Tuning the Crystal Structure of the Epitaxial CdS Shells on Zinc- Blende CdSe Nanocrystals: Lattice Defects and Electronic Traps

摘要

The CdS shells are epitaxially grown onto monodisperse zincblende CdSe core nanocrystals in octadecene mixed with fatty amines, with the volume fraction of fatty amines in the epitaxy solution (V-NH2) varying between 0 and 100%. The shape -except the nanoplatelets from the reactions with medium V-NH2 (especially 20% V-NH2)-and surface ligands of the resulting CdSe/CdS core/shell nanocrystals from all reactions can be unified through a two-step surface treatment. The internal lattice defects originated from zinc-blende/wurtzite stacking fault(s), i.e., wurtzite lattice domain(s) in the CdS shells and twin fault(s) in the zinc-blende region, can be systematically controlled by varying the V-NH2 and remain unaltered during the surface treatments. Both twin faults and wurtzite CdS lattice domains neither affect the electronic structure of the core/shell nanocrystals nor create internal electronic defects for the nanocrystals. Photoluminescence decay dynamics of the dot-shaped core/shell nanocrystals with solely twin faults can be mono-exponential and near-unity radiative decay, but photoluminescence of those with wurtzite CdS domains would always decay with double-exponential even if the photoluminescence quantum yield is unity. The results here imply that the most common lattice defects related to the stacking faults for II-VI and III-V semiconductor nanocrystals can be managed for achieving high-quality optical properties.

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