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    Por favor, use este identificador para citar o enlazar este ítem: https://hdl.handle.net/10259/10768

    Título
    Dataset of the work “Determination of nicotine in e-liquids by electrochemical generation of surface-enhanced Raman scattering substrates”
    Autor
    Romay García, Luis
    Pérez Estébanez, MartínUBU authority Orcid
    Heras Vidaurre, AránzazuUBU authority Orcid
    Colina Santamaría, ÁlvaroUBU authority Orcid
    Editorial
    Universidad de Burgos
    Fecha de publicación
    2025-05-20
    DOI
    10.71486/qf7n-2b15
    Abstract
    Quantitative methods using surface-enhanced Raman scattering (SERS) for analysis in complex matrices are very attractive due to the high sensitivity and selectivity of this technique. In this work, a novel time-resolved electrochemical surface-enhanced Raman scattering (TR-EC-SERS) analytical method has been developed for the determination of nicotine in e-liquids of electronic cigarettes. One of the main challenges of SERS is its inherent lack of reproducibility. Here, this limitation was mitigated by employing an electrochemical pre-treatment step to generate a homogeneous distribution of silver nanoparticles (Ag-NPs) on a silver screen-printed electrode. The enhanced Raman scattering induced by the Ag-NPs enabled the detection of nicotine at nanomolar levels. The high sensitivity of the method allowed the quantitative analysis of diluted e-liquid samples, mitigating potential interferences from other components present in these complex matrices. Moreover, TR-EC-SERS, coupled with parallel factor analysis (PARAFAC), demonstrated the capability of trilinear spectroelectrochemistry data not only to detect nicotine but also to identify potential interfering compounds without prior knowledge of their spectral signatures. This multivariate approach offers significant potential for the detection of outliers in complex samples.
    Palabras clave
    SERS
    Spectroelectrochemistry
    PARAFAC
    Nicotine
    E-liquid
    Materia
    Química analítica
    Chemistry, Analytic
    Electroquímica
    Electrochemistry
    URI
    https://hdl.handle.net/10259/10768
    Referenciado en
    http://hdl.handle.net/10259/10194
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    Atribución 4.0 Internacional
    Documento(s) sujeto(s) a una licencia Creative Commons Atribución 4.0 Internacional
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