Abstract

Photoluminescent quantum dots are used in a range of applications that exploit the unique size tuneable emission, light harvesting and quantum efficient properties of these semiconductor nanocrystals. However, optical instabilities such as photoluminescence intermittency, the stochastic switching between bright, emitting states and dark states, can hinder quantum dot performance. Correlations between this blinking of emission and the dielectric properties of the nanoenvironment between the quantum dot interface and host medium, suggest surface ligands play a role in modulating on-off switching rates. Here we elucidate the nature of the cadmium selenide nanocrystal surface, by combining magic angle spinning NMR and x-ray photoelectron spectroscopy to determine ligand surface densities, with molecular dynamics simulation to assess net ligand filling at the nanocrystal interface. Results support a high ligand coverage and are consistent with photoluminescence intermittency measurements that indicate a dominant contribution from surface ligand to the dielectric properties of the local quantum dot environment.

Highlights

  • Photoluminescent quantum dots are used in a range of applications that exploit the unique size tuneable emission, light harvesting and quantum efficient properties of these semiconductor nanocrystals

  • A number of analytical methods have emerged to study a wide variety of nanoparticles including gold, palladium and platinum nanoparticles using a range of techniques such as thermogravimetric analysis (TGA), Rutherford backscattering spectroscopy (RBS) and x-ray photoelectron spectroscopy (XPS)[17]

  • We show that ligand coverage of the quantum dots (QDs) surface derived from our analysis of high resolution magic angle spinning (HR-MAS) NMR and XPS spectra is consistent with dielectric dependent photoluminescence intermittency (PI) measurements on single CdSe QDs that support a lead contribution of the ligand to the effective dielectric properties of the QD nanoenvironment within the charge-tunnelling and self-trapping (CTST) framework

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Summary

Introduction

Photoluminescent quantum dots are used in a range of applications that exploit the unique size tuneable emission, light harvesting and quantum efficient properties of these semiconductor nanocrystals. We show that ligand coverage of the QD surface derived from our analysis of HR-MAS NMR and XPS spectra is consistent with dielectric dependent PI measurements on single CdSe QDs that support a lead contribution of the ligand to the effective dielectric properties of the QD nanoenvironment within the CTST framework.

Results
Conclusion
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