Surfactant-dependent photoluminescence of CdTe/CdS nanocrystals. Issue 1 (1st January 2017)

• Record Type: Journal Article
• Authors: Virzbickas, Karolis; Rimkute, Laura; Harvie, Andrew J; Critchley, Kevin
• Is Part Of: Journal of experimental nanoscience. Volume 12:Issue 1(2017)
• Page Start: 94
• Page End: 103
• Publication Date: 2017-01-01
• Subjects: CdTe/CdS -- photoluminescence -- TGA -- blinking -- photostability; Nanoscience -- Periodicals; Nanotechnology -- Periodicals; Nanomedicine -- Periodicals; Nanotechnology -- Periodicals; 620.5
• DOI: 10.1080/17458080.2016.1273553
• Languages: English
• ISSNs: 1745-8080

Abstract

ABSTRACT: The photoluminescence of aqueously synthesised core/shell CdTe/CdS quantum dots (QDs) was investigated. Two molar ratios (2.4 and 1.3) of thioglycolic acid (TGA) to Cd 2+ were compared to determine the best synthesis conditions for high photoluminescent quantum yield (PLQY) and photostability. A difference in the PLQY of the CdTe/CdS QDs was observed when CdS shells were grown with different TGA/Cd 2+ ratios. The difference in the observed PLQY was attributed to the quality of the passivation of the CdTe during the CdS shell growth. At TGA/Cd 2+ ratio of 1.3, the CdS shell forms through homogeneous nucleation, which is limited by diffusion of growth material from the solution onto the QDs surface. Due to the lattice mismatch of CdTe and CdS, the core will experience coherence strain resulting in dislocation sites and surface defects between nucleation sites which can result in non-radiative trap states. When the TGA/Cd 2+ ratio is 2.0, the CdS shell grows epitaxially, minimising the number of surface trap states. Finally, we observed that the fluorescence intermittency was supressed for CdTe QDs after UV light illumination, attributed to annealing of deep surface trap states by UV light.