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Ch. Urban1, S. Janson1, U. Ponkratz1,2, O. Kasdorf1, K. Rupprecht1, G. Wortmann1, T. Berthier3, W. Paulus3
1 Universität Paderborn, Department Physik, 33095 Paderborn, GERMANY2 ESRF, 6 rue Jules Horowitz, 38043 Grenoble, FRANCE3 Universitè Rennes, LCSIM, UMR 6511, F-35042 Rennes, FRANCE
Lattice dynamics of SrFeO2.5 studied by 57Fe-ME and 57Fe-NIS
SrFeO2.5
Crystallizes in tetragonal Brownmillerite structure withtwo different iron sites: FeO4 tetrahedrons and FeO6 octahedrons
With ratio FeT : FeO = 1 : 1
The FeO4 tetrahedrons are forming plains containing1D channels of oxygen vacancies. Structural disorder in these plains and chains is attributed to the high oxygenmobility [1, 2].
3. Nuclear Inelastic Scattering (NIS) of Synchrotron Radiation
g(E)
Soft Mode at 7 meVattributed to collective motion of the FeO4-tetrahedrons.
Strong deviations from Deye-like behaviour, i.e. g(E) is not proportional to E2 strong broadening of spectral features with increasing temperature seemingly connected with increasing disorder.
Strong difference between Debye temperatures determined by the initial slop of the phonon DOS (low temperature Debye temperature; D,LT = 250 K) and by integrating the whole phonon DOS (high temperature Debye temperature; D,HT = 425 K)
NIS experiments were carried out at beamline ID18 at ESRF (Grenoble) with an energy resolution of 3 meV. Data were recorded for various temperatures between 15 K and 500 K (see Fig. 2).The derived partial phonon density-of-states (DOS) at the Fe sites are shown in Fig. 3. The spectral features of the DOS at 300 K as well as the derived parameters agree well with Ref. [3].
4. Mössbauer Spectroscopy
Attribution of thesubspectra:
Mössbauer absorption spectroscopy was carried out at Paderborn UniversityAbsorption spectra were recorded for various temperatures between 4 K and 935 K, the magnetic ordering temperature is TN = 705 K. 3+
TFe 3+OFe
Isomer shift as function of temperature
D3 θ /T 3
Bc D y
D 0
9 k T yS = S θ +8T dy
18 Mc θ e -1
S(FeO) > S(FeT)
Larger covalency of the FeT
3+ - oxygen bonding
Calculation of the Debye temperatures by:
D Tθ (Fe ) = 469 K
D Oθ (Fe ) = 362 K
The average of the Debye temperature for both Fe sites, D(FeO+FeT) = 416 K) agrees very well with the high temperature Debye temperature D,HT calculated from the Fe partial phonon DOS.
2. Crystal Structure 1. Introduction / Aims SrFeO2.5+x
Different physical and chemical properties in dependence of oxygen content (x = 0 to 0.5).Ordering of oxygen dislocationspressure and temperature induced phase transitionsOxygen diffusion already at room temperature with possible technical application, e.g. for fuel cells.Here we study the lattice dynamics at the 57Fe sites by nuclearInelastic scattering (NIS) of synchrotron radiation and, complementary, by 57Fe-Mössbauer effect (ME).
Fig.1: (left) Crystal structure of SrFeO2.5
Fig.2: 57Fe-NIS spectra of SrFeO2.5 at various temperatures.
Fig.4: Debye temperatures of SrFeO2.5
Fig.3: Partial phonon DOS of SrFeO2.5 at various temperatures.
Fig.5: 57Fe-Mössbauerspectra of SrFeO2.5 at various temperatures.
Fig.6: Temperature dependence of the isomer shifts of the different Fe sites.
• Additional structures above 700 K can be attributed to oxygen vacancies and formation of metallic iron.• Detailed analysis of combined magnetic dipol / electric quadrupole interaction reveals tilting angels of Vzz with O = 82.5° and T = 77.7° with respect to the magnetic hyperfine field.
5. ConclusionCombined study by NIS and ME on SrFeO2.5 delivers a detailed picture of the lattice dynamics, where ME provides a site selective analysis.From similar NIS [2] and ME studies [4, 5] of CaFeO2.5, which has also the Brownmillerite structure, but without disorder of thetetrahedral sites and without a high oxygen mobility, and which does not show the soft mode peak at 7 meV [2], we attribute the high oxygen mobility in SrFeO2.5 to collective motions of the FeO4 tetrahedrons reflected by the soft mode at 7 meV.
[1] P. Bezdicka et al., Z. anorg. allg. Chem. 619, 1 (1993); F. Girgsdies, R. Schöllhorn, Solid State Commun. 91, 111 (1994); R. Le Toquin et al., (University of Rennes), unpublished[2] A.I. Rykov et al., Physica B 350, 287 (2004)[3] W. Sturhahn and A.I. Chumakov, Hyp. Interact. 123/13234, 809 (1999)[4] Ch. Urban, Diploma thesis (Paderborn 2005)[5] O. Kasdorf, Bachelor thesis (Paderborn 2005)
References