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106  High Temperature SoZid Oxide Fuel Cells: Fundamentals, Design and Applications

         monotonically with increasing content of  Co. In particular, the OCV drop was
         significant for Co concentrations above 10 mol%. This was caused by the onset of
         hole  conduction.  But  power  density  increased  with  Co  concentration  and
         attained a maximum value at 8.5 mol% Co. This was explained by the improved
         ionic conductivity  of  the doped electrolyte. However, current leakage became
         dominant at higher Co levels. When the electrolyte thickness was reduced, the
         power density further increased and at 180 pm thickness the maximum power
         density was 1.58 W/cm2 at 800°C and 0.5 W/cm2 at 600°C. Larger cells of  150
         mm diameter using La~.~Sro.2Gao.sMgo.15C00.0~03 electrolyte have also been
         investigated recently 11921.



         4.7  Oxides with Other Structures



         4.7.1 Brownmillerites  (e.g. BazlnzOd
         Anther perovskite-related structure, which is interesting from the viewpoint of
         oxide ion conduction, is brownmillerite with a general formula of A2B’B1‘05 or
         A2B205. This structure can be viewed as  a perovskite with oxygen vacancies
         ordered along the  [loll direction in alternate layers. Such vacancy ordering
         results in an increased unit cell relative to the perovskite. In other words, Iattice
         parameters of the a and c axis of  the ideal brownmillerite oxide are larger than
         those of  the ideal perovskite oxide by 2 and the b axis of  brownmillerite is the
         same as that of  perovskite. In some cases the oxygen vacancies do not order,
         which results in a perovskite structure with a statistical distribution of  oxygen
         vacancies on the oxygen sites. Therefore, high oxide ion conductivity  is also
         expected in brownmillerites.
           Goodenough  et  al.  [93]  have  reported  the  high  oxide ion  conductivity  in
         several brownmillerite  oxides. A  listing  [94] is  given in  Table  4.5.  All  these
         brownmillerites exhibit oxide ion conductivity and the conductivities are rather


         Table 4.5  Oxide ion conductivity for selected brownmillerite compounds [94]
         Compound           T(g)   o(S/cm)     Compound         T(K)   o(s/cm)
         Ba21n205            973   5x10-3      Ba31n2Hf08       673    1.0~10-3
                            1223   1x10-I      Sr31n2Hf08       973    1x10-4
         BaZr03              973    1x10-6     Ba3SczZrOs       973    7x10-3
         BaZr0.5In0.~02.7~   973   1x10-2      Ba2GdIno.8Gao.205   873   5 x low3
         Ba3h2ZrOg           973   5~10-~  Ba2GdIno.6Gao,405    873    5 x
         Ba3In1.7Zrl ,308.15   973   5x10-2    Ca2Cr205         973    ~xIO-~
         Ba2In1.33Zr0.6705.33   973   1x10-3   Sr2ScAI05        973    1x10-5
         Ba21nl.7~Ceo.250j.125   973   9 x     Sr~Sc1.3A10.705   973   1x10-3
                            1223   6~10-~  Sr2S~A10.8Mg0.204.9   973   5 x
         BasIn2TiOs          973    7x10-4     Sr2SCA10.gZn0.204.9   973   2 x
         Ba31n2ZrOs          673   6.8  x      SrzSco.sYo.2A105   973   1x10-4
         Ba&&Og              673    1.5  x     Srl.8Bao,2ScA10j   973   1x10-4
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