Abstract

The quantum dot, one of the central materials in nanoscience, is a semiconductor crystal with a physical size on the nanometer length scale. It is often called an "artificial atom" because researchers can create nanostructures which yield properties similar to those of real atoms. By virtue of having a size in between molecules and solids, the quantum dot offers a rich palette for exploring new science and developing novel technologies. Although the physical structure of quantum dots is well known, a clear understanding of the resultant electronic structure and dynamics has remained elusive. However, because the electronic structure and dynamics of the dot, the "excitonics", confer its function in devices such as solar cells, lasers, LEDs, and nonclassical photon sources, a more complete understanding of these properties is critical for device development. In this Account, we use colloidal CdSe dots as a test bed upon which to explore four select issues in excitonic processes in quantum dots. We have developed a state-resolved spectroscopic approach which has yielded precise measurements of the electronic structural dynamics of quantum dots and has made inroads toward creating a unified picture of many of the key dynamic processes in these materials. We focus on four main topics of longstanding interest and controversy: (i) hot exciton relaxation dynamics, (ii) multiexcitons, (iii) optical gain, and (iv) exciton-phonon coupling. Using this state-resolved approach, we reconcile long standing controversies related to phenomena such as exciton cooling and exciton-phonon coupling and make surprising new observations related to optical gain and multiexcitons.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.