Investigating the spatial distribution of plasma species using cavity ringdown spectroscopy and simulations
ORAL
Abstract
Advances in semiconductor etching depend on reliable plasma modelling and quantitative knowledge of near-surface behaviour of key reactive species. In this research, cavity ring down spectroscopy is utilised to determine number densities and gas temperatures of key species in technologically relevant low pressure ICPs of pure N2, O2 and Ar. Examples include N2+(X) and N2(A), O(3P) and O-, and Ar+(4P) and Ar metastable and radiative states. Studies on all three gases are extended into the plasma-surface boundary layers to quantify absolute number densities as a function of height above a non-driven electrode. A clear decrease in absolute ion density is observed as the electrode is approached for N2+ and O-. A more gradual decrease is observed for the N2(A) metastable species. In contrast, a modest increase is observed for O(3P). Lifetimes obtained for the neutral N2(A) and O(3P) species in the plasma bulk are contrasted with near-surface lifetimes at a series of pressures. The rotational and vibrational temperatures of N2(A) have also been investigated through a broadband cavity enhanced spectroscopic study at a series of pressures and powers, including within the capacitive regime. 2D-axisymmetric simulations are performed for N2, O2 and Ar, and compared with data in order to enhance reactive chemistry sets and refine simulation parameters.
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Publication:Quantification of N2+ ions in an inductively coupled plasma using Saturated Cavity Ringdown Spectroscopy (in progress)
Spatially resolved sat-CRDS studies on reactive nitrogen species in an inductively coupled plasma (in progress)
Spatially resolved spectroscopic studies on reactive oxygen species in an inductively coupled plasma paired with simulation (in progress)
Presenters
Charlie Kniebe-Evans
Department of Physical & Theoretical Chemistry, University of Oxford
Authors
Charlie Kniebe-Evans
Department of Physical & Theoretical Chemistry, University of Oxford
Nicholas O'Keeffe
Department of Physical & Theoretical Chemistry, University of Oxford
Samuel Rogers
Department of Physical & Theoretical Chemistry, University of Oxford
Gus Hancock
Department of Physical & Theoretical Chemistry, University of Oxford
Robert Peverall
Department of Physical & Theoretical Chemistry, University of Oxford
Grant Ritchie
Department of Physical & Theoretical Chemistry, University of Oxford