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用砷对锗进行单层掺杂:实现最佳掺杂剂激活的新化学途径。

Monolayer Doping of Germanium with Arsenic: A New Chemical Route to Achieve Optimal Dopant Activation.

作者信息

Kennedy Noel, Garvey Shane, Maccioni Barbara, Eaton Luke, Nolan Michael, Duffy Ray, Meaney Fintan, Kennedy Mary, Holmes Justin D, Long Brenda

机构信息

School of Chemistry & AMBER Centre, University College Cork, Cork, T12 YN60, Ireland.

Tyndall National Institute, Lee Maltings, University College Cork, Cork, T12 R5CP, Ireland.

出版信息

Langmuir. 2020 Sep 1;36(34):9993-10002. doi: 10.1021/acs.langmuir.0c00408. Epub 2020 Aug 18.

Abstract

Reported here is a new chemical route for the wet chemical functionalization of germanium (Ge), whereby arsanilic acid is covalently bound to a chlorine (Cl)-terminated surface. This new route is used to deliver high concentrations of arsenic (As) dopants to Ge, via monolayer doping (MLD). Doping, or the introduction of Group III or Group V impurity atoms into the crystal lattice of Group IV semiconductors, is essential to allow control over the electronic properties of the material to enable transistor devices to be switched on and off. MLD is a diffusion-based method for the introduction of these impurity atoms via surface-bound molecules, which offers a nondestructive alternative to ion implantation, the current industry doping standard, making it suitable for sub-10 nm structures. Ge, given its higher carrier mobilities, is a leading candidate to replace Si as the channel material in future devices. Combining the new chemical route with the existing MLD process yields active carrier concentrations of dopants (>1 × 10 atoms/cm) that rival those of ion implantation. It is shown that the dose of dopant delivered to Ge is also controllable by changing the size of the precursor molecule. X-ray photoelectron spectroscopy (XPS) data and density functional theory (DFT) calculations support the formation of a covalent bond between the arsanilic acid and the Cl-terminated Ge surface. Atomic force microscopy (AFM) indicates that the integrity of the surface is maintained throughout the chemical procedure, and electrochemical capacitance voltage (ECV) data shows a carrier concentration of 1.9 × 10 atoms/cm corroborated by sheet resistance measurements.

摘要

本文报道了一种用于锗(Ge)湿化学功能化的新化学路线,通过该路线,对氨基苯胂酸可共价结合到氯(Cl)终止的表面上。这条新路线用于通过单层掺杂(MLD)将高浓度的砷(As)掺杂剂输送到Ge中。掺杂,即将第III族或第V族杂质原子引入第IV族半导体的晶格中,对于控制材料的电子特性以使晶体管器件能够开启和关闭至关重要。MLD是一种基于扩散的方法,用于通过表面结合分子引入这些杂质原子,它为当前行业掺杂标准离子注入提供了一种无损替代方法,使其适用于亚10纳米结构。鉴于其较高的载流子迁移率,Ge是未来器件中替代Si作为沟道材料的主要候选者。将新化学路线与现有的MLD工艺相结合,可产生与离子注入相当的活性掺杂剂载流子浓度(>1×10原子/cm)。结果表明,可以通过改变前驱体分子的大小来控制输送到Ge的掺杂剂剂量。X射线光电子能谱(XPS)数据和密度泛函理论(DFT)计算支持对氨基苯胂酸与Cl终止的Ge表面之间形成共价键。原子力显微镜(AFM)表明在整个化学过程中表面的完整性得以保持,并且电化学电容电压(ECV)数据显示载流子浓度为1.9×10原子/cm,薄层电阻测量结果证实了这一点。

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