The laser ablation of chrysene-d(12) has been investigated by laser desorpt
ion/post-ionization time-of-flight mass spectrometry (L2ToFMS). The early s
tages of plume expansion were probed by locating the focus of the post-ioni
zation laser to within 50 mu m of the surface. A spatial and temporal study
of the desorption plume was carried out by recording positive ion time-of-
flight mass spectra as a function of delay time and position. When the ioni
zation laser focus was moved to-within 50 mu m of the surface the appearanc
e of the chrysene-d(12) parent ion signals changed from being sharply defin
ed with a mass resolution of similar to 700 to broad signals of reduced int
ensity and a significantly lower resolution. Furthermore, the broad ionizat
ion signals were observed at longer delay times on increasing the desorptio
n-laser power. We attribute the observed phenomena to the laser desorption
of molecular clusters, their transient survival, and ultimate evaporation t
o discrete molecules.