Analysis of gas-phase reactions during pulsed laser ablation using laser-induced fluorescence, absorption, and emission spectroscopy

2002 ◽  
Author(s):  
Joerg Hermann ◽  
Christophe Dutouquet
2003 ◽  
Vol 208-209 ◽  
pp. 101-106 ◽  
Author(s):  
A. Santagata ◽  
V. Marotta ◽  
S. Orlando ◽  
R. Teghil ◽  
M. Zaccagnino ◽  
...  

2002 ◽  
Vol 186 (1-4) ◽  
pp. 335-338 ◽  
Author(s):  
R. Teghil ◽  
L. D’Alessio ◽  
A. Santagata ◽  
M. Zaccagnino ◽  
D. Ferro

1983 ◽  
Vol 29 ◽  
Author(s):  
J. F. Osmundsen ◽  
C. C. Abele ◽  
J. G. Eden

ABSTRACTThe gas phase photochemistry of an LCVD reactor used to grow polycrystalline Ge films was studied by absorption and emission spectroscopy. Upon photodissociating GeH4 (5% in an Ar or He carrier) at 248 nm (KrF laser), excited states of Ge and GeH are produced. Spatially, spectrally and temporally resolved atomic and molecular emissions are monitored as a function of gas pressure and laser intensity. These data lead to the conclusion that GeH2 is predominantly produced directly from GeH4 by The simultaneous absorption of two 5 eV (λ = 248 nm) photons.


1996 ◽  
Vol 433 ◽  
Author(s):  
L. G. Coccia ◽  
G. C. Tyrrell ◽  
I. W. Boyd

AbstractA number of factors have been identified as affecting the gas phase oxidation of cations during pulsed laser ablation of lead zirconate titanate (PZT), by using energy dispersive mass spectrometry (EDMS). These phenomena are known to be critical to the deposition of high quality thin films of PZT. However, to isolate the role of each cation species and the influence of its gas phase properties, we have also looked beyond the ablation of the PZT ceramic. In this paper, we detail our observations during pulsed laser ablation of electroceramic and metallic targets, specifically PZT, Pb and Ti. We have observed the evolution and transport of molecular species during gas phase expansion over a wide range of oxygen pressures (10−7 - 10−1 mbar) and laser fluences (0.3 -10 Jcm−2). The yields of the molecular ion species are strongly dependent upon the number density of the background gas. We propose an interpretation of the relative yields of the species based upon their respective gas phase binding energies and their ease of formation based upon the reaction thermodynamics and reaction cross-section of each species.


1996 ◽  
Vol 11 (6) ◽  
pp. 1514-1519 ◽  
Author(s):  
R. Dat ◽  
O. Auciello ◽  
D. J. Lichtenwalner ◽  
A. I. Kingon

La0.5Sr0.5CoO3 (LSCO) thin films have been deposited on (100) MgO substrates using pulsed laser ablation-deposition (PLAD). The crystallographic orientation of LSCO was found to be dependent on the surface treatment of (100) MgO prior to deposition. PLAD deposition parameters were optimized to yield LSCO films with an RMS surface roughness of 40–50 Å. A smooth surface morphology was reproduced as long as the oxygen content of the LSCO target was preserved. Otherwise, “splashing” occurred which resulted in the transfer of condensed particles from molten spherical globules of LSCO from the target to the substrate. Splashing was subsequently eliminated and smooth surface quality was restored after annealing the LSCO target at 550 °C in oxygen for 3 h. Optical emission spectroscopy (OES) of the LSCO's plume identified excited atomic cobalt neutrals, excited singly ionized strontium and lanthanum, and excited molecular LaO species. Oxygen interaction with the plume produced no new species. Furthermore, the OES data suggest that the observed LaO molecules were not created by the chemical reaction between La and O2 during ablation, but were ejected directly from the target during the PLAD process.


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