Синтез, властивості CaCu3Ti4O12 з колосальною величиною діелектричної проникності

Ceramic materials CaCu3Ti4O12 were synthesized by solid-phase reactions technique. The sequence of chemical reactions during the synthesis has been determined. Phase CaCu3Ti4O12 appears at 700 °C. At 800 – 900 °C, the intermediate phases CaTiO3, CuTiO3 and Ca3Ti2O7 are formed. Calcium and copper tit...

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Бібліографічні деталі
Дата:2019
Автори: V'yunov, Oleg, Konchus, Boris, Yanchevskiy, Oleg, Belous, Anatolii
Формат: Стаття
Мова:English
Опубліковано: V.I.Vernadsky Institute of General and Inorganic Chemistry 2019
Онлайн доступ:https://ucj.org.ua/index.php/journal/article/view/59
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Назва журналу:Ukrainian Chemistry Journal

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Ukrainian Chemistry Journal
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institution Ukrainian Chemistry Journal
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datestamp_date 2019-12-11T17:05:09Z
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language English
topic_facet CaCu3Ti4O12 ceramics
colossal dielectric constant
microstructure
format Article
author V'yunov, Oleg
Konchus, Boris
Yanchevskiy, Oleg
Belous, Anatolii
spellingShingle V'yunov, Oleg
Konchus, Boris
Yanchevskiy, Oleg
Belous, Anatolii
Синтез, властивості CaCu3Ti4O12 з колосальною величиною діелектричної проникності
author_facet V'yunov, Oleg
Konchus, Boris
Yanchevskiy, Oleg
Belous, Anatolii
author_sort V'yunov, Oleg
title Синтез, властивості CaCu3Ti4O12 з колосальною величиною діелектричної проникності
title_short Синтез, властивості CaCu3Ti4O12 з колосальною величиною діелектричної проникності
title_full Синтез, властивості CaCu3Ti4O12 з колосальною величиною діелектричної проникності
title_fullStr Синтез, властивості CaCu3Ti4O12 з колосальною величиною діелектричної проникності
title_full_unstemmed Синтез, властивості CaCu3Ti4O12 з колосальною величиною діелектричної проникності
title_sort синтез, властивості cacu3ti4o12 з колосальною величиною діелектричної проникності
title_alt SYNTHESIS, PROPERTIES CaCu3Ti4O12 WITH COLOSSAL VALUE OF THE DIELECTRIC PERMITTIVITY
Синтез, свойства CaCu3Ti4O12 с колоссальной величиной диэлектрической проницаемости
description Ceramic materials CaCu3Ti4O12 were synthesized by solid-phase reactions technique. The sequence of chemical reactions during the synthesis has been determined. Phase CaCu3Ti4O12 appears at 700 °C. At 800 – 900 °C, the intermediate phases CaTiO3, CuTiO3 and Ca3Ti2O7 are formed. Calcium and copper titanates, CaTiO3 and CuTiO3 interact to form CaCu3Ti4O12. Ca3Ti2O7 phase with pyrochlore structure is stable and prevent the formation of final product, CaCu3Ti4O12. A method for the synthesis of CaCu3Ti4O12 by solid-state reactions technique from previously synthesized CaTiO3 (at 1050 °С) and CuTiO3 (at 950  °С), taken in a molar ratio of 1:3, is proposed. This method give the possibility to avoid the appearance of an undesirable Ca3Ti2O7 phase with the pyrochlore structure and to reduce the content of free copper oxide to value less than 0.5 mol.%. In addition, instead of the copper oxide, which is usually used in solid-state reaction technique, the chemically more active form of the copper-containing reagent, CuCO3∙Cu(OН)2 were used. This reduce the synthesis time of the intermediate CuTiO3. The crystal structure, chemical composition, microstructure and electrophysical parameters of ceramics have been analyzed. The synthesized ceramics CaCu3Ti4O12 is cubic body-centered (space group Im-3) with the unit cell parameter a = 7.3932 Å, which agreed with the literature data. The calculated tolerance factor of CaCu3Ti4O12, t = 0.7626 is not sufficient for a stabilization of peroskite ABO3 structure; that is why the crystal structure of this compound contains 3 different cation sites: dodecahedral (Ca2+), octahedral (Ti4+), tetrahedral (Cu2+). At 1150 °C, the density of CaCu3Ti4O12 ceramic sintered has a maximum (90% of the theoretical density). At infra-low frequencies (10-3 Hz), the dielectric constant (ɛ) reaches record values of 107, however, dielectric losses (tg δ) up to 10 were observed. In the frequency range 10-3 - 105 Hz the value of ɛ exceeds 104; and at 105 Hz minimum of the dielectric losses (tg δ ~ 0.1) is observed. A comparative analysis of methods for the synthesis of CaCu3Ti4O12 shows that the synthesis conditions of material of the same chemical composition can be crucial in creating high dense ceramic with uniform grains, high dielectric constant and low dielectric losses in a wide frequency range.
publisher V.I.Vernadsky Institute of General and Inorganic Chemistry
publishDate 2019
url https://ucj.org.ua/index.php/journal/article/view/59
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AT yanchevskiyoleg sintezsvojstvacacu3ti4o12skolossalʹnojveličinojdiélektričeskojpronicaemosti
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spelling oai:ojs2.1444248.nisspano.web.hosting-test.net:article-592019-12-11T17:05:09Z SYNTHESIS, PROPERTIES CaCu3Ti4O12 WITH COLOSSAL VALUE OF THE DIELECTRIC PERMITTIVITY Синтез, свойства CaCu3Ti4O12 с колоссальной величиной диэлектрической проницаемости Синтез, властивості CaCu3Ti4O12 з колосальною величиною діелектричної проникності V'yunov, Oleg Konchus, Boris Yanchevskiy, Oleg Belous, Anatolii CaCu3Ti4O12 ceramics colossal dielectric constant microstructure Ceramic materials CaCu3Ti4O12 were synthesized by solid-phase reactions technique. The sequence of chemical reactions during the synthesis has been determined. Phase CaCu3Ti4O12 appears at 700 °C. At 800 – 900 °C, the intermediate phases CaTiO3, CuTiO3 and Ca3Ti2O7 are formed. Calcium and copper titanates, CaTiO3 and CuTiO3 interact to form CaCu3Ti4O12. Ca3Ti2O7 phase with pyrochlore structure is stable and prevent the formation of final product, CaCu3Ti4O12. A method for the synthesis of CaCu3Ti4O12 by solid-state reactions technique from previously synthesized CaTiO3 (at 1050 °С) and CuTiO3 (at 950  °С), taken in a molar ratio of 1:3, is proposed. This method give the possibility to avoid the appearance of an undesirable Ca3Ti2O7 phase with the pyrochlore structure and to reduce the content of free copper oxide to value less than 0.5 mol.%. In addition, instead of the copper oxide, which is usually used in solid-state reaction technique, the chemically more active form of the copper-containing reagent, CuCO3∙Cu(OН)2 were used. This reduce the synthesis time of the intermediate CuTiO3. The crystal structure, chemical composition, microstructure and electrophysical parameters of ceramics have been analyzed. The synthesized ceramics CaCu3Ti4O12 is cubic body-centered (space group Im-3) with the unit cell parameter a = 7.3932 Å, which agreed with the literature data. The calculated tolerance factor of CaCu3Ti4O12, t = 0.7626 is not sufficient for a stabilization of peroskite ABO3 structure; that is why the crystal structure of this compound contains 3 different cation sites: dodecahedral (Ca2+), octahedral (Ti4+), tetrahedral (Cu2+). At 1150 °C, the density of CaCu3Ti4O12 ceramic sintered has a maximum (90% of the theoretical density). At infra-low frequencies (10-3 Hz), the dielectric constant (ɛ) reaches record values of 107, however, dielectric losses (tg δ) up to 10 were observed. In the frequency range 10-3 - 105 Hz the value of ɛ exceeds 104; and at 105 Hz minimum of the dielectric losses (tg δ ~ 0.1) is observed. A comparative analysis of methods for the synthesis of CaCu3Ti4O12 shows that the synthesis conditions of material of the same chemical composition can be crucial in creating high dense ceramic with uniform grains, high dielectric constant and low dielectric losses in a wide frequency range. Ceramic materials CaCu3Ti4O12 were synthesized by solid-phase reactions technique. The sequence of chemical reactions during the synthesis has been determined. Phase CaCu3Ti4O12 appears at 700 °C. At 800 – 900 °C, the intermediate phases CaTiO3, CuTiO3 and Ca3Ti2O7 are formed. Calcium and copper titanates, CaTiO3 and CuTiO3 interact to form CaCu3Ti4O12. Ca3Ti2O7 phase with pyrochlore structure is stable and prevent the formation of final product, CaCu3Ti4O12. A method for the synthesis of CaCu3Ti4O12 by solid-state reactions technique from previously synthesized CaTiO3 (at 1050 °С) and CuTiO3 (at 950  °С), taken in a molar ratio of 1:3, is proposed. This method give the possibility to avoid the appearance of an undesirable Ca3Ti2O7 phase with the pyrochlore structure and to reduce the content of free copper oxide to value less than 0.5 mol.%. In addition, instead of the copper oxide, which is usually used in solid-state reaction technique, the chemically more active form of the copper-containing reagent, CuCO3∙Cu(OН)2 were used. This reduce the synthesis time of the intermediate CuTiO3. The crystal structure, chemical composition, microstructure and electrophysical parameters of ceramics have been analyzed. The synthesized ceramics CaCu3Ti4O12 is cubic body-centered (space group Im-3) with the unit cell parameter a = 7.3932 Å, which agreed with the literature data. The calculated tolerance factor of CaCu3Ti4O12, t = 0.7626 is not sufficient for a stabilization of peroskite ABO3 structure; that is why the crystal structure of this compound contains 3 different cation sites: dodecahedral (Ca2+), octahedral (Ti4+), tetrahedral (Cu2+). At 1150 °C, the density of CaCu3Ti4O12 ceramic sintered has a maximum (90% of the theoretical density). At infra-low frequencies (10-3 Hz), the dielectric constant (ɛ) reaches record values of 107, however, dielectric losses (tg δ) up to 10 were observed. In the frequency range 10-3 - 105 Hz the value of ɛ exceeds 104; and at 105 Hz minimum of the dielectric losses (tg δ ~ 0.1) is observed. A comparative analysis of methods for the synthesis of CaCu3Ti4O12 shows that the synthesis conditions of material of the same chemical composition can be crucial in creating high dense ceramic with uniform grains, high dielectric constant and low dielectric losses in a wide frequency range. Ceramic materials CaCu3Ti4O12 were synthesized by solid-phase reactions technique. The sequence of chemical reactions during the synthesis has been determined. Phase CaCu3Ti4O12 appears at 700 °C. At 800 – 900 °C, the intermediate phases CaTiO3, CuTiO3 and Ca3Ti2O7 are formed. Calcium and copper titanates, CaTiO3 and CuTiO3 interact to form CaCu3Ti4O12. Ca3Ti2O7 phase with pyrochlore structure is stable and prevent the formation of final product, CaCu3Ti4O12. A method for the synthesis of CaCu3Ti4O12 by solid-state reactions technique from previously synthesized CaTiO3 (at 1050 °С) and CuTiO3 (at 950  °С), taken in a molar ratio of 1:3, is proposed. This method give the possibility to avoid the appearance of an undesirable Ca3Ti2O7 phase with the pyrochlore structure and to reduce the content of free copper oxide to value less than 0.5 mol.%. In addition, instead of the copper oxide, which is usually used in solid-state reaction technique, the chemically more active form of the copper-containing reagent, CuCO3∙Cu(OН)2 were used. This reduce the synthesis time of the intermediate CuTiO3. The crystal structure, chemical composition, microstructure and electrophysical parameters of ceramics have been analyzed. The synthesized ceramics CaCu3Ti4O12 is cubic body-centered (space group Im-3) with the unit cell parameter a = 7.3932 Å, which agreed with the literature data. The calculated tolerance factor of CaCu3Ti4O12, t = 0.7626 is not sufficient for a stabilization of peroskite ABO3 structure; that is why the crystal structure of this compound contains 3 different cation sites: dodecahedral (Ca2+), octahedral (Ti4+), tetrahedral (Cu2+). At 1150 °C, the density of CaCu3Ti4O12 ceramic sintered has a maximum (90% of the theoretical density). At infra-low frequencies (10-3 Hz), the dielectric constant (ɛ) reaches record values of 107, however, dielectric losses (tg δ) up to 10 were observed. In the frequency range 10-3 - 105 Hz the value of ɛ exceeds 104; and at 105 Hz minimum of the dielectric losses (tg δ ~ 0.1) is observed. A comparative analysis of methods for the synthesis of CaCu3Ti4O12 shows that the synthesis conditions of material of the same chemical composition can be crucial in creating high dense ceramic with uniform grains, high dielectric constant and low dielectric losses in a wide frequency range. V.I.Vernadsky Institute of General and Inorganic Chemistry 2019-07-31 Article Article Inorganic Chemistry Неорганическая химия Неорганічна хімія application/pdf https://ucj.org.ua/index.php/journal/article/view/59 10.33609/0041-6045.85.6.2019.77-86 Ukrainian Chemistry Journal; Vol. 85 No. 6 (2019): Ukrainian Chemistry Journal; 77-86 Украинский химический журнал; Том 85 № 6 (2019): Украинский химический журнал; 77-86 Український хімічний журнал; Том 85 № 6 (2019): Український хімічний журнал; 77-86 2708-129X 2708-1281 en https://ucj.org.ua/index.php/journal/article/view/59/36