Photoemission electron microscopy (PEEM) is a well known technique whi
ch was developed along with early electron microscopes. A new version
of this microscope has recently been developed which is compatible wit
h ultrahigh vacuum (UHV) conditions and allows real-time observation o
f the surface work function with a working resolution of 1 mum. The co
ntrast mechanism of this microscope is based on local differences in e
lectronic work function. The adsorption of reactants in many cases lea
ds to a work function change in the surface. During the catalytic oxid
ation of CO on platinum-group metals at oxygen pressures above 10(-5)
Torr, the formation of CO, oxygen and mixed reactive islands can be ob
served. In this study, the reaction kinetics were followed along with
the formation of different reactive structures. The transition from on
e reactive phase to another occurred via island formation and reactive
fronts. The nucleation occurred at a countable number of extended def
ects (several mum in diameter) which had their own characteristic dyna
mics. The growth process of islands on Pt(111) were followed by PEEM a
nd were related to the macroscopic reaction rate measurements of bista
bility. The PEEM measurements showed clearly that there was a range of
parameters where the reaction exhibits bistability and this correspon
ded to the pressure region determined from macroscopic experiments. Fo
r oscillating conditions the extended defects acted as pacemakers for
the formation of target patterns and spirals.