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DOI 10.1016/j.saa.2014.02.020

Медицинская библиотека · Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy · 2014

Kinetic fluorescence quenching of CdS quantum dots in the presence of Cu(II): chemometrics-assisted resolving of the kinetic data and quantitative analysis of Cu(II).

Abdollahi Hamid, Shamsipur Mojtaba, Barati Ali

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Аннотация

In this work, the kinetic fluorescence behavior of CdS quantum dots (QDs) in the presence of Cu(II) was investigated. In contrast to some other transition metal ions such as Ag(I), Ni(II), and Hg(II), a gradual red-shift in the emission spectrum of CdS QDs was observed for Cu(II) during the reaction course. More investigations revealed the existence of two chemical components in the recorded kinetic data in the presence of Cu(II). Multivariate curve resolution-alternating least squares (MCR-ALS) method was applied in order to extract pure emission spectra and time-dependent profiles of these two components at different concentrations of Cu(II). The results obtained from resolving the data by MCR-ALS got some information about the mechanism of the interaction between CdS QDs and Cu(II) ions which were in good agreement with those reported in the literature. Moreover, the multivariate method of analysis, partial least-squares (PLS) method, was used to develop a multivariate calibration model for quantitative analysis of Cu(II) using the entire kinetic data sets. The calibration and validation sets were created ranging from 0.02 to 1μM of Cu(II) and were successfully calibrated and predicted by the PLS model. This method allowed a sensitive determination of Cu(II) ions with a detection limit of 13nM based on three times of the standard deviation corresponding to PLS regression.

Для цитирования: Abdollahi Hamid, Shamsipur Mojtaba, Barati Ali. Kinetic fluorescence quenching of CdS quantum dots in the presence of Cu(II): chemometrics-assisted resolving of the kinetic data and quantitative analysis of Cu(II).. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy. 2014. DOI: 10.1016/j.saa.2014.02.020.

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