利用扫描近场光学拉曼显微镜观测 4H-SiC 沟槽金属氧化物半导体场效应晶体管测试结构的各向异性应力

IF 2.4 3区 化学 Q2 SPECTROSCOPY Journal of Raman Spectroscopy Pub Date : 2024-05-25 DOI:10.1002/jrs.6685
Masanobu Yoshikawa, Masataka Murakami, Tomoyuki Ushida, Junichiro Samejima, Kana Mitsuzawa, Nobuhiro Matoba, Minwho Lim, Oleg Rusch, Mathias Rommel
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引用次数: 0

摘要

我们在 4H 碳化硅(4H-SiC)的 m 面和 a 面制备了两种沟槽测试金属氧化物半导体场效应晶体管(MOSFET)结构,并使用我们开发的扫描近场光学拉曼显微镜(SNOM)研究了深度为 1 μm 的小沟槽的各向异性应力分布。m面沟槽底部σ11(a轴)的应力分布比a面沟槽底部σ11(a轴)的应力分布大约100兆帕,m面沟槽底部σ33(c轴)的应力分布与a面沟槽底部σ33(c轴)的应力分布基本相同。实验结果与有限元法(FEM)的计算结果十分吻合。这些结果表明,4H-SiC 沟道测试 MOSFET 沟道顶点周围的 σ11 各向异性应力分布发生在 m 面和 a 面。因此,m 面和 a 面的迁移率差异可能是各向异性应力造成的。
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Anisotropic stress observation of 4H-SiC trench metal-oxide semiconductor field-effect transistor test structures by scanning near-field optical Raman microscope

We prepared two types of trench-test metal-oxide semiconductor field-effect transistor (MOSFET) structures on m- and a-faces in 4H silicon carbide (4H-SiC) and investigated the anisotropic stress distribution of small trenches with a depth of 1 μm using a scanning near-field optical Raman microscope (SNOM) that we developed. The stress distributions of σ11 (a-axis) under the bottom of the trench for m-face were approximately 100 MPa larger than those for a-face, and the stress distributions of σ33 (c-axis) under the bottom of the trench for m-face were almost the same as those for a-face. The experimental result agrees well with that calculated by the finite element method (FEM). These results indicate that the anisotropic stress distributions of σ11 components around the apex of the trenches of 4H-SiC trench-test MOSFET occur in m- and a-faces. Thus, it is possible that the differences in mobilities for m- and a-faces might be caused by the anisotropic stresses.

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来源期刊
CiteScore
5.40
自引率
8.00%
发文量
185
审稿时长
3.0 months
期刊介绍: The Journal of Raman Spectroscopy is an international journal dedicated to the publication of original research at the cutting edge of all areas of science and technology related to Raman spectroscopy. The journal seeks to be the central forum for documenting the evolution of the broadly-defined field of Raman spectroscopy that includes an increasing number of rapidly developing techniques and an ever-widening array of interdisciplinary applications. Such topics include time-resolved, coherent and non-linear Raman spectroscopies, nanostructure-based surface-enhanced and tip-enhanced Raman spectroscopies of molecules, resonance Raman to investigate the structure-function relationships and dynamics of biological molecules, linear and nonlinear Raman imaging and microscopy, biomedical applications of Raman, theoretical formalism and advances in quantum computational methodology of all forms of Raman scattering, Raman spectroscopy in archaeology and art, advances in remote Raman sensing and industrial applications, and Raman optical activity of all classes of chiral molecules.
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