硅基虚拟衬底上c6h8o7处理和H、cl钝化的ge - mos电容性能(001)

L. Hänel, Y. Elogail, D. Schwarz, I. Fischer, J. Schulze
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引用次数: 2

摘要

随着摩尔定律接近其物理极限,除了经典的金属氧化物半导体场效应晶体管(MOSFET)之外,晶体管概念也被发明出来。隧道效应晶体管(TFET)是一个很有前途的候选者,因为理论上预测该器件的亚阈值摆幅低于60 mV/dec。然而,硅不是tfet的衬底选择-载流子迁移率和由此产生的导通电流太低。因此,建议锗(Ge)作为p沟道TFET (p-TFET)的活性材料,建议化合物III/ v材料作为n-TFET的活性材料,高k材料作为栅极氧化物。这种发展在制造过程中带来了新的问题。这是因为Ge/高k接口不像Si/ sio2接口那样具有天然的高质量,导致gate - mos电容成为TFET的关键部分。需要新的锗表面清洗和钝化方法。然而,硅仍然是衬底材料的选择,这需要这些材料在硅上的协整。作为第一次尝试,我们展示了以Al2O3作为栅极氧化物的ge - mos电容器在Si(001)上的Ge-Virtual-Substrate上具有良好的性能,迟滞率低至0.6 V。我们建议结合常规和非常规的清洗步骤,如H2O2和C6H8O7(柠檬酸),然后是H-和cl -钝化。所讨论的数据对串联电阻进行了校正,并在可能的情况下对寄生电容进行了校正,寄生电容可用作清洗和钝化效率的指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Performance of C6H8O7-treated and H- and Cl-passivated Ge-MOS-capacitances on Ge-virtual-substrate on Si(001)
As Moore's law is approaching its physical limitations, transistor concepts besides the classical Metal Oxide Semiconductor Field-Effect Transistor (MOSFET) have been invented. The Tunneling FET (TFET) is a promising candidate due to the theoretically predicted subthreshold swing below 60 mV/dec of this device concept. However, Si is not the substrate of choice for TFETs — the carrier mobility and the resulting on-currents are too low. Therefore, Germanium (Ge) is suggested as active material for p-channel TFET (p-TFET) as compound III/V-materials are suggested as n-TFET active material with a high-k material as Gate oxide. This development entails new issues in the manufacturing process. That is because the Ge/high-k-interface is not of natural high quality as the Si/SiO2-interface, causing the Gate-MOS-capacitance to be the critical part of the TFET. New cleaning and passivation methods for the Ge surface are necessary. Nevertheless, Si will remain the substrate material of choice, what requires co-integration of those materials on Si. As a first attempt, we show Ge-MOS-capacitors with Al2O3 as Gate Oxide on Ge-Virtual-Substrate on Si(001) of good performance with hysteresis down to 0.6 V. We propose a combination of conventional and unconventional cleaning steps such as H2O2 and C6H8O7 (Citric Acid) followed by H- and Cl-passivation. The discussed data are corrected for series resistance and — when possible — for parasitic capacitances that can be used as indicators for cleaning and passivation efficiencies.
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