首页> 外文OA文献 >HF vapor etching and cleaning of silicon wafer surfaces
【2h】

HF vapor etching and cleaning of silicon wafer surfaces

机译:HF蒸汽蚀刻和硅晶片表面的清洁

摘要

The objectives of this project are to understand the reaction mechanisms for oxide etching by both HF/H2 0 and HF/alcohol processes and to develop a vapor phase HF cleaning process to remove metallic contamination and native oxide on a silicon surface. Although the HF vapor process has been studied intensively for past several decades, the commercial application has not been very successful due to the unknown nature of the process. This study, performed at MIT, has emphasized on finding possible applications to the semiconductor industry as a replacement to the aqueous phase cleaning processes. The ultimate purpose of this project is to demonstrate feasibility of the HF vapor process for a vacuum compatible and clustered cleaning process. In this study, the etching experiments were carried out in a stainless steel vacuum chamber connected to a vacuum wafer transfer system. Samples were introduced through a load lock chamber and transferred to the HF vapor reaction chamber. The base pressure of the system was maintained under 10-7 Torr. The system can handle sample sizes between 1 cm square and 10 cm diameter silicon wafers. The etching rates were measured by an in situ ellipsometer installed on the HF vapor reactor. Ellipsometric measurements suggest that oxide etching can occur without a condensed layer or with a condensed layer on the oxide surface. The etching rates of oxide in the condensed regime were very high (3,000-12,000 A/min) compared to the gas phase regime (0-300 A/min). The etching regime in which a condensed layer is formed is a function of not only the partial pressures of HF and H 20 in the feed gas, but also a function of the mass transport of the products from the sample in the gas phase. We have categorized two different etching regimes: the gas phase regime and the condensed phase regime. In the gas phase etching regime, reactant molecules are adsorbed on the oxide surface in sub-monolayer, monolayer, or multilayer films. In the multilayer adsorption regime, the etching rate is usually low (typically 0-400 A/min) and is linearly proportional to the partial pressure of HF and H20. The etching rate in this regime is greatly affected by the temperature of the substrate. The mass transfer rate limits the etch rate of oxide in the multilayer adsorption regime. In the submonolayer or monolayer adsorption regime the etching rate is described by Langmuir- Hinshelwood kinetics. The etching rate is governed by surface kinetics in this regime. Advantages of this etching regime are: 1) smoother etched surface, 2) low selectivity to TEOS, 3) haze-free etched surface, 4) no metal attack, 5) perfect removal of native oxide, and 6) vacuum compatible process. The HF vapor process in this regime is an ideal process for contact cleaning and polymer removal after metal or via etching. Electrostatic charge on the wafer surface affects the etching reaction significantly in the non-condensed regimes. A positively charged surface enhanced the etching reaction in the submonolayer and monolayer etching regimes. Direct ionization of HF on the oxide surface is responsible for the enhancement in this regime. A negatively charged surface mainly enhanced the etching in the multilayer regime. A thicker multilayer, induced by the formation of fluorosilicate, is responsible for the etching enhancement in this regime. We have demonstrated a successful removal of sodium from both oxide and silicon surfaces using HF/H2 0, HF/IPA, and HF/H20/SiF4 processes in reduced pressure operation. All experiments were performed in a vacuum environment and in-situ XPS was used to measure the surface concentration of sodium. The sodium contamination on oxide surface was successfully removed by both HF/H 20 and HF/IPA processes. The HF/H 20 process could not remove all of sodium contamination on a silicon surface. The addition of SiF4 in the HF/H 20 process greatly enhances the cleaning effect, reducing Na contamination below the detection limit of our XPS, even on a silicon surface. Based on our study, we have reported a true gas phase and vacuum compatible HF vapor process, operated in the monolayer adsorption regime at elevated temperature. A successful removal of RIE residue was performed with a combined cleaning procedure of HF vapor and ashing process. This combined process is a perfect dry cleaning process for contact cleaning method. This process sequence is ideal for a vacuum cluster configuration in which a single wafer is processed at a time and is not exposed in the ambient.
机译:该项目的目的是了解通过HF / H2 0和HF /酒精工艺进行氧化物蚀刻的反应机理,并开发气相HF清洗工艺以去除硅表面的金属污染和天然氧化物。尽管已经对HF蒸气方法进行了数十年的深入研究,但是由于该方法的未知性质,其商业应用还不是很成功。这项在麻省理工学院进行的研究强调了寻找半导体工业的可能应用,以代替水相清洗工艺。该项目的最终目的是证明HF蒸气工艺可用于真空兼容且成簇的清洗工艺。在这项研究中,蚀刻实验是在连接真空晶片传输系统的不锈钢真空室中进行的。样品通过负载锁定室引入并转移到HF蒸气反应室。系统的基本压力保持在10-7 Torr以下。该系统可以处理1平方厘米到10厘米直径的硅晶片。通过安装在HF蒸气反应器上的原位椭圆仪测量蚀刻速率。椭偏测量表明,在氧化物表面上没有凝结层或凝结层的情况下,可以进行氧化物蚀刻。与气相方式(0-300 A / min)相比,在冷凝状态下氧化物的蚀刻速率非常高(3,000-12,000 A / min)。形成冷凝层的蚀刻方式不仅取决于进料气体中HF和H 20的分压,还取决于气相中样品中产物的质量传递。我们对两种蚀刻方式进行了分类:气相方式和冷凝相方式。在气相蚀刻方案中,反应物分子被吸附在亚单层,单层或多层膜中的氧化物表面上。在多层吸附方式中,蚀刻速率通常较低(通常为0-400 A / min),并且与HF和H20的分压成线性比例。在这种情况下,蚀刻速率受衬底温度的影响很大。传质速率限制了多层吸附方案中氧化物的蚀刻速率。在亚单层或单层吸附方式中,蚀刻速率由Langmuir-Hinshelwood动力学描述。在这种情况下,蚀刻速率取决于表面动力学。这种蚀刻方式的优点是:1)蚀刻后的表面更光滑; 2)对TEOS的选择性低; 3)无雾的蚀刻表面; 4)无金属侵蚀; 5)完全去除天然氧化物;以及6)真空兼容工艺。在这种情况下,HF蒸气法是用于金属或蚀刻后接触清洁和聚合物去除的理想方法。晶片表面上的静电荷在非冷凝状态下会显着影响蚀刻反应。带正电的表面增强了亚单层和单层蚀刻方案中的蚀刻反应。 HF在氧化物表面上的直接电离是这种状态下增强的原因。带负电的表面在多层状态下主要增强了蚀刻。由氟硅酸盐的形成引起的较厚的多层负责在这种情况下的蚀刻增强。我们已经证明在减压操作中使用HF / H2 0,HF / IPA和HF / H20 / SiF4工艺可以成功地从氧化物和硅表面去除钠。所有实验均在真空环境中进行,并使用原位XPS测量钠的表面浓度。通过HF / H 20和HF / IPA工艺成功去除了氧化物表面的钠污染。 HF / H 20工艺无法去除硅表面上的所有钠污染。在HF / H 20工艺中添加SiF4可以大大提高清洁效果,即使在硅表面上,也可以将Na污染降低到XPS的检测极限以下。根据我们的研究,我们报告了一种真正的气相和真空兼容的HF蒸气工艺,该工艺在高温下以单层吸附方式进行。使用HF蒸气和灰化工艺的组合清洁程序成功去除了RIE残留物。此组合过程是接触清洗方法的理想干洗方法。该处理顺序对于真空集群配置是理想的,在真空集群配置中,一次要处理单个晶片并且不会暴露在环境中。

著录项

  • 作者

    Han Yong-Pil 1962-;

  • 作者单位
  • 年度 1999
  • 总页数
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类

相似文献

  • 外文文献
  • 中文文献
  • 专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号