4 results match your criteria: "Affiliated to University of Kalyani[Affiliation]"

Herein, we present a pioneering approach to enhancing Förster resonance energy transfer (FRET) efficiency through the synergistic integration of cetyltrimethylammonium bromide (CTAB) surfactants and ZnS quantum dots (QDs) within a zinc quinolate complex (ZQC)-dye (Rhodamine B: RhB) system. FRET efficiency is elevated from 13.1% to 49% with surfactants alone and further to an impressive 93.

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Engineering the surface of metal halide perovskite nanocrystals (MHPNCs) is crucial for optimizing their optical properties, repairing surface defects, enhancing quantum yield, and ensuring long-term stability. These enhancements make surface-engineered MHPNCs ideal for applications in light-emitting devices (LEDs), displays, lasers, and photodetectors, contributing to energy efficiency. This article delves into an introduction to MHPNCs, their structure and types, particularly the ABX type (where A represents monovalent organic/inorganic cations, B represents divalent metal ions mainly Pb metal, and X represents halide ions), synthesis methods, unique optical properties, surface modification techniques using various agents (particularly inorganic molecules/materials, organic molecules, polymers, and biomolecules) to tune optical properties and applications in the aforementioned light-emitting technologies, challenges and opportunities, including advantages and disadvantages of surface-modified APbX MHPNCs, and a summary and future outlook.

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Herein we report the fabrication of a surfactant modified quantum dot complex (S-QDC, having λ = 485 nm) nanocomposite (composed of cetyltrimethylammonium bromide surfactants and a zinc-quinolate complex attached ZnS quantum dot), the donor capability of S-QDC in Förster resonance energy transfer (FRET) with an acceptor organic molecule (λ = 573 nm), and finally their utilization in the FRET-based white light emission having features near to mid-day sunlight. The Förster distance, energy transfer efficiency, donor-acceptor distance, number of binding sites, and binding constant are evaluated to be 3.48 nm, 85.

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Herein we report the formation of a nanometal surface energy transfer (NSET) pair between a donor biologically active heterocyclic luminescent ligand such as 3-(1,3-Dioxoisoindolin-2-yl)-N, N-dimethylpropan-1-ammonium perchlorate (SPNL; λ-408 nm) and an acceptor silver nanoparticle (Ag NP; λ-406 nm). When the SPNL ligand interacts with Ag NPs, the quenching in their luminescence intensity at 408 nm is noticed, with a Stern-Volmer constant of 0.8 × 10 M.

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