Surfactant-dependent photoluminescence of CdTe/CdS nanocrystals

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 Cd2+ were compared to determine the best synthesis conditions for high photoluminescent quantum yield (PLQY) and photostability. A diff...

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Main Authors: Karolis Virzbickas, Laura Rimkute, Andrew J Harvie, Kevin Critchley
Format: Article
Language:English
Published: Taylor & Francis Group 2017-01-01
Series:Journal of Experimental Nanoscience
Subjects:
TGA
Online Access:http://dx.doi.org/10.1080/17458080.2016.1273553
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spelling doaj-1a701f3dd54e42ca8392d17bdf935a822020-11-25T00:18:42ZengTaylor & Francis GroupJournal of Experimental Nanoscience1745-80801745-80992017-01-011219410310.1080/17458080.2016.12735531273553Surfactant-dependent photoluminescence of CdTe/CdS nanocrystalsKarolis Virzbickas0Laura Rimkute1Andrew J Harvie2Kevin Critchley3University of LeedsUniversity of LeedsUniversity of LeedsUniversity of LeedsThe 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 Cd2+ 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/Cd2+ 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/Cd2+ 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/Cd2+ 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.http://dx.doi.org/10.1080/17458080.2016.1273553CdTe/CdSphotoluminescenceTGAblinkingphotostability
collection DOAJ
language English
format Article
sources DOAJ
author Karolis Virzbickas
Laura Rimkute
Andrew J Harvie
Kevin Critchley
spellingShingle Karolis Virzbickas
Laura Rimkute
Andrew J Harvie
Kevin Critchley
Surfactant-dependent photoluminescence of CdTe/CdS nanocrystals
Journal of Experimental Nanoscience
CdTe/CdS
photoluminescence
TGA
blinking
photostability
author_facet Karolis Virzbickas
Laura Rimkute
Andrew J Harvie
Kevin Critchley
author_sort Karolis Virzbickas
title Surfactant-dependent photoluminescence of CdTe/CdS nanocrystals
title_short Surfactant-dependent photoluminescence of CdTe/CdS nanocrystals
title_full Surfactant-dependent photoluminescence of CdTe/CdS nanocrystals
title_fullStr Surfactant-dependent photoluminescence of CdTe/CdS nanocrystals
title_full_unstemmed Surfactant-dependent photoluminescence of CdTe/CdS nanocrystals
title_sort surfactant-dependent photoluminescence of cdte/cds nanocrystals
publisher Taylor & Francis Group
series Journal of Experimental Nanoscience
issn 1745-8080
1745-8099
publishDate 2017-01-01
description 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 Cd2+ 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/Cd2+ 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/Cd2+ 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/Cd2+ 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.
topic CdTe/CdS
photoluminescence
TGA
blinking
photostability
url http://dx.doi.org/10.1080/17458080.2016.1273553
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AT laurarimkute surfactantdependentphotoluminescenceofcdtecdsnanocrystals
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