Interaction of CdTe/CdS quantum dots with antibodies

In the study, we observed the strong adsorption of CdTe/CdS QDs to antibodies and the formation of QDs-antibodies conjugates. Capillary electrophoresis with laser-induced fluorescence detection （CE-LIF）, fluorescence spectrometry and fluorescence correlation spectroscopy （FCS） were used to characterize the QDs conjugates with antibody. We found that the QDs-antibody conjugates possessed high fluorescence, small hydrodynamic radii and good stability in aqueous solution. 2009 Ji Cun Ren. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.

Anti-Reflection Characteristics of Si Nanowires for Enhanced Photoluminescence from CdTe/CdS Quantum Dots

CdTe/CdS quantum dots（QDs） are fabricated on Si nanowires（NWs） substrates with and without Au nanoparticles（NPs）. The formation of Au NPs on Si NWs can be certified as shown in scanning electron microscopy images. The optical properties of samples are also investigated. It is interesting to find that the photoluminescence（PL） intensity of Cd Te/Cd S QD films on Si nanowire substrates with Au NPs is significantly increased,which can reach 8-fold higher than that of samples on planar Si without Au NPs. The results of finite-difference time-domain simulation indicate that Au NPs induce stronger localization of electric field and then boost the PL intensity of QDs nearby. Furthermore, the time-resolved luminescence decay curve shows the PL lifetime, which is about 5.5 ns at the emission peaks of QD films on planar, increasing from 1.8 ns of QD films on Si NWs to4.7 ns after introducing Au NPs into Si NWs.

Novel Hybrid SiO2/ZnS Coated CdTe/CdS Quantum Dots and Their Bioapplications

Novel CdTe/CdS quantum dots(QDs)coated with a hybrid of SiO_2 and ZnS were fabricated through a simple two-step approach.The hybrid SiO_2/ZnS coated CdTe/CdS quantum dots was characterized by transmission electron microscopy(TEM),UV and fluorescence spectrometer.Results indicated that the core-shell structure gave the QDs outstanding photoluminescence properties,includinganarrowphotoluminescencespectrum,high photoluminescence(PL)quantum yield and long emission lifetime(average PL lifetime of increased from 26.4 ns to 49.1 ns).Cellular studies showed the QDs had good cytocompatibility with Hela cells as determined by the 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide(MTT)assay after coating SiO_2/ZnS,and also proved the feasibility of using the hybrid SiO_2/ZnS coated QDs as optical probes for in vitro cell imaging.The synthesis method of QDs is highly promising for the production of robust and functional optical probes for bio-imaging and sensing applications.

Ultrafast Carrier Dynamics in CdSe/CdS/ZnS Quantum Dots

The intra- and inter-band relaxation dynamics of CdSe/CdS/ZnS core/shell/shell quantum dots are investigated with the aid of time-resolved nonlinear transmission spectra which are obtained using femtosecond pump-probe technique. By selectively exciting the core and shell carrier, the dynamics are studied in detail. Carrier relaxation is found faster in the conduction band of the CdS shell （about 130 fs） than that in the conduction band of the CdSe core （about 400 fs）. From the experiments it is distinctly demonstrated the existence of the defect states in the interface between the CdSe core and the CdS shell, indicating that ultrafast spectroscopy might be a suitable tool in studying interface and surface morphology properties in nanosystems.

Investigation of ultrafast dynamics of CdTe quantum dots by femtosecond fluorescence up-conversion spectroscopy

The ultrafast carrier relaxation processes in CdTe quantum dots are investigated by femtosecond fluorescence upconversion spectroscopy.Photo-excited hole relaxing to the edge of the forbidden gap takes a maximal time of ～ 1.6 ps with exciting at 400 nm,depending on the state of the photo-excited hole.The shallow trapped states and deep trap states in the forbidden gap are confirmed for CdTe quantum dots.In addition,Auger relaxation of trapped carriers is observed to occur with a time constant of ～ 5 ps.A schematic model of photodynamics is established based on the results of the spectroscopy studies.Our work demonstrates that femtosecond fluorescence up-conversion spectroscopy is a suitable and effective tool in studying the transportation and conversion dynamics of photon energy in a nanosystem.

CdS Quantum Dots as Fluorescence Probes for Detection of Adriamycin Hydrochloride

Water-soluble CdS quantum dots（CdS-QDs） capped with thioglycohc acid were easily prepared, and a detection method of adriamycin was presented based on the fluorescence quenching of CdS-QDs. It was found that a complex could be formed between cetyhrimethyl ammonium bromide（CTAB） and CdS-QDs by using electrostatic interaction in Britton-Robinson（BR） buffer at pH = 7.00, and the strong fluorescence emission of the complex was observed at 500 nm when the complex was excited at 378 run. The presence of adriamycin, however, could strongly quench the fluorescence through hydrophobic interaction. The overall quenching percentage as a function of adriamycin concentration matches the Stern-Volmer equation very well. These properties make CdS-QDs a potential fluorescence probe for the detection of adriamycin. The detection hmit（3σ） of adriamycin is approximately 10^-9 mol/L.

Adaption of Au Nanoparticles and CdTe Quantum Dots in DNA Detection

A DNA fluorescence probe system based on fluorescence resonance energy transfer （FRET） from CdTe quantum dot （QD） donors to Au nanoparticle （AuNP） acceptors is presented. CdTe QDs, 2.5nm in diameter, as energy donors, were prepared in water. Au nanoparticles, 16nm in diameter, as energy acceptors, were prepared from gold chloride by reduction. CdTe QDs were linked to 5＇-NH2-DNA through 1-ethyl-3-（dimethylaminopropyl）car- bodiimide hydrochloride （EDC） as a linker, and the 3＇-SH-DNA was self-assembled onto the surface of AuNPs. The hybridization of complementary double stranded DNA （dsDNA） bound to the QDs and AuNPs （CdTe-dsDNA-Au） determined the FRET distance of CdTe QDs and Au nanoparticles. Compared to the fluorescence of CdTe-DNA, the fluorescence of CdTe-DNA-Au conjugates decreased extremely, which indicated that the FRET occurred between CdTe QDs and Au nanoparticles. The fluorescence change of this conjugate depended on the ratio of Au-DNA to CdTe-DNA. When the AuNPs-DNA to QD-DNA ratio was 10：1, the FRET efficiency reached a maximum. The probe system would have a certain degree of fluorescence recovery when a complementary single stranded DNA was introduced into this system, which showed that the distance between CdTe QDs and Au nanoparticles was increased.

Using capillary electrophoresis mobility shift assay to study the interaction of CdTe quantum dots with bovine serum albumin

In this work, the capillary electrophoresis mobility shift assay （CEMSA） was first adopted to study the interaction of protein with quantum dots （QDs）. In this study, bovine serum albumin （BSA） and CdTe QDs were used as model samples. We observed that BSA was facilely adsorbed to CdTe QDs surface, and the QD-BSA complex was formed by a 1：1 stoichiometric ratio. A value of 2.17 4-0.27 × 10^6 mol^-1 L^-1 （at 25 ℃） for the association constant was obtained by CEMSA.

Ultrasensitive Detection of Glyphosate Using CdTe Quantum Dots in Sol-Gel-Derived Silica Spheres Coated with Calix[6]arene as Fluorescent Probes

We have developed a simple method for the preparation of highly fluorescent and stable, water-soluble CdTe quantum dots in sol-gel-derived composite silica spheres which were coated with calix[6]arene. The resulting nanoparticles (NPs) were characterized in terms of UV, fluorescence and FT-IR spectroscopy and TEM. The results show that the new NPs display more intense fluorescence intensity and are more stable than its precursors of the type SiO2/CdTe. Under the optimum, the novel NPs exhibit a higher selectivity and ultrasensitive fluorescence probes for the determination of gly-phosate over other pesticides, the fluorescence intensity increase with the concentration of glyphosate in the range from 1.0 to 25.0 nmol/L and the detection limit is low to 0.0725 nmol/L. A mechanism is suggested to explain the inclusion process by a Langmuir binding isotherm.

Citrate-stabilized CdSe/CdS quantum dots as fluorescence probe for protein determination

A rapid, ultrasensitive and convenient fluorescence measurement technology based on the enhancement of the fluorescence intensity resulting from the interaction of functionalized CdSe/CdS quantum dots （QDs） with bov/ne serum albumin （BSA） was proposed. The citrate-stabilized CdSe/CdS （QDs） were synthesized by using Se powder and Na2S as precursors instead of any pyrophoric organometallic precursors. The modified CdSe/CdS QDs are brighter and more stable against photobleaching in comparison with organic fluorophores. At pH 7.0, the fluorescence signal of CdSe/CdS is enhanced by increasing the concentration of BSA in the range of 0.1-10 μg/mL, and the low detection limit is 0.06 μg/mL. A linear relationship between the enhanced fluorescence peak intensity （△F） and BSA concentration （c） is established using equation △F=50.7c＋16.4 （R=0.996 36）. Results of determination for BSA in three synthetic samples are identical with the true values, and the recovery （98.9%-102.4%） and relative standard deviation （RSD, 1.8%-2.5%） are satisfactory.

Study on Interaction between Chitosan and CdS Quantum Dots via Photoluminescence Spectra

The interaction between CdS quantum dots and amino polysaccharide chitosan in aqueous solution was studied via photoluminescence (PL) spectra. The surface binding of chitosan with different molecular weight (MW) quenched the luminescence of QDs due to the elimination of radioactive anion vacancy centers. This process fits well with the Perrin model; lower MW chitosan exhibits higher quenching efficiency due to better availability to the surface.

Quantitative Model for the Surface-related Electron Transfer in CdS Quantum Dots

The influence of surface S^2- dangling bonds and surface doped ions（Se^2-, Cu^2＋, and Hg^2＋） on the photoluminescence of Cd^2＋-rich CdS QDs was investigated. A quantitative model was proposed to understand the complex transfer processes of excited electrons in CdS QDs. The transfer of excited electrons from either the conduction band or the Cd^2＋-related trap-state to the surface S^2-related shallow hole trap-state is effective. However, the trap of excited electrons by surface doped ion trap-states from the Cd^2＋-related trap-state is more effective than that from the conduction band. The efficiency of trapping electrons from both the conduction band and the Cd^2＋-related trap-state can be quantitatively understood with the help of the proposed model. The results show that the transfer efficiency of excited electrons is dependent on the location of the energy-level of the relevant surface-related trap-state. The trap of excited electrons by the surface trap-state with energy-level closer to that of the conduction band is more effective, especially for the trap of excited electrons from Cd^2＋-related trap-state.

Cytotoxicity and DNA Damage Effect of TGA-capped CdTe Quantum Dots

The cytotoxicity and DNA damage caused by thioglycolic acid（TGA）-capped cadmium telluride（CdTe） quantum dots（QDs） to hepatocyte line HL-7702 were investigated.Cell viability was measured by 3-（4,5-dimethylthiazol-2-yl）-2,5-diphenyltetrazolium bromide（MTT） assay;DNA damage was detected by single cell gel electrophoresis（SCGE）;the change of cell cycle progression was examined by propidium iodide（PI）-flow cytometry（FCM）;apoptosis was measured by acridine orange/ethidium bromide（AO/EB） assay and Annexin V-FITC/PI-FCM（FITC：fluorescein isothiocyanate）.The results show that the cytotoxicity induced by CdTe QDs was increased in a dose-dependent and time-dependent manner;after exposure to QDs for 24 h,as the exposure dose increased,the rate of DNA damage was significantly increased（P0.05）,and the degree of DNA damage was elevated.As the dose of CdTe QDs increased,the percentage of G 0 /G 1 phase cells was significantly decreased（P0.001）,while the percenttages of S and G 2 /M phases cells were significantly increased（P0.001）.In AO/EB assay,apoptotic cells could be observed under a fluorescence microscope,and apoptotic rate was increased as exposure dose increased.In Annexin V-FITC/PI-FCM assay,the apoptotic rates of CdTe QDs treated groups were significantly increased compared with that of control group（P0.05）.Our studies indicate that CdTe QDs could influence cell viability,and induce DNA damage,the S and G2 /M phases arrest and apoptosis of HL-7702.

Microwave Synthesis of CdTe/TGA Quantum Dots and Their Thermodynamic Interaction with Bovine Serum Albumin

The thioglycollic acid（TGA） as a capping agent, CdTe/TGA quantum dots（QDs） with excellent properties were synthesized under microwave irradiation. The TGA/Cd/Te molar ratios, reaction time, temperature and p H are the crucial factors for properties of QDs. The QDs were characterized by UVvis absorption and fluorescence spectra, transmission electron microscopy and Fourier transform infrared spectroscopy. The experimental results show that when the p H value is 11.5 and molar ratio of TGA：Cd：Te is 1.2：1：0.4 at 100 ℃ heating for 15 min, the resulted QDs exhibit a high fluorescence quantum yield of 78%. The fluorescence full width at half maximum（FHMW） of QDs is around 23 nm. The products are spherical with average size of 3-5 nm. There is a strong coordination effect between TGA and Cd2＋. Moreover, the results of interaction between as-made QDs and bovine serum albumin（BSA） suggest that the QDs-BSA binding reaction is a static quenching. The negative values of free energy（△G〈0） suggest that the binding process is spontaneous, △H〈0 and △S〈0 show that hydrogen bonds and van der Waals interactions play a major role in the binding reaction between QDs and BSA.

Exploring Feasibility for Application of Luminescent CdTe Quantum Dots Prepared in Aqueous Phase to Live Cell Imaging

This paper explored the feasibility for the application of luminescent CdTe quantum dots prepared in aqueous phase to live cell imaging. The highly luminescent CdTe quantum dots （QDs） were first prepared in aqueous phase, and then were covalentiy coupled to a plant lectin （UEA-1）, as a fluorescent probe. After incubating with of human umbilical vein endothelial cells （HUVECs）, the QD probe with UEA-1 was able to specifically bind the corresponding cell receptor. The good cell images were obtained in live cells using laser confocal scanning microscopy. We predict that QDs prepared in water phase will probably become an attractive alternative probe in cellular imaging and bio-labeling.

Luminescent properties dependence of water-soluble CdTe quantum dots on stabilizing agents and reaction time

The influence of stabilizing agents and reaction time on the luminescent properties of water-soluble CdTe quantum dots(QDs) was discussed.The thioglycolic acid(TGA)-CdTe ODs were characterized by TEM,XRD and FTIR.It is found that larger-size QDs can be synthesized more easily when L-cysteine(Cys) or golutathione(GSH) is chosen as stabilizing agent and TGA is proper to prepare highly luminescent QDs because of the effect between Cd2+ and sulfhydryl group.Furthermore,the absorption wavelength,full width at half maximum(FWHM),stokes shift,photoluminescence(PL) quantum yield and PL stability of TGA-CdTe are strongly dependent on reaction time,in which the absorption wavelength changes against reaction time with an exponential function.The TGA-CdTe QDs prepared at 2 h possess more excellent luminescent properties.

High-quality CdS quantum dots sensitized ZnO nanotube array films for superior photoelectrochemical performance

The surface characteristics of ZnO were synthetically optimized by a self-designed simultaneous etching and W-doping hydrothermal method utilizing as-prepared ZnO nanorod(NR)array films as the template.Benefiting from the etching and regrowth process and the different structural stabilities of the various faces of ZnO NRs,the uniquely etched and W-doped ZnO(EWZ)nanotube(NT)array films with larger surface area,more active sites and better energy band structure were used to improve the photoelectrochemical(PEC)performance and the loading quality of CdS quantum dots(QDs).On the basis of their better surface characteristics,the CdS QDs were uniformly loaded on EWZ NT array film with a good coverage ratio and interface connection;this effectively improved the light-harvesting ability,charge transportation and separation as well as charge injection efficiency during the PEC reaction.Therefore,all the CdS QD-sensitized EWZ NT array films exhibited significantly enhanced PEC performance.The CdS/EWZ-7 composite films exhibited the optimal photocurrent density with a value of 12 mA·cm^(-2),2.5 times higher than that of conventional CdS/ZnO-7 composite films under the same sensitization times with CdS QDs.The corresponding etching and optimizing mechanisms were also discussed.

MTT Detection of the Toxicity on CdTe Quantum Dots

Objective: The quantum dots are the useful materials in microelectronics and biomedical research. However its toxicity has to be considered. We studied the effect of cell inhibition with ZnS core quantum dots and CdTe quantum dots modified with Thioglycolic acid or Cysteine functional group (TGA-CdTe, TGA-CdTe/ZnS, Cys-CdTe, Cys-CdTe/ZnS) on Caco-2 cell proliferation. Methods: We studied the effect of cell inhibition with ZnS core QDs and CdTe QDs modified with functional group on Caco-2 cell proliferation by MTT assay at 0, 12.5, 25, 50, 100 μg/ml and 6, 24, 48 h. Result: Our results showed that all QDs have inhibited cell proliferation and reached maximum 79.21%. The inhibition rate of Cys-modified QDs increased with the increase of concentration and reached maximum 66.72%. The inhibition rate of TGA-modified QDs increased with the increase of time. The ratios of Cys-modified to TGA-modified were less than 1 at all concentrations and three exposure times (P ≤ 0.01). The average ratios of Cys-CdTe/ZnS to Cys-CdTe reached 1.11 only for 48 h (P ≤ 0.05). The ratios of TGA-CdTe/ZnS to TGA-CdTe were closed to 1 at all concentrations and exposure times. Conclusion: The regularity of QDs modified with functional group is that inhibition of TGA-modified higher than Cys-modified. Inhibition exhibited dose-dependent for Cys-modified while exhibited time-dependent for TGA-modified. The regularity of CdTe-QDs with ZnS or not is that the inhibition of Cys-CdTe/ZnS was higher than Cys-CdTe while TGA-CdTe/ZnS and TGA-CdTe were consistent.

All-Optical Reconfigurable Metamaterial Employing the Self-Assembly of CdTe Quantum Dots

Positively and negatively charged polyelectrolytes, namely, Poly(diallyldimethylammonium chloride) and Poly(styrene sulfonate), respectively, were employed to disperse and deploy negatively charged quantum dots on an otherwise passive metamaterial structure with a resonant frequency of 0.62 THz, by employing a layer-by-layer, self-assembly scheme. Upon exposure to a UV source with a wavelength of 365 nm the amplitude modulation was observed to increase with increases in the number of deposited bi-layers, until a modulation maximum of 2.68% was recorded enabling an all-optical, dynamically reconfigurable metamaterial geometry. Furthermore, amplitude modulation was subsequently observed to decrease with further increases in the number of layers employed due to quenching and shadowing effects. The experimental observations reported herein will enable the utilization of all-optical reconfigurable THz devices for communication and data transmission applications.

Alloyed CdTe_0.6S_0.4Quantum Dots Sensitized TiO₂Electrodes for Photovoltaic Applications

The photovoltaic performance of alloyed CdTe0.6S0.4 quantum dot sensitized solar cells (QDSSCs) is investigated. Fluorine doped Tin Oxide (FTO) substrates were coated with 20 nm-diameter TiO2 nanoparticles (NPs). Presynthesized colloidal solution of alloyed CdTe0.6S0.4 quantum dots (QDs) of 4.2 nm was deposited onto TiO2 NPs substrates using direct adsorption (DA) technique, by dipping for different times at ambient conditions. The FTO counter electrodes were coated with platinum, while the electrolyte containing I-/I-3 redox species was sandwiched between the two electrodes. Compared to pure CdTe QDs and CdS QDs, CdTe0.6S0.4 QDs showed better photovoltaic performance. The J-V characteristic curves of the assembled QDSSCs were measured at AM 1.5 simulated sunlight. The short current density (Jsc) and efficiency (η) increase with dipping time. At 24 h dipping time, the open-circuit photovoltage Voc, Jsc, fill factor (FF), and η were 0.46 volts, 1.54 mA/cm2, 0.43% and 0.31%, respectively.