Issue 4, 2011

Luminescent properties of dye–PMMA composite nanospheres

Abstract

The luminescent properties of two types of dye-poly(methyl methacrylate) (PMMA) composite nanospheres were discussed and compared. Dye molecules (Ru(bpy)3Cl2) were combined with PMMA nanospheres in two strategies: embedding dye molecules during PMMA nanosphere formation (Em-PMMA NPs) and adsorbing dye molecules onto the surface of the produced PMMA nanospheres (Ad-PMMA NPs). It has been proved that the electrostatic interaction dominated the load of Ru(bpy)32+ on the PMMA matrix. The luminescence intensity of the Em-PMMA NPs was much higher than that of the Ad-PMMA NPs under same dye concentration due to different dye load distribution in two types of dye-PMMA composite nanospheres. Luminescence lifetime measurement of Ru(bpy)32+ in the Em-PMMA NPs (containing 2.20 × 103Ru(bpy)32+ molecules per NP) indicates that ∼60% of dye molecules loaded in inside of the PMMA matrix and ∼40% located close to/on the surface of NPs. For the Ad-PMMA NPs containing same amount of dye as Em-PMMA Nps, most of dye molecules (∼84%) were on the surface of NPs and only ∼16% of them penetrated into the PMMA matrix. The luminescence of the Em-PMMA NPs had nearly seven fold enhancement and the excited-state lifetime had nearly five fold extension relative to a dye aqueous solution. The mechanism of luminescence enhancement was studied. The results indicate that the larger viscosity and weaker polarity of a PMMA matrix led to the luminescence enhancement of Ru(bpy)32+. These luminescent PMMA nanospheres with high stability, long lifetime and high brightness hold great the potential for being a novel biological label.

Graphical abstract: Luminescent properties of dye–PMMA composite nanospheres

Supplementary files

Article information

Article type
Paper
Submitted
22 Jun 2010
Accepted
08 Oct 2010
First published
22 Nov 2010

Phys. Chem. Chem. Phys., 2011,13, 1560-1567

Luminescent properties of dye–PMMA composite nanospheres

X. Wang, S. Xu and W. Xu, Phys. Chem. Chem. Phys., 2011, 13, 1560 DOI: 10.1039/C0CP00929F

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