excitonic absorption
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Nanoscale ◽  
2022 ◽  
Author(s):  
M. Negri ◽  
L. Francaviglia ◽  
D. Kaplan ◽  
V. Swaminathan ◽  
G. Salviati ◽  
...  

In this work, we study the excitonic absorption and cathodoluminescence emission of MoS2 micro-pyramids grown by chemical vapor deposition on SiO2 substrates, obtained at room and cryogenic temperatures.


2021 ◽  
Vol 104 (12) ◽  
Author(s):  
Kazuki Konishi ◽  
Nobuko Naka
Keyword(s):  

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Anna Ioannou ◽  
Ioanna Vareli ◽  
Andreas Kaltzoglou ◽  
Ioannis Koutselas

Abstract Three new hybrid two-dimensional (2D) organic–inorganic semiconductors are presented, which contain lead halides and a mixture of hexanediamine-based isomers in the stoichiometry [2,2,4(2,4,4)-trimethyl-1,6-hexanediamine]PbX4 (X = I, Br, Cl). These hexanediamine derivatives, with attached methyl groups at the carbon backbone of both isomers, determine the packing of the organic layers between the inorganic 2D sheets, while the optical absorption and photoluminescence spectra reveal excitonic peaks at T = 77 K and room temperature. The as-synthesized semiconductors were stored for three years in the dark and under low humidity and were examined again and the results were compared to those of the fresh materials. The chloride analogue, after the three year storage, displays white-like luminescence. The use of non-equivalent isomer and racemic mixtures in the organic component to form hybrid organic–inorganic semiconductors is an efficient method to alter the properties of 2D perovskites by tuning the isomers’ chemical functionalities. Finally, a comparison of the observed excitonic absorption and photoluminescence signals to that of analogous 2D compounds is discussed.


2021 ◽  
Author(s):  
Reza Tirbandpaya ◽  
Abdolraouf Samadi-Maybodi

Abstract This paper presents a new and fast method for determination of vitamin B1 (thiamine) using functionalized CdSe/ZnS quantum dots (QDs) as a sensor. In this study the core-shell CdSe/ZnS QDs with thioglycolic acid capping agents were synthesized by wet chemical method in aqueous solution. Electronic absorption was applied for size determination of the QDs, the average diameters of the synthesized quantum dots were calculated using wavelength of the first excitonic absorption peak. The methods of FESEM and FTIR were also used for characterization of the prepared samples. The results indicated that vitamin B1 could effectively quench the QDs emission and the fluorescence intensity decreased linearly with the concentration of vitamin B1 ranging from 10-7 to 10-4 molL−1 with limit of detection of 2×10-8 mol L−1. Determination of vitamin B1in pills from two pharmaceutical companies were used as real samples using this method .


Author(s):  
Ramesh Kumar Raji ◽  
Tholkappiyan Ramachandran ◽  
M. Muralidharan ◽  
R. Suriakarthick ◽  
Muthu Dhilip ◽  
...  

Abstract Perovskite structured LaTixFe1-xO3 (x = 0, 0.05, 0.15, 0.25) lanthanum ferrites were synthesized by conventional solid-state reaction. The structural Rietveld refinement and Raman analysis were conducted and confirmed that single-phase orthorhombic phase with Pbnm symmetry formed. The positions of the ions and their bonds of these ferrites were investigated. The spherical shaped morphology of these ferrites was examined. The quantitative chemical composition and distribution of these ferrites were confirmed. The excitonic absorption edge was observed at 590 nm; ascribed to the electronic transition from O2p→Fe3d and optical band gap values increased from 1.85– 2.02 eV as Ti concentration increased. The dielectric and magnetic behavior of these ferrites was studied. It is suggested that synthesized LaTixFe1xO3 powders with different properties could be tailored for different requirements.


2021 ◽  
Vol 27 (S1) ◽  
pp. 122-123
Author(s):  
Steffi Woo ◽  
Robert Schneider ◽  
Johann Preuß ◽  
Ashish Arora ◽  
Benjamin Carey ◽  
...  
Keyword(s):  

2021 ◽  
Author(s):  
Ashley Shin ◽  
Azmain A. Hossain ◽  
Stephanie M. Tenney ◽  
Xuanheng Tan ◽  
Lauren A. Tan ◽  
...  

The influence of external dielectric environments is well understood for 2D semiconductor materials but is overlooked for colloidally-grown II-VI nanoplatelets (NPLs). In this work, we synthesize MX (M=Cd, Hg; X= Se, Te) NPLs of varying thicknesses, and apply a modified Elliott model to fit excitonic absorption features and report exciton binding energies for cadmium telluride and mercury chalcogenides for the first time. Our observations indicate that the exciton binding energy is modulated by the dielectric screening of semiconductor material by the external ligand environment. Furthermore, NPL binding energies show a dependence on the number of monolayers consistent with relative effect of internal vs. external dielectric. To describe this, we derive an analytical electrostatic model, reinforcing the hypothesis that the external environment increases the exciton binding energy relative to the bulk—due to the distortion of the Coulombic potential across the NPL surface. We further confirm this effect by decreasing and recovering the exciton binding energy of HgTe NPLs through washing in polarizable solvents. Our results illustrate that NPLs are colloidal analogues of Van der Waals 2D semiconductors and point to surface modification as an approach to control photophysics and device properties.


2021 ◽  
Author(s):  
Ashley Shin ◽  
Azmain A. Hossain ◽  
Stephanie M. Tenney ◽  
Xuanheng Tan ◽  
Lauren A. Tan ◽  
...  

The influence of external dielectric environments is well understood for 2D semiconductor materials but is overlooked for colloidally-grown II-VI nanoplatelets (NPLs). In this work, we synthesize MX (M=Cd, Hg; X= Se, Te) NPLs of varying thicknesses, and apply a modified Elliott model to fit excitonic absorption features and report exciton binding energies for cadmium telluride and mercury chalcogenides for the first time. Our observations indicate that the exciton binding energy is modulated by the dielectric screening of semiconductor material by the external ligand environment. Furthermore, NPL binding energies show a dependence on the number of monolayers consistent with relative effect of internal vs. external dielectric. To describe this, we derive an analytical electrostatic model, reinforcing the hypothesis that the external environment increases the exciton binding energy relative to the bulk—due to the distortion of the Coulombic potential across the NPL surface. We further confirm this effect by decreasing and recovering the exciton binding energy of HgTe NPLs through washing in polarizable solvents. Our results illustrate that NPLs are colloidal analogues of Van der Waals 2D semiconductors and point to surface modification as an approach to control photophysics and device properties.


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