Synthesis, crystal structure, electric and magnetic properties of new UNiSi2 splat
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11320%2F17%3A10364335" target="_blank" >RIV/00216208:11320/17:10364335 - isvavai.cz</a>
Výsledek na webu
<a href="http://dx.doi.org/10.1063/1.5001301" target="_blank" >http://dx.doi.org/10.1063/1.5001301</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1063/1.5001301" target="_blank" >10.1063/1.5001301</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Synthesis, crystal structure, electric and magnetic properties of new UNiSi2 splat
Popis výsledku v původním jazyce
We explored the crystal structure, magnetic and transport properties of UNiSi2 material, which was prepared by rapid solidification-splat cooling. The UNiSi2 splat is mostly single phase, the refinement of crystal structure indicated orthorhombic CeNiSi2-type structure (space group Cmcm) with lattice parameters a = 4.0082 angstrom, b = 16.0813 angstrom and c = 4.0064 angstrom. Also SEM analysis revealed the morphology exhibiting dendritic grains in the matrix. TEM images indicate mixed structure formed by crystalline particles embedded into amorphous or nanocrystalline matrix. Magnetic and electrical properties of the splat resemble properties of samples, which were prepared by conventional methods, exhibiting a ferromagnetic transition at about 91K and similar temperature dependence of resistivity. The coercive field of mu H-0(c) = 2.25 T is much enhanced due to the magnetic anisotropy introduced by the sample preparation technique. Barkhausen jumps were observed on the hysteresis loop. Magnetization of the sample does not saturate in magnetic fields up to mu H-0 = 18 T. Published by AIP Publishing.
Název v anglickém jazyce
Synthesis, crystal structure, electric and magnetic properties of new UNiSi2 splat
Popis výsledku anglicky
We explored the crystal structure, magnetic and transport properties of UNiSi2 material, which was prepared by rapid solidification-splat cooling. The UNiSi2 splat is mostly single phase, the refinement of crystal structure indicated orthorhombic CeNiSi2-type structure (space group Cmcm) with lattice parameters a = 4.0082 angstrom, b = 16.0813 angstrom and c = 4.0064 angstrom. Also SEM analysis revealed the morphology exhibiting dendritic grains in the matrix. TEM images indicate mixed structure formed by crystalline particles embedded into amorphous or nanocrystalline matrix. Magnetic and electrical properties of the splat resemble properties of samples, which were prepared by conventional methods, exhibiting a ferromagnetic transition at about 91K and similar temperature dependence of resistivity. The coercive field of mu H-0(c) = 2.25 T is much enhanced due to the magnetic anisotropy introduced by the sample preparation technique. Barkhausen jumps were observed on the hysteresis loop. Magnetization of the sample does not saturate in magnetic fields up to mu H-0 = 18 T. Published by AIP Publishing.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10302 - Condensed matter physics (including formerly solid state physics, supercond.)
Návaznosti výsledku
Projekt
<a href="/cs/project/LM2011025" target="_blank" >LM2011025: LMNT - Laboratoře magnetizmu a nízkých teplot - provoz a rozvoj národní výzkumné infrastruktury</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2017
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Low Temperature Physics
ISSN
1063-777X
e-ISSN
—
Svazek periodika
43
Číslo periodika v rámci svazku
8
Stát vydavatele periodika
UA - Ukrajina
Počet stran výsledku
4
Strana od-do
986-989
Kód UT WoS článku
000412369500018
EID výsledku v databázi Scopus
2-s2.0-85025066313