| 1. |
- Chernov, S. V., et al.
(författare)
-
Sr2GaScO5, Sr10Ga6Sc4O25, and SrGa0,75Sc0,25O2,5: a Play in the Octahedra to Tetrahedra Ratio in Oxygen-Deficient Perovskites
- 2012
-
Ingår i: Inorganic Chemistry. - : American Chemical Society (ACS). - 0020-1669 .- 1520-510X. ; 51:2, s. 1094-1103
-
Tidskriftsartikel (refereegranskat)abstract
- Three different perovskite-related phases were isolated in the SrGa(1-x)Sc(x)O(2.5) system: Sr(2)GaScO(5), Sr(10)Ga(6)Sc(4)O(25), and SrGa(0.75)Sc(0.25)O(2.5), Sr(2)GaScO(5) (x = 0.5) crystallizes in a brownrnillerite-type structure [space group (S.G.) Icmm, a = 5.91048(5) angstrom, b = 15.1594(1) angstrom, and c = 5.70926(4) angstrom] with complete ordering of Sc(3+) and Ga(3+) over octahedral and tetrahedral positions, respectively. The crystal structure of Sr(10)Ga(6)Sc(4)O(25) (x = 0.4) was determined by the Monte Carlo method and refined using a combination of X-ray, neutron, and electron diffraction data [S.G. I4(1)/a, a = 17.517(1) angstrom, c = 32.830(3) angstrom]. It represents a novel type of ordering of the B cations and oxygen vacancies in perovskites. The crystal structure of Sr(10)Ga(6)Sc(4)O(25) can be described as a stacking of eight perovskite layers along the c axis ...[-(Sc/Ga)O(1.6)-SrO(0.8)-(Sc/Ga)O(1.8)-SrO(0.8)-](2 center dot center dot center dot) Similar to Sr(2)GaScO(5), this structure features a complete ordering of the Sc(3+) and Ga(3+) cations over octahedral and tetrahedral positions, respectively, within each layer. A specific feature of the crystal structure of Sr(10)Ga(6)Sc(4)O(25) is that one-third of the tetrahedra have one vertex not connected with other Sc/Ga cations. Further partial replacement of Sc(3+) by Ga(3+) leads to the formation of the cubic perovskite phase SrGa(0.75)Sc(0.25)O(2.5) (x = 0.25) with a = 3.9817(4) angstrom. This compound incorporates water molecules in the structure forming SrGa(0.75)Sc(0.25)O(2.5)center dot xH(2)O hydrate, which exhibits a proton conductivity of similar to 2.0 x 10(-6) S/cm at 673 K.
|
|
| 2. |
- Biendicho, Jordi Jacas, et al.
(författare)
-
Synthesis and characterization of perovskite-type SrxY1−xFeO3−δ (0.63≤x<1.0) and Sr0.75Y0.25Fe1−yMyO3−δ (M=Cr, Mn, Ni), (y=0.2, 0.33, 0.5)
- 2013
-
Ingår i: Journal of Solid State Chemistry. - : Elsevier BV. - 0022-4596 .- 1095-726X. ; 200, s. 30-38
-
Tidskriftsartikel (refereegranskat)abstract
- Oxygen-deficient ferrates with the cubic perovskite structure SrxY1-xFeO3-d were prepared in air (0.71 ≤ x ≤ 0.91) as well as in N2 (x=0.75 and 0.79) at 1573K. The oxygen content of the compounds prepared in air increases with increasing strontium content from 3-δ=2.79(2) for x=0.75 to 3-δ=2.83(2) for x=0.91. Refinement of the crystal structure of Sr0.75Y0.25FeO2.79 using TOF neutron powder diffraction (NPD) data shows high anisotropic atomic displacement parameter (ADP) for the oxygen atom resulting from a substantial cation and anion disorder. Electron diffraction (ED) and high-resolution electron microscopy (HREM) studies of Sr0.75Y0.25FeO2.79 reveal a modulation along <100>p with G± ~0.4<100>p indicating a local ordering of oxygen vacancies. Magnetic susceptibility measurements at 5-390K show spin-glass behaviour with dominating antiferromagnetic coupling between the magnetic moments of Fe cations. Among the studied compositions, Sr0.75Y0.25FeO2.79 shows the lowest thermal expansion coefficient (TEC) of 10.5 ppm K-1 in air at 298-673K. At 773-1173K TEC increases up to 17.2 ppm K-1 due to substantial reduction of oxygen content. The latter also results in a dramatic decrease of the electrical conductivity in air above 673K. Partial substitution of Fe by Cr, Mn and Ni according to the formula Sr0.75Y0.25Fe1-yMyO3-δ (y=0.2, 0.33, 0.5) leads to cubic perovskites for all substituents with y=0.2. Their TECs are higher in comparison with un-doped Sr0.75Y0.25FeO2.79. Only M=Ni has increased electrical conductivity compared to un-doped Sr0.75Y0.25FeO2.79.
|
|
| 3. |
|
|
| 4. |
|
|
| 5. |
- Gunawidjaja, Philips N., et al.
(författare)
-
Biomimetic Apatite Mineralization Mechanisms of Mesoporous Bioactive Glasses as Probed by Multinuclear ³¹P, ²⁹Si, ²³Na and ¹³C Solid State NMR
- 2010
-
Ingår i: The Journal of Physical Chemistry C. - : American Chemical Society (ACS). - 1932-7447 .- 1932-7455. ; 114:45, s. 19345-19356
-
Tidskriftsartikel (refereegranskat)abstract
- An array of magic-angle spinning (MAS) nuclear magnetic resonance (NMR) spectroscopy experiments is applied to explore the surface reactions of a mesoporous bioactive glass (MBG) of composition Ca0.10Si0.85P0.04O1.90 when subjected to a simulated body fluid (SBF) for variable intervals. Powder X-ray diffraction and 31P NMR techniques are employed to quantitatively monitor the formation of an initially amorphous calcium phosphate surface layer and its subsequent crystallization into hydroxycarbonate apatite (HCA). Prior to the onset of HCA formation, 1H → 29Si cross-polarization (CP) NMR evidence dissolution of calcium ions; a slightly increased connectivity of the speciation of silicate ions is observed at the MBG surface over 1 week of SBF exposure. The incorporation of carbonate and sodium ions into the bioactive orthophosphate surface layer is explored by 1H → 13C CPMAS and 23Na NMR, respectively. We discuss similarities and distinctions in composition−bioactivity relationships established for traditional melt-prepared bioglasses compared to MBGs. The high bioactivity of phosphorus-bearing MBGs is rationalized to stem from an acceleration of their surface reactions due to presence of amorphous calcium orthophosphate clusters of the MBG pore wall.
|
|
| 6. |
- Shafeie, Samrand, 1984-, et al.
(författare)
-
Phase formation, crystal structures and magnetic properties of perovskite-type phases in the system La2Co1+z(MgxTi1-x)1-zO6
- 2011
-
Ingår i: Journal of Solid State Chemistry. - : Elsevier BV. - 0022-4596 .- 1095-726X. ; 184:1, s. 177-190
-
Tidskriftsartikel (refereegranskat)abstract
- Perovskite-type cobaltates in the system La(2)Co(1+z) (Mg(x)Ti(1-x))(1-z)O(6) were studied for z=0 <= x <= 0.6 and 0 <= x <= 0.9, using X-ray and neutron powder diffraction, electron diffraction (ED), magnetic susceptibility measurements and X-ray absorption near-edge structure (XANES) spectroscopy. The samples were synthesised using the citrate route in air at 1350 degrees C. The space group symmetry of the structure changes from P2(1)/n via Pbnm to R (3) over barc with both increasing Mg content and increasing Co content. The La(2)Co(Mg(x)Ti(1-x))O(6) (z=0) compounds show anti-ferromagnetic couplings of the magnetic moments for the Co below 15 K for x=0, 0.1 and 0.2. XANES spectra show for the compositions 0 <= x <= 0.5 a linear decrease in the L(3)/(L(3)+ L(2))Co-L(2.3) edge branching ratio with x, in agreement with a decrease of the average Co ion spin-state, from a high-spin to a lower-spin-state, with decreasing nominal Co(2+) ion content.
|
|
| 7. |
- Svensson, Gunnar, 1960-, et al.
(författare)
-
Synthesis and characterisation of the novel double perovskites La2CrB2/3Nb1/3O6, B = Mg, Ni, Cu
- 2012
-
Ingår i: Materials Research Bulletin. - : Elsevier BV. - 0025-5408 .- 1873-4227. ; 47:9, s. 2449-2454
-
Tidskriftsartikel (refereegranskat)abstract
- The novel perovskites La2CrB2/3Nb1/3O6, B = Mg, Ni, and Cu have been synthesised at 1350 degrees C in air via the citrate route. Rietveld refinements using neutron powder diffraction (NPD) data showed that the compounds adopt the GdFeO3 type structure with space group Pbnm, and unit cell parameters a approximate to b approximate to root 2 x a(p) and c approximate to 2 x a(p), where a(p) approximate to 3.8 angstrom. Selected area electron diffraction (SAED) of B = Ni and Cu samples confirmed space group Pbnm. However, distinct reflections forbidden in Pbnm symmetry, but allowed in the monoclinic sub-group P2(1)/n and unit cell parameters a approximate to b approximate to root 2 x a(p) and c approximate to 2 x a(p), beta approximate to 90 degrees were present in SAED patterns of B = Mg sample. This indicates an ordering of the B-cations within the crystal structure of La2CrMg2/3Nb1/3O6. High-resolution electron microscopy (HREM) study indicating uniform, without formation of clusters, ordering of B-cations in the crystallites of La2CrMg2/3Nb1/3O6. Magnetic susceptibility measurements show that the compounds are antiferromagnetic (with some glass or spin clustering effects due to additional ferromagnetic interactions between the B-cations) with T-N for La2CrB2/3Nb1/3O6, B = Mg, Ni, Cu being 90, 125 and 140K, respectively.
|
|
| 8. |
|
|
