Sodium intercalation into the n=2 Ruddlesden-Popper type host Y2Ti2O5S2: Synthesis, structure, and properties of alpha-NaxY2Ti2O5S2 (0 < x <= 1)
Sodium intercalation into the oxide slabs of the cation-deficient n = 2 Ruddlesden-Popper oxysulfide Y2Ti2O5S 2 to produce α-NaxY2Ti2O 5S2 (0 < x ≤ 1.0) is reported. These materials have been probed as a function of the amount of intercalated sodium using high-resolution neutron powder diffra...
| Main Authors: | , , , , , , |
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| Format: | Journal article |
| Language: | English |
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2003
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| _version_ | 1826288972018483200 |
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| author | Clarke, S Denis, S Rutt, O Hill, T Hayward, M Hyett, G Gal, Z |
| author_facet | Clarke, S Denis, S Rutt, O Hill, T Hayward, M Hyett, G Gal, Z |
| author_sort | Clarke, S |
| collection | OXFORD |
| description | Sodium intercalation into the oxide slabs of the cation-deficient n = 2 Ruddlesden-Popper oxysulfide Y2Ti2O5S 2 to produce α-NaxY2Ti2O 5S2 (0 < x ≤ 1.0) is reported. These materials have been probed as a function of the amount of intercalated sodium using high-resolution neutron powder diffraction. At all levels of sodium intercalation the tetragonal symmetry of the host is retained, for example: Na0.35(5)Y2Ti2O5S2, I4/mmm, a = 3.80171(2) Å, c = 22.6270(2) Å, Z = 2; Na 0.84(2)Y2Ti2O5S2, I4/mmm, a = 3.84429(6) Å, c = 22.5440(4) Å, Z = 2 at 298 K. The sodium ion occupies a site coordinated by twelve oxide ions which corresponds to the "A"-site in the perovskite-like oxide slabs of the structure. At levels of sodium intercalation up to the maximum α-Na1.0Y 2Ti2O5S2 the cell volume increases approximately linearly with x as electrons enter bands which are antibonding with respect to the Ti-O framework. The effects on the structural details of electrostatic repulsion between the yttrium and intercalated sodium ions is discussed, and these materials are compared with the analogous lithium intercalates. Magnetic susceptibility and electrical resistivity measurements are consistent with delocalization of the intercalated electrons especially for large x. The insertion of lithium into α-Na0.5Y 2Ti2O5S2 and of magnesium into Y2Ti2O5S2 are also reported. |
| first_indexed | 2024-03-07T02:21:48Z |
| format | Journal article |
| id | oxford-uuid:a42ef4c9-e60d-461a-a9df-641609762bc3 |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-07T02:21:48Z |
| publishDate | 2003 |
| record_format | dspace |
| spelling | oxford-uuid:a42ef4c9-e60d-461a-a9df-641609762bc32022-03-27T02:32:11ZSodium intercalation into the n=2 Ruddlesden-Popper type host Y2Ti2O5S2: Synthesis, structure, and properties of alpha-NaxY2Ti2O5S2 (0 < x <= 1)Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:a42ef4c9-e60d-461a-a9df-641609762bc3EnglishSymplectic Elements at Oxford2003Clarke, SDenis, SRutt, OHill, THayward, MHyett, GGal, ZSodium intercalation into the oxide slabs of the cation-deficient n = 2 Ruddlesden-Popper oxysulfide Y2Ti2O5S 2 to produce α-NaxY2Ti2O 5S2 (0 < x ≤ 1.0) is reported. These materials have been probed as a function of the amount of intercalated sodium using high-resolution neutron powder diffraction. At all levels of sodium intercalation the tetragonal symmetry of the host is retained, for example: Na0.35(5)Y2Ti2O5S2, I4/mmm, a = 3.80171(2) Å, c = 22.6270(2) Å, Z = 2; Na 0.84(2)Y2Ti2O5S2, I4/mmm, a = 3.84429(6) Å, c = 22.5440(4) Å, Z = 2 at 298 K. The sodium ion occupies a site coordinated by twelve oxide ions which corresponds to the "A"-site in the perovskite-like oxide slabs of the structure. At levels of sodium intercalation up to the maximum α-Na1.0Y 2Ti2O5S2 the cell volume increases approximately linearly with x as electrons enter bands which are antibonding with respect to the Ti-O framework. The effects on the structural details of electrostatic repulsion between the yttrium and intercalated sodium ions is discussed, and these materials are compared with the analogous lithium intercalates. Magnetic susceptibility and electrical resistivity measurements are consistent with delocalization of the intercalated electrons especially for large x. The insertion of lithium into α-Na0.5Y 2Ti2O5S2 and of magnesium into Y2Ti2O5S2 are also reported. |
| spellingShingle | Clarke, S Denis, S Rutt, O Hill, T Hayward, M Hyett, G Gal, Z Sodium intercalation into the n=2 Ruddlesden-Popper type host Y2Ti2O5S2: Synthesis, structure, and properties of alpha-NaxY2Ti2O5S2 (0 < x <= 1) |
| title | Sodium intercalation into the n=2 Ruddlesden-Popper type host Y2Ti2O5S2: Synthesis, structure, and properties of alpha-NaxY2Ti2O5S2 (0 < x <= 1) |
| title_full | Sodium intercalation into the n=2 Ruddlesden-Popper type host Y2Ti2O5S2: Synthesis, structure, and properties of alpha-NaxY2Ti2O5S2 (0 < x <= 1) |
| title_fullStr | Sodium intercalation into the n=2 Ruddlesden-Popper type host Y2Ti2O5S2: Synthesis, structure, and properties of alpha-NaxY2Ti2O5S2 (0 < x <= 1) |
| title_full_unstemmed | Sodium intercalation into the n=2 Ruddlesden-Popper type host Y2Ti2O5S2: Synthesis, structure, and properties of alpha-NaxY2Ti2O5S2 (0 < x <= 1) |
| title_short | Sodium intercalation into the n=2 Ruddlesden-Popper type host Y2Ti2O5S2: Synthesis, structure, and properties of alpha-NaxY2Ti2O5S2 (0 < x <= 1) |
| title_sort | sodium intercalation into the n 2 ruddlesden popper type host y2ti2o5s2 synthesis structure and properties of alpha naxy2ti2o5s2 0 lt x lt 1 |
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