二氧化碳微波放电流出物中原子氧的空间分辨 TALIF 研究

Arne Meindl, Ante Hecimovic, U. Fantz
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摘要

本研究开发了一种用于一维空间分辨 TALIF 检测基态氧原子(2p4 3P2,1,0)的诊断装置。本研究的目的是研究氧原子的温度和绝对数量密度沿低压二氧化碳微波放电流出物的演变,以深入了解放电后机制的一些情况。等离子体源在 600 W-1200 W 的吸收功率条件下运行,纯 CO2 流量为 74 sccm 和 370 sccm,压力介于 1.2 mbar 和 5 mbar 之间,比能量输入高达 111.9 eV/分子。在这些操作条件下,二氧化碳的转化率很高(高达 90%),而能效却很低(2-7.4%),这是由于电子直接撞击解离推动了转化过程,导致二氧化碳分裂为一氧化碳和逸散氧原子。TALIF 测量得出的空间分辨率平移温度在 1000 K-1600 K 之间,适用于大多数运行条件和流出物的轴向位置。使用氙 6p′ [3/2]2 进行的参考测量用于绝对数量密度校准。所得到的基态原子氧的轴向分辨数密度曲线沿着流出物增加,甚至在距离活动排放口几厘米的相当大的距离上也是如此,然后根据条件的不同,在 5×1020 m-3 和 2.2×1021 m-3 之间达到最大值,之后便开始下降。这种行为表明,在所研究的二氧化碳放电过程中,在放电后状态下淬灭逸散氧原子可能具有重要意义。测量到的空间分辨数量密度演变与通过壁碰撞淬灭是主要失活机制的定性一致,强调了粒子与壁相互作用的重要性。
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Spatially resolved TALIF investigation of atomic oxygen in the effluent of a CO2 microwave discharge
A diagnostic setup for one-dimensionally spatially resolved TALIF detection of ground state oxygen atoms (2p4 3P2,1,0) is developed. The goal of this study is to investigate the evolution of temperatures and absolute number densities of oxygen atoms along the effluent of a low-pressure CO2 microwave discharge in order to gain insights into some of the mechanisms governing the post-discharge regime. The plasma source is operated at conditions of 600 W−1200 W of absorbed power with flow rates of 74 sccm and 370 sccm pure CO2 at pressures between 1.2 mbar and 5 mbar with specific energy inputs up to 111.9 eV/molecule. These operating conditions exhibit high CO2 conversions (up to 90 %) at low energy efficiencies (2−7.4 %), due to direct electron impact dissociation driving the conversion process resulting in splitting of CO2 into CO and metastable oxygen atoms. The TALIF measurements yield spatially resolved translational temperatures between 1000 K−1600 K for most operating conditions and axial positions along the effluent. Reference measurements with xenon 6p′ [3/2]2 are used for absolute number density calibration. The resulting axially resolved number density profiles of ground state atomic oxygen increase along the effluent, even at considerable distances of several centimeters from the active discharge, before they reach a maximum between 5×1020 m−3 and 2.2×1021 m−3 depending on the condition, and decrease after that. This behavior indicates the potential significance of quenching of metastable oxygen atoms within the post-discharge regime of the investigated CO2 discharges. The measured spatially resolved number density evolutions are qualitatively consistent with quenching via wall collisions being the dominant deactivation mechanism, underlining the importance of particle-wall interactions.
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