Two-color Quantum Research Articles

Development of a Dual Fluorescence Signal-Enhancement Immunosensor Based on Substrate Modification for Simultaneous Detection of Interleukin-6 and Procalcitonin.

High-sensitivity detection of biomarkers is of great significance to improve the accuracy of disease diagnosis and the rate of occult disease diagnosis. Using a substrate modification and two-color quantum dot (QD) nanobeads (QBs), we have developed a dual fluorescence signal-enhancement immunosensor for sensitive, simultaneous detection of interleukin 6 (IL-6) and procalcitonin (PCT) at low volumes (∼20 μL). First, the QBs compatible with QDs with different surface ligands were prepared by optimizing surfactants based on the microemulsion method. Through the use of a fluorescence-linked immunosorbent assay (FLISA), the feasibility of a dual signal-enhancement immunosensor was verified, and a 5-fold enhancement of fluorescence intensity was achieved after the directional coating of the antibodies on sulfhydryl functionalization (-SH) substrates and the preparation of QBs by using a polymer and silica double-protection method. Next, a simple polydimethylsiloxane (HS-PDMS) immunosensor with a low volume consumption was prepared. Under optimal conditions, we achieved the simultaneous detection of IL-6 and PCT with a linear range of 0.05-50 ng/mL, and the limit of detection (LOD) was 24 and 32 pg/mL, respectively. The result is comparable to two-color QBs-FLISA with a sulfhydryl microplate, even though only 20% of its volume was used. Thus, the dual fluorescence signal-enhancement HS-PDMS immunosensor offers the capability of early microvolume diagnosis of diseases, while the detection of inflammatory factors is clinically important for assisting disease diagnosis and determining disease progression.

Patternable quantum dot color conversion film based on photolithography technique

This paper presents a patternable two-color quantum dot (QD) color conversion film based on photolithography technique. Toluene-assisted dispersion of QD powder with the best performance matching was selected from four typical dispersions by experimental comparison. On this basis, the color conversion film of QD was prepared by photolithography technique. The experimental results show that the height of the patternable QD microstructures has good consistency. At the same time, the monochromatic spectrum test shows that the spectral characteristics of QDs are not significantly affected by the photolithographic process. Therefore, the preparation methods described in this paper can provide a reference for related research.

Velocity of sound beyond the high-density relativistic limit from lattice simulation of dense two-color QCD

Abstract We obtain the equation of state (EoS) for two-color quantum chromodynamics (QCD) at low temperature and high density from the lattice Monte Carlo simulation. We find that the velocity of sound exceeds the relativistic limit ($c_s^2/c^2=1/3$) after BEC-BCS (Bose-Einstein condensation–Bardeen–Cooper–Schrieffer) crossover in the superfluid phase. Such an excess of the sound velocity is previously unknown from any lattice calculations for QCD-like theories. This finding might have a possible relevance to the EoS of neutron star matter revealed by recent measurements of neutron star masses and radii.

Switchable two-color graphene quantum dot as a promising fluorescence probe to highly sensitive pH detection and bioimaging

Graphene quantum dots have been widely applied in biosensing, fluorescence imaging, biomedicine, energy storage and conversion and catalysis, but design and synthesis of polychromatic graphene quantum dot with high luminous efficiency still faces great challenges. The study reports synthesis of histidine, serine and pentaethylenehexamine-functionalized and boron-doped graphene quantum dot (HSPB-GQD) via one-step pyrolysis. The resulting HSPB-GQD consists of graphene sheets of 2–5 nm with carboxyl, hydroxyl, amino, imino and imidazole. Synergy of histidine, serine, pentaethylenehexamine and boron atoms improves the luminescence behavior. This realizes unique switchable two-color luminescence. UV excitation of 370 nm produces one strong blue fluorescence with the maximum emission wavelength of 455 nm and quantum yield of 72.34%. Vis. excitation of 480 nm produces one strong yellow fluorescence with the maximum emission wavelength of 560 nm and quantum yield of 72.59%. The multiple proton dissociation system constructed by nitrogen-containing and oxygen-containing groups makes yellow fluorescence sensitive to environmental pH value. The intensity linearly increases with increasing pH in the range of 4.5–10.0. Organic molecules and inorganic ions do not interfere pH detection. HSPB-GQD as a promising fluorescence probe with negligible effect on cell viability was successfully applied to pH detection in biological and environmental water samples and cell imaging.

Three dimensional orientation of small polyatomic molecules excited by two-color femtosecond pulses

We study the excitation of asymmetric-top (including chiral) molecules by two-color femtosecond laser pulses. In the cases of non-chiral asymmetric-top molecules excited by an orthogonally polarized two-color pulse, we demonstrate, classically and quantum mechanically, three-dimensional orientation. For chiral molecules, we show that the orientation induced by a cross-polarized two-color pulse is enantioselective along the laser propagation direction, namely, the two enantiomers are oriented in opposite directions. The classical and quantum simulations are in excellent agreement on the short time scale, whereas on the longer time scale, the enantioselective orientation exhibits quantum beats. These observations are qualitatively explained by analyzing the interaction potential between the two-color pulse and molecular (hyper-)polarizability. The prospects for using the enantioselective orientation for enantiomers’ separation is discussed.

Growth and characterization of II-VI semiconductor multilayer quantum-well structures for two-color quantum well infrared photodetector applications

The design, growth, and characterizations of ZnCdSe/ZnCdMgSe semiconductor multilayer quantum-well structures for two-color quantum-well infrared photodetectors (QWIPs) are reported. The energy band and quantum well states are computed in a ZnCdSe/ZnCdMgSe single quantum well for both infrared detection regions. The sample has been grown in a multichamber molecular beam epitaxy system. The good crystalline quality of sample and its lattice matching to the InP substrate are investigated by high-resolution x-ray diffraction and transmission electron microscopy analysis. These structural measurements also confirm the good agreement between the design and the grown structure. The band-to-band and interband transition energies are experimentally determined by photoluminescence and contactless electroreflectance, respectively. The intersubband absorption spectra are investigated by Fourier transform infrared spectroscopy at room temperature. This multilayer structure represents a significant technological validation of the capabilities and potential of InP-based II-VI materials for engineering two-color QWIP devices. This paper provides a detailed methodology for the growth and in-depth characterization of such a complex high precision multilayered structure.

Relative scale setting for two-color QCD with $N_f=2$ Wilson fermions

Abstract We determine the scale-setting function and the pseudocritical temperature on the lattice in $N_f=2$ two-color quantum chromodynamics (QCD) using the Iwasaki gauge and Wilson fermion actions. Although two-color QCD does not correspond to the real world, it is very useful as a good testing ground for three-color QCD. The scale-setting function gives the relative lattice spacings of simulations performed at different values of the bare coupling. It is a necessary tool for taking the continuum limit. First, we measure the meson spectra for various combinations of ($\beta,\kappa$) and find a line of constant physics in the $\beta$–$\kappa$ plane. Next, we determine the scale-setting function via $w_0$ scale in the gradient flow method. Furthermore, we estimate the pseudocritical temperature at zero chemical potential from the chiral susceptibility. Combining these results, we can discuss the QCD phase diagram in which both axes are given by dimensionless quantities, namely the temperature normalized by the pseudocritical temperature on the lattice and the chemical potential normalized by the pseudoscalar meson mass. This makes it easy to compare among several lattice studies, and also makes it possible to compare theoretical analyses and lattice studies in the continuum limit.

Fluctuation-induced higher-derivative couplings and infrared dynamics of the quark-meson-diquark model

In a qualitative study, the low-energy properties of the $\text{SO}\!\left(6\right)$-symmetric Quark-Meson-Diquark Model as an effective model for two-color Quantum Chromodynamics are investigated within the Functional Renormalization Group (FRG) approach. In particular, we compute the infrared scaling behavior of fluctuation-induced higher-derivative couplings of the linear Quark-Meson-Diquark Model and map the resulting renormalized effective action onto its nonlinear counterpart. The higher-derivative couplings of the nonlinear model, which we identify as the low-energy couplings of the Quark-Meson-Diquark Model, are therefore entirely determined by the FRG flow of their linear equivalents. This grants full access to their scaling behavior and provides insights into conceptual aspects of purely bosonic effective models, as they are treated within the FRG. In this way, the presented work is understood as an immediate extension of our recent advances in the $\text{SO}\!\left(4\right)$-symmetric Quark-Meson Model beyond common FRG approximations.

Distinct spatiotemporal imaging of femtosecond surface plasmon polaritons assisted with the opening of the two-color quantum pathway effect.

Accurately capturing the spatiotemporal information of surface plasmon polaritons (SPPs) is the basis for expanding SPP applications. Here, we report spatio-temporal evolution imaging of femtosecond SPPs launched from a rectangular trench in silver film with a 400-nm light pulse assisted femtosecond laser interferometric time-resolved (ITR) photoemission electron microscopy. It is found that introducing the 400nm light pulse in the spatially separated near-infrared (NIR) laser pump-probe ITR scheme enables distinct spatiotemporal imaging of the femtosecond SPPs with a weak probe pulse in the ITR scheme, which is free from the risk of sample damage due to the required high monochromatic field for a clear photoelectron image as well as the entangled interference fringe (between the SPPs and probe pulse) in the usual spatially overlapped pump-probe ITR scheme. The demonstrated great improvement of the visibility of the SPPs spatiotemporal image with an additional 400nm light pulse scheme facilitates further analysis of the femtosecond SPPs, and carrier wavelength (785nm), group velocity (0.94C) and phase velocity (0.98C) of SPPs are extracted from the distinct spatio-temporal evolution images of SPPs. Furthermore, the modulation of photoemission induced by the quantum pathway interference effect in the 400nm-assisted scheme is proposed to play a major role in the distinct visualization for SPPs. The probabilities of electrons in different quantum pathways are obtained quantitatively through fitting the experimental results with the quantum pathway interference model. The probability that electrons emit through the quantum pathway allows us to quantitatively analyze the contribution to electron emission from the different quantum pathways. These findings pave a way for the spatiotemporal imaging of the near-infrared light-induced SPPs, such as the communication wave band using PEEM.

Two-Color Quantum Correlation between Down-Conversion Beams at 1.5 and 3.3 μm from a Singly Resonant Optical Parametric Oscillator

We demonstrated a two-color quantum correlation between the down-conversion beams with a telecommunication wavelength at 1.5 μm and mid-infrared wavelength at 3.3 μm generated by a singly resonant optical parametric oscillator (SRO) operated above the pump threshold with a magnesium-oxide doped periodically-poled lithium niobate crystal in the cavity. A maximum of 1.8 dB noise reduction of the intensity difference of the twin beams was measured at the analysis frequency of 5 MHz. Based on a theoretical model for the quantum correlation between the twin beams given by a semi-classical approach, the influence of the analysis frequency and pump parameter on the quantum correlation between the twin beams was discussed theoretically and experimentally. The quantum correlation between the twin beams was degraded at the analysis frequencies above 5 MHz due to the limitation of the bandwidth of SRO cavity and was degraded at the analysis frequencies below 5 MHz due to the excess intensity noise of the pump. The two-color quantum correlated twin beams at 1.5 and 3.3 μm have potential applications in high-precision measurements beyond the shot noise level.

Switchable Multi-Color Solution-Processed QD-laser

In this paper, for the first time, the switchable two-color quantum dot laser has been realized considering solution process technology, which has both simultaneous and lonely lasing capability exploiting selective energy contacts. Furthermore, both channels can be modulated independently, which is a significant feature in high-speed data transmission. To this end, utilizing superimposed quantum dots with various radii in the active layer provides the different emission wavelengths. In order to achieve the different sizes of QDs, solution process technology has been used as a cost-effectiveness and fabrication ease method. Moreover, at the introduced structure to accomplish the idea, the quantum wells are used as separate selective energy contacts to control the lasing channels at the desired wavelength. It makes the prominent device have simultaneous lasing at different emission wavelengths or be able to lase just at one wavelength. The performance of the proposed device has been modeled based on developed rate equation by assuming inhomogeneous broadening of energy levels as a consequence of the size distribution of quantum dots and considering tunnel injection of carriers into the quantum dots via selective energy contacts. Based on simulation results, the simultaneous lasing in both or at one of two wavelengths 1.31 μm and 1.55 μm has been realized by the superimposition of two different sizes of InGaAs quantum dots in a single cavity and accomplishment of selective energy contacts. Besides, controlling the quantum dot coverage leads to managing the output power and modulation response at the desired wavelengths. By offering this idea, one more step is actually taken to approach the switchable QD-laser by the simple solution process method.

A highly sensitive fluorescent immunosensor for sensitive detection of nuclear matrix protein 22 as biomarker for early stage diagnosis of bladder cancer.

A novel strategy is reported for highly sensitive, rapid, and selective detection of nuclear matrix protein NMP22 using two-color quantum dots based on fluorescence resonance energy transfer (FRET). Quantum dots (QDs) are highly advantageous for biological imaging and analysis, particularly when combined with (FRET) properties of semiconductor quantum dot (QDs) are ideal for biological analysis to improve sensitivity and accuracy. In this FRET system narrowly dispersed green emitting quantum dot CdTe core is used as a donor and labelled by monoclonal (mAb) antibody, while orange emitting quantum dot CdTe/CdS core shell is used as an accepter and labelled by polyclonal (pAb) antibody. The quantum dots are labelled by antibodies using EDC/NHS as crosslinking agent. Bovine serum albumin (BSA) solution was added to block nonspecific binding sites. The fluorescence intensity of QDs accepter decreased linearly with the increasing concentrations of NMP22 from 2–22 pg mL−1 due to FRET system and fluoroimmunoassay reaction. This method has good regression coefficient (R2 = 0.998) and detection limit was 0.05 pg mL−1. The proposed FRET-based immunosensor provides a quick, simple and sensitive immunoassay tool for protein detection, and can be considered as a promising approach for clinical applications. The proposed FRET-based immunosensor provides a quick, simple and sensitive immunoassay tool for protein detection, and can be considered as a promising approach for clinical applications.

A simple FRET system using two‐color CdTe quantum dots assisted by cetyltrimethylammonium bromide and its application to Hg(II) detection

In this study, we developed a novel simple fluorescence resonance-energy transfer (FRET) system between two-color CdTe quantum dots (QDs) assisted by cetyltrimethylammonium bromide (CTAB). Mercaptopropionic (MPA)-capped CdTe QDs serving as both donors and acceptors were successfully synthesized by changing the refluxing time in aqueous solution. CTAB micelles formed in water and minimized the distance between the donors and acceptors significantly by electrostatic interactions, improving FRET efficiency. Several factors that affected the fluorescence spectra of the FRET system were investigated. The prepared FRET system was feasible as an effective fluorescent probe to detect Hg(II) in aqueous solution. At pH7.0, a linear relationship between the quenched fluorescence intensity of orange-emitting acceptors (QDs(A) ) and Hg(II) concentration was acquired in the range 5-250nmol/L with a detection limit of 1.95nmol/L. The developed method showed excellent analytical performance for Hg(II) with high sensitivity and acceptable selectivity, reproducibility and stability. This finding indicated that the method has a promising potential application for environmental monitoring. This study demonstrated the great promise of QDs for expedient, low-cost and high-sensitivity detection of Hg(II).

A Single-Molecule Homogeneous Immunoassay by Counting Spatially "Overlapping" Two-Color Quantum Dots with Wide-Field Fluorescence Microscopy.

We developed a single-molecule homogeneous immunoassay by counting spatially "overlapping" two-color quantum dots (QD) under a wide-field fluorescence microscope. QD 655 with red fluorescence and QD 565 with green fluorescence were modified with capture and detection antibodies, respectively. A capture antibody-modified QD 655 and a detection antibody-modified QD 565 were conjugated by a corresponding antigen molecule to form a "sandwich" immunocomplex. The conjugated QD 655 could not be distinguished from the conjugated QD 565 by fluorescent microscopy because the distance between them was smaller than the resolution of an optical microscope (approximately 200 nm). The immunocomplex color became yellow because of the spatial "overlap" of the red and green fluorescence. The number of the yellow spots was equal to the number of immunocomplex molecules, while the concentration of the antigen was related to the ratio of the yellow dots to the red dots. The successful quantification of two model proteins in the human plasma, namely, alpha-fetoprotein and carcinoembryonic antigen, demonstrated the accuracy and reliability of our approach.

Two-color multiphoton emission for comprehensive reveal of ultrafast plasmonic field distribution

We experimentally demonstrate comprehensive reveal of the ultrafast plasmonic field distribution in a bowtie nanostructure by two-color photoemission electron microscopy (PEEM). We attribute the comprehensive reveal of the field distribution to an effective opening of the two-color quantum channel in multiphoton photoemission, which leads to a dramatic reduction of the nonlinear order (from 4.07 down to 2.01) of the plasmon-assisted photoelectrons and a huge increment of the photoemission yields (typically 20-fold enhancement). Furthermore, we have found that opening extent of the quantum channel strongly related with the photoemission yields generated from one-color 400 and 800 nm laser pulse illumination, and the optimized ratio between the yields for effective opening of two-color quantum channel in our experiment is also achieved. Additionally, benefiting from the high spatial resolution of PEEM, we found there exists a large difference in the nonlinear order of two-color photoemission under the plasmonic excitation within a nanostructure, which has not been reported yet. This work introduces multicolor quantum channel photoemission into the PEEM imaging and offers new way to flexibly control the nonlinear order of the plasmon-assisted photoemission, and it will enable PEEM as a versatile tool in many potential applications.

Infrared Spectroscopy and Structures of Boron-Doped Silicon Clusters (SinBm, n = 3–8, m = 1–2)

Binary nanoclusters are of great interest for understanding fundamental phenomena related to applied materials science. Herein, neutral silicon-rich silicon–boron clusters (SinBm, n = 3–8, m = 1–2) are characterized by means of resonant infrared-ultraviolet two-color ionization (IR-UV2CI) spectroscopy, mass spectrometry, and quantum chemical calculations. Global energy optimizations are employed to find the most stable SinBm structures. By comparing the IR-UV2CI spectrum with the calculated linear IR absorption spectra of the corresponding low-energy isomers, the geometries of the observed SinBm clusters are determined. Based on this structural information, different physical properties of the detected SinBm clusters such as charge distributions and ionization energies are investigated. Natural bond orbital analysis shows that significant negative charge (∼−1e) is localized at the boron atom(s). As the B–B bond is stronger than the B–Si and Si–Si bonds, boron segregation is observed for SinBm clusters with m = 2.

Multiscale Monte Carlo equilibration: Two-color QCD with two fermion flavors

We demonstrate the applicability of a recently proposed multiscale thermalization algorithm to two-color quantum chromodynamics (QCD) with two mass-degenerate fermion flavors. The algorithm involves refining an ensemble of gauge configurations that had been generated using a renormalization group (RG) matched coarse action, thereby producing a fine ensemble that is close to the thermalized distribution of a target fine action; the refined ensemble is subsequently rethermalized using conventional algorithms. Although the generalization of this algorithm from pure Yang-Mills theory to QCD with dynamical fermions is straightforward, we find that in the latter case, the method is susceptible to numerical instabilities during the initial stages of rethermalization when using the hybrid Monte Carlo algorithm. We find that these instabilities arise from large fermion forces in the evolution, which are attributed to an accumulation of spurious near-zero modes of the Dirac operator. We propose a simple strategy for curing this problem, and demonstrate that rapid thermalization--as probed by a variety of gluonic and fermionic operators--is possible with the use of this solution. In addition, we study the sensitivity of rethermalization rates to the RG matching of the coarse and fine actions, and identify effective matching conditions based on a variety of measured scales.

A surface plasmonic coupled mid-long-infrared two-color quantum cascade detector

A novel mid-long-infrared two-color photodetector is proposed. It combines quantum cascade detector (QCD) and surface plasmonic coupling structure. The reflection spectrum and electric field are analyzed by algorithm of finite difference time domain method (FDTD). This QCD is sensitive to 4.4μm and 9.0μm infrared light. Mid-infrared and long-infrared pixels are interlaced arranged with specific plasmonic micro-cavity structures integrated. 7.1 and 7 times enhancement in optical absorption are obtained for mid-infrared and long-infrared pixels, respectively. Besides, a polarization-discriminating detection performance has been observed.

Energy exchange between modes in a multimode two-color quantum dot laser with optical feedback.

We investigate experimentally and theoretically the multimode dynamics of a two-color quantum dot laser subject to time-delayed optical feedback. We unveil energy exchanges between the longitudinal modes of the excited state triggered by variations of the feedback phase, and observe that the modal competition between longitudinal modes appears independently within the ground state and excited state emission. These features are accurately reproduced with a quantum dot laser model extended to take into account multiple modes for both ground and excited states. Finally, we discuss the significant impact of such behavior on feedback-based control of two-color quantum dot lasers.

Enhanced dimerization drives ligand-independent activity of mutant epidermal growth factor receptor in lung cancer.

Mutations within the epidermal growth factor receptor (EGFR/erbB1/Her1) are often associated with tumorigenesis. In particular, a number of EGFR mutants that demonstrate ligand-independent signaling are common in non-small cell lung cancer (NSCLC), including kinase domain mutations L858R (also called L834R) and exon 19 deletions (e.g., ΔL747-P753insS), which collectively make up nearly 90% of mutations in NSCLC. The molecular mechanisms by which these mutations confer constitutive activity remain unresolved. Using multiple subdiffraction-limit imaging modalities, we reveal the altered receptor structure and interaction kinetics of NSCLC-associated EGFR mutants. We applied two-color single quantum dot tracking to quantify receptor dimerization kinetics on living cells and show that, in contrast to wild-type EGFR, mutants are capable of forming stable, ligand-independent dimers. Two-color superresolution localization microscopy confirmed ligand-independent aggregation of EGFR mutants. Live-cell Förster resonance energy transfer measurements revealed that the L858R kinase mutation alters ectodomain structure such that unliganded mutant EGFR adopts an extended, dimerization-competent conformation. Finally, mutation of the putative dimerization arm confirmed a critical role for ectodomain engagement in ligand-independent signaling. These data support a model in which dysregulated activity of NSCLC-associated kinase mutants is driven by coordinated interactions involving both the kinase and extracellular domains that lead to enhanced dimerization.