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Revisiting the Anion Framework Conservation in Cation Exchange Processes
Author(s) -
Noga Meir,
Beatriz MartínGarcía,
Iwan Moreels,
Dan Oron
Publication year - 2016
Publication title -
chemistry of materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.741
H-Index - 375
eISSN - 1520-5002
pISSN - 0897-4756
DOI - 10.1021/acs.chemmater.6b03332
Subject(s) - dopant , nanorod , exciton , ion exchange , ion , doping , chemistry , chemical physics , fluorescence , exchange interaction , crystal structure , materials science , crystallography , inorganic chemistry , nanotechnology , condensed matter physics , physics , optics , optoelectronics , ferromagnetism , organic chemistry
We investigated the effect of cation exchange on the anionic framework of lightly doped CdSe:Te/CdS nanorods. In contrast with previously studied core/shell systems, the Te dopant, located in the center of the CdSe core, provides an extremely sensitive indicator for any structural changes of the anionic framework that may occur as a result of the cation exchange process. We first optimized the cation exchange procedure in order to retain the fluorescence properties of the CdSe:Te/CdS nanorods after exchange of Cd2+ for Cu+ and back to Cd2+. Next, using multiexciton spectroscopy, we were able to probe the magnitude of the exciton–exciton repulsion interaction and use that to assess the degree of crystal structure conservation. Our findings provide a much stronger proof that the anion framework is indeed rigid, showing no evidence of significant migration of the anionic dopant.

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