Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14279/19922
Title: Exciton–Ligand Interactions in PbS Quantum Dots Capped with Metal Chalcogenides
Authors: Papagiorgis, Paris 
Tsokkou, Demetra 
Kushagra, Gahlot 
Protesescu, Loredana 
Manoli, Andreas 
Hermerschmidt, Felix 
Christodoulou, Constantinos 
Choulis, Stelios A. 
Kovalenko, Maksym V. 
Othonos, Andreas S. 
Itskos, Grigorios 
Major Field of Science: Engineering and Technology
Field Category: Electrical Engineering - Electronic Engineering - Information Engineering
Keywords: Colloidal quantum dots;Surface passivation;Colloidal solubility;Spectroscopic investigation
Issue Date: 2020
Source: The Journal of Physical Chemistry C, 2020, vol. 124. no. 50, pp. 27848–27857
Volume: 125
Issue: 50
Start page: 27848
End page: 27857
Journal: The Journal of Physical Chemistry C 
Abstract: Colloidal quantum dots (CQDs) are typically decorated with organic molecules that provide surface passivation and colloidal solubility. An alternate but less studied surface functionalization approach via inorganic complexes can produce stable CQDs with attractive transport and optical properties. Further development of such all-inorganic CQD solids is dependent on the deeper understanding of the energetic and dynamic interactions of the new ligands with the CQD excitons. Herein, a series of four metal chalcogenide (MCC) ligands of the KzXS4 type were attached to PbS CQDs. Out of the four MCC complexes studied, we find that only K4GeS4 ligands yield robust PbS CQD films with bright photoluminescence (PL) in the solid state. A systematic spectroscopic investigation of the K4GeS4-capped CQD films provides evidence of the temperature-dependent ligand-mediated exciton delocalization and trapping processes. At low temperatures, efficient trapping at ligand-induced states is found to occur within ∼6 ns after photoexcitation, followed by a considerably slower exciton back transfer to the CQD core. At elevated temperatures, the CQD films become photoconductive, providing evidence of exciton dissociation via carrier transfer within adjacent dots. The addition of a thin CdS shell suppresses the delocalization and trapping of excitons, resulting in brighter emission and significantly slower transient absorption and PL dynamics.
URI: https://hdl.handle.net/20.500.14279/19922
ISSN: 19327447
DOI: 10.1021/acs.jpcc.0c09790
Rights: © American Chemical Society
Type: Article
Affiliation : Cyprus University of Technology 
University of Cyprus 
Institute of Inorganic Chemistry 
University of Groningen 
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