Quantum dots can absorb light and transfer it to graphene, but the efficiency of the transfer depends on how far the QDs and the graphene are separated from each other. This study demonstrated that the thickness of the organic molecule layer that typically surrounds the QDs is crucial in attaining sufficiently high efficiency of this light/energy transfer into the graphene. In other works, the thinner the organic layer, the better.
This transfer can be further optimized by engineering the interface between the two nanomaterials, specifically optimizing the thickness of the organic capping molecules on the quantum dots. Based on this work, further improvement of the performance of these nano-photonic devices can be expected.
Commercial cadmium selenide (CdSe) quantum dots have long insulating organic ligands that prevent their utilization in energy and charge transfer applications for which short distances between the QDs and other materials are critical. Short, chlorine ligands that passivated CdSe QDs are an intriguing alternative material to enhance the interaction with materials into which charge carriers, such as electrons, can easily conduct.
Graphene is such a material. The combination of CdSe quantum dots and graphene could hold the key to the development and implementation of nanoscale materials systems in flexible electronics and photodetectors.
What Are The Details?
— CFN Capabilities: The Advanced Optical Microscopy Facility measured the time-resolved photoluminescence from isolated CdSe quantum dots deposited on graphene.
— The team discovered that short, chloride-capped CdSe quantum dots, deposited on chemical-vapor-deposited, monolayer layer graphene, exhibited highly efficient energy transfer to the graphene with a 4x observed reduction in the excitonic lifetime. This demonstrated significant near-field coupling between quantum dots and the graphene.
More information: “Time-resolved energy transfer from single chloride-terminated nanocrystals to graphene.” O. A. Ajayi, et al. Appl. Phys. Lett. 104, 171101 (2014); dx.doi.org/10.1063/1.4874298