Structural, magnetic and thermal characterization of Fe50Se50 powders obtained by mechanical alloying

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F20%3A10410666" target="_blank" >RIV/00216208:11310/20:10410666 - isvavai.cz</a>

Výsledek na webu

<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=LxRf6JnjUp" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=LxRf6JnjUp</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1007/s10973-019-08772-x" target="_blank" >10.1007/s10973-019-08772-x</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Structural, magnetic and thermal characterization of Fe50Se50 powders obtained by mechanical alloying

Popis výsledku v původním jazyce

In this paper, Fe50Se50 alloy powders were synthesized from pure elemental powder by mechanical allowing. The structure, microstructure, morphology, chemical composition and thermal behavior at a function of milling times (0-39 h) were investigated by X-ray diffraction (XRD), scanning electron microscopy attached with energy-dispersive spectroscopy and differential scanning calorimetry (DSC). In addition, the interaction hyperfine and magnetic proprieties was examined by transmission Mossbauer spectroscopy (TMS) and thermomagnetic measurements (VSM) respectively. For milling times up to 6 h, the results of refinement of the X-ray diffraction pattern by MAUD software reveal the formation of the beta-FeSe hexagonal, amorphous selenium and nanocrystalline alpha-Fe. The DSC curves show several exothermic and endothermic peaks associated with various phases&apos; transitions such as the exothermic peak at 103 degrees C related to crystallization amorphous selenium. However, after prolonging the milling time to 39 h, the XRD shows the formation of alpha-FeSe phase tetragonal which has plenty of technological interests especially the superconductivity. The Mossbauer spectroscopy confirmed the formation the two-phase paramagnetic hexagonal beta-FeSe and alpha-FeSe tetragonal, according to the XRD and DSC. Measurement of magnetization (VSM) displays that saturation magnetization (MS) decreases as the milling time increases.

Název v anglickém jazyce

Structural, magnetic and thermal characterization of Fe50Se50 powders obtained by mechanical alloying

Popis výsledku anglicky

In this paper, Fe50Se50 alloy powders were synthesized from pure elemental powder by mechanical allowing. The structure, microstructure, morphology, chemical composition and thermal behavior at a function of milling times (0-39 h) were investigated by X-ray diffraction (XRD), scanning electron microscopy attached with energy-dispersive spectroscopy and differential scanning calorimetry (DSC). In addition, the interaction hyperfine and magnetic proprieties was examined by transmission Mossbauer spectroscopy (TMS) and thermomagnetic measurements (VSM) respectively. For milling times up to 6 h, the results of refinement of the X-ray diffraction pattern by MAUD software reveal the formation of the beta-FeSe hexagonal, amorphous selenium and nanocrystalline alpha-Fe. The DSC curves show several exothermic and endothermic peaks associated with various phases&apos; transitions such as the exothermic peak at 103 degrees C related to crystallization amorphous selenium. However, after prolonging the milling time to 39 h, the XRD shows the formation of alpha-FeSe phase tetragonal which has plenty of technological interests especially the superconductivity. The Mossbauer spectroscopy confirmed the formation the two-phase paramagnetic hexagonal beta-FeSe and alpha-FeSe tetragonal, according to the XRD and DSC. Measurement of magnetization (VSM) displays that saturation magnetization (MS) decreases as the milling time increases.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10402 - Inorganic and nuclear chemistry

Projekt

—

Návaznosti

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2020

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Journal of Thermal Analysis and Calorimetry

ISSN

1388-6150

e-ISSN

—

Svazek periodika

140

Číslo periodika v rámci svazku

1

Stát vydavatele periodika

HU - Maďarsko

Počet stran výsledku

10

Strana od-do

53-62

Kód UT WoS článku

000520712700003

EID výsledku v databázi Scopus

2-s2.0-85073956877