Single nanoscopic emitters embedded in the crystalline matrix have become a valuable resource for emerging nanophotonics and quantum technologies. The generally anisotropic nature of the matrix strongly affects the emission properties of the quantum emitters, in particular, when the matrix is assembled in nanophotonic structures. We report on rigorous analysis and engineering of spontaneous emission from single emitters coupled to nanoantenna and planar anisotropic antenna structures. By developing a convenient theoretical method with efficient numerical implementation, we show that accurate modeling of the anisotropy is essential in predicting the emission pattern for many important systems, such as single molecules in the solid-state matrix, isolated defects in 2D materials and so on. In particular, we illustrate the amplified effects of material anisotropy and geometrical anisotropy for emitters coupled to planar antenna and nanoantenna structures. We show that with an appropriate design of the anisotropy, a strong enhancement of the emission rate and a nearly collimated beam from single emitters can be simultaneously achieved.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1039/c9nr00235a | DOI Listing |
J Fluoresc
January 2025
Department of Physics, Jnanabharathi, Bangalore University, Bengaluru, 560056, Karnataka, India.
In this report the photophysical property of newly synthesized fluorescein based derivative 2-(5-((2,4-dichlorophenyl)diazenyl)-6-hydroxy-3-oxo-3H-xanthen-9-yl)benzoic acid has studied by spectroscopic and theoretical that is by Density Functional Theory technique. The structural and functional group of the synthesized molecule was confirmed by nuclear magnetic resonance and fourier transform infrared spectroscopy technique, and from the result so far obtained has been confirmed that molecule has a stable structure and confirmed the presence the functional groups present in the sample. The optical properties of the molecule are studied using the spectroscopic technique and it has revealed the solute-solvent interaction behaviour of the molecule and it has been observed that the bathochromic shift was of about 5 nm, from the fluorescence measurement it has revealed that the emission has been observed at green region and from the power spectra it has been confirmed the same.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
East China University of Science and Technology, Insitute of Fine Chemicals, Meilong Road 130, Shanghai, China, 200237, Shanghai, CHINA.
Protein clustering/disassembling is a fundamental process in biomolecular condensates, playing crucial roles in cell fate decision and cellular homeostasis. However, the inherent features of protein clustering, especially for its reversible behavior and subtle microenvironment variation, present significant hurdles in probe chemistry for tracking protein clustering dynamics. Herein, we report a bilateral-tailored chemigenetic probe, in which an "amphiphilic" AIEgen QMSO3Cl is covalently conjugated to a protein tag that is genetically fused to protein-of-interest (POI).
View Article and Find Full Text PDFChem Asian J
January 2025
JNCASR: Jawaharlal Nehru Centre for Advanced Scientific Research, New Chemistry Unit, Jakkur, 560064, Bangalore, INDIA.
This study investigates the photophysical behaviour of Mn/Fe and Mn/Sn co-doped CsPbCl3 perovskite nanocrystals (NCs) to explore carrier dynamics and dopant interactions. Using gated photoluminescence (PL) and temperature-dependent measurements, we elucidate the impact of dopant chemistry on exciton behaviour, focusing on vibrationally assisted delayed fluorescence (VADF) and energy transfer mechanisms. The efficiency of VADF is influenced by factors such as the bandgap, temperature, quantum confinement, and host composition.
View Article and Find Full Text PDFChemistry
January 2025
Budapest University of Technology and Economics, Department of Inorganic and Analytical Chemistry, Muegyetem rkp 3, 1111, Budapest, HUNGARY.
New hybrids were synthesised by linking carboranes and siloles, both of which are known as aggregation-induced emission active units. Although most of the newly synthesised systems do not display notable quantum yield either in solution or in the aggregated state, they emit strongly in the solid-state, and a quantum yield of up to 100% can be achieved. The tailorable quantum yield can be attributed to the packing of the molecules in the crystal lattice ruled by the carborane and phenyl moieties according to the SC-XRD data.
View Article and Find Full Text PDFRSC Adv
January 2025
Institute of Polymer and Dye Technology, Lodz University of Technology Stefanowskiego 16 Lodz 90537 Poland.
This study investigates the structure-property relationships of a series of phenylhydrazones bearing various electron-donating and electron-withdrawing substituents, such as methoxy, dimethylamino, morpholinyl, hydroxyl, chloro, bromo, and nitro groups. The compounds were synthesized, and their structures were characterized using single-crystal X-ray diffraction, powder X-ray diffraction, FTIR spectroscopy, NMR spectroscopy, and DSC. Three-dimensional excitation-emission matrix (3D-EEM) fluorescence spectroscopy and UV-Vis spectroscopy were employed to elucidate the complex interplay between the molecular skeleton, substituents, and the resulting photophysical properties.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!