Page 173 - High Temperature Solid Oxide Fuel Cells Fundamentals, Design and Applications
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150  High Temperature Solid Oxide Fuel Cells: Fundamentals,  Design and Applications

           6.2  Requirements for an Anode

           The role of an anode in a solid oxide fuel cell is to provide the sites for the fuel gas
           to react with the oxide ions delivered by the electrolyte, within a structure which
           also facilitates the necessary charge neutralisation by its electronic conductivity.
           These functional considerations together with the operating environment of the
           anode  are the  key  factors  in the materials  selection  for  the  anode.  It  must
           evidently be refractory, given the high cell operating temperature to be sustained
           over a commercially useful lifetime, and be compliant with thermal cycling to
           ambient  temperature.  In  addition,  the  equilibrium  between  fuel  gas  and
           oxidation products within the anode compartment results in an oxygen partial
           pressure  which  is  very  low,  but  variable  over  several  orders  of  magnitude
           depending  on  the  precise  reactant  and  product  conditions.  Chemical  and
           physical  stability  despite  such  variations  is  essential  since  certain  metallic
           components of the anode could suffer corrosion by fuel oxidation products, while
           electrical properties and lattice geometry of oxide components of the anode could
           change by variation of stoichiometry.
             For simplicity and reliability of operation, including start-up and shut-down as
           well as tolerance of transients, redox stability is a further desirable attribute of an
           anode material to permit brief excursions to high oxygen concentrations, even to
           air,  without  irreversible  loss  of  structural  coherence  and  electrochemical
           functionality. Stability implies the maintenance  of  structural integrity  of  the
           anode  itself  over  the whole  temperature range  to  which  it  is  exposed, from
           the  fabrication  temperature  through  normal  operating  conditions,  to  the
           repeated cycling down to ambient temperature.
             Throughout these ranges of temperature and gas environment there should
           also be maintained the necessary  compatibility with the other materials with
           which the anode comes into contact, specifically the electrolyte, the interconnect
           and  any  relevant  structural  components.  Physical  compatibility  requires  a
           match of  thermomechanical  properties such as thermal expansion  coefficient
           and  an  absence  of  phase-change  effects  which  could  generate  stresses
           during temperature variations. For chemical compatibility there should be no
           solid-state  contact  reaction,  interdiffusion of  constituent  elements  of  those
           materials or formation of reaction product layers which would increase resistive
           losses or otherwise interfere with anode functionality, despite the extremes of
           temperature. After assembly into a series connected stack, of  course the same
           applies to the anode-interconnect  interface. Compatibility must extend also to
           the behaviour of the material towards the ambient gases including corrosion or
           poisoning by trace impurities such as sulphur.
             Obviously the  anode  material  should  not  only  be  an adequate electronic
           conductor, but also electrocatalytically active such that a rapid charge exchange
           can be  established. Resistive and overpotential losses are thereby minimised.
           However, the catalytic behaviour of  anode materials should not extend to the
           promotion  of  unwanted  side  reactions,  hydrocarbon  pyrolysis  followed  by
           deposition of carbon being an example. The electrochemical reaction takes place
           in the region (Figure 6.1) where oxygen ions available from the electrolyte can
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