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Charge transfer dynamics of the CdTe quantum dots fluorescence quenching induced by ferrous (II) ions
12
Citations
31
References
2020
Year
EngineeringColloidal NanocrystalsChemistryPhosphorescence ImagingCharge Transfer DynamicsQuantum DotsBioimagingCharge SeparationCation SensingPhotophysical PropertyBiophysicsPhotochemistryNanotechnologySingle-molecule DetectionFe2+ AdditionExcited State PropertyCdte QdsApplied PhysicsCdte Quantum Dots
Size dependence of glutathione capped CdTe quantum dots (GSH-CdTe QDs) on the sensitivity and selectivity in the fluorometric detection of ferrous (II) ions (Fe2+) has been systematically investigated. Smaller-size QDs show higher sensitivity in the detection of Fe2+, resulting in higher quenching efficiency and red shift of the fluorescence peak of QDs. Stern–Volmer plots indicate that the charge transfer model can be employed to account for the observed fluorescence quenching effect. Fe2+ is bound to the surface of QDs by GSH and excited electrons are transferred from QDs to Fe2+, which facilitates a nonradiative recombination process and a decrease in the PL efficiency. In addition, the results from time resolved photoluminescence and a confocal scanning fluorescence microscope have shown that smaller-size QDs have a faster decrease in the fluorescence lifetime compared with that of larger-size QDs with Fe2+ addition, suggesting that the fast charge transfer in smaller-size QDs should be responsible for the observed fluorescence quenching effect. This Letter provides a comprehensive understanding of the mechanism of the fluorescence for the CdTe QDs quenched by Fe2+.
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