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Constraints on micro-Raman strain metrology for highly doped strained Si materials

机译:高掺杂应变Si材料的微拉曼应变计量学约束

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Ultraviolet (UV), low penetration depth, micro-Raman spectroscopy, and high-resolution x-ray diffraction (HRXRD) are utilized as complementary, independent stress characterization tools for a range of strained Si samples doped by low energy (2 keV) Sb ion implantation. Following dopant implantation, good agreement is found between the magnitudes of strain measured by the two techniques. However, following dopant activation by annealing, strain relaxation is detected by HRXRD but not by micro-Raman. This discrepancy mainly arises from an anomalous redshift in the Si Raman peak position originating from the high levels of doping achieved in the samples. This has serious implications for the use of micro-Raman spectroscopy for strain characterization of highly doped strained Si complementary metal-oxide semiconductor devices and structures therein. We find a direct correlation between the Si Raman shift and peak carrier concentration measured by the differential Hall technique, which indicates that UV micro-Raman may become a useful tool for nondestructive dopant characterization for ultrashallow junctions in these Si-based materials.
机译:紫外线(UV),低穿透深度,显微拉曼光谱和高分辨率X射线衍射(HRXRD)被用作互补的,独立的应力表征工具,用于一系列掺杂有低能(2 keV)Sb的应变Si样品离子注入。在掺杂剂注入之后,通过两种技术测得的应变大小之间发现了很好的一致性。但是,在通过退火激活掺杂剂之后,HRXRD可以检测到应变松弛,而微拉曼检测不到。这种差异主要是由于样品中实现的高掺杂水平导致的Si Raman峰位置出现异常红移。这对于使用微拉曼光谱法对高掺杂的应变Si互补金属氧化物半导体器件及其结构进行应变表征具有严重的意义。我们发现通过差分霍尔技术测得的Si拉曼位移与峰值载流子浓度之间存在直接相关性,这表明UV微拉曼可能成为这些Si基材料中超浅结的无损掺杂剂表征的有用工具。

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