Strain Imaging of GaAs by Stimulated Raman Scattering Microscopy

IF 2.2 3区 化学 Q2 SPECTROSCOPY
Journal of Raman Spectroscopy Pub Date : 2026-08-03 Epub Date: 2026-04-26 DOI:10.1002/jrs.70147
Yuki Sano, Yasuyuki Ozeki
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引用次数: 0

Abstract

Gallium arsenide (GaAs) is a key compound semiconductor used in high-speed and optoelectronic devices, where strain and defect characterization are essential for improving device reliability and performance. However, the conventional approach based on spontaneous Raman spectroscopy suffers from inherently low signal intensity, which severely limits measurement speed. Although stimulated Raman scattering (SRS) offers orders-of-magnitude signal enhancement and faster imaging, the excitation wavelengths commonly used in conventional setups (typically below 1  μm) are strongly absorbed, hindering SRS signal generation. Here, we overcome this limitation by employing telecom-wavelength SRS microscopy. Clear SRS spectra corresponding to the longitudinal optical (LO) phonon mode near 292 cm − 1 were successfully obtained. The technique enables detection of phonon peak shifts with < 0.2 cm − 1 spectral precision and visualization of local phonon frequency variations associated with surface damage. Compared with conventional Raman mapping, the present method achieves more than two orders of magnitude higher measurement throughput. These results establish telecom-wavelength SRS microscopy as a promising and versatile tool for nondestructive characterization of GaAs.

Abstract Image

受激拉曼散射显微镜下砷化镓的应变成像
砷化镓(GaAs)是用于高速光电器件的关键化合物半导体,应变和缺陷表征对于提高器件的可靠性和性能至关重要。然而,基于自发拉曼光谱的传统方法固有的信号强度低,严重限制了测量速度。虽然受激拉曼散射(SRS)提供了数量级的信号增强和更快的成像,但传统装置中常用的激发波长(通常低于1 μm)被强烈吸收,阻碍了SRS信号的产生。在这里,我们克服了这一限制,采用电信波长SRS显微镜。在292 cm−1附近成功获得了纵向光学(LO)声子模式对应的清晰SRS光谱。该技术能够以<; 0.2 cm−1的光谱精度检测声子峰移,并可视化与表面损伤相关的局部声子频率变化。与传统的拉曼映射相比,该方法的测量吞吐量提高了两个数量级以上。这些结果建立了电信波长SRS显微镜作为一个有前途的和通用的工具,非破坏性表征砷化镓。
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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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