Controlling the europium oxidation state in diopside through flux concentration

This paper explores the connection between the H 3 BO 3 flux concentration and the co-existence of Eu 2+ and Eu 3+ dopants within CaMgSi 2 O 6 crystals (diopside). The samples were synthesised using a solid-state synthesis method under varying atmospheric conditions, including oxidative (air), neutr...

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Veröffentlicht in:Dalton transactions : an international journal of inorganic chemistry 2024-04, Vol.53 (14), p.6386-6398
Hauptverfasser: Górecka, N, Le niewski, T, Mahlik, S, api ski, M, Tsai, Y.-T, Bielicka-Gie do, A, Szczodrowski, K
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container_issue 14
container_start_page 6386
container_title Dalton transactions : an international journal of inorganic chemistry
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creator Górecka, N
Le niewski, T
Mahlik, S
api ski, M
Tsai, Y.-T
Bielicka-Gie do, A
Szczodrowski, K
description This paper explores the connection between the H 3 BO 3 flux concentration and the co-existence of Eu 2+ and Eu 3+ dopants within CaMgSi 2 O 6 crystals (diopside). The samples were synthesised using a solid-state synthesis method under varying atmospheric conditions, including oxidative (air), neutral (N 2 ), and reductive (H 2 /N 2 mixture) environments. Additionally, some materials underwent chemical modification by partially substituting Si 4+ with Al 3+ ions acting as charge compensation defects stabilizing Eu 3+ luminescence. Depending on the specific synthesis conditions, the materials predominantly displayed either the orange-red luminescence of Eu 3+ (under oxidising conditions) or the blue luminescence of Eu 2+ ; however, the comprehensive results confirmed the co-existence of Eu 3+ /Eu 2+ luminescence in both cases. This work shows that varying flux concentrations added during synthesis significantly affect the relative strength of Eu 2+ and Eu 3+ emissions in a manner dependent on the synthesis atmosphere. The emission of Eu 2+ increases with a higher flux concentration in materials synthesised under oxidative and neutral atmospheres independent of the chemical modification. In contrast, for materials obtained under a reductive atmosphere, the changes in the Eu 3+ emission intensity depended on the presence or absence of Al 3+ ions namely the increase of flux increased the Eu 3+ intensity in the case of unmodified materials and decreased in the Al-modified ones. All observed effects were qualitatively explained considering the double role of the flux in the studied system, which besides facilitating the diffusion of chemical species during synthesis acts as a charge compensating agent by creating B′ Si centres stabilizing Eu 3+ emission. The reduction of lanthanides (Ln 3+ ) incorporated into alkali earth sites in a matrix, , requires the creation of electron donating defects, e.g. , and elimination of charge compensation defects, e.g. V′′ Me , from the vicinity of the .
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The samples were synthesised using a solid-state synthesis method under varying atmospheric conditions, including oxidative (air), neutral (N 2 ), and reductive (H 2 /N 2 mixture) environments. Additionally, some materials underwent chemical modification by partially substituting Si 4+ with Al 3+ ions acting as charge compensation defects stabilizing Eu 3+ luminescence. Depending on the specific synthesis conditions, the materials predominantly displayed either the orange-red luminescence of Eu 3+ (under oxidising conditions) or the blue luminescence of Eu 2+ ; however, the comprehensive results confirmed the co-existence of Eu 3+ /Eu 2+ luminescence in both cases. This work shows that varying flux concentrations added during synthesis significantly affect the relative strength of Eu 2+ and Eu 3+ emissions in a manner dependent on the synthesis atmosphere. The emission of Eu 2+ increases with a higher flux concentration in materials synthesised under oxidative and neutral atmospheres independent of the chemical modification. In contrast, for materials obtained under a reductive atmosphere, the changes in the Eu 3+ emission intensity depended on the presence or absence of Al 3+ ions namely the increase of flux increased the Eu 3+ intensity in the case of unmodified materials and decreased in the Al-modified ones. All observed effects were qualitatively explained considering the double role of the flux in the studied system, which besides facilitating the diffusion of chemical species during synthesis acts as a charge compensating agent by creating B′ Si centres stabilizing Eu 3+ emission. 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The samples were synthesised using a solid-state synthesis method under varying atmospheric conditions, including oxidative (air), neutral (N 2 ), and reductive (H 2 /N 2 mixture) environments. Additionally, some materials underwent chemical modification by partially substituting Si 4+ with Al 3+ ions acting as charge compensation defects stabilizing Eu 3+ luminescence. Depending on the specific synthesis conditions, the materials predominantly displayed either the orange-red luminescence of Eu 3+ (under oxidising conditions) or the blue luminescence of Eu 2+ ; however, the comprehensive results confirmed the co-existence of Eu 3+ /Eu 2+ luminescence in both cases. This work shows that varying flux concentrations added during synthesis significantly affect the relative strength of Eu 2+ and Eu 3+ emissions in a manner dependent on the synthesis atmosphere. The emission of Eu 2+ increases with a higher flux concentration in materials synthesised under oxidative and neutral atmospheres independent of the chemical modification. In contrast, for materials obtained under a reductive atmosphere, the changes in the Eu 3+ emission intensity depended on the presence or absence of Al 3+ ions namely the increase of flux increased the Eu 3+ intensity in the case of unmodified materials and decreased in the Al-modified ones. All observed effects were qualitatively explained considering the double role of the flux in the studied system, which besides facilitating the diffusion of chemical species during synthesis acts as a charge compensating agent by creating B′ Si centres stabilizing Eu 3+ emission. 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The samples were synthesised using a solid-state synthesis method under varying atmospheric conditions, including oxidative (air), neutral (N 2 ), and reductive (H 2 /N 2 mixture) environments. Additionally, some materials underwent chemical modification by partially substituting Si 4+ with Al 3+ ions acting as charge compensation defects stabilizing Eu 3+ luminescence. Depending on the specific synthesis conditions, the materials predominantly displayed either the orange-red luminescence of Eu 3+ (under oxidising conditions) or the blue luminescence of Eu 2+ ; however, the comprehensive results confirmed the co-existence of Eu 3+ /Eu 2+ luminescence in both cases. This work shows that varying flux concentrations added during synthesis significantly affect the relative strength of Eu 2+ and Eu 3+ emissions in a manner dependent on the synthesis atmosphere. The emission of Eu 2+ increases with a higher flux concentration in materials synthesised under oxidative and neutral atmospheres independent of the chemical modification. In contrast, for materials obtained under a reductive atmosphere, the changes in the Eu 3+ emission intensity depended on the presence or absence of Al 3+ ions namely the increase of flux increased the Eu 3+ intensity in the case of unmodified materials and decreased in the Al-modified ones. All observed effects were qualitatively explained considering the double role of the flux in the studied system, which besides facilitating the diffusion of chemical species during synthesis acts as a charge compensating agent by creating B′ Si centres stabilizing Eu 3+ emission. 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source Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
subjects Calcium magnesium silicates
Chemical synthesis
Crystal defects
Diopside
Europium
Inert atmospheres
Luminescence
Oxidation
Species diffusion
Valence
title Controlling the europium oxidation state in diopside through flux concentration
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