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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 >CW measurements of resonance Raman profiles, line-widths, and cross-sections of fluorescent dyes: Application to Nile Blue A in water and ethanol
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CW measurements of resonance Raman profiles, line-widths, and cross-sections of fluorescent dyes: Application to Nile Blue A in water and ethanol

机译:共振拉曼光谱,线宽和荧光染料截面的连续波测量:在水和乙醇中的尼罗蓝A的应用

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The aim of this work is to illustrate the power of recently developed methods for measuring resonance Raman scattering (RRS) spectra of efficient fluorophores (using a standard continuous wave excitation and a charge-coupled device (CCD)-based Raman spectrometer), by applying them to a detailed study of a specific fluorophore: Nile Blue A. A combination of methods are used to measure the RRS properties of Nile Blue A in water (quantum yield (QY) of 4%) and ethanol (QY of 22%) at excitation wavelengths between 514 and 647 nm, thus covering both pre-resonance and RRS conditions. Standard Raman measurements are used in situations where the fluorescence background is small enough to clearly observe the Raman peaks, while the recently introduced polarization-difference RRS and continuously shifted Raman scattering are used closer to (or at) resonance. We show that these relatively straightforward methods allow us to determine the Raman cross-sections of the most intense Raman peaks and provide an accurate measurement of their line-width; even for broadenings as low as ~ 4 cm ~(- 1). Moreover, the obtained Raman excitation profiles agree well with those derived from the optical absorption by a simple optical transform model. This study demonstrates the possibility of routine RRS measurements using standard Raman spectrometers, as opposed to more complicated time-resolved techniques.
机译:这项工作的目的是通过应用以下方法来说明最近开发的用于测量有效荧光团的共振拉曼散射(RRS)光谱的方法(使用标准的连续波激发和基于电荷耦合器件(CCD)的拉曼光谱仪)他们将对特定的荧光团:尼罗蓝A进行详细研究。使用多种方法来测量水中尼罗蓝A的RRS特性(量子产率(QY)为4%)和乙醇(量子产率为22%)。激发波长在514和647 nm之间,因此涵盖了预谐振和RRS条件。在荧光背景足够小以清楚地观察拉曼峰的情况下使用标准拉曼测量,而最近引入的偏振差RRS和连续移动的拉曼散射则用于接近(或处于)共振的情况。我们表明,这些相对简单的方法使我们能够确定最强烈的拉曼峰的拉曼横截面,并提供其线宽的准确测量值。甚至低至〜4 cm〜(-1)的展宽。此外,所获得的拉曼激发轮廓与通过简单的光学变换模型从光学吸收中得出的轮廓非常吻合。这项研究证明了使用标准拉曼光谱仪进行常规RRS测量的可能性,而不是更复杂的时间分辨技术。

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