Abstract
We demonstrate the formation and spatial modulation of strongly coupled gallium selenide quantum dot (QD) nanoassemblies suspended in a nematic liquid-crystal (NLC) matrix at room temperature. Using static and dynamic optical techniques we show that the coupled QDs aggregate with a well-defined directionality commensurate with the NLC director axis. This results in highly anisotropic spectral properties of the QD assembly. The spatial orientation of the aggregates is selectively controlled in situ by the application of in-plane electric fields. The strong interdot coupling further increases the excitonic recombination rate which is both direction and electric field dependent. This electrical modulation, a noninvasive process, could potentially be an important functionality for the design and creation of building blocks for novel optoelectronic devices.
- Received 7 June 2010
DOI:https://doi.org/10.1103/PhysRevB.82.165428
©2010 American Physical Society