Oxygen reduction sites and diffusion paths at La0.9Sr0.1MnO3-x/yttria-stabilized zirconia interface for different cathodic overvoltages by secondary-ion mass spectrometry
T. Horita et al., Oxygen reduction sites and diffusion paths at La0.9Sr0.1MnO3-x/yttria-stabilized zirconia interface for different cathodic overvoltages by secondary-ion mass spectrometry, SOL ST ION, 127(1-2), 2000, pp. 55-65
Oxygen reduction active sites were investigated at the interface of O-2/La-
0.9,Sr-0.1,MnO3-x (LSM)/yttria-stabilized zirconia (YSZ) for three differen
t overvoltages of cathodic polarization (n = - 0.336 V, n = - 0.185 V, and
n = - 0.090 V versus reference electrode). Isotopic oxygen (O-16/O-18) exch
ange under cathodic polarization and secondary ion mass spectrometry (SIMS)
technique were examined to visualize the oxygen incorporation/reduction ac
tive sites. The LSM mesh pattern electrode was prepared to define the area
and length of contact between LSM mesh and YSZ. Under cathodic polarization
of n = - 0.336 V, oxide ions can diffuse through the LSM to take part in t
he electrode reaction. From the SIMS images of YSZ surface, the active site
s for oxygen reduction/incorporation are distributed in spots at the positi
on where the LSM mesh was attached. Especially, O-2/LSM/YSZ three phase bou
ndary (TPB) is the main active site for oxygen incorporation/ reduction, al
though some spots of high O-18 concentration were observed at the center of
the LSM mesh part. Under the lower polarization (n = - 0.185 V, and n = -
0.090 V), oxide ions did not diffuse through the LSM mesh. SIMS imaging ana
lysis of YSZ surface showed high O-18 concentration spots around the center
of the LSM mesh part. The distribution of ionic currents at the surface of
YSZ affects the distribution of active sites for oxygen incorporation. (C)
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