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High-pressure stabilisation of R = Y member of R2CuTiO6 double perovskite series

Double perovskite oxides of the A2B’B″O6 type with Jahn-Teller active Cu2+ as the B′ constituent have gained considerable research interest in recent years. For fundamental studies, the rare earth element (R) based systems such as R2CuTiO6 form an intriguing research platform as they allow systemati...

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Published in:Journal of solid state chemistry 2023-01, Vol.317, p.123646, Article 123646
Main Authors: Sederholm, Linda, Tiittanen, Taneli, Karppinen, Maarit
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description Double perovskite oxides of the A2B’B″O6 type with Jahn-Teller active Cu2+ as the B′ constituent have gained considerable research interest in recent years. For fundamental studies, the rare earth element (R) based systems such as R2CuTiO6 form an intriguing research platform as they allow systematic chemical-pressure studies by simply controlling the size of the R constituent. However, for the R2CuTiO6 compounds conventional ambient-pressure high-temperature synthesis yields an orthorhombic (Pnma) double perovskite structure for the largest R constituents (La–Gd) only, while the compounds with the smaller R:s adopt a hexagonal structure. Here we demonstrate a hexagonal-to-perovskite structure conversion for the R ​= ​Y compound achieved through a high-pressure (HP) high-temperature treatment at 4 ​GPa and 1000 ​°C. Structural details of the thus stabilized new double perovskite phase of Y2CuTiO6 are addressed through a combined DFT simulation and Rietveld refinement study, revealing signs towards the rare layered-type ordering of the B-site (Cu and Ti) cations. Similar to the previously reported R2CuTiO6 perovskite phases with R ​= ​La, Pr, and Nd, the R ​= ​Y member is found paramagnetic throughout the measured temperature range of 5–300 ​K. From UV–vis absorption measurements the optical bandgap is estimated to be ca 3.4 ​eV. With high pressure treatment at 4 ​GPa and 1000 ​°C, hexagonal Y2CuTiO6 can be transformed into orthorhombic perovskite. This extends the known R2CuTiO6 (R ​= ​La–Gd) perovskite family to considerably smaller rare earth element (R) constituents and allows new properties to be discovered: here, partial layer-type B-site order which is rare for perovskites. [Display omitted] •Hexagonal Y2CuTiO6 is converted to orthorhombic perovskite via high pressure treatment.•This extends the R2CuTiO6 perovskite series (R ​= ​La–Gd) to the smaller Rs.•Combined Rietveld and DFT analysis points towards partial layer-type B-site order.•Magnetic measurement shows paramagnetic behaviour down to 5 ​K.•Strongly negative Weiss temperature indicates antiferromagnetic spin interactions.
doi_str_mv 10.1016/j.jssc.2022.123646
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For fundamental studies, the rare earth element (R) based systems such as R2CuTiO6 form an intriguing research platform as they allow systematic chemical-pressure studies by simply controlling the size of the R constituent. However, for the R2CuTiO6 compounds conventional ambient-pressure high-temperature synthesis yields an orthorhombic (Pnma) double perovskite structure for the largest R constituents (La–Gd) only, while the compounds with the smaller R:s adopt a hexagonal structure. Here we demonstrate a hexagonal-to-perovskite structure conversion for the R ​= ​Y compound achieved through a high-pressure (HP) high-temperature treatment at 4 ​GPa and 1000 ​°C. Structural details of the thus stabilized new double perovskite phase of Y2CuTiO6 are addressed through a combined DFT simulation and Rietveld refinement study, revealing signs towards the rare layered-type ordering of the B-site (Cu and Ti) cations. 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For fundamental studies, the rare earth element (R) based systems such as R2CuTiO6 form an intriguing research platform as they allow systematic chemical-pressure studies by simply controlling the size of the R constituent. However, for the R2CuTiO6 compounds conventional ambient-pressure high-temperature synthesis yields an orthorhombic (Pnma) double perovskite structure for the largest R constituents (La–Gd) only, while the compounds with the smaller R:s adopt a hexagonal structure. Here we demonstrate a hexagonal-to-perovskite structure conversion for the R ​= ​Y compound achieved through a high-pressure (HP) high-temperature treatment at 4 ​GPa and 1000 ​°C. Structural details of the thus stabilized new double perovskite phase of Y2CuTiO6 are addressed through a combined DFT simulation and Rietveld refinement study, revealing signs towards the rare layered-type ordering of the B-site (Cu and Ti) cations. Similar to the previously reported R2CuTiO6 perovskite phases with R ​= ​La, Pr, and Nd, the R ​= ​Y member is found paramagnetic throughout the measured temperature range of 5–300 ​K. From UV–vis absorption measurements the optical bandgap is estimated to be ca 3.4 ​eV. With high pressure treatment at 4 ​GPa and 1000 ​°C, hexagonal Y2CuTiO6 can be transformed into orthorhombic perovskite. This extends the known R2CuTiO6 (R ​= ​La–Gd) perovskite family to considerably smaller rare earth element (R) constituents and allows new properties to be discovered: here, partial layer-type B-site order which is rare for perovskites. [Display omitted] •Hexagonal Y2CuTiO6 is converted to orthorhombic perovskite via high pressure treatment.•This extends the R2CuTiO6 perovskite series (R ​= ​La–Gd) to the smaller Rs.•Combined Rietveld and DFT analysis points towards partial layer-type B-site order.•Magnetic measurement shows paramagnetic behaviour down to 5 ​K.•Strongly negative Weiss temperature indicates antiferromagnetic spin interactions.</abstract><pub>Elsevier Inc</pub><doi>10.1016/j.jssc.2022.123646</doi><orcidid>https://orcid.org/0000-0001-7209-0509</orcidid><oa>free_for_read</oa></addata></record>
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subjects Cation ordering
Chemical pressure
Double perovskite
High-pressure conversion
title High-pressure stabilisation of R = Y member of R2CuTiO6 double perovskite series
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