Multicolor Quantum Dots Research Articles

Solvent mediated synthesis of multicolor narrow bandwidth emissive carbon quantum dots and their potential in white light emitting diodes

The development of efficient and environmentally sustainable materials for white light-emitting diodes (WLEDs) is of paramount importance in the field of lighting technology. In this study, we present a solvent-modulated synthesis approach for the fabrication of multicolor narrow-bandwidth emissive carbon quantum dots (CQDs) as a promising solution for constructing WLEDs. The synthesis method involves the controlled reaction of organic precursors in different solvent environments, leading to the formation of CQDs with distinct emission wavelengths with a relatively small full width at half maximum, ranging from 28 to 42 nm. Moreover, these synthesized multicolor CQDs demonstrate a remarkably high fluorescence quantum yield of up to 65%, indicating their potential for constructing efficient WLED when incorporated in polymer matrix and coated on the surface of blue light-emitting diode (LED).

Early Steps of Individual Multireceptor Viral Interactions Dissected by High-Density, Multicolor Quantum Dot Mapping in Living Cells.

Viral capture and entry to target cells are the first crucial steps that ultimately lead to viral infection. Understanding these events is essential toward the design and development of suitable antiviral drugs and/or vaccines. Viral capture involves dynamic interactions of the virus with specific receptors in the plasma membrane of the target cells. In the last years, single virus tracking has emerged as a powerful approach to assess real time dynamics of viral processes in living cells and their engagement with specific cellular components. However, direct visualization of the early steps of multireceptor viral interactions at the single level has been largely impeded by the technical challenges associated with imaging individual multimolecular systems at relevant spatial (nanometer) and temporal (millisecond) scales. Here, we present a four-color, high-density quantum dot spatiotemporal mapping methodology to capture real-time interactions between individual virus-like-particles (VLPs) and three different viral (co-) receptors on the membrane of primary living immune cells derived from healthy donors. Together with quantitative tools, our approach revealed the existence of a coordinated spatiotemporal diffusion of the three different (co)receptors prior to viral engagement. By varying the temporal-windows of cumulated single-molecule localizations, we discovered that such a concerted diffusion impacts on the residence time of HIV-1 and SARS-CoV-2 VLPs on the host membrane and potential viral infectivity. Overall, our methodology offers the possibility for systematic analysis of the initial steps of viral-host interactions and could be easily implemented for the investigation of other multimolecular systems at the single-molecule level.

Aptamer-Loop DNA Nanoflower Recognition and Multicolor Fluorescent Carbon Quantum Dots Labeling System for Multitarget Living Cell Imaging.

Visualization of multiple targets in living cells is important for understanding complex biological processes, but it still faces difficulties, such as complex operation, difficulty in multiplexing, and expensive equipment. Here, we developed a nanoplatform integrating a nucleic acid aptamer and DNA nanotechnology for living cell imaging. Aptamer-based recognition probes (RPs) were synthesized through rolling circle amplification, which were further self-assembled into DNA nanoflowers encapsulated by an aptamer loop. The signal probes (SPs) were obtained by conjugation of multicolor emission carbon quantum dots with oligonucleotides complementary to RPs. Through base pairing, RPs and SPs were hybridized to generate aptamer sgc8-, AS1411-, and Apt-based imaging systems. They were used for individual/simultaneous imaging of cellular membrane protein PTK7, nucleolin, and adenosine triphosphate (ATP) molecules. Fluorescence imaging and intensity analysis showed that the living cell imaging system can not only specifically recognize and efficiently bind their respective targets but also provide a 5-10-fold signal amplification. Cell-cycle-dependent distribution of nucleolin and concentration-dependent fluorescence intensity of ATP demonstrated the utility of the system for tracking changes in cellular status. Overall, this system shows the potential to be a simple, low-cost, highly selective, and sensitive living cell imaging platform.

Multicolor nitrogen-doped carbon quantum dots and its application in the detection of Fe3+ ion.

In this paper, nitrogen-doped carbon quantum dots (N-CQDs) are synthesized by the hydrothermal method. N-CQDs exhibit strong fluorescence, and N-CQDs are well dispersed in water as well as in various organic solvents. N-CQDs emit multi-color fluorescence from blue to red, with wavelengths in the range of 450-650 nm without the need for purification. Furthermore, the fluorescence emission of N-CQDs was selectively quenched after adding Fe3+ ions. N-CQDs were used as a nanoprobe for the detection of Fe3+ ions, showing a good linear correlation between the fluorescence emission and the concentration of Fe3+ in the Fe3+ concentration range from 0 to 100 μM. The limit of detection (LOD) was 55.7μM for Fe3+ in water and 40.2μM in fetal bovine serum (FBS) samples. The study shows that the synthesized N-CQDs have low cost and great potential for application in biological analysis.

The controllable synthesis of multi-color carbon quantum dots modified by polythiophene and their application in fluorescence detection of Au3+ and Hg2+

Herein, hydrothermal method was used to prepare a series of multi-color polythiophene modified carbon quantum dots. Under UV excitation, fluorescence their maximum emission wavelengths appear at 612 nm, 570 nm, and 540 nm respectively. The prepared CD-BTH and CD-BN can have specific detection of Au3+ and Hg2+ through fluorescence quenching effect. The detection limits for Au3+ are 3 nM and 5.4 nM respectively, and for Hg2+ are 23 nM and 90 nM respectively. CD-KN detects Au3+ specifically through fluorescence resonance, with a detection limit of 33 nM. Under the interference of other metal ions, three types of polythiophene modified quantum carbon dots exhibit excellent selectivity for the responsive ions. Meanwhile, this article also elucidates the law that as the electron withdrawing ability of the side chains of polythiophene derivatives increasing, the fluorescence emission peaks of the prepared polythiophene modified carbon dots shifts red and the fluorescence quantum yield is higher.

Miniaturization of Multicolor Quantum Dots Lasing Based on 2D Constrained Resonator (Advanced Optical Materials 20/2024)

Miniaturization of Multicolor Quantum Dots Lasing Based on 2D Constrained Resonator (Advanced Optical Materials 20/2024)

Real-Time Detection of Multiple Intracellular MicroRNAs using an Ultrasound-Propelled Nanomotor-Based Dynamic Fluorescent Probe.

Multiple intracellular microRNA (miRNA) detection is essential for disease diagnosis and management. Nonetheless, the real-time detection of multiple intracellular miRNAs has remained challenging. Herein, we have developed an ultrasound (US)-powered nanomotor-based dynamic fluorescent probe for the real-time OFF-ON fluorescent determination of multiple intracellular miRNAs. The new probe relies on the utilization of multicolored quantum dot (QD)-labeled single-stranded DNA (ssDNA)/graphene oxide (GO)-coated US-powered gold nanowire (AuNW) nanomotors. The fluorescence of QDs is quenched due to π-π interactions with the GO. Upon binding to target miRNAs, the QDs-ssDNA is now distant from the AuNWs, resulting in effective OFF-ON QD fluorescence switching. Compared with conventional passive probes, the dynamic fluorescent probe enhances probe-target interactions by using the US-propelled nanomotor, resulting in exceptionally efficient and prompt hybridization. Simultaneous quantitative analysis of miR-10b and miR-21 in vitro can be achieved within 15 min with high sensitivity and specificity. Additionally, multicolor QDs provide strong signal intensity and multiplexed detection, enabling one-step real-time discrimination between cancer cells (A549) and normal cells (L02). The obtained results are in good agreement with those from qRT-PCR. This dynamic fluorescent probe based on a nanomotor and QDs enables rapid "on the move" specific detection of multiple intracellular miRNAs in intact cells, facilitating real-time monitoring of diverse intracellular miRNA expression, and it could pave the way for novel applications of nanomotors in biodetection.

Investigation of the luminescence mechanism of multi-color nitrogen-doped carbon quantum dots and their application in the detection of Fe3+

This study reports the successful preparation of nitrogen-doped carbon quantum dots (N-CQDs) with a quantum yield of 15 % utilizing the hydrothermal method. Citric acid was employed as the carbon source, while 1,3-Diamino-2-propanol was utilized as the dopant. It was discovered that the emission of synthesized N-CQDs was dependent on concentration and excitation. By altering the N-CQDs concentration, the fluorescence emission peak was shifted from 453 to 574 nm, causing the emission to transition from blue to orange. The presence of multiple fluorescence emission centers within N-CQDs was confirmed through two-dimensional fluorescence matrix scanning. As the concentration of N-CQDs increased, the distance between these centers decreased, ultimately leading to aggregation. The energy or electrons were transferred as a result of the surface functional groups' interaction, which ultimately causes the fluorescence emission peak to shift to the red. Furthermore, an increase in concentration results in the formation of larger aggregates and larger sp2 carbon domains, ultimately resulting in longer wavelengths. Because of the convenience of use, high sensitivity, and rapid response of the fluorescent probe detection approach, multi-color N-CQDs with tunable concentration were used for the identification of Fe3+, with a 10–200 μM linear detection range and limits of detection (LOD) of 0.56 μM.

Optically Readable, Physically Unclonable Subwavelength Pixel via Multicolor Quantum Dot Printing for Anticounterfeiting.

We present a secure and user-friendly ultraminiaturized anticounterfeiting labeling technique─the color-encoded physical unclonable nanotag. These nanotags consist of subwavelength spots formed by random combinations of multicolor quantum dots, which are fabricated using a cost-efficient printing method developed in this study. The nanotags support over 170,000 different colors and are inherently resistant to cloning. Moreover, their high brightness and color purity, owing to the quantum dots, ensure an ease of readability. Additionally, these nanotags can function as color-encrypted pixels, enabling the incorporation of labels (such as QR codes) into ultrasmall physically unclonable hidden tags with a resolution exceeding 100,000 DPI. The unique blend of compactness, flexibility, and security positions the color-encoded nanotag as a potent and versatile solution for next-generation anticounterfeiting applications.

Multiplex fluorescence quenching immunoassay based on multicolor magnetic quantum dot and dual spectral-overlapped polydopamine nanospheres for ultrasensitive detection of aflatoxin B1, zearalenone, ochratoxin A, and fumonisin B1

Due to the increasing fungal infections and the implementation of strict food safety regulations, the demand for sensitive, rapid, and easy assays for testing co-contaminated mycotoxins in food has grown in recent years. In this study, a multiplex fluorescence quenching immunoassay is developed to simultaneously detect prevalent mycotoxins in cereals, namely aflatoxin B1 (AFB1), zearalenone (ZEN), ochratoxin A (OTA), and fumonisin B1 (FB1). Four spherical nanocomposites with magnetic core and three-layer quantum dot (QD) shell (MagTQD) are fabricated. These nanocomposites exhibit different maximum emission peaks without overlap and interference at the same excitation wavelength. Four MagTQD conjugated with corresponding coating antigens to prepare four fluorescence signal probes with rapid magnetic enrichment ability, respectively. Moreover, polydopamine nanospheres (PDANs) with dual-spectral overlapped fluorescence quenching properties are conjugated with four mycotoxin antibodies to prepare four fluorescence quenching probes, respectively. The established immunoassay has the low detection limit at 1.29 pg mL−1 for AFB1, 0.80 pg mL−1 for ZEN, 1.97 pg mL−1 for OTA, and 13.89 pg mL−1 for FB1, respectively. This developed assay can provide a new approach to realize the efficient detection of multi-mycotoxins in food safety supervision.

Multicolor lignin-derived carbon quantum dots: Controllable synthesis and photocatalytic applications

The cost-effective, high-performance fabrication of multicolor carbon quantum dots (CQDs) from biomass is critical to its prospective application. Lignin, with its phenylpropane structural unit and abundant functional groups, is a reliable precursor for the formation of high-quality CQDs. Here, CQDs from renewable lignin were successfully prepared via a two-step method, and controllable preparation of CQDs to emit blue, green, yellow, and red fluorescence was achieved by adjusting the N-containing acid dopant. The investigated fluorescence mechanism revealed that the energy bandgap of the lignin-derived CQDs decreased and the emission wavelength redshifted as the graphitization degree and number of C=O surface groups increased. The light absorption region of the Bi7O9I3 photocatalysts modified with blue CQDs to red CQDs gradually broadened in the redshifted direction. In particular, compared with pure Bi7O9I3 (70.9%), the red CQDs-modified Bi7O9I3 (RCQD/BOI) can remove 94.7% of antibiotics within 60 min of light irradiation. The superior photocatalytic activity of RCQD/BOI is attributed to the established internal electric field that accelerates charge transfer and effectively separates the photogenerated e+-h+ inside Bi7O9I3. Furthermore, through radical capture, electron paramagnetic resonance (EPR) experiments validated the photocatalytic mechanism of RCQD/BOI and revealed that h+, O2− and OH are key reactants in the photocatalytic degradation process. This promising and sustainable approach for the synthesis of multicolor lignin-derived CQDs opens the avenue of high-value utilization of biomass resources, green production of CQDs nanomaterials, and efficient development of CQDs-based photocatalysts for wastewater treatment.

Miniaturization of Multicolor Quantum Dots Lasing Based on 2D Constrained Resonator

AbstractElevated expectations for laser performance, encompassing broadband tunability, integration, low power consumption, and a low threshold, have emerged within the realms of photonic chips and optoelectronic devices. Nevertheless, achieving multicolor miniaturized lasers within a singular micro‐nano structure remains challenging, hindered by constraints in geometric structure, optical gain, and bandgap considerations. Here, an approach to obtain integrated multicolor lasing beam output simultaneously in a desired direction from a 2D‐constrained micro‐resonator is proposed. The wavelength of the lasing beam is tuned by controlling the size of quantum dots (QDs) in the resonator. Owing to the high density of power within the cavity and the localized surface plasmon resonance on the surface of the Au‐Ag nanowires (NWs), a notably low laser threshold is realized in the micro‐resonator channel. This work introduces a method for realizing an integrated multicolor micro‐laser, providing a pathway toward the implementation of active photonic chips and advanced optoelectronic devices.

Preparation of lignin-based full-color carbon quantum dots and their multifunctionalization with waterborne polyurethanes

Lignin is a popular material for energy transition and high-value utilization due to its low cost, non-toxicity, renewability, and widespread availability. However, its complex structure has hindered its application. Waterborne polyurethane (WPU) uses water as a dispersion medium, which is safer for humans and the environment but also leads to disadvantages such as poor mechanical properties and water resistance. In this study, we prepared multicolor photoluminescent carbon quantum dots (CQDs) in a wide range of wavelengths from lignin. We successfully prepared panchromatic CQDs by additive mixing. The redshift of the emission wavelength is attributed to the synergistic effect of the sp2 conjugated structure and the surface functional groups. The full-color solid-state luminescence of the CQDs was successfully achieved, and most importantly, the application of full-color CQDs in light-emitting diodes was realized. Moreover, the embedding of the multicolor CQDs in WPU not only makes WPU luminescent but also improves the water resistance and mechanical properties of WPUs. The hydrogen-bonding interactions between the functional groups on the surface of the CQDs and the urethane were responsible for the high performance of the composite. We investigated the UV and strong blue light shielding abilities of WPU/yellow CQDs films, which resulted from the unique absorption peaks of yellow CQDs in the UV region and the strong blue light region. This work provides an efficient method for the high-value utilization of biomass materials and paves the way for the multifunctional application of WPU.

One-Step Dual-Color Labeling of Viral Envelope and Intraviral Genome with Quantum Dots Harnessing Virus Infection.

Labeling the genome and envelope of a virus with multicolor quantum dots (QDs) simultaneously enables real-time monitoring of viral uncoating and genome release, contributing to our understanding of virus infection mechanisms. However, current labeling techniques require genetic modification, which alters the virus's composition and infectivity. To address this, we utilized the CRISPR/Cas13 system and a bioorthogonal metabolic method to label the Japanese encephalitis virus (JEV) genome and envelopes with different-colored QDs in situ. This technique allows one-step two-color labeling of the viral envelope and intraviral genome with QDs harnessing virus infection. In combination with single-virus tracking, we visualized JEV uncoating and genome release in real time near the endoplasmic reticulum of live cells. This labeling strategy allows for real-time visualization of uncoating and genome release at the single-virus level, and it is expected to advance the study of other viral infection mechanisms.

Driving multicolor lignin-based carbon quantum dots into selective metal-ion recognition and photocatalytic antibiotic decomposition

Achieving a waste-treats-pollutant vision, rationally designed lignin valorization that encompasses a shining story of multicolor carbon dots is proposed to promote selective metal-ion sensing and photocatalytic antibiotic removal.

Fabrication of anthracite-derived multicolor graphene quantum dots for their potential application in nanomedicine

Aim: This study aims to discover an alternative precursor with abundant source and low cost for multicolor graphene quantum dots (GQDs) preparation and application. Methods: In the current study, anthracite-derived multicolor GQDs were prepared at different reaction temperatures (100°–150°C), referring to the GQDs 100, GQDs 120, GQDs 130, and GQDs 150. Results: The GQDs 100, GQDs 120, GQDs 130, and GQDs 150 solutions were found to be orange-red, yellow-green, green, and blue under 365 nm excitation UV (ultraviolet) lamp, respectively. The X-ray photoelectron spectroscopy (XPS) data suggests high temperature intensifies oxidation of the amorphous sp3 carbon, resulting in GQDs with higher crystalline structure (Csp2). Compared with the GQDs 100 and GQDs 120, the GQDs 130 and GQDs 150 showed much better biocompatibility, which may attribute to their higher Csp2 composition and smaller size. Conclusions: The results suggest that GQDs 130 and GQDs 150 are ideal candidates for nanomedicine applications, e.g., drug/gene delivery and bio-imaging, etc.

Homogeneous fluorescence immunoassay based on AuNPs quenching dendritic silica assembled with multicolor QDs for the simultaneous determination of four mycotoxins in cereals

In this work, a novel homogeneous fluorescence immunoassay for the simultaneous detection of ochratoxin A (OTA), aflatoxin B1 (AFB1), fumonisins B1 (FB1), and zearalenone (ZEN) in cereal samples is established. Here, amino groups and thiol groups are grafted onto the surface of dendritic mesoporous silica nanoparticles (DMSNs) to improve loading rate and fluorescence preservation rate of quantum dots (QDs), enabling enrichment and amplification of fluorescence signals. In this test system, the fluorescence of the signal probe (DMSNs@QDs@Ab) is quenched by AuNPs, and then the presence of the targets makes the fluorescence of the signal probes recover. The correlation between the recovered fluorescence value and mycotoxin concentration is applied to achieve quantitative detecting mycotoxins. This assay displays good linear correlation in range of 0.01–100 μg L-1, with the limit of detection (LOD) of 0.0001 μg L-1 for OTA, 0.0008 μg L-1 for AFB1, 0.001 μg L-1 for FB1, and 0.0006 μg L-1 for ZEN, respectively. The proposed assay is applied to detect multiple mycotoxins in contaminated cereal samples and the test results is confirmed by liquid chromatography-tandem mass spectrometry (UPLC-MS/MS). Avail of silica with high loading capacity for assembling multicolor QDs to achieve simultaneous multi-signal output, a simple and efficient homogeneous fluorescence immunoassay is proposed for the first time. This multiplex test strategy provides a good idea for simultaneous, rapid, and sensitive detection of multiple hazardous substances in food and environment samples.

Preparation of multicolor carbon quantum dots by hydrothermal method and their functionalization applications

Carbon quantum dots (CQDs) have become a popular research topic because of their many unique virtues, especially the significance of tunable photoluminescence properties. However, the synthesis of multicolor CQDs is still at an exploratory stage, and there are many dilemmas that have not yet been well resolved, such as long-wavelength emission and solid-state luminescence. Here, we selected suitable carbon and dopant sources as precursors for the synthesis of CQDs through the rational design of the experiments in an aqueous system, and the as-prepared CQDs possessed blue, green, yellow and red emissions, with optimal emissions of approximately 475 nm, 530 nm, 580 nm, and 645 nm, respectively. Furthermore, the corresponding PLQYs were 30.13 %, 36.84 %, 39.16 % and 21.36 %, respectively. It was found that the redshift of the emission wavelengths can be attributed to the synergistic effect of the increase in the sp2 conjugate size and the surface states. To conquer the aggregation caused quenching (ACQ) of CQDs and realize the solid-state luminescence of CQDs, we successfully prepared solid-state fluorescent films and solid-state phosphors. Finally, multicolor CQDs were successfully applied to prepare monochromatic and white light-emitting diodes (WLEDs). The adopted green synthesis technology can provide a good technical support for the future development of CQDs synthesis.

Acid catalyzed microwave-assisted production of full-color light emissive carbon quantum dots for CCT-tunable WLEDs

Many studies have examined the use of multicolor light emissive carbon quantum dots (CQDs) in toxic metal-free optoelectronic devices, but it is still limited to obtain desirable optical properties. Here, we present a straightforward synthetic route for producing multicolor light emissive nitrogen-doped carbon quantum dots (NCQDs) using a microwave-assisted process, thus yielding individual color emissions of NCQDs in a batch. The emissive colors from NCQDs can be controlled by adjusting the molar ratios of citric acid and urea from 1 to 6 for blue and green-light emission, respectively. When o-phenylenediamine (oPDA) was chosen as a precursor, the resulting NCQDs can emit yellow light, while the red light emissive NCQDs can be obtained in the presence of a diluted HCl as a catalyst for accelerating and extending sp2-carbon bonding. The doped nitrogen in NCQDs was found to be formed as a graphitic nitrogen in the core, leading to red-shifted photoluminescent emissions from 450 nm to 620 nm. To fabricate white-light emitting diodes (WLEDs), the mixing ratios of NCQDs with different light emissions in polydimethylsiloxane (PDMS) were varied to control the correlated color temperature (CCT) from 3386 K to 7151 K and CIE coordinates of (0.30, 0.32), (0.32, 0.36), and (0.40, 0.37).

Opening band gap of multi-color graphene quantum dots using D-fructose as a green precursor

Graphene was successfully isolated by Professors Andre Geim and Kostya Novoselov in 2004. Graphene has attracted considerable research importance for its distinctive properties and potential applications. In this study, low-cost and high blue, yellow, and green photoluminescent (PL) graphene quantum dots (GQDs) were synthesized with deionized water (DI) and D-fructose as precursors by the dehydration method in the presence of hydrochloric acid. Transmission electron microscopy imaging proved the changing size of the GQDs and, by nuclear magnetic resonance spectroscopy, we observed the hydrogen-functionalized GQDs. The highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) of the synthesized GQDs were determined, and an energy bandgap was obtained from optical investigations.