Enthalpy relaxation kinetics of Ge20Te(80-y)Sey far-infrared glasses in the glass transition range
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F16%3A39901209" target="_blank" >RIV/00216275:25310/16:39901209 - isvavai.cz</a>
Výsledek na webu
<a href="http://dx.doi.org/10.1080/14786435.2016.1177227" target="_blank" >http://dx.doi.org/10.1080/14786435.2016.1177227</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1080/14786435.2016.1177227" target="_blank" >10.1080/14786435.2016.1177227</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Enthalpy relaxation kinetics of Ge20Te(80-y)Sey far-infrared glasses in the glass transition range
Popis výsledku v původním jazyce
Differential scanning calorimetry was used to study enthalpy relaxation kinetics of the Ge20Te(80-y)Sey infrared chalcogenide glasses for the compositional range y=0-8. The relaxation behaviour was described in terms of the phenomenological Tool-Narayanaswamy-Moynihan (TNM) model. The direct curve-fitting procedure was used to determine the values of TNM parameters. Compositional evolution of the TNM parameters was interpreted with respect to the involved structural entities and their motions. Based on the joint Raman scattering study, the addition of Se leads to increased amount of edge-shared GeTe4-xSex tetrahedra. While the primary structural basis for the relaxation movements appears not to be affected by addition of Se (constant value of non-linearity), changes of the non-exponentiality parameter indicate increased structural variability occurring within the groups of directly interlinked tetrahedra, which were found to carry the main portion of relaxation movements. Increased activation energy was explained by the presence of significantly stronger Ge-Se bonds and increased amount of edge-shared tetrahedra.
Název v anglickém jazyce
Enthalpy relaxation kinetics of Ge20Te(80-y)Sey far-infrared glasses in the glass transition range
Popis výsledku anglicky
Differential scanning calorimetry was used to study enthalpy relaxation kinetics of the Ge20Te(80-y)Sey infrared chalcogenide glasses for the compositional range y=0-8. The relaxation behaviour was described in terms of the phenomenological Tool-Narayanaswamy-Moynihan (TNM) model. The direct curve-fitting procedure was used to determine the values of TNM parameters. Compositional evolution of the TNM parameters was interpreted with respect to the involved structural entities and their motions. Based on the joint Raman scattering study, the addition of Se leads to increased amount of edge-shared GeTe4-xSex tetrahedra. While the primary structural basis for the relaxation movements appears not to be affected by addition of Se (constant value of non-linearity), changes of the non-exponentiality parameter indicate increased structural variability occurring within the groups of directly interlinked tetrahedra, which were found to carry the main portion of relaxation movements. Increased activation energy was explained by the presence of significantly stronger Ge-Se bonds and increased amount of edge-shared tetrahedra.
Klasifikace
Druh
J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
CEP obor
CF - Fyzikální chemie a teoretická chemie
OECD FORD obor
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Návaznosti výsledku
Projekt
<a href="/cs/project/GAP106%2F11%2F1152" target="_blank" >GAP106/11/1152: Reverzibilní krystalizace a strukturni relaxace amorfních materiálů pro záznam informace</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2016
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Philosophical Magazine
ISSN
1478-6435
e-ISSN
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Svazek periodika
96
Číslo periodika v rámci svazku
16
Stát vydavatele periodika
GB - Spojené království Velké Británie a Severního Irska
Počet stran výsledku
9
Strana od-do
1623-1631
Kód UT WoS článku
000375918800001
EID výsledku v databázi Scopus
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