Atomistic effect of laterally and vertically growth shell on physical behaviours of CdSe/CdTe type-II core/crown and core/shell nanoplatelets: tight-binding theory

Utilizing the atomistic tight-binding theory, the impact of the lateral and vertical potential confinement by the coated shell on the CdSe/CdTe core/crown and core/shell nanoplatelets (NPLs) is attained. The spatial charge separation and encapsulated shell have a noteworthy impact on the electronic structures and optical properties because of the type-II band profile. The reduced band gaps with the growing laterally and vertically passivated shell thicknesses are due to the quantum confinement phenomena. The optical band gaps adjusted across the visible light are achieved by the shell thickness change. The excitonic binding energies of CdSe/CdTe core/shell NPLs are larger than those of CdSe/CdTe core/crown NPLs. Thanks to the spatial charge separation, a shortening of the oscillation strengths is concomitant with an increase of the radiative lifetimes. Overall, this scientific research underlines the importance of the theoretical understanding and practical control by lateral and vertical confinement of heterostructure NPLs.

Efficiency Study of PbTe/CdTe Core/Shell Quantum Dots Solar Cells

In this work we theoretically study how to optimize the efficiency of an intermediate band solar cell based on IV-VI PbTe/CdTe semiconductor materials. We focus our attention on how control structural parameters, such as the height and radius in cylindrical quantum dots and the radius in spherical quantum dots to obtain the inter and intraband transition energies that provide the highest efficiency values of the solar cell. The calculation of the energy levels, the selection rules for transitions energies were performed using the 4×4 k.p Kane-Dimmok Hamiltonian.

Rapid Synthesis of Thiol-Co-Capped-CdTe/CdSe/ZnSe Core Shell-Shell Nanoparticles: Their Optical and Structural Morphology

CdTe QDs has been demonstrated in many studies to possess good outstanding optical and photo-physical properties. However, it has been established from literature that the toxic Cd2+ that tends to leak out into nearby solutions can be protected by less toxic ZnS or ZnSe shells leading to the synthesis of core-shells and multi-core-shells. Hence, this has allowed the synthesis of CdTe multi-core-shells to have gained much interest. The preparation of most CdTe multi-core-shells reported from various studies usually has a longer reaction time (6–24 h) in reaching their highest emission maxima. The synthesis of CdTe multi-core-shells in this study only took 35 min to obtain a highest emission maximum compared to what has been reported from the literature. CdTe multi-core-shells were synthesized by injecting 7, 14, and 21 mL each of Zn complex solution and Se ions into the reacting mixture containing CdTe core-shells (3 h) at 5 min intervals over a 35 min reaction time. The emission maxima of the MPA-TGA-CdTe multi-core-shells at 21 mL injection was recorded around 625 nm. Therefore, we are reporting the rapid synthesis of five different thiol co-capped CdTe/CdSe/ZnSe multi-core-shell QDs with the highest emission maxima obtained at 35 min reaction time.

Phonon Characterization, Structural and Optical Properties of Type-II CdSe/CdTe core/shell and Type-II/type-I CdSe/CdTe/ZnS core/shell/shell Quantum Dots

The CdSe, type-II CdSe/CdTe core/shell and type-II/type-I CdSe/CdTe/ZnS core/shell/shell quantum dots (QDs) were successfully synthesized in a noncoordinating solvent. The phonon characterizations, optical properties and structures of the synthesized QDs were characterized by Raman scattering (RS) spectra, photoluminescence (PL) spectroscopy, PL-decay lifetime, absorption spectroscopy (Abs), and X-ray diffraction (XRD). The growth of QDs was monitored by using RS, which demonstrated the formation of correct of the core/shell and core/shell/shell structures. Observation results from XRD reveal that all QDs crystallize in the cubic phase with zinc-blende structure. The typical characteristics of spatially indirect recombination for type-II QDs were observed through Abs and PL spectroscopy. The ZnS shell significantly enhanced the PL quantum yeild (QY), the optical durability, the chemical stability and separating CdSe/CdTe QDs from the surroundings. The effect of excitation power on the PL properties of the CdSe core, CdSe/CdTe and CdSe/CdTe/ZnS QDs has been investigated.

68Ga CdTe/CdS fluorescent quantum dots for detection of tumors: investigation on the effect of nanoparticle size on stability and in vivo pharmacokinetics

BackgroundQuantum dots (QDs)-based theranostics offer exciting new approaches to diagnose and therapy of cancer. To take advantage of the unique properties of these fluorescent QDs for different biomedical applications, their structures, size and/or surface chemistry need to be optimized, allowing their stability and functionalities to be tailored for different biomedical applications.MethodologyCadmium telluride/Cadmium sulfide QDs (CdTe/CdS QDs) were synthesized and their structure, size, photostability and functionalities as a bioprobe for detection of Fibrosarcoma tumors were studied and compared with Cadmium telluride (CdTe) QDs. Hence, CdTe/CdS QDs were labeled with 68Ga radionuclide for fast in vivo biological nuclear imaging. Using gamma paper chromatography (γ-PC), the physicochemical properties of the prepared labeled QDs were assessed. In vivo biodistribution and positron emission tomography (PET) imaging of the 68Ga@ CdTe/CdS QDs nanocrystals were investigated in Sprague Dawley® rats bearing Fibrosarcoma tumor.ResultsCdS shell on the surface of CdTe core increases the size and photostability against high energy radiations; therefore, CdTe/CdS QDs show prolonged fluorescence as compared to CdTe QDs.ConclusionExcellent accumulation in tumor was observed for core/shell quantum dots, but this study showed that small changes in the size of the QDs (+1 nm), after adding the CdS shell around CdTe core, greatly change their biodistribution (especially the liver uptake).

Template-free electrochemical synthesis of Cd/CdTe core/shell nanowires and CdTe nanotubes

Template-free electrodeposition was utilized to prepare Cd/CdTe nanowires and CdTe nanotubes for the first time, where the formation of one-dimensional structures was due to the highly anisotropic crystal structure and the Kirkendall effect.