Lellinger Dirk, Thomson James, Coca-Lopez Nicolas, Ntziouni Afroditi, Nikoloudakis Nikolaos, Fernández-Álvarez María, Jeliazkova Nina, Bañares Miguel A, Portela Raquel, Diz Enrique Lozano
Fraunhofer LBF, Darmstadt, Germany.
ELODIZ Ltd., High Wycombe, UK.
Appl Spectrosc. 2025 Apr 24:37028251330654. doi: 10.1177/00037028251330654.
Raman spectroscopy is a powerful characterization technique with increasing applications that would greatly benefit from data harmonization. Several standards deal with calibration in Raman spectroscopy, but no detailed procedure covers the complete calibration of an instrument, including both spectral axes, from reference material spectra generation to data processing. Moreover, the type of reference materials, the quality of the recorded spectra and the choice of the fitting functions are critical for obtaining precise and reliable reference data for calibration. This report describes the challenges and importance of peak fitting for Raman signal calibration based on an interlaboratory study with 10 different instruments. Spectra of neon emission, silicon, calcite, and polystyrene were fitted using common peak shapes, observing that Gaussian, Pearson IV, Voigt, and Voigt shapes are preferred for these materials, respectively. An analysis of the effect on the fitting of the signal-to-noise ratio (S/N) recommends a minimum value of 100 for a Raman peak if it should be used to calibrate a Raman instrument. Some factors that might affect the peak shape of the Raman signal, such as the physical and chemical properties of the sample, the nature of the electronic transitions, the instrument response and the spectral resolution are discussed. The results highlight the role of peak fitting analysis in improving the quality and reliability of Raman spectra calibration and, thus, enhancing data transfer and comparability, especially for handheld and portable Raman analyzers, as well as applications based on quantification, multivariate data analysis, and other complex processing steps.
拉曼光谱是一种强大的表征技术,其应用日益广泛,数据协调将使其受益匪浅。有几项标准涉及拉曼光谱的校准,但没有详细程序涵盖仪器的完整校准,包括从参考物质光谱生成到数据处理的两个光谱轴。此外,参考物质的类型、记录光谱的质量以及拟合函数的选择对于获得精确可靠的校准参考数据至关重要。本报告基于对10台不同仪器的实验室间研究,描述了拉曼信号校准中峰拟合的挑战和重要性。使用常见峰形对氖发射、硅、方解石和聚苯乙烯的光谱进行拟合,观察到高斯、皮尔逊IV、沃伊特和沃伊特峰形分别适用于这些材料。对信噪比(S/N)对拟合的影响分析表明,如果要用于校准拉曼仪器,拉曼峰的最小值应为100。讨论了一些可能影响拉曼信号峰形的因素,如样品的物理和化学性质、电子跃迁的性质、仪器响应和光谱分辨率。结果突出了峰拟合分析在提高拉曼光谱校准质量和可靠性方面的作用,从而增强数据传输和可比性,特别是对于手持式和便携式拉曼分析仪,以及基于定量、多变量数据分析和其他复杂处理步骤的应用。