高光谱成像
拉曼散射
化学成像
光学
显微镜
拉曼光谱
光谱成像
材料科学
光谱分辨率
飞秒
激光器
相干反斯托克斯拉曼光谱
散射
光谱特征
分辨率(逻辑)
物理
计算机科学
谱线
人工智能
量子力学
天文
作者
Matthew G. Clark,Kent A. Brasseale,Gil A. Gonzalez,Gregory Eakins,Chi Zhang
摘要
Stimulated Raman scattering (SRS) and coherent anti-Stokes Raman scattering (CARS) microscopy are the most widely used coherent Raman scattering imaging technologies. Hyperspectral SRS and CARS imaging offer Raman spectral information at every pixel, which enables better separation of different chemical compositions. Although both techniques require two excitation lasers, their signal detection schemes and spectral properties are quite different. The goal of this protocol is to perform both hyperspectral SRS and CARS imaging on a single platform and compare the two microscopy techniques for imaging different biological samples. The spectral focusing method is employed to acquire spectral information using femtosecond lasers. By using standard chemical samples, the sensitivity, spatial resolution, and spectral resolution of SRS and CARS in the same excitation conditions (i.e., power at the sample, pixel dwell time, objective lens, pulse energy) are compared. The imaging contrasts of CARS and SRS for biological samples are juxtaposed and compared. The direct comparison of CARS and SRS performances would allow for optimal selection of the modality for chemical imaging.
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