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Steady state and time resolved spectroscopic study of C-dots―MEH―PPV polymer nanoparticles composites
Fluorescent carbon dots (C-dots) have been found to be a new class of nanomaterial for potential applications. Herein, polyethylenimine branched (BPEI) functionalized carbon dots (C-dots) are synthesized by changing the synthesis time using a microwave pyrolysis method. The photoluminescence intensi...
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Published in: | Physical chemistry chemical physics : PCCP 2013-10, Vol.15 (39), p.16834-16840 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Fluorescent carbon dots (C-dots) have been found to be a new class of nanomaterial for potential applications. Herein, polyethylenimine branched (BPEI) functionalized carbon dots (C-dots) are synthesized by changing the synthesis time using a microwave pyrolysis method. The photoluminescence intensity and average decay time of C-dots are found to be increased with increasing the crystallinity of the C-dots. C-dots-MEH-PPV polymer nanoparticles composites are formed by electrostatic interaction between these particles. The intensity of C-dots quenches dramatically with increasing the concentration of MEH-PPV nanoparticles (PNPs) and the intensity of PNPs increases gradually under excitation at 370 nm. This phenomenon may be due to energy transfer from C-dots to PNPs because there is a good spectral overlap between the emission spectra of C-dots and the absorption spectra of PNPs. The drastic photoluminescence quenching and the shortening of the decay time of C-dots in the composites confirms the efficient resonance energy transfer from C-dots to polymer nanoparticles. The energy transfer efficiency (66% to 89%) and rate of energy transfer are found to depend strongly on the time of pyrolysis. These C-dots-polymer composites will open up a way for developing new challenging materials for potential applications. |
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ISSN: | 1463-9076 1463-9084 |
DOI: | 10.1039/c3cp51547h |