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Effects of Plume Hydrodynamics and Oxidation on the Composition of a Condensing Laser-Induced Plasma
Author(s) -
David G. Weisz,
Jonathan C. Crowhurst,
Mikhail Finko,
Timothy P. Rose,
Batikan Köroğlu,
R. Trappitsch,
Harry B. Radousky,
W. J. Siekhaus,
Michael R. Armstrong,
Brett H. Isselhardt,
Magdi Azer,
Davide Curreli
Publication year - 2018
Publication title -
the journal of physical chemistry a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.756
H-Index - 235
eISSN - 1520-5215
pISSN - 1089-5639
DOI - 10.1021/acs.jpca.7b11994
Subject(s) - plume , laser ablation , ablation , condensation , plasma , chemistry , analytical chemistry (journal) , laser , chemical physics , materials science , optics , environmental chemistry , thermodynamics , physics , engineering , quantum mechanics , aerospace engineering
High-temperature chemistry in laser ablation plumes leads to vapor-phase speciation, which can induce chemical fractionation during condensation. Using emission spectroscopy acquired after ablation of a SrZrO 3 arget, we have experimentally observed the formation of multiple molecular species (ZrO and SrO) as a function of time as the laser ablation plume evolves. Although the stable oxides SrO and ZrO 2 are both refractory, we observed emission from the ZrO intermediate at earlier times than SrO. We deduced the time-scale of oxygen entrainment into the laser ablation plume using an 18 O 2 environment by observing the in-growth of Zr 18 O in the emission spectra relative to Zr 16 O, which was formed by reaction of Zr with 16 O from the target itself. Using temporally resolved plume-imaging, we determined that ZrO formed more readily at early times, volumetrically in the plume, while SrO formed later in time, around the periphery. Using a simple temperature-dependent reaction model, we have illustrated that the formation sequence of these oxides subsequent to ablation is predictable to first order.

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