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http://elar.urfu.ru/handle/10995/140708
Полная запись метаданных
Поле DC | Значение | Язык |
---|---|---|
dc.contributor.author | Animitsa, I. E. | en |
dc.contributor.author | Korona, D. V. | en |
dc.contributor.author | Bushueva, A. V. | en |
dc.contributor.author | Andreev, R. D. | en |
dc.contributor.author | Nokhrin, S. S. | en |
dc.date.accessioned | 2025-01-15T06:55:17Z | - |
dc.date.available | 2025-01-15T06:55:17Z | - |
dc.date.issued | 2024 | - |
dc.identifier.citation | The Novel Zn-Doped Hexagonal Perovskite Ba7In6Al2O19: Electrical Conductivity and Hydration / I. E. Animitsa, D. V. Korona, A. V. Bushueva, R. D. Andreev, S. S. Nokhrin // Chimica Techno Acta. — 2024. — Vol. 11, No. 4. — № 202411403. | ru |
dc.identifier.issn | 2411-1414 | online |
dc.identifier.uri | http://elar.urfu.ru/handle/10995/140708 | - |
dc.description | Received: 24.08.2024. Revised: 09.09.2024. Accepted: 11.09.2024. Available online: 30.09.2024. | en |
dc.description | A novel hexagonal perovskite Ba7In5.9Zn0.1Al2O18.95 has been synthesized. | en |
dc.description | Ba7In5.9Zn0.1Al2O18.95 is capable of dissociative water molecule incorporation. | en |
dc.description | Ba7In5.9Zn0.1Al2O18.95 is able to exhibit proton conductivity. | en |
dc.description | Ba7In5.9Zn0.1Al2O18.95 demonstrates predominant proton transport at T ≤ 500 °C in wet air. | en |
dc.description | The Zn2+-doping of Ba7In6Al2O19 increases the oxide-ion and proton conductivities. | en |
dc.description.abstract | The novel phase Ba7In5.9Zn0.1Al2O18.95 with hexagonal perovskite structure was obtained by solid-state technique. The substitution of In3+ by the Zn2+leads to the expansion of the lattice parameters and cell volume. It was established that the investigated sample is capable of water incorporation from the gas phase; the degree of hydration reaches 1.42 mol H2O, which is significantly higher than that for the undoped phase (0.41 mol H2O). This is a result of the expansion of the hexagonal layer that facilitates the placement of OH–-groups. The oxide-ion and proton conductivities for the doped Ba7In5.9Zn0.1Al2O18.95 sample were higher than those for the undoped composition, Ba7In6Al2O19, by 0.50 and 0.75 orders of magnitude (500 °C), respectively. The new phase Ba7In5.9Zn0.1Al2O18.95 demonstrates the predominant protonic conductivity at Т ≤ 500 °C and pH2O = 1.93·10−2 atm. | en |
dc.description.sponsorship | This work was supported by the Russian Science Foundation and Government of the Sverdlovsk region (grant № 24-13-20026), https://rscf.ru/project/24-13-20026/. | en |
dc.format.mimetype | application/pdf | en |
dc.language.iso | en | en |
dc.publisher | Уральский федеральный университет | ru |
dc.publisher | Ural Federal University | en |
dc.relation.ispartof | Chimica Techno Acta. 2024. Vol. 11. № 4 | en |
dc.subject | HEXAGONAL PEROVSKITE | en |
dc.subject | PROTON CONDUCTIVITY | en |
dc.subject | HYDRATION | en |
dc.subject | TRANSPORT NUMBERS | en |
dc.title | The Novel Zn-Doped Hexagonal Perovskite Ba7In6Al2O19: Electrical Conductivity and Hydration | en |
dc.type | Article | en |
dc.type | info:eu-repo/semantics/article | en |
dc.type | info:eu-repo/semantics/publishedVersion | en |
dc.identifier.rsi | https://elibrary.ru/item.asp?id=79161823 | - |
dc.identifier.doi | 10.15826/chimtech.2024.11.4.03 | - |
local.contributor.employee | Animitsa I. E. | en |
local.contributor.employee | Korona D V. | en |
local.contributor.employee | Bushueva A. V. | en |
local.contributor.employee | Andreev R. D. | en |
local.contributor.employee | Nokhrin S. S. | en |
local.contributor.employee | Анимица, Ирина Евгеньевна | ru |
local.contributor.employee | Корона, Даниил Валентинович | ru |
local.contributor.employee | Бушуева, Арина Викторовна | ru |
local.contributor.employee | Андреев, Роман Дмитриевич | ru |
local.contributor.employee | Нохрин, Сергей Семенович | ru |
local.description.order | 202411403 | - |
local.fund.rsf | 24-13-20026 | - |
Располагается в коллекциях: | Chimica Techno Acta |
Файлы этого ресурса:
Файл | Описание | Размер | Формат | |
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cta-2024-4-03.pdf | 710,93 kB | Adobe PDF | Просмотреть/Открыть |
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