Chloride-Induced Thickness Control in CdSe Nanoplatelets
Impact
![Google Scholar](/xmlui/themes/Mirage2/images/uji/logo_google.png)
![Microsoft Academico](/xmlui/themes/Mirage2/images/uji/logo_microsoft.png)
Metadata
Show full item recordcomunitat-uji-handle:10234/9
comunitat-uji-handle2:10234/7013
comunitat-uji-handle3:10234/8638
comunitat-uji-handle4:
INVESTIGACIONThis resource is restricted
http://dx.doi.org/10.1021/acs.nanolett.8b02361 |
Metadata
Title
Chloride-Induced Thickness Control in CdSe NanoplateletsAuthor (s)
Date
2018Publisher
ACS PublicationsISSN
1530-6984; 1530-6992Bibliographic citation
CHRISTODOULOU, Sotirios, et al. Chloride-Induced Thickness Control in CdSe Nanoplatelets. Nano letters, 2018, vol. 18, no 10, p. 6248-6254.Type
info:eu-repo/semantics/articlePublisher version
https://pubs.acs.org/doi/10.1021/acs.nanolett.8b02361Version
info:eu-repo/semantics/publishedVersionSubject
Abstract
Current colloidal synthesis methods for CdSe
nanoplatelets (NPLs) routinely yield samples that emit, in
discrete steps, from 460 to 550 nm. A significant challenge lies
with obtaining thicker NPLs, to further widen ... [+]
Current colloidal synthesis methods for CdSe
nanoplatelets (NPLs) routinely yield samples that emit, in
discrete steps, from 460 to 550 nm. A significant challenge lies
with obtaining thicker NPLs, to further widen the emission
range. This is at present typically achieved via colloidal atomic
layer deposition onto CdSe cores, or by synthesizing NPL
core/shell structures. Here, we demonstrate a novel reaction
scheme, where we start from 4.5 monolayer (ML) NPLs and
increase the thickness in a two-step reaction that switches
from 2D to 3D growth. The key feature is the enhancement of
the growth rate of basal facets by the addition of CdCl2, resulting in a series of nearly monodisperse CdSe NPLs with
thicknesses between 5.5 and 8.5 ML. Optical characterization yielded emission peaks from 554 nm up to 625 nm with a line
width (fwhm) of 9−13 nm, making them one of the narrowest colloidal nanocrystal emitters currently available in this spectral
range. The NPLs maintained a short emission lifetime of 5−11 ns. Finally, due to the increased red shift of the NPL band edge
photoluminescence excitation spectra revealed several high-energy peaks. Calculation of the NPL band structure allowed us to
identify these excited-state transitions, and spectral shifts are consistent with a significant mixing of light and split-off hole states.
Clearly, chloride ions can add a new degree of freedom to the growth of 2D colloidal nanocrystals, yielding new insights into
both the NPL synthesis as well as their optoelectronic properties [-]
Is part of
Nano Lett. 2018, 18.Investigation project
CTQ2017-83781-P; B2017-59; Grant 696656 GrapheneCore1; Grant 714876 PHOCONARights
© 2018 American Chemical Society
http://rightsstatements.org/vocab/InC/1.0/
info:eu-repo/semantics/restrictedAccess
http://rightsstatements.org/vocab/InC/1.0/
info:eu-repo/semantics/restrictedAccess
This item appears in the folowing collection(s)
- QFA_Articles [829]