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Symmetry control of cation substitution in ‘antizeolite’ borates. / Rashchenko, Sergey V.; Davydov, Alexey; Sagatov, Nursultan E. и др.

в: Materials Research Bulletin, Том 167, 112398, 11.2023.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

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Rashchenko SV, Davydov A, Sagatov NE, Podborodnikov IV, Arkhipov SG, Romanenko AV и др. Symmetry control of cation substitution in ‘antizeolite’ borates. Materials Research Bulletin. 2023 нояб.;167:112398. doi: 10.1016/j.materresbull.2023.112398

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BibTeX

@article{b483f89b1e4b460fb768c764395f8fa7,
title = "Symmetry control of cation substitution in {\textquoteleft}antizeolite{\textquoteright} borates",
abstract = "{\textquoteleft}Antizeolite{\textquoteright} borates are a family of inorganic compounds with structure based on fixed (pseudo)tetragonal [Ba12(BO3)6]6+ sublattice, and various anionic clusters occupying {\textquoteleft}channels{\textquoteright} in the sublattice. An ability to host different anionic clusters provides a convenient way to tune such functional properties of materials based of {\textquoteleft}antizeolite{\textquoteright} borates as dichroism, luminescence etc. We demonstrated the dependence of extent of Sr2+→Ba2+ substitution in the cationic sublattice of antizeolite barium borates on the symmetry of initial compound. The latter is controlled by {\textquoteleft}guest{\textquoteright} anionic clusters in the channels of sublattice. In the case of initially orthorhombic [Ba12-xSrx(BO3)6](BO3)2 solid solution, the structure adapts to the increase in Sr2+ content (up to Sr/(Ba+Sr) ratio of at least 39 wt. %) by tetragonalization of the sublattice. In contrast, in tetragonal [(Ba1-xSrx)12(BO3)6](BO3)[LiF4] solid solution another structural mechanism of Sr2+ accommodation takes place, which results in the (2a,2c) modulation and is limited by maximum Sr/(Ba+Sr) ratio of 10-20 wt. %.",
keywords = "Antizeolite borates, Cation substitution, Modulation",
author = "Rashchenko, {Sergey V.} and Alexey Davydov and Sagatov, {Nursultan E.} and Podborodnikov, {Ivan V.} and Arkhipov, {Sergey G.} and Romanenko, {Alexandr V.} and Bekker, {Tatyana B.}",
note = "Acknowledgments: This work was supported by the Russian Science Foundation, grant № 21-19-00097, https://www.rscf.ru/project/21-19-00097/. The SEM and EDS studies were performed in the Analytical Center for Multi-element and Isotope Research SB RAS. The XRD study was done using the equipment of Research and Education Centre “Molecular Design and Ecologically Safe Technologies” at Novosibirsk State University.",
year = "2023",
month = nov,
doi = "10.1016/j.materresbull.2023.112398",
language = "English",
volume = "167",
journal = "Materials Research Bulletin",
issn = "0025-5408",
publisher = "Elsevier Ltd",

}

RIS

TY - JOUR

T1 - Symmetry control of cation substitution in ‘antizeolite’ borates

AU - Rashchenko, Sergey V.

AU - Davydov, Alexey

AU - Sagatov, Nursultan E.

AU - Podborodnikov, Ivan V.

AU - Arkhipov, Sergey G.

AU - Romanenko, Alexandr V.

AU - Bekker, Tatyana B.

N1 - Acknowledgments: This work was supported by the Russian Science Foundation, grant № 21-19-00097, https://www.rscf.ru/project/21-19-00097/. The SEM and EDS studies were performed in the Analytical Center for Multi-element and Isotope Research SB RAS. The XRD study was done using the equipment of Research and Education Centre “Molecular Design and Ecologically Safe Technologies” at Novosibirsk State University.

PY - 2023/11

Y1 - 2023/11

N2 - ‘Antizeolite’ borates are a family of inorganic compounds with structure based on fixed (pseudo)tetragonal [Ba12(BO3)6]6+ sublattice, and various anionic clusters occupying ‘channels’ in the sublattice. An ability to host different anionic clusters provides a convenient way to tune such functional properties of materials based of ‘antizeolite’ borates as dichroism, luminescence etc. We demonstrated the dependence of extent of Sr2+→Ba2+ substitution in the cationic sublattice of antizeolite barium borates on the symmetry of initial compound. The latter is controlled by ‘guest’ anionic clusters in the channels of sublattice. In the case of initially orthorhombic [Ba12-xSrx(BO3)6](BO3)2 solid solution, the structure adapts to the increase in Sr2+ content (up to Sr/(Ba+Sr) ratio of at least 39 wt. %) by tetragonalization of the sublattice. In contrast, in tetragonal [(Ba1-xSrx)12(BO3)6](BO3)[LiF4] solid solution another structural mechanism of Sr2+ accommodation takes place, which results in the (2a,2c) modulation and is limited by maximum Sr/(Ba+Sr) ratio of 10-20 wt. %.

AB - ‘Antizeolite’ borates are a family of inorganic compounds with structure based on fixed (pseudo)tetragonal [Ba12(BO3)6]6+ sublattice, and various anionic clusters occupying ‘channels’ in the sublattice. An ability to host different anionic clusters provides a convenient way to tune such functional properties of materials based of ‘antizeolite’ borates as dichroism, luminescence etc. We demonstrated the dependence of extent of Sr2+→Ba2+ substitution in the cationic sublattice of antizeolite barium borates on the symmetry of initial compound. The latter is controlled by ‘guest’ anionic clusters in the channels of sublattice. In the case of initially orthorhombic [Ba12-xSrx(BO3)6](BO3)2 solid solution, the structure adapts to the increase in Sr2+ content (up to Sr/(Ba+Sr) ratio of at least 39 wt. %) by tetragonalization of the sublattice. In contrast, in tetragonal [(Ba1-xSrx)12(BO3)6](BO3)[LiF4] solid solution another structural mechanism of Sr2+ accommodation takes place, which results in the (2a,2c) modulation and is limited by maximum Sr/(Ba+Sr) ratio of 10-20 wt. %.

KW - Antizeolite borates

KW - Cation substitution

KW - Modulation

UR - https://www.scopus.com/record/display.uri?eid=2-s2.0-85162085834&origin=inward&txGid=bcced48342704efafb5099b231da1316

UR - https://www.mendeley.com/catalogue/ba25276a-6125-3c60-8489-fcf5520b9801/

U2 - 10.1016/j.materresbull.2023.112398

DO - 10.1016/j.materresbull.2023.112398

M3 - Article

VL - 167

JO - Materials Research Bulletin

JF - Materials Research Bulletin

SN - 0025-5408

M1 - 112398

ER -

ID: 53935837