The purpose of our study was to develop methods for creating hybrid nanostructures based on colloidal Ag2S quantum dots, pyramidal silver nanoparticles, Au nanorods, and to determine the spectral-luminescent manifestations of exciton-plasmon interactions in these structures. The objects of the study were Ag2S quantum dots passivated with thioglycolic acid (Ag2S/TGA QDs) and 2-mercaptopropionic acid (Ag2S/2-MPA QDs), gold nanorods (Au NRs), silver nanoparticles with pyramidal geometry (Ag NPs), and their mixtures. The spectral properties were studied using a USB2000+ with a PMC-100-20 photomultiplier system (Becker & Hickl Germany). The article considers the transformation of the luminescence spectra of colloidal Ag2S/TGA QDs and Ag2S/2-MPA QDs in mixtures with pyramidal Ag NPs and Au NRs. The study demonstratedthe presence of the effects of the contour transformation of the luminescence spectra due to the Fano effect, as well as the luminescence quenching following direct contact between QDs and NPs
A technique of obtaining plexitonic structures based on Ag2S quantum dots passivated with l-cysteine (Ag2S/l-Cys QDs) in the presence of Au nanorods passivated with cetyltrimethylammonium bromide molecules (Au/CTAB NRs) with controlled luminescence was developed.
The aim of the study is to establish spectral-luminescent interaction effects in mixtures of colloidal Zn0.5Cd0.5S quantum dots passivated with 2-mercaptopropionic acid and Au and Au/SiO2nanoparticles. The studied samples of Zn0.5Cd0.5S quantum dots, Au and Au/SiO2 nanoparticles and their mixtures were obtained by methods of colloidal synthesis and were characterised using transmission electron microscopy. The absorption, luminescence and time-resolved luminescence spectroscopy were used as the main investigation methods. The measurements were carried out at temperatures of 77 K and 300 K. The spectral-luminescent properties of “free” Zn0.5Cd0.5S quantum dots and those interacting with Au and Au/SiO2 nanoparticles were compared. It was found that the luminescence properties of Zn0.5Cd0.5S quantum dots can be controlled under conditions of changing plasmon-exciton coupling achieved during the formation of a dielectric SiO2 shell on the surface of Au nanoparticles as well as a result of a polymer introduced into the colloidal mixture.
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