2020
DOI: 10.1016/j.jcrysgro.2020.125723
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Flux crystal growth of Cu2GaBO5 and Cu2AlBO5

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Cited by 10 publications
(3 citation statements)
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“…Previously, flux systems based on Bi 2 Mo 3 O 12 were used to grow several transition metal oxyborate compounds with warwickite and ludwigite structures. [20][21][22][23][24][25][26] Thus, the ratio of Bi : Mo = 2 : 3 was constant. However, owing to the discovery of the special role of molybdenum oxide in HTCP formation and its influence on the valence of manganese cations, there arose a need to study flux systems with the ratio Bi : Mo, which is different from 2 : 3.…”
Section: Flux Growthmentioning
confidence: 99%
See 1 more Smart Citation
“…Previously, flux systems based on Bi 2 Mo 3 O 12 were used to grow several transition metal oxyborate compounds with warwickite and ludwigite structures. [20][21][22][23][24][25][26] Thus, the ratio of Bi : Mo = 2 : 3 was constant. However, owing to the discovery of the special role of molybdenum oxide in HTCP formation and its influence on the valence of manganese cations, there arose a need to study flux systems with the ratio Bi : Mo, which is different from 2 : 3.…”
Section: Flux Growthmentioning
confidence: 99%
“…18 In addressing these problems, multicomponent fluxes based on Bi 2 O 3 -MoO 3 -B 2 O 3 -Na 2 O proved to be efficient upon the crystallization of heterovalent oxyborates of warwickite 18,[20][21][22] and ludwigite. 18,[23][24][25][26] The change in the valence composition of the manganese cations in the crystallizing phases was shown in the case of using the solvent components MoO 3 (or WO 3 ) and Na 2 O (or Li 2 O). An assumption was made that manganese was fixed in the valence state 2+ by MoO 3 , and it was impossible to obtain the Mn 3+ -containing phase without the addition of Na 2 O to the fluxes based on Bi 2 Mo 3 O 12 .…”
Section: Introductionmentioning
confidence: 99%
“…This is the most widelyused method for obtaining single crystal samples of the oxyborates with a ludwigite structure due to the presence of growth anisotropy. Natural faceting of single crystals and the possibility of using different solvent types for individual synthesis of different compounds are undoubtedly some merits of this technique [7].…”
Section: Introductionmentioning
confidence: 99%