Field Pulse Desorption Mass-Spectrometry is applied to investigate intermediates of surface reactions. The formation of metal-subcarbonyl compounds is studied at rhodium-and ruthenium field emitters. Electrostatic field effects, field-induced reactions and field fragmentation are measured. The decomposition of methanol on rhodium and ruthenium shows two temperature regimes. At lower temperatures chemisorbed CO hinders the catalytic decomposition. Above the CO-desorption temperatures the C-H-bond cleavage of surface methoxy groups is rate determining. With photon-pulses the field-induced polymerization of ethylene is studied. Adsorbed water -layers form cluster ions (H 2 O) z · H+ with 3 7 eV is needed for the formation of these cluster ions.A special version of the atom probe can be used to study dynamic processes on an atomic scale (1). In the field ion microscope section, a particular area of a tip emitter (=catalyst-)surface is selected. Depending on the tip radius, the tip to screen distance and the probe hole diameter, either single surface atoms or up to several hundred surface sites can be analyzed in the time-of-flight mass spectrometer. With its high detection sensitivity, this technique is able to identifying individual chemisorbed species at characterized crystallographic sites on low-or high-index single crystal surfaces.