Nanopowders of R2Fe14B -type compounds in high magnetic fields: The effects of substitutional and interstitial atoms on inter-sublattice exchange interaction
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F26722445%3A_____%2F20%3AN0000177" target="_blank" >RIV/26722445:_____/20:N0000177 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/68378271:_____/20:00538875
Výsledek na webu
<a href="https://www.confer.cz/proceedings/metal/2020.pdf" target="_blank" >https://www.confer.cz/proceedings/metal/2020.pdf</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.37904/metal.2020.3597" target="_blank" >10.37904/metal.2020.3597</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Nanopowders of R2Fe14B -type compounds in high magnetic fields: The effects of substitutional and interstitial atoms on inter-sublattice exchange interaction
Popis výsledku v původním jazyce
The fundamental magnetic characteristics of R2Fe14B intermetallics are highly sensitive to atomic substitutions and interstitial absorption of light elements. In this work, both were combined, and the influence of the substitutions in the R-sublattice and hydrogen absorption on the magnetization of (RR’)2Fe14BHx (R is Tm or Er, and R’ is Nd) in magnetic fields up to 58T was studied. (Tm0.5Nd0.5)2Fe14B and (Er0.5Nd0.5)2Fe14B were prepared. By using direct hydrogen absorption, (R0.5Nd0.5)2Fe14BHx compounds were obtained with hydrogen content 0≤x≤5.5. Magnetic measurements of both the parent alloys and their hydrides were carried out on nanopowders. The strength of the inter-sublattice coupling in (Tm0.5Nd0.5)2Fe14B, (Er0.5Nd0.5)2Fe14B and their hydrides is estimated by analysing high-field magnetization data. Itis shown that hydrogenation weakens the inter-sublattice exchange interaction up to 45 %. (Tm0.5Nd0.5)2Fe14B, with the maximum hydrogen content of 5.5 at.H/f.u., reaches the field-induced ferromagnetic state at about 55 T.
Název v anglickém jazyce
Nanopowders of R2Fe14B -type compounds in high magnetic fields: The effects of substitutional and interstitial atoms on inter-sublattice exchange interaction
Popis výsledku anglicky
The fundamental magnetic characteristics of R2Fe14B intermetallics are highly sensitive to atomic substitutions and interstitial absorption of light elements. In this work, both were combined, and the influence of the substitutions in the R-sublattice and hydrogen absorption on the magnetization of (RR’)2Fe14BHx (R is Tm or Er, and R’ is Nd) in magnetic fields up to 58T was studied. (Tm0.5Nd0.5)2Fe14B and (Er0.5Nd0.5)2Fe14B were prepared. By using direct hydrogen absorption, (R0.5Nd0.5)2Fe14BHx compounds were obtained with hydrogen content 0≤x≤5.5. Magnetic measurements of both the parent alloys and their hydrides were carried out on nanopowders. The strength of the inter-sublattice coupling in (Tm0.5Nd0.5)2Fe14B, (Er0.5Nd0.5)2Fe14B and their hydrides is estimated by analysing high-field magnetization data. Itis shown that hydrogenation weakens the inter-sublattice exchange interaction up to 45 %. (Tm0.5Nd0.5)2Fe14B, with the maximum hydrogen content of 5.5 at.H/f.u., reaches the field-induced ferromagnetic state at about 55 T.
Klasifikace
Druh
D - Stať ve sborníku
CEP obor
—
OECD FORD obor
20501 - Materials engineering
Návaznosti výsledku
Projekt
Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2020
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název statě ve sborníku
METAL 2020 : 29th International Conference on Metallurgy and Materials : Conference Proceedings, May 20 - 22, 2020 / Brno, Czech Republic, EU
ISBN
978-80-87294-97-0
ISSN
2694-9296
e-ISSN
—
Počet stran výsledku
7
Strana od-do
1000-1006
Název nakladatele
Tanger, Ltd.
Místo vydání
Brno
Místo konání akce
Brno
Datum konání akce
20. 5. 2020
Typ akce podle státní příslušnosti
WRD - Celosvětová akce
Kód UT WoS článku
—