电容耦合氩氧等离子体中随频率变化的电子功率吸收模式转换

A Derzsi, M Vass, R Masheyeva, B Horváth, Z Donkó, P Hartmann
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引用次数: 0

摘要

相位分辨光学发射光谱(PROES)测量结合 1d3v 粒子胞中/蒙特卡罗碰撞模拟,研究了氩氧混合物中低压电容耦合等离子体(CCP)的激发动力学。该研究使用的系统是一个几何对称的 CCP 反应器,在 120 Pa 的 70% Ar-30% O2 混合物中运行,峰峰电压为 350 V,驱动射频频率范围很宽(2 MHz ⩽f⩽ 15 MHz)。从氩基态到氩 2p1 电平的电子碰撞激发率的测量和计算时空分布显示出良好的定性一致性。这些分布显示出明显的频率依赖性,一般认为这可以预测主要放电工作模式的转变。可以区分出三个频率范围,显示出明显不同的激发特性:(i) 在低频范围(f⩽ 3 MHz),鞘的激发很强,而体部区域的激发很弱;(ii) 在中间频率(3.5 MHz ⩽f⩽ 5 MHz),体部区域的激发率增强,并显示出条纹的形成;(iii) 在 6 MHz 以上,体部的激发随着频率的增加而逐渐减弱。通过玻尔兹曼项分析,可以量化欧姆项和伏极项对电子功率吸收的频率贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Frequency-dependent electron power absorption mode transitions in capacitively coupled argon-oxygen plasmas
Phase Resolved Optical Emission Spectroscopy (PROES) measurements combined with 1d3v Particle-in-Cell/Monte Carlo Collisions simulations are performed to investigate the excitation dynamics in low-pressure capacitively coupled plasmas (CCPs) in argon-oxygen mixtures. The system used for this study is a geometrically symmetric CCP reactor operated in a 70% Ar-30% O2 mixture at 120 Pa, applying a peak-to-peak voltage of 350 V, with a wide range of driving RF frequencies (2 MHz  f 15 MHz). The measured and calculated spatio-temporal distributions of the electron impact excitation rates from the Ar ground state to the Ar 2p1 level show good qualitative agreement. The distributions show significant frequency dependence, which is generally considered to be predictive of transitions in the dominant discharge operating mode. Three frequency ranges can be distinguished, showing distinctly different excitation characteristics: (i) in the low frequency range ( f 3 MHz), excitation is strong at the sheaths and weak in the bulk region; (ii) at intermediate frequencies (3.5 MHz f 5 MHz), the excitation rate in the bulk region is enhanced and shows striation formation; (iii) above 6 MHz, excitation in the bulk gradually decreases with increasing frequency. Boltzmann term analysis was performed to quantify the frequency-dependent contributions of the Ohmic and ambipolar terms to the electron power absorption.
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