Si-Cl2-Ar 原子层蚀刻中的反应器壁效应

Joseph R. Vella, M. A. I. Elgarhy, Qinzhen Hao, Vincent M. Donnelly, David B. Graves
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引用次数: 0

摘要

这项工作是对我们以前的手稿[J. Vac. Sci. Technol. A41, 062602 (2023)]的补充,其中将硅-氯-氩(Si-Cl2-Ar)原子层刻蚀(ALE)的分子动力学(MD)模拟预测与实验进行了比较。最初将原子氯(Cl)和硅氯化物的蚀刻产物分布与光学发射光谱(OES)信号进行比较时发现,在较高离子通量下,MD 预测与实验结果之间存在差异。实验结果表明,离子轰击表面释放的含 Cl 蚀刻产物(称为 "高原")在一段相对较长的时间内几乎保持不变,但在 MD 模拟中却没有观察到这种效应。在本报告中,我们证明了在 OES 信号中观察到的 "高原 "很可能是由于含 Cl 的蚀刻产物从反应器壁上解吸并随后吸附在硅基底上造成的。在保持输入气体浓度和压力不变的情况下,改变气体在反应室中的停留时间的实验支持了这一解释。我们还进行了实验,在反应室中增加了仅含 Ar 的气流,以降低反应室壁上含 Cl 物种的浓度。在这两组流量调节实验中,我们观察到的结果与假设一致,即从腔室壁上解吸的含 Cl 物种是造成 MD 预测值与实验观测值之间差异的重要原因。如果根据表面含 Cl 物种的 "额外 "来源对测量的 OES 信号进行校正,则 MD 预测结果和测量的 OES 信号非常一致。这进一步证明了 MD 模拟的预测能力,可以准确捕捉等离子体辅助 ALE 过程中的相关物理和化学过程。我们提供了含 Cl 物种所需密度的数量级估计值,以解释所观察到的额外蚀刻产物。最后,我们讨论了这种效应对等离子纳米制造中 ALE 的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reactor wall effects in Si–Cl2–Ar atomic layer etching
This work complements our previous manuscript [J. Vac. Sci. Technol. A41, 062602 (2023)] where predictions from molecular dynamics (MD) simulations of silicon–chlorine–argon (Si–Cl2–Ar) atomic layer etching (ALE) are compared to experiments. When etch product distributions for atomic chlorine (Cl) and silicon chlorides were initially compared to optical emission spectroscopy (OES) signals, it appeared that there was a discrepancy between the MD predictions and experimental results at higher ion fluences. Experiments showed a relatively long period of nearly constant Cl-containing etch products released from the ion-bombarded surface (referred to as the “plateau”) but this effect was not observed in MD simulations. In this report, we demonstrate that the “plateau” observed in the OES signals is most likely due to the desorption of Cl-containing etch products from the walls of the reactor and subsequent adsorption on the Si substrate. Experiments varying the gas residence time in the chamber while keeping incoming gas concentrations and pressure constant support this interpretation. We also conducted experiments with an additional Ar-only flow in the chamber to reduce the concentration of Cl-containing species on the chamber walls. For both sets of flow modification experiments, we observe results consistent with the hypothesis that Cl-containing species desorbing from chamber walls are a significant cause of the observed discrepancy between MD predictions and experimental observations. If the measured OES signals are corrected for this “additional” source of Cl-containing species at the surface, the MD predictions and measured OES signals are in excellent agreement. This further supports the predictive capability of MD simulations to accurately capture the relevant physical and chemical processes in plasma-assisted ALE processes. We provide an order of magnitude estimate of the required density of Cl-containing species that would account for the additional etch products observed. Finally, we discuss the implications of this effect on ALE in plasma nanofabrication.
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