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拉曼峰拟合及其在拉曼定量研究中的应用实证研究

An Empirical Study on Raman Peak Fitting and Its Application to Raman Quantitative Research.

作者信息

Yuan Xueyin, Mayanovic Robert A

机构信息

1 MLR Key Laboratory of Metallogeny and Mineral Assessment, Institute of Mineral Resources, Chinese Academy of Geological Sciences, Beijing, China.

2 Department of Physics, Astronomy and Material Science, Missouri State University, Springfield, MO, USA.

出版信息

Appl Spectrosc. 2017 Oct;71(10):2325-2338. doi: 10.1177/0003702817721527. Epub 2017 Aug 7.

Abstract

Fitting experimentally measured Raman bands with theoretical model profiles is the basic operation for numerical determination of Raman peak parameters. In order to investigate the effects of peak modeling using various algorithms on peak fitting results, the representative Raman bands of mineral crystals, glass, fluids as well as the emission lines from a fluorescent lamp, some of which were measured under ambient light whereas others under elevated pressure and temperature conditions, were fitted using Gaussian, Lorentzian, Gaussian-Lorentzian, Voigtian, Pearson type IV, and beta profiles. From the fitting results of the Raman bands investigated in this study, the fitted peak position, intensity, area and full width at half-maximum (FWHM) values of the measured Raman bands can vary significantly depending upon which peak profile function is used in the fitting, and the most appropriate fitting profile should be selected depending upon the nature of the Raman bands. Specifically, the symmetric Raman bands of mineral crystals and non-aqueous fluids are best fit using Gaussian-Lorentzian or Voigtian profiles, whereas the asymmetric Raman bands are best fit using Pearson type IV profiles. The asymmetric O-H stretching vibrations of HO and the Raman bands of soda-lime glass are best fit using several Gaussian profiles, whereas the emission lines from a florescent light are best fit using beta profiles. Multiple peaks that are not clearly separated can be fit simultaneously, provided the residuals in the fitting of one peak will not affect the fitting of the remaining peaks to a significant degree. Once the resolution of the Raman spectrometer has been properly accounted for, our findings show that the precision in peak position and intensity can be improved significantly by fitting the measured Raman peaks with appropriate profiles. Nevertheless, significant errors in peak position and intensity were still observed in the results from fitting of weak and wide Raman bands having unnormalized intensity/FWHM ratios lower than 200 counts/cm.

摘要

将实验测量的拉曼光谱带与理论模型轮廓进行拟合,是对拉曼峰参数进行数值测定的基本操作。为了研究使用各种算法进行峰建模对峰拟合结果的影响,对矿物晶体、玻璃、流体的代表性拉曼光谱带以及荧光灯的发射线进行了拟合,其中一些是在环境光下测量的,而另一些是在高压和高温条件下测量的,使用了高斯、洛伦兹、高斯 - 洛伦兹、沃伊特、皮尔逊IV型和贝塔轮廓进行拟合。从本研究中所研究的拉曼光谱带的拟合结果来看,所测拉曼光谱带的拟合峰位置、强度、面积和半高宽(FWHM)值会因拟合中使用的峰轮廓函数不同而有显著变化,应根据拉曼光谱带的性质选择最合适的拟合轮廓。具体而言,矿物晶体和非水流体的对称拉曼光谱带使用高斯 - 洛伦兹或沃伊特轮廓拟合效果最佳,而非对称拉曼光谱带使用皮尔逊IV型轮廓拟合效果最佳。HO的不对称O - H伸缩振动和钠钙玻璃的拉曼光谱带使用多个高斯轮廓拟合效果最佳,而荧光灯的发射线使用贝塔轮廓拟合效果最佳。如果一个峰拟合中的残差不会对其余峰的拟合产生显著影响,那么未清晰分离的多个峰可以同时进行拟合。一旦正确考虑了拉曼光谱仪的分辨率,我们的研究结果表明,通过用适当的轮廓拟合测量的拉曼峰,可以显著提高峰位置和强度的精度。然而,在拟合强度/半高宽比低于200计数/cm的弱且宽的拉曼光谱带的结果中,仍观察到峰位置和强度存在显著误差。

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