Abstract

The purpose of this study is to investigate the time dependent growth of silica shells on CdTe quantum dots to get their optimum thicknesses for practical applications. The core/shell structured silica-coated CdTe quantum dots (CdTe/SiO2 QDs) were synthesized by the Ströber process, which used CdTe QDs co-stabilized by mercaptopropionic acid. The coating procedure used silane primer (3-mercaptopropyltrimethoxysilane) in order to make the quantum dots (QDs) surface vitreophilic. The total size of QDs was dependent on both the time of silica shell growth in the presence of sodium silicate, and on the presence of ethanol during this growth. The size of particles was monitored during the first 72 h using two principally different methods: Dynamic Light Scattering (DLS), and Scanning Electron Microscopy (SEM). The data obtained by both methods were compared and reasons for differences discussed. Without ethanol precipitation, the silica shell thickness grew slowly and increased the nanoparticle total size from approximately 23 nm up to almost 30 nm (DLS data), and up to almost 60 nm (SEM data) in three days. During the same time period but in the presence of ethanol, the size of CdTe/SiO2 QDs increased more significantly: up to 115 nm (DLS data) and up to 83 nm (SEM data). The variances occurring between silica shell thicknesses caused by different methods of silica growth, as well as by different evaluation methods, were discussed.

Highlights

  • Quantum dots (QDs) are fluorescent semiconductor nanocrystals which are being extensively developed because of their unique size-dependent optical and photophysical properties [1]

  • The purpose of this study is to investigate the time dependent growth of silica shells on CdTe quantum dots to get their optimum thicknesses for practical applications

  • We have presented a method to coat luminescent quantum dots (QDs) with silica shells based on the Ströber process

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Summary

Introduction

Quantum dots (QDs) are fluorescent semiconductor nanocrystals which are being extensively developed because of their unique size-dependent optical and photophysical properties [1]. These properties have made QDs ideal for applications in mainstream market products [2], but most importantly, in science as labels for tagging and imaging in biological systems [3]. The following problems remain when using QDs as fluorescent biological labels: (i) strong dependence of the fluorescence on surface states [7], (ii) cytotoxicity as a result of the release of heavy metal ions [8], (iii) chemical and colloidal instabilities of QDs in harsh environments, as well as (iv) toxicity for non-target organisms in the environment [9,10]. The most commonly used are ZnS [11], various polymers [12], and silicates [13,14]

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