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   <subfield code="a">Oxygen incorporation in porous thin films of strontium doped lanthanum ferrite</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Martin Søgaard, Anja Bieberle-Hütter, Peter Hendriksen, Mogens Mogensen, Harry Tuller]</subfield>
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   <subfield code="a">Electrical conductivity relaxation measurements were carried out on thin films of (La0.6Sr0.4)0.99 FeO3 − δ deposited on MgO (100) substrates by pulsed laser deposition in order to determine the surface exchange coefficient, k Ex, of the oxygen incorporation process in the temperature range 550-700°C. The composition of the films was verified using wavelength dispersive x-ray and Rutherford backscattering spectroscopy. Scanning electron microscopy showed small triangular crystallites with the largest dimension 80 nm and the smallest dimension 10 nm. X-ray diffraction showed a cubic perovskite structure and significant texturing. At a constant temperature, k Exwas found to be a function only of the final $p_{\mathrm{O_{2}}}$ of the $p_{\mathrm{O_{2}}}$ -changes the sample was subjected to during conductivity relaxation experiments, confirming that the magnitude of the exchange coefficient was not influenced by changes in ionic defect concentrations. The k Ex-values determined for these thin films were significantly lower than for bulk samples. A value of 3.6 × 10 − 6 cm s − 1 was obtained at 702°C and a final $p_{\mathrm{O_{2}}}$ of 0.048 atm, approximately a factor of six lower than that obtained for bulk samples. An activation energy of 282 ± 20 kJ mol − 1 was found for the surface exchange coefficient at $p_{\mathrm{O_{2}}}$ = 0.048 atm. Possible reasons for the reduced magnitude of k Exare discussed including the role of thermal history in influencing surface morphology and chemistry.</subfield>
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   <subfield code="a">Thin film</subfield>
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   <subfield code="a">Conductivity relaxation</subfield>
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