Crystal growth and structure of a high temperature polymorph of Sr2TiO4 with tetrahedral Ti-coordination, and transition to the Ruddlesden-Popper tetragonal phase
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388980%3A_____%2F22%3A00557344" target="_blank" >RIV/61388980:_____/22:00557344 - isvavai.cz</a>
Výsledek na webu
<a href="http://hdl.handle.net/11104/0331605" target="_blank" >http://hdl.handle.net/11104/0331605</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1039/d2ce00366j" target="_blank" >10.1039/d2ce00366j</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Crystal growth and structure of a high temperature polymorph of Sr2TiO4 with tetrahedral Ti-coordination, and transition to the Ruddlesden-Popper tetragonal phase
Popis výsledku v původním jazyce
Single crystals of transition metal oxides forming the Ruddlesden-Popper series are necessary for complete studies of their often exciting physical properties. In the strontium titanate family, crystal growth of all compounds apart from SrTiO3 has been elusive so far. We have successfully grown crystals of the high-temperature polymorph of Sr2TiO4, by using a floating-zone melt growth followed by a rapid cooling procedure. We report the crystal structure of the new modification, which is isostructural to the orthorhombic Sr2VO4 and Sr2CrO4. This structure hosts an uncommon layered sub-lattice of TiO4 tetrahedra and transforms into the tetragonal low-temperature polymorph via a complex reconstructive transition. The transformation mechanism between the two phases was studied and explains the reasons for the unsuccessful growth of tetragonal Sr2TiO4. The orthorhombic Sr2TiO4 is an insulator, with a band gap of 3.9 eV. It has a large (approximate to 40) dielectric constant, but despite its polar structure does not show any signatures of a ferroelectric order.
Název v anglickém jazyce
Crystal growth and structure of a high temperature polymorph of Sr2TiO4 with tetrahedral Ti-coordination, and transition to the Ruddlesden-Popper tetragonal phase
Popis výsledku anglicky
Single crystals of transition metal oxides forming the Ruddlesden-Popper series are necessary for complete studies of their often exciting physical properties. In the strontium titanate family, crystal growth of all compounds apart from SrTiO3 has been elusive so far. We have successfully grown crystals of the high-temperature polymorph of Sr2TiO4, by using a floating-zone melt growth followed by a rapid cooling procedure. We report the crystal structure of the new modification, which is isostructural to the orthorhombic Sr2VO4 and Sr2CrO4. This structure hosts an uncommon layered sub-lattice of TiO4 tetrahedra and transforms into the tetragonal low-temperature polymorph via a complex reconstructive transition. The transformation mechanism between the two phases was studied and explains the reasons for the unsuccessful growth of tetragonal Sr2TiO4. The orthorhombic Sr2TiO4 is an insulator, with a band gap of 3.9 eV. It has a large (approximate to 40) dielectric constant, but despite its polar structure does not show any signatures of a ferroelectric order.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10402 - Inorganic and nuclear chemistry
Návaznosti výsledku
Projekt
<a href="/cs/project/LM2018124" target="_blank" >LM2018124: Nanomateriály a nanotechnologie pro ochranu životního prostředí a udržitelnou budoucnost</a><br>
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2022
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
CrystEngComm
ISSN
1466-8033
e-ISSN
—
Svazek periodika
24
Číslo periodika v rámci svazku
20
Stát vydavatele periodika
GB - Spojené království Velké Británie a Severního Irska
Počet stran výsledku
10
Strana od-do
3731-3740
Kód UT WoS článku
000790698200001
EID výsledku v databázi Scopus
2-s2.0-85131395906