Nanocrystalline ceria is under study to i
mprove perfor
mance in high-te
mperature catalysis and fuelcells. We synthesize porous ceria
monolithic nanoarchitectures by reacting Ce(III) salts and epoxide-based proton scavengers. Varying the
means of pore-fluid re
moval yields nanoarchitectures with differentpore-solid structures: aerogels, a
mbigels, and xerogels. The dried ceria gels are initially X-ray a
morphous,high-surface-area
materials, with the aerogel exhibiting 225
m2 g
-1. Calcination produces nanocrystalline
materials that, although
moderately densified, still retain the desirable characteristics of high surfacearea, through-connected porosity in the
mesopore size range and nanoscale particle sizes (~10 n
m). Theelectrical properties of calcined ceria a
mbigels are evaluated fro
m 300 to 600
mages/entities/deg.gif">C and co
mpared to thoseof co
mmercially available nanoscale CeO
2. The pressed pellets of both ceria sa
mples exhibit co
mparablesurface areas and void volu
mes. The conductivity of the ceria a
mbigel is 5 ti
mes greater than theco
mmercial sa
mple and both
materials exhibit an increase in conductivity in argon relative to oxygen at600
mages/entities/deg.gif">C, suggesting an electronic contribution to conductivity at low oxygen partial pressures. The ceriaa
mbigel nanoarchitecture responds to changes in at
mosphere at 600
mages/entities/deg.gif">C faster than does the nanocrystalline,non-networked ceria. We attribute the higher relative conductivity of CeO
2 a
mbigels to the bondedpathways inherent to the bicontinuous pore-solid networks of these nanoarchitectures.