Synthesis and Characterization of Highly Luminescent (CdSe)ZnS Quantum Dots

1996 ◽  
Vol 452 ◽  
Author(s):  
F. V. Mikulec ◽  
B. O. Dabbousi ◽  
J. Rodriguez-Viejo ◽  
J. R. Heine ◽  
H. Mattoussi ◽  
...  

AbstractWe report the synthesis of a series of nearly monodisperse ZnS-overcoated CdSe quantum dots whose room temperature photoluminescence quantum yield approaches 50%. This spectrally narrow (FWHM < 40nm) band edge luminescence spans the visible region from blue to red light. We use a two-step synthesis based on the high temperature decomposition of organometallic precursors in a coordinating solvent. We characterize our composite quantum dots using optical spectroscopies, wavelength dispersive x-ray spectroscopy, x-ray photoelectron spectroscopy, high resolution transmission electron microscopy, small angle x-ray scattering, and wide angle x-ray diffraction. The data indicate that samples displaying the highest quantum yield are those which have just achieved a closed shell of ZnS encapsulating the CdSe core. As more ZnS is added, the quantum yield decreases somewhat, possibly due to the many defects present in larger ZnS shells.

2019 ◽  
Vol 26 (1) ◽  
pp. 104-113 ◽  
Author(s):  
Xian-sheng Wang ◽  
Yu-duo Zhang ◽  
Qiao-chu Wang ◽  
Bo Dong ◽  
Yan-jia Wang ◽  
...  

AbstractZnO is modified by Cu2O by the process of precipitation and calcination. X-ray diffraction has shown that Cu2O/ZnO catalysts are made of highly purified cubic Cu2O and hexagonal ZnO. Scanning electron microscopy and transmission electron microscopy have shown that ZnO adhered to the surface of Cu2O. Due to the doping of Cu2O, the absorption range of the Cu2O/ZnO catalyst is shifted from the ultraviolet to the visible region due to diffuse reflection. X-ray photoelectron spectroscopy and photoluminescence spectra have confirmed that there is a substantial interaction between the two phases of the resultant catalyst. The degradation efficiency of Cu2O/ZnO on methyl orange solution is obviously enhanced compared to Cu2O and ZnO. The maximum degradation efficiency is 98%. The degradation efficiency is affected by the pH of the solution and initial concentration. After three rounds of recycling, the degradation rate is almost same. This shows a consistent performance of Cu2O/ZnO. The increase in catalytic ability is related to the lattice interaction caused by the doping of Cu2O.


2019 ◽  
Vol 2019 ◽  
pp. 1-9 ◽  
Author(s):  
Qianchun Zhang ◽  
Xiaolan Zhang ◽  
Linchun Bao ◽  
Yun Wu ◽  
Li Jiang ◽  
...  

Ginkgo leaves were used as precursors for the hydrothermal synthesis of carbon quantum dots (CQDs), which were subsequently characterized by transmission electron microscopy as well as Fourier-transform infrared, X-ray powder diffraction, and X-ray photoelectron spectroscopy. The prepared CQDs exhibited a fluorescence quantum yield of 11% and superior water solubility and fluorescence stability, as well as low cytotoxicities and excellent biocompatibilities with A549 and HeLa cells; these CQDs were also used to bioimage HeLa cells. Moreover, owing to the experimental observation that Hg2+ quenches the fluorescence of the CQDs in a specific and sensitive manner, we developed a method for the detection of Hg2+ using this fluorescence sensor. The sensor exhibited a linear range for Hg2+ of 0.50–20 μM, with an excellent coefficient of determination (R2 = 0.9966) and limit of detection (12.4 nM). In practice, the proposed method was shown to be highly selective and sensitive for the monitoring of Hg2+ in lake water and serum samples.


2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Xiaowen Zou ◽  
Xiaoli Dong ◽  
Limei Wang ◽  
Hongchao Ma ◽  
Xinxin Zhang ◽  
...  

Herein, Ni doped ZnO-TiO2composites were prepared by facile sol-gel approach and were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), UV-visible diffuse reflectance spectroscopy (UV-Vis DRS), X-ray photoelectron spectroscopy (XPS), and photoluminescence spectroscopy (PL). The results indicated that the Ni ions can be incorporated into the lattice of TiO2structure and replace Ti. The introduction of Ni expanded light absorption of TiO2to visible region, increased amount of surface hydroxyl groups and physically adsorbed oxygen (as the electronic scavenges), and then enhanced separation rate of photogenerated carriers. The photodegradation test of reactive brilliant blue (KN-R) under simulated solar light indicated that Ni doped ZnO-TiO2composites have better photocatalytic activities, as compared to those of TiO2and ZnO-TiO2.


2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Xuewei Dong ◽  
Fan Zhang ◽  
Chuan Rong ◽  
Hongchao Ma

The ZnS-Bi-TiO2composites were prepared by the sol-gel method and were characterized by X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), X-ray diffraction (XRD) and UV-visible diffuse reflectance spectroscopy (UV-Vis DRS). It is found that the doped Bi as Bi4+/Bi3+species existed in composites, and the introducing of ZnS enhanced further the light absorption ability of TiO2in visible region and reduced the recombination of photogenerated electrons and holes. As compared to pure TiO2, the ZnS-Bi-TiO2exhibited enhanced photodegradation efficiency under xenon lamp irradiation, and the kinetic constant of methyl orange removal with ZnS-Bi-Ti-0.005 (0.0141 min−1) was 3.9 times greater than that of pure TiO2(0.0029 min−1), which could be attributed to the existence of Bi4+/Bi3+species, the ZnS/TiO2heterostructure.


1999 ◽  
Vol 571 ◽  
Author(s):  
Yun-Wei Cao ◽  
Julia Aksenton ◽  
Victor Soloviev ◽  
Uri Banin

ABSTRACTHigh-temperature colloidal synthesis of InAs/InP and InAs/CdSe core/shell nanocrystal quantum dots is reported. InP and CdSe shells with several thicknesses were grown on InAs cores ranging in diameter between 20 to 50 Å. Optical spectra, X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), and X-ray diffraction (XRD) were used to analyze the core/shell quantum dots and determine their chemical composition, average size, size distributions, and structures. The experimental results indicate that shell growth is uniform, expitaxial, and controllable. For both InP and CdSe shells, growth is accompanied by a red shift of the band gap energy as a result of the extension of the electron wavefunction into the shell region. An increase of the room temperature photoluminescence quantum yield by a factor of∼4 is observed with CdSe shell growth on InAs Cores. The growth of InP shells, however, quenches the photoluminescence quantum yield. The difference is assigned to outer surface effects in core/shell nanocrystals.


2019 ◽  
Vol 14 (12) ◽  
pp. 1796-1803
Author(s):  
Jaber El Ghoul ◽  
Naglaa Abdel All

Pure Zn2SiO4 and Vanadium doped Zn2SiO4 green nanophosphor materials were synthesized using sol–gel method and thermally annealed at 1500 °C. The structural, morphology and optical properties were characterized using various techniques; X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Scanning electron microscope (SEM), high resolution transmission electron microscopy (HTEM), and photoluminescence spectroscopy (PL). XRD results shown β-Zn2SiO4 phase with triclinic structure that obtained after the heat treatment of samples at 1500 °C. The PL spectrum of V-Zn2SiO4 shows an intensive emission band in the visible region centered at 526 nm. This band is related to presence of vanadium in the interfaces between Zn2SiO4 nanoparticles and the host matrix, SiO2. The interesting of these nanophosphors were attributed for its capability of showing color-tunable emissions in visible region under a single-wavelength excitation.


2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Florian Weigert ◽  
Anja Müller ◽  
Ines Häusler ◽  
Daniel Geißler ◽  
Dieter Skroblin ◽  
...  

AbstractControlling thickness and tightness of surface passivation shells is crucial for many applications of core–shell nanoparticles (NP). Usually, to determine shell thickness, core and core/shell particle are measured individually requiring the availability of both nanoobjects. This is often not fulfilled for functional nanomaterials such as many photoluminescent semiconductor quantum dots (QD) used for bioimaging, solid state lighting, and display technologies as the core does not show the application-relevant functionality like a high photoluminescence (PL) quantum yield, calling for a whole nanoobject approach. By combining high-resolution transmission electron microscopy (HR-TEM) and X-ray photoelectron spectroscopy (XPS), a novel whole nanoobject approach is developed representatively for an ultrabright oleic acid-stabilized, thick shell CdSe/CdS QD with a PL quantum yield close to unity. The size of this spectroscopically assessed QD, is in the range of the information depth of usual laboratory XPS. Information on particle size and monodispersity were validated with dynamic light scattering (DLS) and small angle X-ray scattering (SAXS) and compared to data derived from optical measurements. In addition to demonstrating the potential of this novel whole nanoobject approach for determining architectures of small nanoparticles, the presented results also highlight challenges faced by different sizing and structural analysis methods and method-inherent uncertainties.


2014 ◽  
Vol 170 ◽  
pp. 155-167 ◽  
Author(s):  
Monika J. Rak ◽  
Tomislav Friščić ◽  
Audrey Moores

A versatile, low-energy and solvent-free method to access nanoparticles (NPs) of four different transition metals, based on a bottom-up mechanochemical procedure involving milling of inorganic precursors, is presented. Lignin, a biomass waste, was used effectively as a reducing agent, for the first time in a mechanochemical context, to access MNPs where M = Au, Pd, Ru, Re. A series of metal precursors was used for this reaction and their nature was shown to be integral in determining whether NPs became incorporated within the organic lignin matrix, M@lignin, or not. Specifically, organometallic precursors resulted in extensive encapsulation of the NPs, as well as improved control over their size and shape, while ionic precursors afforded matrix-free NPs. The resulting NP-containing composites were characterized through Fourier-transform infrared attenuated total reflectance (FTIR-ATR) spectroscopy, transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and powder X-ray diffraction (PXRD). This mechanochemical grinding method for accessing M@lignin (M = Au, Pd, Ru and Re) is significantly more sustainable than the traditional solvent batch syntheses of metal NPs because it relies on the use of a biomass-based polymer, it is highly atom economical, it eliminates the need for solvents and it reduces drastically the energy input.


Polymers ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 581
Author(s):  
Gajanan S. Ghodake ◽  
Surendra K. Shinde ◽  
Ganesh D. Saratale ◽  
Rijuta G. Saratale ◽  
Min Kim ◽  
...  

The utilization of waste-paper-biomass for extraction of important α-cellulose biopolymer, and modification of extracted α-cellulose for application in enzyme immobilization can be extremely vital for green circular bio-economy. Thus, in this study, α-cellulose fibers were super-magnetized (Fe3O4), grafted with chitosan (CTNs), and thiol (-SH) modified for laccase immobilization. The developed material was characterized by high-resolution transmission electron microscopy (HR-TEM), HR-TEM energy dispersive X-ray spectroscopy (HR-TEM-EDS), X-ray diffraction (XRD), vibrating sample magnetometer (VSM), X-ray photoelectron spectroscopy (XPS), and Fourier transform infrared spectroscopy (FT-IR) analyses. Laccase immobilized on α-Cellulose-Fe3O4-CTNs (α-Cellulose-Fe3O4-CTNs-Laccase) gave significant activity recovery (99.16%) and laccase loading potential (169.36 mg/g). The α-Cellulose-Fe3O4-CTNs-Laccase displayed excellent stabilities for temperature, pH, and storage time. The α-Cellulose-Fe3O4-CTNs-Laccase applied in repeated cycles shown remarkable consistency of activity retention for 10 cycles. After the 10th cycle, α-Cellulose-Fe3O4-CTNs possessed 80.65% relative activity. Furthermore, α-Cellulose-Fe3O4-CTNs-Laccase shown excellent degradation of pharmaceutical contaminant sulfamethoxazole (SMX). The SMX degradation by α-Cellulose-Fe3O4-CTNs-Laccase was found optimum at incubation time (20 h), pH (3), temperatures (30 °C), and shaking conditions (200 rpm). Finally, α-Cellulose-Fe3O4-CTNs-Laccase gave repeated degradation of SMX. Thus, this study presents a novel, waste-derived, highly capable, and super-magnetic nanocomposite for enzyme immobilization applications.


Molecules ◽  
2021 ◽  
Vol 26 (6) ◽  
pp. 1512
Author(s):  
Yuhan Liu ◽  
Meiling Zhang ◽  
Jinjun Cheng ◽  
Yue Zhang ◽  
Hui Kong ◽  
...  

Glycyrrhizae Radix et Rhizoma (GRR) is one of the commonly used traditional Chinese medicines in clinical practice, which has been applied to treat digestive system diseases for hundreds of years. GRR is preferred for anti-gastric ulcer, however, the main active compounds are still unknown. In this study, GRR was used as precursor to synthesize carbon dots (CDs) by a environment-friendly one-step pyrolysis process. GRR-CDs were characterized by using transmission electron microscopy, high-resolution TEM, fourier transform infrared, ultraviolet-visible and fluorescence spectroscopy, X-ray photoelectron spectroscopy, X-ray diffraction and high-performance liquid chromatography. In addition, cellular toxicity of GRR-CDs was studied by using CCK-8 in RAW264.7 cells, and the anti-gastric ulcer activity was evaluated and confirmed using mice model of acute alcoholic gastric ulcer. The experiment confirmed that GRR-CDs were the spherical structure with a large number of active groups on the surface and their particle size ranged from 2 to 10 nm. GRR-CDs had no toxicity to RAW264.7 cells at concentration of 19.5 to 5000 μg/mL and could reduce the oxidative damage of gastric mucosa and tissues caused by alcohol, as demonstrated by restoring expression of malondialdehyde, superoxide dismutase and nitric oxide in serum and tissue of mice. The results indicated the explicit anti-ulcer activity of GRR-CDs, which provided a new insights for the research on effective material basis of GRR.


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