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Optical design for laser tweezers Raman spectroscopy setups for increased sensitivity and flexible spatial detection

机译:用于激光镊子拉曼光谱设置的光学设计,提高灵敏度和灵活的空间检测

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摘要

We demonstrate a method to double the collection efficiency in laser tweezers Raman spectroscopy (LTRS) by collecting both the forward-scattered and backscattered light in a single-shot multitrack measurement. Our method can collect signals at different sample volumes, granting both the pinpoint spatial selectivity of confocal Raman spectroscopy and the bulk sensitivity of non-confocal Raman spectroscopy simultaneously. Further, we display that our approach allows for reduced detector integration time and laser power. To show this, we measure the Raman spectra of both polystyrene beads and bacterial spores. For spores, we can trap them at 2.5m Wlaser power and acquire a high signal-to-noise ratio power spectrum of the calcium-dipicolinic acid peaks using an integration time of 2 x 30 s. Thus, our method will enable the monitoring of biological samples sensitive to high intensities for longer times. Additionally, we demonstrate that by a simple modification, we can add polarization sensitivity and retrieve extra biochemical information. (C) 2021 Optical Society of America under the terms of the OSA Open Access Publishing Agreement
机译:我们展示了一种在激光镊子拉曼光谱(LTRS)中通过在单次激发多轨测量中收集前向散射光和后向散射光来提高收集效率的方法。我们的方法可以在不同的样品体积下采集信号,同时提供共焦拉曼光谱的精确空间选择性和非共焦拉曼光谱的整体灵敏度。此外,我们还表明,我们的方法可以减少探测器集成时间和激光功率。为了证明这一点,我们测量了聚苯乙烯微球和细菌孢子的拉曼光谱。对于孢子,我们可以以2.5m Wlaser功率捕获它们,并使用2 x 30 s的积分时间获取二吡啶甲酸钙峰的高信噪比功率谱。因此,我们的方法将使对高强度敏感的生物样品的监测时间更长。此外,我们还证明,通过一个简单的修改,我们可以增加极化灵敏度和检索额外的生化信息。(c)OSA开放获取出版协议条款下的美国2021光学学会

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