4.8 Article

Probing the Wave Function Delocalization in CdSe/CdS Dot-in-Rod Nanocrystals by Time- and Temperature-Resolved Spectroscopy

Journal

ACS NANO
Volume 5, Issue 5, Pages 4031-4036

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/nn2005969

Keywords

colloidal nanocrystals; band alignment; exciton dynamics

Funding

  1. European Community [214954 (HERODOT)]

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Colloidal semiconductor quantum structures allow controlling the strong confinement of charge carriers through material composition and geometry. Besides being a unique platform to study fundamental effects, these materials attracted considerable interest due to their potential in opto-electronic and quantum communication applications. Heteronanostructures like CdSe/CdS offer new prospects to tailor their optical properties as they take advantage of a small conduction band offset allowing tunability of the electron delocalization from type-I toward quasi-type-II. Here, we report on a detailed study of the exciton recombination dynamics in CdSe/CdS heterorods. We observed a clear size-dependent radiative lifetime, which can be linked to the different degree of electron wave function (de)localization. Moreover, by increasing the temperature from 70 to 300 K, we observed a considerable increase of the radiative lifetime, clearly demonstrating a reduction of the conduction band offset at higher temperatures. Understanding and controlling electron delocalization In such heterostructures will be pivotal for realizing efficient and low-cost photonic devices.

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