Emission Spectra Research Articles

Expanding the genetic and clinical spectrum of Tatton-Brown-Rahman syndrome in a series of 24 French patients

BackgroundTatton-Brown-Rahman syndrome (TBRS; OMIM 615879), also known as DNA methyltransferase 3 alpha (DNMT3A)-overgrowth syndrome (DOS), was first described by Tatton-Brown in 2014. This syndrome is characterised by overgrowth, intellectual disability...

Plasmon-enhanced fluorescence for biophotonics and bio-analytical applications.

Fluorescence spectroscopy serves as an ultrasensitive sophisticated tool where background noises which serve as a major impediment to the detection of the desired signals can be safely avoided for detections down to the single-molecule levels. One such way of bypassing background noise is plasmon-enhanced fluorescence (PEF), where the interactions of fluorophores at the surface of metals or plasmonic nanoparticles are probed. The underlying condition is a significant spectral overlap between the localized surface plasmon resonance (LSPR) of the nanoparticle and the absorption or emission spectra of the fluorophore. The rationale being the coupling of the excited state of the fluorophore with the localized surface plasmon leads to an augmented emission, owing to local field enhancement. It is manifested in enhanced quantum yields concurrent with a decrease in fluorescence lifetimes, owing to an increase in radiative rate constants. This improvement in detection provided by PEF allows a significant scope of expansion in the domain of weakly emitting fluorophores which otherwise would have remained unperceivable. The concept of coupling of weak emitters with plasmons can bypass the problems of photobleaching, opening up avenues of imaging with significantly higher sensitivity and improved resolution. Furthermore, amplification of the emission signal by the coupling of free electrons of the metal nanoparticles with the electrons of the fluorophore provides ample opportunities for achieving lower detection limits that are involved in biological imaging and molecular sensing. One avenue that has attracted significant attraction in the last few years is the fast, label-free detection of bio-analytes under physiological conditions using plasmonic nanoparticles for point-of-care analysis. This review focusses on the applications of plasmonic nanomaterials in the field of biosensing, imaging with a brief introduction on the different aspects of LSPR and fabrication techniques.

Influence of O-H⋅⋅⋅Pt interactions on photoluminescent response in the (Et4N)2{[Pt(bph)(CN)2][phenylene-1,4-diresorcinol]} framework.

Tunable photoluminescence (PL) is one of the hot topics in current materials science, and research performed on the molecular phases is at the forefront of this field. We present the new (Et4N)2[PtII(bph)(CN)2]⋅rez3⋅1/3H2O (Pt2rez3) (bph=biphenyl-2,2'-diyl; rez3=3,3",5,5"-tetrahydroxy-1,1':4',1"-terphenyl, phenylene-1,4-diresorcinol coformer, a linear quaternary hydrogen bond donor) co-crystal salt based on the recently appointed promising [PtII(bph)(CN)2]2- luminophore. Within the extended hydrogen-bonded subnetwork [PtII(bph)(CN)2]2- complexes and rez3 coformer molecules form two types of contacts: the rez3O-H⋅⋅⋅Ncomplex ones in the equatorial plane of the complex and non-typical rez3O-H⋅⋅⋅Pt ones along its axial direction. The combined structural, PL, and DFT approach identified the rez3O-H⋅⋅⋅Pt synthons to be crucial in promoting the noticeable uniform redshift of bph ligand centered (LC) emission compared to the LC emission of the (Et4N)2[PtII(bph)(CN)2]⋅H2O (Pt2) precursor, owing to the direct interference of the phenol group with the PtII-bph orbital system via altering the CT processes within. The high-resolution emission spectra for Pt2 and Pt2rez3 were successfully reproduced at 77 K by using the Franck-Cordon expressions. The possibility to tune PL properties along the plausible continuum of rez3O-H⋅⋅⋅Pt synthons is indicated, considering various scenarios of molecular occupation of the space above and below the complex plane.

Crystal structure and photophysical properties of (κ2‐(N,O)‐5,7‐dichloro‐2‐methyl‐8‐quinolinolate)di(pentafluorophenyl)borane: Experiment and density functional theory calculations

AbstractOver the past decade, the boron Schiff bases (BOSCHIBAs) have garnered significant attention due to their facile and eco‐friendly synthesis, nonlinear and linear optical properties, and sensitivity in solar cells. Recently, luminescent boron(III) complexes have been successfully employed as emitters in organic light‐emitting diodes (OLEDs). The [B(C6F5)2(MeClQ)] complex was synthesized by reacting 5,7‐dichloro‐2‐methylquinoline‐8‐ol with tripentafluorophenylborane, and its structure was determined via single‐crystal X‐ray diffraction (SC‐XRD). The photophysical properties of the compound in various solvents were investigated using UV–Vis and fluorescence spectra in combination with DFT calculations. Analysis based on HOMO‐LUMO energy, emission and absorption spectra, and other parameters indicates that [B(C6F5)2(MeClQ)] exhibits great potential as a blue light emitter in OLEDs.

Improving the performance of resonator-based optical sensors using time-lagged correlation and Fourier phase shift analysis

The performance of time-lagged correlation and Fourier phase shift analysis in resonator-based optical sensors was evaluated and compared to centroiding algorithms. 100 emission spectra of an Er3+ oxyfluoride microsphere were recorded and the average of all data was used as a noiseless spectrum. The Whispering Gallery Mode (WGM) signal, superimposed on the Er3+ emission band, was subtracted and shifted to simulate sensor measurements. Additive random Gaussian noise with different values of the variance was added to the original and WGM-shifted spectra, and the WGM shift was estimated using time-lagged correlation, Fourier phase shift analysis and centroiding algorithms. The procedure was repeated 10000 times to evaluate the accuracy and precision of all numerical methods, and different values of the noise level and WGM shift were considered. These pseudo-experimental studies show that the use of time-lagged correlation and Fourier phase shift analysis can improve the accuracy and precision of the sensor when compared to traditional centroiding algorithms. Additionally, signal analysis can be automated without the need for peak identification and matching.

Self-consistent calculation of the optical emission spectrum of an argon capacitively coupled plasma based on the coupling of particle simulation with a collisional-radiative model

We report the development of a computational framework for the calculation of the optical emission spectrum of a low-pressure argon capacitively coupled plasma (CCP), which is based on the coupling of a particle-in-cell/Monte Carlo collision simulation code with a diffusion-reaction-radiation code for Ar I excited levels. In this framework, the particle simulation provides the rates of the direct and stepwise electron-impact excitation and electron-impact de-excitation for 30 excited levels, as well as the rates of electron-impact direct and stepwise ionization. These rates are used in the solutions of the diffusion equations of the excited species in the second code, along with the radiative rates for a high number of Ar-I transitions. The calculations also consider pooling ionization, quenching reactions, and radial diffusion losses. The electron energy distribution function and the population densities of the 30 excited atomic levels are computed self-consistently. The calculations then provide the emission intensities that reproduce reasonably well the experimentally measured optical emission spectrum of a symmetric CCP source operated at 13.56 MHz with 300 V peak-to-peak voltage, in the 2–100 Pa pressure range. The accuracy of the approach appears to be limited by the one-dimensional nature of the model, the treatment of the radiation trapping through the use of escape factors, and the effects of radiative cascades from higher excited levels not taken into account in the model.

Physical properties of the southwest outflow streamer in the starburst galaxy NGC 253 with ALCHEMI

Aims. The physical properties of galactic molecular outflows are important as they could constrain outflow formation mechanisms. In this work, we study the properties of the southwest (SW) outflow streamer including gas kinematics, optical depth, dense gas fraction, and shock strength through molecular emission in the central molecular zone of the starburst galaxy NGC 253. Methods. We imaged the molecular emission in NGC 253 at a spatial resolution of 1.6″(∼27 pc at D ∼ 3.5 Mpc) based on data from the ALMA Comprehensive High-resolution Extragalactic Molecular Inventory (ALCHEMI) large program. We traced the velocity and velocity dispersion of molecular gas with the CO(1–0) line and studied the molecular spectra in the region of the SW streamer, the brightest CO streamer in NGC 253. We constrained the optical depth of the CO emission with the CO/13CO(1–0) ratio, the dense gas fraction with the HCN/CO(1–0), H13CN/13CO(1–0) and N2H+/13CO(1–0) ratios, as well as the shock strength with the SiO(2–1)/13CO(1–0) and CH3OH(2k–1k)/13CO(1–0) ratios. Results. The CO/13CO(1–0) integrated intensity ratio is ∼21 in the SW streamer region, which approximates the C/13C isotopic abundance ratio. The higher integrated intensity ratio compared to the disk can be attributed to the optically thinner environment of CO(1–0) emission inside the SW streamer. The HCN/CO(1–0) and SiO(2–1)/13CO(1–0) integrated intensity ratios both approach ∼0.2 in three giant molecular clouds (GMCs) at the base of the outflow streamers, which implies a higher dense gas fraction and strength of fast shocks in those GMCs than in the disk, while the HCN/CO(1–0) integrated intensity ratio is moderate in the SW streamer region. The contours of those two integrated intensity ratios are extended in the directions of outflow streamers, which connect the enhanced dense gas fraction and shock strength with molecular outflow. Moreover, the molecular gas with an enhanced dense gas fraction and shock strength located at the base of the SW streamer shares the same velocity as the outflow. Conclusions. The enhanced dense gas fraction and shock strength at the base of the outflow streamers suggest that star formation inside the GMCs can trigger shocks and further drive the molecular outflow. The increased CO/13CO(1–0) integrated intensity ratio coupled with the moderate HCN/CO(1–0) integrated intensity ratio in the SW streamer region are consistent with the picture that the gas velocity gradient inside the streamer may decrease the optical depth of CO(1–0) emission, as well as the dense gas fraction in the extended streamer region.

Redshift and Photon Energy Attenuation Constant in Vacuum

There obtained an estimate of the minimum value of the photon energy attenuation constant in vacuum α: α = 8 · 10–19 m–1 based on quantum concepts of the structure of vacuum and data on the red shift of the emitter spectra of distant galaxies. Presumably, the cosmic microwave radiation is partly the thermal vacuum radiation heated by the photon fluxes from the infinite universe. Despite the universe infinity, the sky is dark precisely due to the photon’s energy absorption from distant and ultra-distant galaxies in vacuum, and not only the photon absorption during various interactions with the gas or dust components of intergalactic clusters. Thus, the emission spectrum of these ultra-distant objects is transformed into the microwave range, which complements the intensity of thermal radiation in this range. The inconsistency of alternative explanations for the red shift is shown: the Doppler effect in the cosmological model of the expanding universe and the Big Bang, and the gravitational shift.

Cross-correlation Techniques to Mitigate the Interloper Contamination for Line Intensity Mapping Experiments

Line intensity mapping (LIM) serves as a potent probe in astrophysics, relying on the statistical analysis of integrated spectral line emissions originating from distant star-forming galaxies. While LIM observations hold the promise of achieving a broad spectrum of scientific objectives, a significant hurdle for future experiments lies in distinguishing the targeted spectral line emitted at a specific redshift from undesired line emissions originating at different redshifts. The presence of these interloping lines poses a challenge to the accuracy of cosmological analyses. In this study, we introduce a novel approach to quantify line–line cross-correlations (LIM-LLX), enabling us to investigate the target signal amid instrumental noise and interloping emissions. For example, at a redshift of z ∼ 3.7, we observed that the measured auto-power spectrum of C ii 158 exhibited substantial bias, from interloping line emission. However, cross-correlating C ii 158 with CO(6–5) lines using an FYST-like experiment yielded a promising result, with a signal-to-noise ratio of ∼10. This measurement is notably unbiased. Additionally, we explore the extensive capabilities of cross-correlation by leveraging various CO transitions to probe the tomographic Universe at lower redshifts through LIM-LLX. We further demonstrate that incorporating low-frequency channels, such as 90 and 150 GHz, into FYST’s EoR-Spec-like experiment can maximize the potential for cross-correlation studies, effectively reducing the bias introduced by instrumental noise and interlopers.

A potential optical approach for diagnosis of the local magnetic field near the surface of the first wall/divertor tiles by Zeeman effect using polarization-resolved laser-induced breakdown spectroscopy

Magnetic field measurement is the basic diagnosis to obtain the physical engineering parameters of magnetic confinement fusion device and the macro information of plasma discharge. The real-time diagnosis of magnetic field distribution near the plasma-facing components (PFCs) surface provides the important information on the migration and transport model of key elements. In this work, a remote, in-situ approach for the magnetic field measurement near the surface of PFCs by the polarization-resolved laser-induced breakdown spectroscopy (LIBS) based on Zeeman effect is proposed and implemented. The Zeeman characteristics of the emission spectra of laser-induced W, Mo and C plasmas were verified in the laboratory by using different magnetic field configurations. According to the polarization characteristics of the Zeeman sublines of the LIBS spectrum, the intensity and direction of the external local magnetic field were successively identified by using a linear polarizer. Subsequently, a linear array fiber was utilized to determine the polarity of the external magnetic field. And finally, the magnetic field intensity near the lower edge surface of the tungsten baffle of the Experimental Advanced Superconducting Tokamak (EAST) upper divertor was measured when the field coils were demagnetized. This method can supplement the experimental data near the PFCs for the magnetic field configuration of the magnetic confinement fusion device and provide a reference for the wall element analysis model diagnosed by LIBS.

Fine-tuning photophysical properties in pyrene derivatives: Unravelling the impact of substitution patterns with incorporation of a strong electron-donating group

To investigate the impact of substitution patterns on the photophysical properties of pyrene derivatives, six novel pyrene derivatives A1-A6 were synthesised by directly coupling anthracene with pyrene units. The objective was to explore the influence of strong electron-donating groups and substitution patterns on their photophysical behaviour. Experimental and theoretical studies were conducted to analyse the photophysical properties of these compounds, revealing a clear dependence on the position of substitution within the pyrene core. Analysis of molecular orbitals revealed significant contributions from both pyrene and anthracene moieties, with deviations from typical electronic distributions attributed to the presence of electron-donating groups. The energy gap values remained consistent across derivatives, contrary to previous findings involving acceptor motif substitutions. Structural analyses indicated deviations from planarity with significant changes in angles upon excitation. The emission spectra of mono- and disubstituted pyrene derivatives predominantly exhibited a single broad maximum with slight shoulders in each solvent. However, the emission spectra of the tetrasubstituted compound (A6) displayed a vibrational structure with three maxima in all solvents, reminiscent of pyrene itself but red-shifted by approximately 30 nm. Furthermore, the central maximum for compound A6 was around 20 nm blue-shifted compared to the other compounds, although its shoulder at around 440 nm corresponded to a maximum observed in other pyrene derivatives. Typically, 1,3,6,8-tetrasubstituted pyrene derivatives, compared to their disubstituted analogues, exhibited red-shifted emission maxima associated with increased π-conjugation due to additional units on the pyrene core. A comprehensive analysis was performed on the absorption and emission spectra of the pyrene derivatives in solvents of various polarities and in the solid state. The fluorescence intensity was influenced by solvent polarity, with A6 showing limited sensitivity (similar quantum efficiency of approximately 45 % in all solvents). Moreover, the quantum yield decreases with the increasing number of anthracene substituents, being the lowest for tetrasubstituted A6. Bi-exponential decay and shorter lifetimes were observed for A1-A6 compared to known compounds, with quantum yields decreasing as solvent polarity increased. In the solid state, emission peaks shifted towards longer wavelengths, with A1 exhibiting the highest quantum yield attributed to steric hindrance. At low temperatures (77 K), emission spectra displayed redshifts, and longer lifetimes were observed. Spectrometric tests in THF/water mixtures indicated luminescence quenching at higher water fractions.

ESIPT-associated fluorescent property and AIE characteristic of multifunctional nanoprobe DPNAP

The DPNAP is a multifunctional nanoprobe designed for selective illumination of fungi and targeted antimicrobial applications. By introducing hydroxyl groups into the DPNAP, the aggregation-induced emission (AIE) characteristic can be obtained. However, its optical properties and underlying theoretical mechanisms are not fully understood. In this work, we explored the stable DPNAP configurations by constructing the potential energy surfaces and elucidated the mechanism of the proton transfer reaction. Our findings indicate that proton transfer occurs through a stepwise reaction with energy barriers of < 10 kcal/mol, owing to the variation in hydrogen-bonding strength as revealed by hydrogen-bond parameters and infrared vibrational analyses. The theoretical fluorescence peak (λcal = 541 nm) based on the optimized structures is consistent with the experimental peak (λexp = 500 nm). The experimental single-fluorescence band is attributed to the overlap of emission spectra of normal structure and single- and double-proton transfer isomers. Moreover, the hydroxyl-induced AIE mechanism is attributed to increased molecular planarity and restricted intramolecular charge transfer in the aggregate state. Understanding of the AIE characteristic and ESIPT mechanism is of fundamental importance in molecular electronics and photonics, and is also beneficial to the development of novel biomedical materials.

Study on Spatial-Temporal Evolution, Decoupling Effect and Influencing Factors of Tourism Transportation Carbon Emissions: Taking North China as an Example

As global warming intensifies, reducing carbon emissions has become a global common mission. Tourism transportation is one of the important sources of carbon emissions, and reducing its carbon emissions is a key part of achieving China’s carbon reduction goals. Based on the panel data of various provinces and cities in North China from 2000 to 2022, this paper calculates the carbon emissions of tourism transportation by using the carbon emission coefficients of different transportation modes in different segments. Moreover, the temporal and spatial evolution of the tourism economy is systematically analyzed. The Tapio decoupling model and LMDI addition decomposition model are used to analyze the relationship between carbon emissions and tourism economic growth and the effects of 11 influencing factors on carbon emissions. The results show that: ① The carbon emission of tourism transportation in North China has experienced four stages: a steady growth period, a transitional adaptation period, a stable equilibrium period, and a drastic decline period. The overall carbon emission level of tourism transportation is as follows: Hebei Province &gt; Shanxi Province &gt; Inner Mongolia Autonomous Region &gt; Beijing City &gt; Tianjin City. ② The decoupling coefficient between tourism traffic carbon emissions and economic development fluctuates but mainly shows a weak decoupling state. ③ In terms of influencing factors, passenger size and passenger density have the greatest impact on the carbon emissions of tourism transportation.

Multidimensional Spectral Phasors of LAURDAN's Excitation-Emission Matrices: The Ultimate Sensor for Lipid Phases?

The impact of lipid diversity on the lateral organization of biological membranes remains a topic of debate. While the existence of domains in lamellar membranes is well-established, the nonlamellar phases occurring in biological systems are less explored due to technical constraints. Here, we present the measurement of the excitation-emission matrices (EEM) of LAURDAN in several lipid structures. LAURDAN is a fluorescence probe widely used for characterizing lipid assemblies. The EEMs were analyzed by multidimensional spectral phasors (MdSP), an approach that seizes information from both the excitation and emission spectra. We developed a computer algorithm to construct EEM data based on a model for LAURDAN's photophysics. The MdSP calculated from the simulated EEMs reveals that all feasible possibilities lie inside a universal triangle in the phasor's plot. We use this triangle to propose a ternary representation for the phasors, allowing a better assessment of LAURDAN's surroundings in terms of hydration, water mobility, and local electronic environment. Building upon this foundation, we constructed a theoretical "phase map" that can assess both lamellar and nonlamellar membranes. We thoroughly validated this theory using well-known lipid mixtures under different phase-state conditions and enzymatically generated systems. Our results confirm that the use of MdSP is a powerful tool for obtaining quantitative information on both lamellar and nonlamellar structures. This study not only advances our understanding of the impact of lipid diversity on membrane organization but also provides a robust and general framework for the assessment of fluorescence properties that can be further extended to other probes.

Vibration‐Dependent Dual‐Phosphorescent Cu4 Nanocluster with Remarkable Piezochromic Behavior

AbstractThe dual emission (DE) characteristics of atomically precise copper nanoclusters (Cu NCs) are of significant theoretical and practical interest. Despite this, the underlying mechanism driving DE in Cu NCs remains elusive, primarily due to the complexities of excited state processes. Herein, a novel [Cu4(PPh3)4(C≡C−p−NH2C6H4)3]PF6 (Cu4) NC, shielded by alkynyl and exhibiting DE, was synthesized. Hydrostatic pressure was applied to Cu4, for the first time, to investigate the mechanism of DE. With increasing pressure, the higher‐energy emission peak of Cu4 gradually disappeared, leaving the lower‐energy emission peak as the dominant emission. Additionally, the Cu4 crystal exhibited notable piezochromism transitioning from cyan to orange. Angle‐dispersive synchrotron X‐ray diffraction results revealed that the reduced inter‐cluster distances under pressure brought the peripheral ligands closer, leading to the formation of new C−H⋅⋅⋅N and N−H⋅⋅⋅N hydrogen bonds in Cu4. It is proposed that these strengthened hydrogen bond interactions limit the ligands′ vibration, resulting in the vanishing of the higher‐energy peak. In situ high‐pressure Raman and vibrationally resolved emission spectra demonstrated that the benzene ring C=C stretching vibration is the structural source of the DE in Cu4.

Electrifying the Road to Net-Zero: Implications of Electric Vehicles and Carbon Emission Coefficient Factors in European Power Systems

The global trend is shifting towards adopting low-carbon transportation solutions, with electrification emerging as a prominent approach. The effectiveness of this transition in mitigating climate change hinges significantly on the source of electricity used for charging electric vehicles. This study focuses on four European Union countries: Switzerland, Italy, Germany, and Poland, each characterized by varying levels of carbon emissions from their power systems. Assumptions are made for the short-term (10%), medium-term (30%), and long-term (60%) penetration of electric vehicles, aligning with the 2050 net zero emissions targets. The study investigates the impact of these penetration levels on energy demand, exploring scenarios ranging from 100% renewable source-generated electricity to 100% coal-generated electricity for EV charging. Finally, utilizing PSS®E 35.5 simulation software, the study assesses the implications of the electric vehicles’ load on medium-voltage transmission lines. The findings highlight the substantial influence of electrifying the transport sector on both environmental sustainability and the power system infrastructure, underscoring the critical role of regional energy mixes and the power system carbon emissions coefficient factor. Regions with lower carbon emission coefficient factors witness significant benefits even with a modest transition to electric vehicles, whereas regions with high carbon emission coefficient factors experience minimal impact despite large-scale EV adoption. Additionally, densely populated urban areas may encounter challenges related to transmission line congestion to meet the growing demand for electric vehicle charging.

EDOT substitution site effect on fluorenone acceptor units: electrochemical polymerization and electrochromic properties of D-A systems

A series of donor-acceptor-donor type molecules (P(2,7-DEF) and P(3,6-DEF)) based on fluorenone acceptor units and 3,4-ethylenedioxythiophene (EDOT) donor units were successfully obtained by Stille coupling reaction in this work, and then generated their corresponding D-A polymers by electrodeposition method. As prepared P(2,7-DEF) and P(3,6-DEF) were characterized by CV, UV–vis spectroscopy, SEM, spectroelectrochemistry, and kinetic studies. Both of these two monomers revealed bright red/yellow light-emitting property in dilute solution. Since the π-conjugation length is longer, the oxidation potential of 2,7-DEF was reduced to 0.85 V, accompanied with red-shifted electronic spectra and emission spectra. The resulting P(2,7-DEF) demonstrated distinct electrochromic properties under various potentials with two different colors from dark-brown to blue-purple. Due to its more porous structure, P(2,7-DEF) also showed favorable optical contrast (26.3 %), very fast switching time (0.32 s), and decent coloration efficiency (221.25 cm2 C−1). However, P(3,6-DEF) displayed much worse electrochromic performances due to its bad electroactivity. P(2,7-DEF) also displayed better redox stability (remaining 79 % electroactivity after 1000 cycles), good optical stability (6 % reduction in optical contrast after 3200 s), and stable optical memory. From these results, P(2,7-DEF) can be further used as a promising near-infrared electrochromic materials.

Unbiased method for spectral analysis of cells with great diversity of autofluorescence spectra.

Autofluorescence is an intrinsic feature of cells, caused by the natural emission of light by photo-excitatory molecular content, which can complicate analysis of flow cytometry data. Different cell types have different autofluorescence spectra and, even within one cell type, heterogeneity of autofluorescence spectra can be present, for example, as a consequence of activation status or metabolic changes. By using full spectrum flow cytometry, the emission spectrum of a fluorochrome is captured by a set of photo detectors across a range of wavelengths, creating an unique signature for that fluorochrome. This signature is then used to identify, or unmix, that fluorochrome's unique spectrum from a multicolor sample containing different fluorescent molecules. Importantly, this means that this technology can also be used to identify intrinsic autofluorescence signal of an unstained sample, which can be used for unmixing purposes and to separate the autofluorescence signal from the fluorophore signals. However, this only works if the sample has a singular, relatively homogeneous and bright autofluorescence spectrum. To analyze samples with heterogeneous autofluorescence spectral profiles, we setup an unbiased workflow to more quickly identify differing autofluorescence spectra present in a sample to include as "autofluorescence signatures" during the unmixing of the full stained samples. First, clusters of cells with similar autofluorescence spectra are identified by unbiased dimensional reduction and clustering of unstained cells. Then, unique autofluorescence clusters are determined and are used to improve the unmixing accuracy of the full stained sample. Independent of the intensity of the autofluorescence and immunophenotyping of cell subsets, this unbiased method allows for the identification of most of the distinct autofluorescence spectra present in a sample, leading to less confounding autofluorescence spillover and spread into extrinsic phenotyping markers. Furthermore, this method is equally useful for spectral analysis of different biological samples, including tissue cell suspensions, peripheral blood mononuclear cells, and in vitro cultures of (primary) cells.

Simultaneous retrieval of orbital phase resolved JWST/MIRI emission spectra of the hot Jupiter WASP-43b: Evidence of water, ammonia and carbon monoxide

Simultaneous retrieval of orbital phase resolved <i>JWST</i>/MIRI emission spectra of the hot Jupiter WASP-43b: Evidence of water, ammonia and carbon monoxide

Efficient and stable hybrid perovskite-organic light-emitting diodes with external quantum efficiency exceeding 40 per cent

Light-emitting diodes (LEDs) based on perovskite semiconductor materials with tunable emission wavelength in visible light range as well as narrow linewidth are potential competitors among current light-emitting display technologies, but still suffer from severe instability driven by electric field. Here, we develop a stable, efficient and high-color purity hybrid LED with a tandem structure by combining the perovskite LED and the commercial organic LED technologies to accelerate the practical application of perovskites. Perovskite LED and organic LED with close photoluminescence peak are selected to maximize photon emission without photon reabsorption and to achieve the narrowed emission spectra. By designing an efficient interconnecting layer with p-type interface doping that provides good opto-electric coupling and reduces Joule heating, the resulting green emitting hybrid LED shows a narrow linewidth of around 30 nm, a peak luminance of over 176,000 cd m−2, a maximum external quantum efficiency of over 40%, and an operational half-lifetime of over 42,000 h.