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Controlling the spatial location of photoexcited electrons in semiconductor CdSe/CdS core/shell nanorods

Published

Author(s)

Chunxing She, Garnett W. Bryant, Arnaud Demorti?, Elena V. Shevchenko, Matthew Pelton

Abstract

It is commonly assumed that, after an electron-hole pair is created in a semiconductor by absorption of a photon, the electron and hole rapidly relax to their respective lowest-energy states before recombining with one another. In semiconductor heterostructure nanocrystals, however, intraband relaxation can be inhibited to the point where recombination occurs primarily from an excited state. We demonstrate this using time-resolved optical measurements for CdSe/CdS core/shell nanorods. For nanorods with large CdSe cores, an electron photoexcited into the lowest-energy state in the core remains in the core, and an electron photoexcited into an excited state in the CdS shell remains in the shell, until the electron recombines with the hole.
Citation
Physical Review B
Volume
87
Issue
15

Keywords

core-shell nanorods, quantum dots, tight-binding theory, transient absorption, emission

Citation

She, C. , Bryant, G. , Demorti?, A. , Shevchenko, E. and Pelton, M. (2013), Controlling the spatial location of photoexcited electrons in semiconductor CdSe/CdS core/shell nanorods, Physical Review B, [online], https://doi.org/10.1103/PhysRevB.87.155427, https://tsapps.nist.gov/publication/get_pdf.cfm?pub_id=910771 (Accessed April 17, 2024)
Created April 21, 2013, Updated October 12, 2021