Polystyrene nanoparticles doped with a luminescent europium complex

[Display omitted] ► Polymer nanoparticles can be doped during miniemulsion polymerization. ► PS particles can be doped with Eu(tta)3phen at levels up to 2% by weight. ► Luminescence of the complex is unchanged by the polymer matrix. ► No self-quenching is found despite relatively high local Eu3+ con...

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Veröffentlicht in:Journal of colloid and interface science 2012-06, Vol.376 (1), p.12-19
Hauptverfasser: Desbiens, Jessie, Bergeron, Benjamin, Patry, Maxime, Ritcey, Anna M.
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Sprache:eng
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Zusammenfassung:[Display omitted] ► Polymer nanoparticles can be doped during miniemulsion polymerization. ► PS particles can be doped with Eu(tta)3phen at levels up to 2% by weight. ► Luminescence of the complex is unchanged by the polymer matrix. ► No self-quenching is found despite relatively high local Eu3+ concentrations. Polystyrene nanoparticles doped with a luminescent europium complex, Eu(tta)3phen, are prepared by miniemulsion polymerization. The influence of the complex on the miniemulsion polymerization is investigated by the systematic variation of the initial concentration of Eu(tta)3phen from 2 to 7wt% relatively to styrene. A maximum doping level of about 2% by weight in the final particles can be achieved. At higher doping levels, destabilization of the miniemulsion leads to a loss of reproducibility with respect to both the degree of conversion and the final Eu content of the particles. Doped nanoparticles of varying diameter, ranging from 19 to 94nm, are successfully prepared. Steady-state and time-resolved luminescence measurements indicate that the luminescence properties of Eu(tta)3phen in the doped latexes are unchanged from those found in THF solution. Aqueous dispersions of the doped particles exhibit characteristic red emission under UV light irradiation. The luminescence intensity increases linearly with Eu(tta)3phen content, indicating the absence of self-quenching despite the relatively high local concentrations within the particles.
ISSN:0021-9797
1095-7103
DOI:10.1016/j.jcis.2012.02.020