, and paramagnetic ordering in the temperature range of 2 to 390 K. Interestingly, the low-temperature ferromagnetism is enhanced by the addition of ferroelectric PT up to x = 0.27.


2020 ◽  
Vol 235 (1-2) ◽  
pp. 7-13
Author(s):  
Jutta Kösters ◽  
Christian Paulsen ◽  
Frank Stegemann ◽  
Birgit Heying ◽  
Valérie Galéa-Clolus ◽  
...  

AbstractSystematically twinned olivenite (Cu2(AsO4)OH) single crystals from Cap Garonne, Mine du Pradet, France, were studied by X-ray diffraction: P 21/n, a = 822.69(6) pm, b = 861.88(9) pm, c = 594.06(9) pm, β = 90.000(6)°, wR = 0.0224, 1621 F2 values, 79 variables and a domain ratio of 0.501(1)/0.499(1). The temperature dependence of the magnetic susceptibility was well reproduced with a square-spin cluster model and an antiferromagnetic spin-exchange parameter of J/kB = 157(3) K.


RSC Advances ◽  
2015 ◽  
Vol 5 (47) ◽  
pp. 37818-37822 ◽  
Author(s):  
K. Vinod ◽  
C. S. Deepak ◽  
Shilpam Sharma ◽  
D. Sornadurai ◽  
A. T. Satya ◽  
...  

In this study we examine the phase transitions in single crystals of [(CH3)2NH2]Co(HCOO)3, using magnetization and specific heat measurements as a function of temperature and magnetic field.


2018 ◽  
Vol 27 (9) ◽  
pp. 097503 ◽  
Author(s):  
S Rizwan Ali ◽  
Farah Naz ◽  
Humaira Akber ◽  
M Naeem ◽  
S Imran Ali ◽  
...  

1996 ◽  
Vol 53 (13) ◽  
pp. 8473-8480 ◽  
Author(s):  
D. X. Li ◽  
Y. Haga ◽  
H. Shida ◽  
T. Suzuki ◽  
T. Koide ◽  
...  

1999 ◽  
Vol 581 ◽  
Author(s):  
L.L. Isaacs ◽  
V. Petricevic ◽  
BaoPing Wang ◽  
Jinpin Ying ◽  
R.R. Alfano

ABSTRACTSol - gel technology is used to prepare sub-micron to micron size particles of Chromium (IV) doped materials. These materials show strong luminescence, as single crystals, in the 1-2 μm range. Such materials include; Cr (IV): (Ca2GeO4, Mg2SiO4, LiScGeO4). The optically active particles are dispersed into glassy matrixes to form optical composites. Ongoing research is aimed at, a) reducing the size and the size distribution of the optically active particles, and b) finding suitable matrix materials.


2020 ◽  
Author(s):  
Quentin Evrard ◽  
Felix Houard ◽  
Carole Daiguebonne ◽  
guillaume calvez ◽  
yan suffren ◽  
...  

<p> Size, morphology and purity control of coordination compounds powders is a key stage for their conversion into materials and devices. In particular, surface science techniques require highly pure bulk materials with a narrow crystallite‑size distribution together with straightforward, scalable and reproducible crystallization procedures. In this work we demonstrate how sonocrystallization, <i>i.e.</i> application of ultrasounds during the crystallization process, can afford, very quickly, powders made of crystallites with controlled size, morphology and purity. We show that this process drastically diminishes the crystallite‑size distribution (low Polydispersity Indexes, PDI) and crystallite aspect ratio. By comparing sonicated samples with various silent crystallization conditions, we unambiguously show that the improvement of the crystallite morphologies and size‑distribution is not due to any thermal effect but to the sonication of the crystallizing media. The application of sonocrystallization on crystallization batches of Single‑Chain Magnets (SCM) maintains SCMs chemical integrity together with their original magnetic behavior. Moreover, luminescent measurements show that sonocrystallization induces an efficient micromixing that drastically enhances the purity of the SCMs powders. We thus propose that sonocrystallization, which is already used on organic or MOF compounds, can be applied to (magnetic) coordination compounds to readily afford bulk powders for characterization or shaping techniques that require pure, morphology‑ and crystallite‑size‑controlled powder samples.</p> <p><br> </p>


1992 ◽  
Vol 57 (4) ◽  
pp. 756-766 ◽  
Author(s):  
Jan Kornatowski ◽  
Beate Kanz-Reuschel ◽  
Gerd Finger ◽  
Werner H. Baur ◽  
Martin Bülow ◽  
...  

The kinetics of hydrothermal crystallization of microporous silicoaluminophosphate SAPO-5 have been studied as a function of water content using the templates tripropylamine (TPA) and triethylamine (TEA). The investigation included the formation of the SAPO-5 phase, its growth in large single crystals, and the size distribution of the crystals. An attempt to fit the experimental data to kinetic models of crystallization is presented. The systems studied have been found to be very similar except for the nucleation stage which is mainly responsible for both the dimensions of the resulting crystals and for the purity of the SAPO-5 phase.


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