Types Of Quantum Dots Research Articles

Quantum Dots-caused Retinal Degeneration in Zebrafish Regulated by Ferroptosis and Mitophagy in Retinal Pigment Epithelial Cells through Inhibiting Spliceosome.

Quantum dots (QDs) are widely used, but their health impact on the visual system is little known. This study aims to elucidate the effects and mechanisms of typical metallic QDs on retinas using zebrafish. Comprehensive histology, imaging, and bulk RNA sequencing reveal that InP/ZnS QDs cause retinal degeneration. Furthermore, single-cell RNA-seq reveals a reduction in the number of retinal pigment epithelial cells (RPE) and short-wave cone UV photoreceptor cells (PR(UV)), accompanied by an increase in middle- and long-wave cone red, green, and blue photoreceptor cells [PR(RGB)]. Mechanistically, after endocytosis by RPE, InP/ZnS QDs inhibit the expression of splicing factor prpf8, resulting in gpx4b mRNA unsplicing, which finally decrease glutathione and induce ferroptosis and mitophagy. The decrease of RPE fails to engulf the damaged outer segments of PR, possibly promoting the differentiation of PR(UV) to PR(RGB). Knockout prpf8 or gpx4b with CRISPR/Cas9 system, the retinal damage is also observed. Whereas, overexpression of prpf8 or gpx4b, or supplement of glutathione can rescue the retinal degenerative damage caused by InP/ZnS QDs. In conclusion, this study illustrates the potential health risks of InP/ZnS QDs on eye development and provides valuable insights into the underlying mechanisms of InP/ZnS QDs-caused retinal degeneration.

Peptide-mediated targeting of Quantum Dots in a 3D model of head and neck cancer

BackgroundOral squamous cell carcinoma (OSCC) treatment mainly relies on surgery. The status of surgical margin is a major prognostic factor for patients as positive margins are associated with lower survival. However, the anatomical particularities of this area complicate margin establishment. Fluorescence guided surgery (FGS) could be employed as an intraoperative technique to improve tumor resection and margin investigation. Quantum dots (QDs) serve as ideal contrast agents in this technique due to their brightness and stability. Since αVβ6 integrin is overexpressed in OSCC, coupling QDs with A20FMDV2 peptide (QDs-A20) targeting the αVβ6 integrin constitute a real opportunity. This study investigates the accumulation of QDs-A20 in 2D and 3D tongue cancer models, as well as QDs coupled to a scrambled version of this peptide (QDs-Scr) or without peptide (QDs-SPP), for imaging purposes. MethodsCdSeCdS/ZnS quantum dots were coated with sulfobetaine polymers (QDs-SPP) and conjugated to A20FMDV2 peptide (QDs-A20) or its scrambled version (QDs-Scr). Two-dimensional (2D) and three-dimensional (3D) tongue cancer cells HSC-3 were employed to test the effectiveness of intracellular accumulation of all types of QDs. Targeting ability of each QDs was assessed by flow cytometry, while the depth of penetration into cancerous spheroids was assessed by fluorescence microscopy. ResultsQDs coating with sulfobetaines polymers (QDs-SPP) completely prevented their internalization by HSC-3 cells in 2D and 3D models, making QDs stealthy and preventing their non-specific accumulation. Conversely, peptides conjugated QDs (QDs-A20 & QDs-Scr) labeled HSC-3 monolayers and managed to label spheroid periphery up to 23 µm deep. However, no difference in accumulation was found between these two QDs whereas only A20 peptide could potentially target αVβ6 integrin. It appears that peptide conjugation increased QDs zeta potential, promoting their adsorption and subsequent endocytosis by cells, independently from αVβ6 integrin. ConclusionsThe present study highlighted the impact of peptide conjugation on QDs internalization in 2D and 3D tongue cancer cell models. QDs-SPP were stealthy and did not accumulate in cells. Peptides conjugated QDs could be used as contrast agents, but in a passive targeting approach. Modifications to surface chemistry are required to target αVβ6 integrin through active targeting. This study also highlights the need for controls such as scrambled peptides, the absence of which can lead to misinterpretation of results.

Versatile Approaches of Quantum Dots in Biosensing and Imaging.

Cancer is considered a formidable global health threat, despite substantial strides in diagnosis, detection, and therapeutic strategies. Remarkable progress has been achieved in these realms, yet the survival rates for cancer patients have persisted at suboptimal levels over decades. Acknowledging the need to address the ongoing challenges in cancer survival rates, research efforts are being made to push the boundaries of innovation in diagnostic techniques, bioimaging, and drug delivery technologies. Over the past few years, nano(bio)technology-based approaches have been applied for biosensing and imaging applications to detect biochemical substances in various matrices. Among various nanoengineered particulates, quantum dots (QDs) have been recognized as versatile agents for these applications. QDs, often called artificial atoms, are characterized by the remarkable optical and electrical features which are essential for cytosensing, localized bioimaging and therapeutics. Here in this review, we have discussed various QDs as sensitive and selective agents for precise sensing and imaging of cancer cells. Both electrochemical and optical approaches have been used to describe the cytosensing detection methods. Furthermore, the bioimaging of malignant tumor cells and the drug delivery with therapeutic responses of QDs have also been highlighted. This review also lists the several kinds of QDs that are frequently used for such kinds of applications, such as carbon, graphene, zinc, and other types of hybrid-based QDs. Finally, to shed insight on prospective research, the advantages and potential of QDs are also highlighted. In this article, we also emphasize the limitations and address the difficulties associated with QDs in clinical applications in order to provide insights for potential solutions.

Investigating the effect of Zn doping and temperature on the photoluminescence behaviour of CuLaSe2 quantum dots.

In this study, CuLaSe2 and ZnCuLaSe2 quantum dots (QDs) with a mean size of ~4nm were synthesized and characterized, and their temperature-dependent photoluminescence (PL) properties were studied in the temperature range from 90 to 300 K for the first time. The results show that the obtained QDs were spherical and revealed excitonic band gaps. The PL intensity for both types of materials decreased when increasing the temperature to 300 K, which was attributed to the nonradiative relaxation and thermal escape mechanisms. As the temperature was increased, the PL linewidths broadened, and PL peak energies were red shifted for both types of QDs due to the exciton-phonon coupling and lattice deformation potential mechanisms. In addition, we found that as the temperature was decreased, the PL spectrum of ZnCuLaSe2 QDs contained two extra components, which could be attributed to the shallow defect sites (low energy peak) and the crystal phase transition process (high energy peak). The spectrum of CuLaSe2 QDs contained one extra component, which could be attributed to the crystal phase transition process.

One-step fast fabrication of multi-layer quantum dot diffusion plate for stable display and ultra-long life, a novel quantum dot packaging strategy

Quantum dots (QDs), renowned for their distinctive optical and physical attributes, are extensively employed in diverse fields such as lighting, displays, electronics, sensors, and solar cells. Nonetheless, the susceptibility to light, oxygen, and moisture is a major obstacle to the development of QDs. Achieving simple, efficient, and universal modification or encapsulation for enhanced stability remains a challenge. Herein, a one-step fast fabrication of multi-layer quantum dot diffusion plate (QD-DP) with excellent barrier and optical properties was proposed, which is alternately stacked by MS-EVOH and MS-QDs layers. The barrier phase morphology undergoes a fiber-flake transition induced by the bidirectional tensile force field during multiplication, and layer-by-layer encapsulation synergistically enhances the barrier performance, photo-oxygen stability, thermal-oxygen stability, and fluorescence lifetime of QD-DP in backlight applications. Under high-power UV irradiation, the fluorescence intensity ofMS/MS-QD 128L dropped to 90 % (T90) in only about 10 minutes, while the T90 of MS-E/MS-QD 128L was close to 216 hours, improved more than 1200 times. Concurrently, the quantum dot diffusion plate (QD-DP), characterized by an alternating multi-layer structure, demonstrated an elevated backlight color gamut value of ∼ 120 % NTSC, outperforming conventional quantum dot light emitting diodes (QLED). Compared with existing QDs backlight modules, a simpler structure, more efficient preparation process, and longer fluorescence lifetime of QD-DP were achieved.Moreover, unlike prevalent modification or packaging technologies that only target specific QD types, our alternating multilayer coextrusion packaging technology is applicable to all kinds of QDs and is simple, efficient, and universal.It was believed that this work could provide new opportunities for all kinds of QDs encapsulation and application in many fields and will be the dawn of large-scale commercialization of QDs.

Bright Semiconductor Quantum Dots Shed New Light on Precision Nanomedicine for Various Diseases

Nanomaterials with diagnostic and therapeutic functions have exciting potential to reshape the landscape of precision medicine. Impressive progress has been made toward the design and production of innovative theranostic nanomaterials that improve disease care, motivated by their ability to simultaneously provide diagnostic information and therapeutic benefits. Herein, the state‐of‐the‐art theranostic semiconductor quantum dots (QDs) are summarized, and the diverse types of QDs designed for the diagnosis and treatment of different diseases are discussed. The opportunities and benefits of QDs are highlighted throughout using in vitro and in vivo examples aimed at addressing various clinical challenges, including cancer, vascular dysfunctions, microbial infections, and medical tattoos. Over the past several years, this area has experienced enormous growth, particularly in preclinical animal imaging and therapy, which has brought the field closer to reaching human patients. Unfortunately, several barriers to clinical translation remain. Therefore, in addition to summarizing the key results from previous in vivo studies, the lessons learned from these studies are synthesized, perspective on the future steps needed for both fundamental studies and the clinical translation of theranostic QD nanotechnology to inform future QD design is provided.

Zwitterionic carbon quantum dots incorporated ultrafiltration membrane for efficient removal of copper ion

Copper, prized for its excellent thermal and electrical conductivity, poses risks when present in wastewater. Treating copper ion-containing wastewater is vital for human and environmental safety. Membrane separation technology offers an eco-friendly and energy-efficient solution. In this study, a mixture of cellulose acetate (CA) and thermoplastic polyurethane (TPU) was used to fabricate the tubular membrane, with quantum dots (QDs) added. Three types of QDs were introduced into the tubular membrane: carbon quantum dots (CQDs), tertiary amine CQDs (TQDs), and zwitterionic CQDs (ZQDs). At pH = 10, copper ions were chelated with sodium dimethyldithiocarbamate (SDDC) at a ratio of SDDC/Cu2+=10 (w/w), signifying a molar concentration (mol.L-1) ratio of SDDC:Cu2+=3:16. This process achieved a 99.8% removal rate of copper ion. The ZQDs-M exhibited high pure water flux of 6,227.4 L.m−2.h−1.bar−1 and 95.4% copper ion-complex rejection rate. The ZQDs-M also demonstrated excellent anti-adhesion properties, with only 4.55% relative fluorescence intensity of E. coli and 34.58% BSA adsorption. The BSA dynamic anti-fouling property of the ZQDs-M was also superior to that of tubular membrane without QDs addition.

Gallium Sulfide Quantum Dots with Zinc Sulfide and Alumina Shells Showing Efficient Deep Blue Emission.

Solution-processed quantum dot (QD) based blue emitters are of paramount importance in the field of optoelectronics. Despite large research efforts, examples of efficient deep blue/near UV-emitting QDs remain rare due to lack of luminescent wide band gap materials and high defect densities in the existing ones. Here, we introduce a novel type of QDs based on heavy metal free gallium sulfide (Ga2 S3 ) and their core/shell heterostructures Ga2 S3 /ZnS as well as Ga2 S3 /ZnS/Al2 O3 . The photoluminescence (PL) properties of core Ga2 S3 QDs exhibit various decay pathways due to intrinsic defects, resulting in a broad overall PL spectrum. We show that the overgrowth of the Ga2 S3 core QDs with a ZnS shell results in the suppression of the intrinsic defect-mediated states leading to efficient deep-blue emission at 400 nm. Passivation of the core/shell structure with amorphous alumina yields a further enhancement of the PL quantum yield approaching 50 % and leads to an excellent optical and colloidal stability. Finally, we develop a strategy for the aqueous phase transfer of the obtained QDs retaining 80 % of the initial fluorescence intensity.

Cellular uptake, intracellular behavior, and acute/sub-acute cytotoxicity of a PEG-modified quantum dot with promising in-vivo biomedical applications

Quantum Dots (QDs) modified with branched Polyethylene Glycol-amine (6- or 8-arm PEG-amine) coupled with methoxy PEG (mPEG) hold great promise for in vivo biomedical applications due to a long half-life in blood and negligible toxicity. However, the potential risks regarding their concomitant prolonged co-incubation with cardiovascular and blood cells remains inconclusive. In the present study, the feasible, effective and convenient proliferating-restricted cell line models representing the circulatory system were established to investigate the cellular internalization followed by intracellular outcomes and resulting acute/sub-acute cytotoxicity of the 6-arm PEG-amine/mPEG QDs. We found a dose-, time- and cell type-dependent cellular uptake of the 6-arm PEG-amine/mPEG QDs, which was ten-fold lower compared to the traditional linear PEG-modified counterpart. The QDs entered cells via multiple endocytic pathways and were mostly preserved in Golgi apparatus for at least one week instead of degradation in lysosomes, resulting in a minimal acute cytotoxicity, which is much lower than other types of PEG-modified QDs previously reported. However, a sub-acute cytotoxicity of QDs were observed several days post exposure using the concentrations eliciting no-significant acute cytotoxic effects, which was associated with elevated ROS generation caused by QDs remained inside cells. Finally, a non-cytotoxic concentration of the QDs was identified at the sub-acute cytotoxic level. Our study provided important information for clinical translation of branched PEG-amine/mPEG QDs by elucidating the QDs-cell interactions and toxicity mechanism using the proliferation-restricted cell models representing circulatory system. What's more, we emphasized the indispensability of sub-acute cytotoxic effects in the whole biosafety evaluation process of nanomaterials like QDs.

Dangling Bonds as Possible Contributors to Charge Noise in Silicon and Silicon-Germanium Quantum Dot Qubits.

Spin qubits based on Si and Si1-xGex quantum dot architectures exhibit among the best coherence times of competing quantum computing technologies, yet they still suffer from charge noise that limit their qubit gate fidelities. Identifying the origins of these charge fluctuations is therefore a critical step toward improving Si quantum-dot-based qubits. Here, we use hybrid functional calculations to investigate possible atomistic sources of charge noise, focusing on charge trapping at Si and Ge dangling bonds (DBs). We evaluate the role of global and local environment in the defect levels associated with DBs in Si, Ge, and Si1-xGex alloys, and consider their trapping and excitation energies within the framework of configuration coordinate diagrams. We additionally consider the influence of strain and oxidation in charge-trapping energetics by analyzing Si and GeSi DBs in SiO2 and strained Si layers in typical Si1-xGex quantum dot heterostructures. Our results identify that Ge dangling bonds are more problematic charge-trapping centers both in typical Si1-xGex alloys and associated oxidation layers, and they may be exacerbated by compositional inhomogeneities. These results suggest the importance of alloy homogeneity and possible passivation schemes for DBs in Si-based quantum dot qubits and are of general relevance to mitigating possible trap levels in other Si, Ge, and Si1-xGex-based metal-oxide-semiconductor stacks and related devices.

Tailoring Eco-Friendly Colloidal Quantum Dots for Photoelectrochemical Hydrogen Generation.

A photoelectrochemical (PEC) cell is able to realize effective solar-to-hydrogen energy conversion from water by using the semiconductor photoelectrode. Semiconducting colloidal quantum dots (QDs) with captivating features of size-tunable optoelectronic properties and broad light absorption are regarded as promising photosensitizers in solar-driven PEC systems. Up to now, different types of QDs have been developed to achieve high-efficiency PEC H2 generation, while the majority of state-of-the-art QDs-PEC systems are still fabricated from QDs consisting of heavy metals (e.g., Cd and Pb), which are extremely harmful to the human health and natural environment. In this context, substantial efforts have been made to mitigate the usage of highly toxic heavy metals and concurrently promote the development of alternative environment-friendly QDs with comparable features. This review presents recent advances of solar-driven PEC devices based on several typical environment-friendly QDs (e.g., carbon QDs, I-III-VI QDs and III-V QDs). A variety of techniques (e.g., shell thickness tuning, alloying/doping, and ligands exchange, etc.) to engineer these QD's optoelectronic properties and achieve high-efficiency PEC H2 production are thoroughly discussed. Furthermore, the critical challenges and future perspectives of advanced eco-friendly QDs-PEC systems in terms of QDs' synthesis, photo-induced charge kinetics, and operation stability/efficiency are briefly proposed.

High-Throughput Characterization of Single-Quantum-Dot Emission Spectra and Spectral Diffusion by Multiparticle Spectroscopy

In recent years, quantum dots (QDs) have emerged as bright, color-tunable light sources for various applications such as light-emitting devices, lasing, and bioimaging. One important next step to advance their applicability is to reduce particle-to-particle variations of the emission properties as well as fluctuations of a single QD’s emission spectrum, also known as spectral diffusion (SD). Characterizing SD is typically inefficient as it requires time-consuming measurements at the single-particle level. Here, however, we demonstrate multiparticle spectroscopy (MPS) as a high-throughput method to acquire statistically relevant information about both fluctuations at the single-particle level and variations at the level of a synthesis batch. In MPS, we simultaneously measure emission spectra of many (20–100) QDs with a high time resolution. We obtain statistics on single-particle emission line broadening for a batch of traditional CdSe-based core–shell QDs and a batch of the less toxic InP-based core–shell QDs. The CdSe-based QDs show significantly narrower homogeneous line widths, less SD, and less inhomogeneous broadening than the InP-based QDs. The time scales of SD are longer in the InP-based QDs than in the CdSe-based QDs. Based on the distributions and correlations in single-particle properties, we discuss the possible origins of line-width broadening of the two types of QDs. Our experiments pave the way to large-scale, high-throughput characterization of single-QD emission properties and will ultimately contribute to facilitating rational design of future QD structures.

Biological Applications of Aqueous CuInS Quantum Dots: Overview

Quantum dots (QDs), a type of semiconductor nanomaterial, have drawn a lot of attention because of their exceptional optical characteristics and prospective uses in biology and medicine. However, the presence of heavy hazardous metals in typical QDs, such as Cd, Pb and Hg, has posed a significant obstacle to their use. Therefore, it is essential to look for a workable substitute that would be nontoxic and have comparable optical characteristics to the traditional QDs. It has been determined that ternary I–III–VI QDs are appropriate substitutes. They emit light in the near-infrared range and have adjustable optical characteristics. They are valuable in a variety of biological applications because of their optical characteristics and can be easily bioconjugated with biomolecules for targeted imaging. Therefore, this review concentrates on the most recent developments in the usage of aqueous CIS QDs in biological, bioconjugated with biomolecules, nanomedical and drug delivery system applications.

InP/ZnSeS/ZnS Quantum Dots with High Quantum Yield and Color Purity for Display Devices

To achieve the quantum yield and color purity suitable for applications to the visible emitters in display devices, the optical features of indium phosphide (InP) quantum dots (QDs) are improved. Two types of InP cores are synthesized with two kinds of the phosphorus precursors, tris(trimethylsilyl)phosphine and tris(dimethylamino)phosphine. The prepared cores are fabricated for the gradient-alloyed inner shell (ZnSeS) and outer shell (ZnS) to complete the environmentally benign QDs with the structures of core/inner-shell/outer-shell. The quantum yields in the two types of QDs are 95 and 85% with the bandwidths of 35 and 36 nm, respectively, comparable to the characteristics of state-of-the-art InP QDs. The band-to-band transition of the neutral states in QDs turns out to be more efficient than the band-to-hole transition, whereas the optical transitions of the charged states are not strong. Despite the similar peak shapes with the equivalent Stokes shift, the optical features investigated by temperature-dependent and time-resolved spectroscopy are distinctive in the two types of QDs. In particular, the formation of the charged states and localized states, in addition to the dark states, is influenced by the precursors. These findings suggest strategies to enhance the quantum yield and color purity of InP QDs for applications to display devices with a green chemistry approach.

How structural and vibrational features affect optoelectronic properties of non-stoichiometric quantum dots: computational insights.

While stoichiometric quantum dots (QDs) have been well studied, a significant knowledge gap remains in the atomistic understanding of the non-stoichiometric ones, which are predominantly present during the experimental synthesis. Here, we investigate the effect of thermal fluctuations on structural and vibrational properties of non-stoichiometric cadmium selenide (CdSe) nanoclusters: anion-rich (Se-rich) and cation-rich (Cd-rich) using ab initio molecular dynamics (AIMD) simulations. While the excess atoms on the surface fluctuate more for a given QD type, the optical phonon modes are mostly composed of Se atoms dynamics, irrespective of the composition. Moreover, Se-rich QDs have higher bandgap fluctuations compared to Cd-rich QDs, suggesting poor optical properties of Se-rich QDs. Additionally, non-adiabatic molecular dynamics (NAMD) suggests faster non-radiative recombination for Cd-rich QDs. Altogether, this work provides insights into the dynamic electronic properties of non-stoichiometric QDs and proposes a rationale for the observed optical stability and superiority of cation-rich candidates for light emission applications.

Перспективы применения наночастиц Ag(10%):InP/ZnS MPA в лечении дрожжевых кератомикозов

Relevance. Resistant fungal keratitis (keratomycosis) is a big current problem in ophthalmology. The limited arsenal of drugs and the low efficiency of surgical treatment often leads to extremely low anatomical and functional results. One of the alternative approaches to the management of fungal keratitis can be the use of nanoparticles, in monotherapy, or as a catalyst for a more effective effect of a native drug. Quantum dots (QDs) act as nanoparticles. Under the action of light in the visible region of the spectrum, QDs are capable of participating in redox reactions and the simulated formation of reactive oxygen species (ROS) by changing the electronic interactions with the surrounding atoms. Purpose. Synthesis of QDs potentially active against fungal microflora, study of the ability of this type of QDs and analogues to produce ROS and analysis of their fungicidal activity against yeast microflora in vitro. Material and methods. The study determined the effectiveness of the QDs solution in suppressing the growth of colonies of resistant species of fungi of the genus Candida spp (C. albicans, C. glabrata, C. tropicalis, C. Parapsilosis) in vitro. QDs Ag(10%):InP/ZnS MPA were used in the form of a native solution (10%) and at a dilution of 1:100 (0.1%). Results. It was possible to reveal the complete suppression of the visible growth of Candida spp. in the area treated with QDs, regardless of concentration. The diameter of the growth inhibition zone (GIZ) in all cases exceeded 24 mm, which corresponded to a high degree of sensitivity. Conclusion. The synthesized Ag(10%):InP/ZnS MPA QDs showed high antiinfective activity against the resistant yeast microbiota Candida spp. in laboratory conditions, playing one of the primary roles in the course of keratomycosis. It is necessary to consider QDs Ag(10%):InP/ZnS MPA as one of the alternative/additional agents for the treatment of resistant ophthalmomycosis, in particular keratomycosis, after limited clinical trials in various variations. Key words: fungal keratitis, yeast fungi, quantum dots, nanoparticles.

Atomic-scale characterization of single and double layers of InAs and InAlAs Stranski-Krastanov quantum dots

We report a detailed structural characterization of single and double layers of InAs and InAlAs quantum dots (QDs) and their wetting layers (WLs) by atomic force microscopy (AFM) and cross-sectional scanning tunneling microscopy (X-STM). The X-STM analysis with atomic resolution showed that the InAlAs WL consists of two distinct layers: a bottom part where all the Al atoms of the InAlAs alloy settled, and a top part containing exclusively In and Ga atoms. The QDs formed from the InAlAs layer contains no Al atoms at all and lie on top of the Al-rich WL. In the double layers of QDs, the InAlAs QDs were used as a seed to influence the nucleation of the InAs QDs grown on top. A gradual decrease in the density of the top InAs QDs was observed in the AFM images with increasing thickness of the GaAs spacer. The X-STM images showed that both QDs layers were completely intermixed for a 2-nm-thick spacer, while effective strain-induced stacking of both types of QDs was observed for a GaAs spacer thickness of 4 nm. However, both QD layers were completely decoupled for a GaAs spacer thickness of 8 nm and could thus be treated as individual layers.

Monitoring leaching of Cd2+ from cadmium-based quantum dots by an Cd aptamer fluorescence sensor

Quantum Dots (QDs) have been demonstrated with outstanding optical properties and thus been widely used in many biological and biomedical studies. However, previous studies have shown that QDs can cause cell toxicity, mainly attributable to the leached Cd2+. Therefore, identifying the leaching kinetics is very important to understand QD biosafety and cytotoxicity. Toward this goal, instrumental analyses such as inductively coupled plasma mass spectrometry (ICP-MS) have been used, which are time-consuming, costly and do not provide real-time or spatial information. To overcome these limitations, we report herein a fast and cost-effective fluorescence sensor based a Cd2+-specific aptamer for real-time monitoring the rapid leaching kinetics of QDs in vitro and in living cells. The sensor shows high specificity towards Cd2+ and is able to measure the Cd2+ leached either from water-dispersed CdTe QDs or two-layered CdSe/CdS QDs. The sensor is then used to study the stability of these two types of QDs under conditions to mimic cellular pH and temperature and the results from the sensor are similar to those obtained from ICP-MS. Finally, the sensor is able to monitor the leaching of Cd2+ from QDs in HeLa cells. The fluorescence aptamer sensor described in this study may find many applications as a tool for understanding biosafety of numerous other Cd-based QDs, including leaching kinetics and toxicity mechanisms in living systems.

The use and detection of quantum dots as nanotracers in environmental fate studies of engineered nanoparticles

Investigations of the behavior and effects of engineered nanoparticles (ENPs) on human health and the environment need detailed knowledge of their fate and transport in environmental compartments. Such studies are highly challenging due to low environmental concentrations, varying size distribution of the particles and the interference with the natural background. A strategy to overcome these limits is to use mimics of ENPs with unique detectable properties that match the properties of the ENPs as nanotracers. A special class of ENPs that can be tracked are quantum dots (QDs). QDs are composed of different metals, metalloids, or more recently also carbon (e.g., graphene), that result in unique optical properties. This allows the tracking of such particles by fluorescence microscopic and photometric techniques. Many types of QDs consist of heavy elements, allowing to track and visualize these particles also by electron microscopy and to quantitate the particles indirectly based on these elements. QDs can also be surface modified in various ways which enable them to be used as a label or as traceable mimics for ENPs. This review reflects a broad range of methods to synthesize and modify QDs based on metals, metalloids, and graphene for studying the environmental fate of nanoparticles and discusses and compares analytical methods that can be used for tracking and quantifying QDs. In addition, we review applications of QDs as ENP mimics in environmental studies of surface waters, soils, microorganisms, and plants with respect to the applied analytical techniques.

Electrochemically Determining Electronic Structure of ZnO Quantum Dots with Different Surface Ligands.

The electronic structure of quantum dots (QDs) including band edges and possible trap states is an important physical property for optoelectronic applications. The reliable determination of the energy levels of QDs remains a big challenge. Herein we employ cyclic voltammetry (CV) to determine the energy levels of three types of ZnO QDs with different surface ligands. Coupled with spectroscopic techniques, it is found that the onset potential of the first reductive wave is likely related to the conduction band edges while the first oxidative wave originates from the trap states. The determined specific energy levels in CV further demonstrates that the ZnO QDs without surface ligands mainly have oxygen interstitial defects whilst the ZnO QDs covered with ligands contain oxygen vacancies. The present electrochemical method offers a powerful and effective way to determine the energy levels of wide bandgap ZnO QDs, which will boost their device performance.