Alexandre Chapotot, Jérémie Chrétien, O. Fesiienko, E. Pargon, Jinyoun Cho, Kristof Dessein, A. Boucherif, G. Hamon, Maxime Darnon
{"title":"Enhancing minority carrier lifetime in Ge: Insights from HF and HCl cleaning procedures","authors":"Alexandre Chapotot, Jérémie Chrétien, O. Fesiienko, E. Pargon, Jinyoun Cho, Kristof Dessein, A. Boucherif, G. Hamon, Maxime Darnon","doi":"10.1116/6.0003236","DOIUrl":null,"url":null,"abstract":"Efficiently passivating germanium (Ge) surfaces is crucial to reduce the unwanted recombination current in high-performance devices. Chemical surface cleaning is critical to remove surface contaminants and Ge oxides, ensuring effective surface passivation after dielectric deposition. However, Ge oxides can rapidly regrow upon air exposure. To understand the surface evolution after wet cleaning, we present a comprehensive study comparing HF and HCl deoxidation steps on p-type Ge surfaces and monitor the surface as a function of air exposure time. Distinct oxide regrowth dynamics are observed: HF-treated samples exhibit swift regrowth of all Ge oxide states, whereas HCl-treated Ge surfaces exhibit a lower concentration of low degrees of oxidation and slower or no regrowth of high oxide states even after 110 min of air exposure. In addition, the presence of Ge–Cl bonds induces different oxidation dynamics compared to the Ge–OH bonds resulting from HF cleaning. This leads to varying surface electronic band structures, with HF-treated Ge exhibiting a strong positive band bending (+0.20 eV). Conversely, HCl-treated samples display a lower band curvature (+0.07 eV), mostly due to the presence of Ge–Cl bonds on the Ge surface. During air exposure, the increased GeOx coverage significantly reduces the band bending after HF, while a constant band bending is observed after HCl. Finally, these factors induce a reduction in the surface recombination velocity after wet etching. Combining both chemical and field-induced passivation, HF-treated Ge without rinsing exceeds 800 μs.","PeriodicalId":509398,"journal":{"name":"Journal of Vacuum Science & Technology A","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Vacuum Science & Technology A","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1116/6.0003236","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Efficiently passivating germanium (Ge) surfaces is crucial to reduce the unwanted recombination current in high-performance devices. Chemical surface cleaning is critical to remove surface contaminants and Ge oxides, ensuring effective surface passivation after dielectric deposition. However, Ge oxides can rapidly regrow upon air exposure. To understand the surface evolution after wet cleaning, we present a comprehensive study comparing HF and HCl deoxidation steps on p-type Ge surfaces and monitor the surface as a function of air exposure time. Distinct oxide regrowth dynamics are observed: HF-treated samples exhibit swift regrowth of all Ge oxide states, whereas HCl-treated Ge surfaces exhibit a lower concentration of low degrees of oxidation and slower or no regrowth of high oxide states even after 110 min of air exposure. In addition, the presence of Ge–Cl bonds induces different oxidation dynamics compared to the Ge–OH bonds resulting from HF cleaning. This leads to varying surface electronic band structures, with HF-treated Ge exhibiting a strong positive band bending (+0.20 eV). Conversely, HCl-treated samples display a lower band curvature (+0.07 eV), mostly due to the presence of Ge–Cl bonds on the Ge surface. During air exposure, the increased GeOx coverage significantly reduces the band bending after HF, while a constant band bending is observed after HCl. Finally, these factors induce a reduction in the surface recombination velocity after wet etching. Combining both chemical and field-induced passivation, HF-treated Ge without rinsing exceeds 800 μs.
有效钝化锗(Ge)表面对于减少高性能器件中不必要的重组电流至关重要。化学表面清洁对于去除表面污染物和锗氧化物至关重要,可确保介电沉积后表面的有效钝化。然而,Ge 氧化物在暴露于空气后会迅速再生。为了了解湿法清洁后的表面演变,我们对 p 型 Ge 表面的 HF 和 HCl 脱氧步骤进行了全面的研究比较,并监测了表面与空气暴露时间的函数关系。我们观察到了不同的氧化物再生动态:经过高频处理的样品显示出所有 Ge 氧化物状态的快速再生,而经过盐酸处理的 Ge 表面则显示出较低的低度氧化物浓度和较慢的高氧化物状态再生,甚至在暴露于空气中 110 分钟后仍没有再生。此外,与高频清洗产生的 Ge-OH 键相比,Ge-Cl 键的存在引起了不同的氧化动力学。这导致了不同的表面电子能带结构,HF 处理过的 Ge 具有很强的正带弯曲(+0.20 eV)。相反,盐酸处理过的样品显示出较低的带弯曲度(+0.07 eV),这主要是由于 Ge 表面存在 Ge-Cl 键。在暴露于空气中期间,GeOx 覆盖率的增加显著降低了高频后的带弯曲,而盐酸后则观察到恒定的带弯曲。最后,这些因素导致湿法蚀刻后表面重组速度降低。结合化学钝化和场诱导钝化,经过高频处理的 Ge 在不冲洗的情况下,其表面钝化速度超过 800 μs。