首页> 外文期刊>Journal of Raman Spectroscopy: An International Journal for Original Work in All Aspects of Raman Spectroscopy, Including Higher Order Processes, and Also Brillouin- and Rayleigh Scattering >Implementation of a novel low-noise InGaAs detector enabling rapid near-infrared multichannel Raman spectroscopy of pigmented biological samples
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Implementation of a novel low-noise InGaAs detector enabling rapid near-infrared multichannel Raman spectroscopy of pigmented biological samples

机译:实施新型低噪声InGaAs检测器,可对有色生物样品进行快速近红外多通道拉曼光谱分析

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Pigmented tissues are inaccessible to Raman spectroscopy using visible laser light because of the high level of laser-induced tissue fluorescence. The fluorescence contribution to the acquired Raman signal can be reduced by using an excitation wavelength in the near infrared range around 1000nm. This will shift the Raman spectrum above 1100nm, which is the principal upper detection limit for silicon-based CCD detectors. For wavelengths above 1100nm indium gallium arsenide detectors can be used. However, InGaAs detectors have not yet demonstrated satisfactory noise level characteristics for demanding Raman applications. We have tested and implemented for the first time a novel sensitive InGaAs imaging camera with extremely low readout noise for multichannel Raman spectroscopy in the short-wave infrared (SWIR) region. The effective readout noise of two electrons is comparable to that of high quality CCDs and two orders of magnitude lower than that of other commercially available InGaAs detector arrays. With an in-house built Raman system we demonstrate detection of shot-noise limited high quality Raman spectra of pigmented samples in the high wavenumber region, whereas a more traditional excitation laser wavelength (671nm) could not generate a useful Raman signal because of high fluorescence. Our Raman instrument makes it possible to substantially decrease fluorescence background and to obtain high quality Raman spectra from pigmented biological samples in integration times well below 20s. Copyright (c) 2015 John Wiley & Sons, Ltd.
机译:由于激光诱导的组织荧光水平高,因此使用可见激光对色素沉着的组织无法进行拉曼光谱分析。通过使用在1000nm附近的近红外范围内的激发波长,可以减少对获取的拉曼信号的荧光贡献。这会将拉曼光谱移到1100nm以上,这是硅基CCD检测器的主要检测上限。对于1100nm以上的波长,可以使用砷化铟镓探测器。然而,对于苛刻的拉曼应用,InGaAs检测器尚未表现出令人满意的噪声水平特性。我们首次测试并实现了一种新颖的灵敏InGaAs成像相机,该相机具有极低的读出噪声,可用于短波红外(SWIR)区域的多通道拉曼光谱。两个电子的有效读出噪声与高质量CCD的噪声相当,并且比其他市售InGaAs检测器阵列低两个数量级。使用内部构建的拉曼系统,我们展示了在高波数区域中发色样品的散粒噪声有限的高质量拉曼光谱的检测,而更传统的激发激光波长(671nm)由于高荧光而无法生成有用的拉曼信号。我们的拉曼仪器可以大大降低荧光背景,并在远低于20s的积分时间内从有色生物样品中获得高质量的拉曼光谱。版权所有(c)2015 John Wiley&Sons,Ltd.

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