4.6 Article

Spatially and temporally resolved atomic oxygen densities in a micro cavity plasma array

Journal

PLASMA SOURCES SCIENCE & TECHNOLOGY
Volume 32, Issue 2, Pages -

Publisher

IOP Publishing Ltd
DOI: 10.1088/1361-6595/acb9b9

Keywords

atmospheric pressure plasma; micro plasma; dielectric barrier discharge; micro cavity plasma array; optical emission spectroscopy; helium state enhanced actinometry; atomic oxygen density

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Micro cavity plasma arrays have various applications, including treatment of volatile organic compounds and generation of new species. The focus has shifted to plasma catalysis, where catalytic surfaces are combined with plasmas. The key is generating reactive species like atomic oxygen within the plasma, typically measured using laser spectroscopic methods. In the case of micro plasma arrays, limited optical access led to the use of optical emission spectroscopy and helium state enhanced actinometry.
Micro cavity plasma arrays have numerous applications, such as the treatment of volatile organic compounds or the generation of new species. In recent years, the focus has also shifted to plasma catalysis, in which catalytic surfaces are combined with plasmas. The key to all of these applications is the generation of reactive species such as atomic oxygen within the plasma. Typically, atomic oxygen densities can be measured by laser spectroscopic methods. In the case of a micro plasma array, which consists of thousands of cavities with a diameter between 50 and 200 mu m, optical access is limited. For this reason, an optical emission spectroscopy approach, helium state enhanced actinometry, is used. 2D resolved narrow bandwidth measurements are performed by using an ICCD camera in combination with a tunable bandpass filter (550-1000 nm). The discharge is operated in helium with an oxygen admixture of 0.1%. An argon admixture of 0.05% is used as actinometer gas. The triangular excitation voltage is varied between amplitudes of 400 and 800 V at a frequency of 15 kHz. Very high dissociation degrees up to nearly complete dissociation are observed. Time resolved measurements show significant differences in oxygen density between the increasing and the decreasing potential phase.

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