Colloidal quantum dots (QDs) have attracted interest as materials for opto-electronic applications, wherein their efficient energy use requires the understanding of carrier relaxation. In QDs capped by bifunctional thiols, used to attach the QDs to a surface, the relaxation is complicated by carrier traps. Using 2D spectroscopy at 77 K, we follow excitations in thiol-capped CdSe QDs with state specificity and high time resolution. We unambiguously identify the lowest state as an optically allowed hole trap, and identify an electron trap with excited-state absorption. The presence of traps changes the initial dynamics entirely by offering a different relaxation channel. 2D electronic spectroscopy enables us to pinpoint correlations between states and to easily separate relaxation from different starting states. We observe the direct rapid trapping of 1S, 2S, and 1S holes, and several competing electron relaxation processes from the 1P state.
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http://dx.doi.org/10.1039/c6cp04190f | DOI Listing |
Nanomaterials (Basel)
April 2019
Jiangsu Engineering Laboratory of Nuclear Energy Equipment Materials, College of Material Science and Technology, Nanjing University of Aeronautics and Astronautics, Nanjing 210016, China.
Quantum dots (QDs) have attracted great attention due to their unique optical properties. High fluorescence efficiency is very important for their practical application. In this study, we report a simple and efficient strategy to enhance the photoluminescence of water-dispersed thiol-capped QDs using γ-radiation.
View Article and Find Full Text PDFPhys Chem Chem Phys
February 2019
Siberian Federal University, Svobodny Prospect 79, 660041 Krasnoyarsk, Russia.
The photoluminescence (PL) properties of composites obtained by embedding green-emitting semiconductor nanocrystals (NCs) of two different types (thiol-capped CdTe and CdSe/ZnS) into chitosan-based biopolymer particles were investigated. The synthesis of self-assembled particles from oppositely charged polysaccharides involved a preliminary electrostatic binding of positively charged chitosan chains by negatively charged functional groups of NC stabilizing ligands. The amount of NCs and the acidity of the solution were found to be important parameters influencing the PL.
View Article and Find Full Text PDFSpectrochim Acta A Mol Biomol Spectrosc
November 2018
Department of Chemistry, Faculty of Natural and Agricultural Sciences, University of Pretoria, Lynnwood Road, Pretoria 0002, South Africa. Electronic address:
Triclosan (TCS) is a common antimicrobial found in many personal care products. A large amount of TCS thus enters the wastewater system leading to the accumulation thereof in water sources. In this work, core-shell structured GSH-CdSe/ZnS fluorescent quantum dots (QDs) were synthesized based on organometallic synthesis with a thiol ligand capping agent.
View Article and Find Full Text PDFNanoscale
July 2018
Department of Chemical Science and U.R. INSTM, University of Padova, Via Marzolo 1, I-35131, Padova, Italy.
Here we present a comprehensive study on the photophysics of QDs-fullerene blends, aiming to elucidate the impact of ligands on the extraction of carriers from QDs. We investigated how three different ligands (oleylamine, octadecanethiol and propanethiol) influence the dynamics of charge generation, separation, and recombination in blends of CdSe/CdS core/shell QDs and PCBM. We accessed each relevant process directly by combining the results from both optical and magnetic spectroscopies.
View Article and Find Full Text PDFPhys Chem Chem Phys
September 2016
Department of Chemical Physics, Lund University, PO Box 124, 221 00 Lund, Sweden.
Colloidal quantum dots (QDs) have attracted interest as materials for opto-electronic applications, wherein their efficient energy use requires the understanding of carrier relaxation. In QDs capped by bifunctional thiols, used to attach the QDs to a surface, the relaxation is complicated by carrier traps. Using 2D spectroscopy at 77 K, we follow excitations in thiol-capped CdSe QDs with state specificity and high time resolution.
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