Concentration Of Quantum Dots Research Articles

Fluorescence Enhancement of CdS:Ag Quantum Dots Co-Assembled with Au Nanoparticles in a Hollow Nanosphere Form.

Colloidal quantum dots (QDs) have exceptional fluorescence properties. Overcoming aggregation-induced quenching and enhancing the fluorescence of colloidal QDs have remained a challenging issue in this field. In this study, composite hollow nanospheres composed of Au nanoparticles (NPs) and CdS:Ag-doped QDs were successfully constructed through controlled microemulsion-based cooperative assembly. This method harnessed the localized surface plasmon resonance (LSPR) effect of Au NPs nearby doped QDs, resulting in enhanced doped QD fluorescence and the observation of the Purcell effect. The composite hollow nanospheres show a fluorescence enhancement compared to that of the pure CdS:Ag QDs. The enhanced fluorescence was demonstrated to come from the synergetic enhancement of the absorption and emission transition of the doped QDs. This approach provides a feasible technological pathway to address the challenge of improving the fluorescence performance of the doped QDs.

Brilliant quantum dots’ photoluminescence from a dual-resonance plasmonic grating

Semiconductor quantum dots (QDs) have recently caused a stir as a promising and powerful lighting material applied in real-time fluorescence detection, display, and imaging. Photonic nanostructures are well suited for enhancing photoluminescence (PL) due to their ability to tailor the electromagnetic field, which raises both radiative and nonradiative decay rate of QDs nearby. However, several proposed structures with a complicated manufacturing process or low PL enhancement hinder their application and commercialization. Here, we present two kinds of dual-resonance gratings to effectively improve PL enhancement and propose a facile fabrication method based on holographic lithography. A maximum of 220-fold PL enhancement from CdSe/CdS/ZnS QDs are realized on 1D Al-coated photoresist (PR) gratings, where dual resonance bands are excited to simultaneously overlap the absorption and emission bands of QDs, much larger than those of some reported structures. Giant PL enhancement realized by cost-effective method further suggests the potential of better developing the nanostructure to QD-based optical and optoelectronic devices.

Two-photon absorption in quantum dots with Hellmann potential

Abstract We study the nonlinear optical absorption properties of a spherical quantum dot with Hellmann potential, focusing on the two-photon absorption (TPA) process, using GaAs/AlGaAs material as an example. { The radial Schr"{o}dinger equation is solved using the Nikiforov-Uvarov method, while the two-photon absorption coefficient is determined through second-order perturbation theory concerning the electron-photon interaction}. Our study shows that the intraband transition has a smaller energy transition than the interband transition, leading to TPA spectra for the intraband transition that is restricted within a smaller energy range and exhibits a higher peak value than those for the interband transition. The peak corresponding to $\ell=2$ consistently appears to the left of the peak corresponding to $\ell=1$ in both intraband and interband transition cases. Additionally, the dependence of the absorption peak position on the order of transition, $n$, differs between intra- and inter-band transitions. We also observe blue shift behavior in the TPA spectra as all three parameters, $r_0$, $V_{0e}$, and $\eta$, increase. Our investigation has the potential to enable the design of novel photonic devices, ultra-fast optical switches, and highly efficient solar cells through the optimization of quantum dot material properties.

Maximization of cytochrome C oxidase enzyme activity by optimizing color conversion from red organic light-emitting diodes

Photobiomodulation (PBM) therapy using red and near-infrared (NIR) light can effectively activate cytochrome C oxidase (CCO) enzyme to promote wound healing in living organisms. To maximize this therapeutic effect, the use of a light source with a spectrum absorbed by the CCO enzyme is necessary. A red/NIR light source optimized for CCO enzyme was obtained by partially color-converting a red organic light-emitting diode with copper indium sulfide/zinc sulfide quantum dots (QDs). To increase color conversion efficiency, the dispersion of QDs was improved by using a fibrous color conversion layer (FCCL). By optimizing the QD content in the FCCL, a red/NIR light source similar to the absorption spectrum of CCO enzyme was obtained with a spectral matching ratio of 81.7 %. When this light source was used in PBM therapy, it was experimentally verified that it showed a much faster wound closure effect compared to general red light, and it was proven that this was due to increased activity of the CCO enzyme. This study is a method of obtaining a red/NIR light source for PBM suitable for a specific enzyme performing a specific function, and is particularly useful due to its excellent form factor of being large, thin, and flexible.

Polyvalent Aptamer-Functionalized NIR-II Quantum Dots for Targeted Theranostics in High PD-L1-Expressing Tumors.

Ag2S quantum dots (QDs) show superior optical properties in the NIR-II region and display significant clinical potential with favorable biocompatibility. However, inherent defects of low targeting and poor solubility necessitate practical modification methods to achieve the theranostics of Ag2S QDs. Herein, we used rolling circle amplification (RCA) techniques to obtain long single-stranded DNA containing the PD-L1 aptamer and C-rich DNA palindromic sequence. The C-rich DNA palindromic sequences can specifically chelate Ag2+ and thus serve as a template to result in biomimetic mineralization and formation of pApt-Ag2S QDs. These QDs enable specific targeting and illuminate hot tumors with high PD-L1 expression effectively, serving as excellent molecular targeted probes. In addition, due to the high NIR-II absorption of Ag2S QDs, pApt-Ag2S QDs exhibit remarkable photothermal properties. And besides, polyvalent PD-L1 aptamers can recognize PD-L1 protein and effectively block the inhibitory signal of PD-L1 on T cells, enabling efficient theranostics through the synergistic effect of photothermal therapy and immune checkpoint blocking therapy. Summary, we enhance the biological stability and antibleaching ability of Ag2S QDs using long single-stranded DNA as a template, thereby establishing a theranostic platform that specifically targets PD-L1 high-expressing inflamed tumors and demonstrates excellent performance both in vitro and in vivo.

Exploring the electro-optical properties of nematic liquid crystal through incorporation of ZnCuGaS2 core/shell quantum dots

ABSTRACT The current study focuses on elucidating the interaction mechanisms between ZnCuGaS2 quantum dots (QDs) and nematic liquid crystals (NLCs) (5CB), intending to comprehend how this interaction leads to the alteration of electro-optical properties of the host material. Various concentrations of QDs were incorporated into NLCs and investigated to examine their emission and transmittance characteristics. Remarkably, an enhancement (~68%) in photoluminescence was observed for the concentration of 0.04 wt. %, adding an intriguing aspect to the findings. A notable decrease in the threshold voltage, from 1.5 V (in pure NLC) to 0.5 V, was observed for the optimised concentration (0.04 wt. %) calculated using transmittance-voltage measurement. This sample exhibited a noteworthy improvement in optical transmission, showing an increase by 2.7 times compared to pure NLC. Fundamentally, the introduction of QDs leads to a reduction in light leakage centres and ionic impurities, consequently enhancing radiative recombination. Moreover, the memory effect of the sample was evident in the capacitance-voltage data, revealing that the NLC with QDs significantly increased the capacitance value from 290 pF to 466 pF when compared to the pure NLC. The objective of the present research is to examine the impact of QDs on NLC concerning key parameters such as mentioned above.

CdSe/ZnS Quantum Dots' Impact on In Vitro Actin Dynamics.

Quantum dots (QDs) are a novel type of nanomaterial that has unique optical and physical characteristics. As such, QDs are highly desired because of their potential to be used in both biomedical and industrial applications. However, the mass adoption of QDs usage has raised concerns among the scientific community regarding QDs' toxicity. Although many papers have reported the negative impact of QDs on a cellular level, the exact mechanism of the QDs' toxicity is still unclear. In this investigation, we study the adverse effects of QDs by focusing on one of the most important cellular processes: actin polymerization and depolymerization. Our results showed that QDs act in a biphasic manner where lower concentrations of QDs stimulate the polymerization of actin, while high concentrations of QDs inhibit actin polymerization. Furthermore, we found that QDs can bind to filamentous actin (F-actin) and cause bundling of the filament while also promoting actin depolymerization. Through this study, we found a novel mechanism in which QDs negatively influence cellular processes and exert toxicity.

Study of Laser-Induced Multi-Exciton Generation and Dynamics by Multi-Photon Absorption in CdSe Quantum Dots.

Multi-exciton generation by multi-photon absorption under low-energy photons can be thought a reasonable method to reduce the risk of optical damage, especially in photoelectric quantum dot (QD) devices. The lifetime of the multi-exciton state plays a key role in the utilization of photon-induced carriers, which depends on the dynamics of the exciton generation process in materials. In this paper, the exciton generation dynamics of the photon absorption under low-frequency light in CdSe QDs are successfully detected and studied by the temporal resolution transient absorption (TA) spectroscopy method. Since the cooling time of hot excitons extends while the rate of auger recombination is accelerated when incident energy is increased, the filling time of defect states is irregular, and exciton generation experiences a transition from single-photon absorption to multi-photon absorption. This result shows how to change the excitation. Optical parameters can prolong the lifetime of excitons, thus fully extracting excitons and improving the photoelectric conversion efficiency of QD optoelectronic devices, which provides theoretical and experimental support for the development of QD optoelectronic devices.

Перспективы использования наночастиц (квантовых точек) в офтальмологии

Review Prospects for the use of nanoparticles (quantum dots) in ophthalmology V.O. Ponomarev, K.A. Tkachenko Eye Microsurger y Ekaterinburg Center, Ekaterinburg, Russian Federation Purpose. A systematic analysis of domestic and foreign literature devoted to the potential use of quantum dots (QD) in ophthalmology, as well as the identification of the main problems regarding the implementation of QD in ophthalmic practice. Material and methods. To carry out the review, a systematic analysis of scientific publications of domestic and foreign authors was carried out on the resources of PubMed, Medline, eLibrary from 2008 to 2021, devoted to the determination of physicochemical parameters, as well as the practical use of QD. Results. QD-based semiconductor nanoparticles are increasingly entrenched in modern science and medicine, in particular ophthalmology. This review defines the main physical parameters and physical and chemical properties of QD. Their potential applications are wide enough and focused on imaging, drug delivery, electrical stimulation and broad spectrum of anti-infective activity. Conclusion. To date, the existing limitations in the sphere of active QD application in ophthalmic practice are related to fundamental research in the field of acute and chronic cytotoxicity, selection of safe doses and concentrations of QD, working out mechanisms of their delivery, as well as in the study of mechanisms of chemical and biological interaction with the structures of the visual analyzer at dynamically changing physical parameters of QD (shape, size, features of functionalization and silanization). Interdisciplinary interactions between the pillars of fundamental medicine, physics, biology, chemistry, and ophthalmology, in particular, will probably allow us to realize in the nearest five years in clinical practice all the fundamental principles laid down in the previous studies. Key words: nanoparticles, quantum dots, anti-infective activity, imaging method, fluorescence

A Multistate Thermoresponsive Smart Window Based on a Multifunctional Luminescent Solar Concentrator.

Conventional luminescent solar concentrators (LSCs) usually only have the ability to absorb solar energy and convert it to electricity but are not able to regulate the transmitted light. Herein, a multistate thermoresponsive smart window (SW) based on LSC has been fabricated, in which the stimuli-responsive host layer consists of polydimethylsiloxane (PDMS) and ethylene glycol solution (EGS) microdroplets stacking with LSC layer-based on near-infrared (NIR) CuInSe2-xSx/ZnS core/shell quantum dots (QDs) and PDMS matrix. As-synthesized CISSe/ZnS QDs with broad NIR absorption in LSC exhibit controllable emission spectra over 833-1088 nm and high photoluminescence (PL) quantum yield from 45 to 83%. Coupling with Si solar cells as a reference, optimized LSC-SW devices with dimensions of 5 × 5 × 0.9 cm3 exhibit higher power conversion efficiency (PCE) of 1.19-1.36% with increased temperature from 0 to 50 °C than those of sole LSC and SW devices. The corresponding visible light transmissions are regulated from 75.1 to 48.1% accordingly. The improvement of PCEs in an opaque state is mainly due to enhanced absorption of QDs originating from rescattered photons from the EGS/PDMS layer, leading to more emitted photons reaching photovoltaics. This work is expected to bring up new opportunities for applications in greenhouses, building facades, and energy-efficient smart windows.

Ultrafast Electron Transfer from CuInS2 Quantum Dots to a Molecular Catalyst for Hydrogen Production: Challenging Diffusion Limitations.

Systems integrating quantum dots with molecular catalysts are attracting ever more attention, primarily owing to their tunability and notable photocatalytic activity in the context of the hydrogen evolution reaction (HER) and CO2 reduction reaction (CO2RR). CuInS2 (CIS) quantum dots (QDs) are effective photoreductants, having relatively high-energy conduction bands, but their electronic structure and defect states often lead to poor performance, prompting many researchers to employ them with a core-shell structure. Molecular cobalt HER catalysts, on the other hand, often suffer from poor stability. Here, we have combined CIS QDs, surface-passivated with l-cysteine and iodide from a water-based synthesis, with two tetraazamacrocyclic cobalt complexes to realize systems which demonstrate high turnover numbers for the HER (up to >8000 per catalyst), using ascorbate as the sacrificial electron donor at pH = 4.5. Photoluminescence intensity and lifetime quenching data indicated a large degree of binding of the catalysts to the QDs, even with only ca. 1 μM each of QDs and catalysts, linked to an entirely static quenching mechanism. The data was fitted with a Poissonian distribution of catalyst molecules over the QDs, from which the concentration of QDs could be evaluated. No important difference in either quenching or photocatalysis was observed between catalysts with and without the carboxylate as a potential anchoring group. Femtosecond transient absorption spectroscopy confirmed ultrafast interfacial electron transfer from the QDs and the formation of the singly reduced catalyst (CoII state) for both complexes, with an average electron transfer rate constant of <kET> ≈ (10 ps)-1. These favorable results confirm that the core tetraazamacrocyclic cobalt complex is remarkably stable under photocatalytic conditions and that CIS QDs without inorganic shell structures for passivation can act as effective photosensitizers, while their smaller size makes them suitable for application in the sensitization of, inter alia, mesoporous electrodes.

Reduced Surface Trap States of PbS Quantum Dots by Acetonitrile Treatment for Efficient SnO2-Based PbS Quantum Dot Solar Cells.

The solution-phase ligand-exchange strategy offers a simple pathway to prepare PbS quantum dots (QDs) and their corresponding solar cells. However, the production of high-quality PbS QDs with reduced surface trap state density for efficient PbS QD solar cells (QDSCs) still faces challenges. As the hydroxyl group (-OH) has been demonstrated to be the primary source of the surface trap states on PbS QDs in the general oleic acid method, here, we present an effective and facile strategy for reducing the surface -OH content of PbS QDs by using acetonitrile (ACN) as precipitant to wash the surface of QDs, which significantly decreases the trap state density and enables the preparation of superior PbS QDs. The resulting solar cell with an ITO/SnO2/n-PbS/p-PbS/Au structure obtained an improved photoelectric conversion efficiency (PCE) from 8.53 to 10.49% with an enhanced air storage stability, realizing a high PCE for SnO2-based PbS QDSCs.

Enhanced dielectric, electrical and electro-optical properties: Towards understanding the interaction in mesophases of 8OCB liquid crystal dispersed with CdSe/ZnS quantum dots

The current advancements in developing new liquid crystalline materials for the next generation applications focus mainly on improving the physical characteristics of the liquid crystal (LC) systems. Recent progress has shown that the functionalized nanoparticles embedded in LC matrices can significantly alter the characteristics of the LC material based on the mutual interaction between the host molecules and guest particles. In this aspect, the present study reports the impact of dispersing core-shell type CdSe/ZnS quantum dots (QDs) on the dielectric, electrical and electro-optical properties of the 8OCB LC doped at various concentrations. The doped samples exhibit an ion releasing behavior and this effect becomes more evident as the doping concentration increases up to 0.2 wt% in the LC system. It is explained as a result of the growing tactoid-like ellipsoidal form acquired by QDs owing to the enhanced mutual interaction among QD ligands and rod-like LC molecules. The temperature variation of the diffusion constant, conductivity, ionic mobility and mean relaxation time of ions significantly follows each other in all the studied samples. Moreover, thermal profiles of the dielectric anisotropy, threshold voltage and splay elastic constant show a decreasing pattern with an increment in doping concentration. A dual-relaxation regime is experimentally investigated, corresponding to the contribution of nematic director and dimers, providing two kinds of rotational viscosity in the pristine and QDs dispersed LC samples. The transmittance-voltage curve reveals the presence of residual value in the dispersed samples and is related to the volatile memory effect. A slight enhancement is observed in the photoluminescence intensity for the lower doped sample and reduces further with increasing doping concentration in the pristine LC system. All these findings suggest the considerable contribution of functionalized QDs to the studied properties in terms of interaction between the LC and dopant material. This study will further elucidate the selection of optimal QDs concentration based on the required properties for their potential applications in futuristic devices based on LCs.

Unique properties of titanium dioxide quantum dots assisted regulation of growth and biochemical parameters of Hibiscus sabdariffa plants

Owing to the uniqueness of quantum dots (QDs) as a potential nanomaterial for agricultural application, hence in the present study, titanium dioxide quantum dots (TiO2 QDs) were successfully synthesized via sol-gel technique and the physico-chemical properties of the prepared TiO2 QDs were analyzed. Based on the results, the TiO2 QDs showed the presence of anatase phase of TiO2. TEM examination revealed spherical QDs morphology with an average size of 7.69 ± 1.22 nm. The large zeta potential value (-20.9 ± 2.3 mV) indicate greater stability of the prepared TiO2 QDs in aqueous solutions. Moreover, in this work, the application of TiO2 QDs on Hibiscus sabdariffa plants was conducted, where H. sabdariffa plants were foliar sprayed twice a week in the early morning with different concentrations of TiO2 QDs (0, 2, 5, 10, 15 and 30 ppm) to evaluate their influence on these plants in terms of morphological indexes and biochemical parameters. The results exhibited an increasing impact of the different used concentrations of TiO2 QDs on morphological indexes, such as fresh weight, dry weight, shoot length, root length, and leaf number, and physio-biochemical parameters like chlorophyll a, chlorophyll b, carotenoid contents, total pigments and total phenolic contents. Remarkably, the most prominent result was recorded at 15 ppm TiO2 QDs where plant height, total protein and enzymatic antioxidants like catalase and peroxidase were noted to increase by 47.6, 20.5, 29.5 and 38.3%, respectively compared to control. Therefore, foliar spraying with TiO2 QDs positively serves as an effective strategy for inducing optimistic effects in H. sabdariffa plants.

Interactions of CdSe Nanocrystals with Cationic Proteins Extracted from Moringa oleifera Seeds

Even with significant developments in nanoscience, relatively little is known about the interactions of nanocrystal semiconducting materials with bio-macromolecules. To investigate the interfacial phenomena of cadmium selenide quantum dot (CdSe QD) nanocrystals with proteins extracted from Moringa oleifera seeds, different concentrations of cadmium selenide quantum dots–Moringa oleifera seed protein (CdSe–MSP) complexes were prepared. Respective CdSe QDs with hexagonal phase and crystalline size in the range of 4–7 nm were synthesized and labelled with the purified mesoporous MSP having a surface area of 8.4 m2/g. The interaction mechanism between CdSe QDs and MSP was studied using UV–Vis absorption, fluorescence emission and Fourier Transform Infrared spectroscopies. The UV–Vis absorption spectra showed absorption bands of CdSe–MSP complexes at 546.5 nm. The fluorescence intensity of CdSe QDs was found to decrease with increasing concentration of MSP. The thermodynamic potentials ∆Hθ (−321.3 × 103 Jmol−1); ∆Sθ (156.0 JK−1mol−1) and ∆Gθ (−46.6 × 103 Jmol−1) were also calculated. The stability of the complex found is strongly influenced by electrostatics interaction and surface-bound complexation equilibrium attraction. This information can help to elucidate the surface characteristics of MSP and its potential interactions with other molecules or nanoparticles.

Triplet energy transfer from quantum dots increases Ln(iii) photoluminescence, enabling excitation at visible wavelengths.

Europium(iii) complexes are promising for bioimaging because of their long-lived, narrow emission. The photoluminescence (PL) from europium(iii) complexes is usually low. Thus, the effective utilization of low-energy light >400 nm and enhancement of PL are long-standing goals. Here, we show for the first time that 1-naphthoic acid triplet transmitter ligands bound to CdS quantum dots (QDs) and europium(iii) complexes create an energy transfer cascade that takes advantage of the strong QD absorption. This is confirmed by transient absorption spectroscopy, which shows hole mediated triplet energy transfer from QDs to 1-NCA, followed by triplet transfer from 1-NCA to europium(iii) complexes with an efficiency of 65.9 ± 7.7%. Smaller CdS QDs with a larger driving force lead to higher triplet transfer efficiency, with Eu(iii) PL intensity enhanced up to 21.4 times, the highest value ever reported. This hybrid QD system introduces an innovative approach to enhance the brightness of europium complexes.

Size control of MoS2 quantum dots by varying the crystallographic orientation of sapphire substrates

The phenomena in size-dependent optoelectronic and catalytic properties of MoS2 quantum dots make them attractive in fabricating optoelectronic devices and processing water-splitting. However, growing monolayered MoS2 quantum dots with controlled sizes is challenging and has never been realized on a solid-state substrate. Herein, we experimentally demonstrate the size of monolayered MoS2 quantum dots can be thermodynamically manipulated by varying the orientation of the sapphire substrate from c plane, m plane to r plane and the size can be tuned from 10 nm to 2 nm. An apparent shift in the optical absorption and outstanding size-dependent electrocatalytic capability of the MoS2 quantum dots can be featured. The DFT results verify that the size modulation is associated with the interaction strength between the MoS2 quantum dots and the sapphire substrate. This work provides a new benchmark in the growth of size-tunable monolayered MoS2 quantum dots on a solid-state substrate.

Design of Quantum Dot Color Convertors for Inkjet‐Printed Optoelectronic Devices: Violet‐Converted Full Color Mini‐LED

AbstractThis study presents a strategy of design and development of inkjet‐printable and UV‐curable quantum dot (QD) polymer‐based inks and color conversion (CC) film for use in optoelectronic devices. At first, the preparation of a QD ink is focused on two key aspects, that are QD chemical compatibility and ink printability. In the hybrid organic–inorganic polymer/QDs system, it must be formulated to a well‐dispersed ink, in which a dispersant additive without negative effect on QDs is introduced to enhance the QD suspension. As the optical density of final dried QD film is one of the most critical concerns in color conversion, QD concentration should be as high as possible in the ink, which increases the ink viscosity. Consequently, a trade‐off between QD concentration and the ink viscosity associated with the ink‐jetting temperature is considered to ensure the ink printability. Finally, the designed QD ink is printed as color conversion film on a mini‐LED panel composed of two violet mini‐chips to produce red and green emissions, while blue emission directly comes from a blue mini‐chip. The final conversion efficiency of QDCC on mini‐LED panel are between 35% and 45%, showing the promising applications in optoelectronic devices.

Photoelectric properties of thin layers of Ag2S quantum dots passivated with thiol-containing molecules

In this work, we studied the electrophysical properties of condensates of colloidal Ag2S quantum dots (QDs), passivated with thiol-containing molecules (thioglycolic acid and L-cysteine) (further, Ag2S/TGA QDs and Ag2S/L-Cys QDs) on indium tin oxide (ITO) substrates. The temperature dependences of the electrical characteristics (conductivity) are analyzed in the temperature range from 300 to 360 K. Facts of the formation of the Schottky barrier structures is obtained. Activation energies of 0.2 eV (Ag2S/L-Cys QDs) and 0.66 eV (Ag2S/TGA QDs) were obtained by the use of linear approximations of current–voltage (I–V) characteristics in Arrhenius coordinates. It is shown that the conductivity of ITO - Ag2S QDs film - Al structure is mainly determined by the Schottky barrier that is formed at the Al-Ag2S QDs film junction. The rectifying contact is formed at the Ag2S film -Al junction due to the lower work function of Al. The I–V characteristics under the optical radiation action were analyzed for the studied sandwich structures. They turned out to be similar for Ag2S/TGA and Ag2S/L-Cys QDs. When a reverse or forward bias voltage is applied to a sandwich structure, in the case of the optical radiation action with a wavelength starting from the its value, corresponding to the most probable exciton transition in the QDs absorption the photocurrent is observed. The found difference (by an order of magnitude) in the photocurrent values of the sandwich structure, based on Ag2S/TGA QDs and Ag2S/L-Cys QDs is related to the smaller thickness of the Ag2S/TGA QDs film.

Impact of Surface Ligand on the Biocompatibility of InP/ZnS Quantum Dots with Platelets.

InP/ZnS quantum dots (QDs) have received a large focus in recent years as a safer alternative to heavy metal-based QDs. Given their intrinsic fluorescent imaging capabilities, these QDs can be potentially relevant for in vivo platelet imaging. The InP/ZnS QDs are synthesized and their biocompatibility investigated through the use of different phase transfer agents. Analysis of platelet function indicates that platelet-QD interaction can occur at all concentrations and for all QD permutations tested. However, as the QD concentration increases, platelet aggregation is induced by QDs alone independent of natural platelet agonists. This study helps to define a range of concentrations and coatings (thioglycolic acid and penicillamine) that are biocompatible with platelet function. With this information, the platelet-QD interaction can be identified using multiple methods. Fluorescent lifetime imaging microscopy (FLIM) and confocal studies have shown QDs localize on the surface of the platelet toward the center while showing evidence of energy transfer within the QD population. It is believed that these findings are an important stepping point for the development of fluorescent probes for platelet imaging.