Filtering Effect Research Articles

Flexible Ag2Se/Ag2S nanocomposite on carbon fabric optimized via interfaced engineered energy filtering effect for a textile based wearable thermoelectric generator

Wearable devices have become increasingly attractive in wearable electronics due to their advantages of environmental friendliness and foldability. The state-of-the-art thermoelectric system depends on inorganic semiconductors that show high electron mobility but lack mechanical stability and thermoelectric performance. Here, We have proposed a solvothermal method to grow Ag2Se/Ag2S nanocomposite on carbon fabric with outstanding properties, demonstrating excellent flexibility. The crystallographic analysis was performed for all samples through XRD and confirmed the orthorhombic Ag2Se and mono-clinic Ag2S. Further, the morphological analysis revealed the enhanced growth on the carbon fabric. We investigated the thermoelectric properties of Ag2Se/Ag2S nanocomposite and achieved a high power factor of 8.1 μW/mK2 which is twice as high as the percentage of the pure Ag2Se. Additionally, thermoelectric legs were fabricated using Ag2Se/Ag2S nanocomposite in a 2-pair module. They produced an output voltage of 0.1 mV to 7.4 mV at a temperature gradient (ΔT) of 3–8 K. This work is a promising approach for obtaining high-performance wearable thermoelectric device.

Ratiometric fluorescence sensing and discrimination of tetracycline analogs by using coumarin-embedded Eu-MOF nanosensor

As widely used antibiotics, tetracycline residues exist in food and environmental media, which pose certain hidden dangers and negative effects on public health. Therefore, the sensing and discrimination of tetracycline analogs (TCs) have great significance for improving food safety and preventing environmental pollution. Herein, a 7-hydroxycoumarin-3-carboxylic acid-embedded Eu-MOF (HC@Eu-MOF) material was constructed and then developed for the detection of TCs. Upon addition of TCs, the synthesized sensor displays opposite fluorescence changes at two different wavelengths due to the simultaneous presence of the inner filter effect (IFE) and the antenna effect (AE), and achieves a stable ratio signal response within 90 s. In addition, six important tetracycline analogs, including chlortetracycline (CTC), oxytetracycline (OTC), tetracycline (TC), metacycline (MC), doxycycline (DC) and demeclocycline (DMC) can be discriminated with 100 % accuracy through the principal component analysis even in extremely complicated mixtures. Further, a smartphone-assisted portable device was applied for visual sensing of TCs. The as-developed platform possessed the characteristics of simple synthesis, fast response, high sensitivity, and high stability, which further lays a further foundation for the on-site visual detection and discrimination of TCs in real samples.

Ratiometric fluorescence sensor based on dye-encapsulated Zn-MOF for highly sensitive detection of diquat in tap water and apple samples

The development of convenient and intelligent visualization of rapid pesticide detection methods is key to ensuring food quality and safety. This paper presents a smartphone-based ratiometric fluorescence sensor for smart field visualization and detection of diquat (DQ). Three-dimensional Zn-MOFs are prepared by the solvothermal method using the rigid ligand 4,4′,4″-s-triazine-2,4,6-triyltribenzoic acid (H3TATB), the flexible ligand 1,4-bis((1H-imidazol-1-yl)methyl)benzene (bimb), and the transition metal (Zn2+), which shows good structural and thermal stability. Zn-MOF is a three-dimensional framework crystallizing in a triclinic crystal system in the Pī space group. Then, RhB@Zn-MOF is obtained by introducing rhodamine B (RhB) into the Zn-MOF framework using the same method. Internal Filter Effect (IFE) quenches red fluorescence and Fluorescence Resonance Energy Transfer (FRET) enhances blue fluorescence, enabling high sensitivity and visual detection of DQ. The sensor has a low detection limit of 10.50 nM and is linear over the 0–70.00 μM concentration range. Compared to Zn-MOF (detection limit of 16.90 nM), the introduction of RhB significantly improved the precision and sensitivity of DQ detection. The combination of a smartphone and RGB analysis enables fast and accurate quantitative analysis of DQ in tap water and apple samples. The sensor platform has the advantages of convenience, intelligent real-time detection, etc. It has a wide prospect of practical application and consolidates a solid foundation for food safety control.

Cobalt oxyhydroxide nanoflakes enable ratiometric fluorescent assay of gallic acid

Gallic acid (GA) is widely used in beverages, food, and other fields as antioxidant. However, GA is slightly toxic and the accumulation of GA is harmful to human body. Therefore, it's vital to develop simple and sensitive detection methods for GA. In this work, a novel ratiometric fluorescent nanoprobe (named CoOOH/OPD/SiNPs) for the GA detection in different foods was designed and prepared. The fluorescence of silicon nanoparticles (SiNPs) at 443 nm would be quenched by cobalt oxyhydroxide (CoOOH) nanoflakes. o-phenylenediamine (OPD) would be oxidized to 2,3-diaminophenazine (DAP) by CoOOH nanoflakes that have peroxidase-like activity, which produces a new fluorescent peak at 556 nm. Meanwhile, SiNPs' fluorescence would be quenched through DAP due to inner filter effect (IFE). With the addition of GA, the reductive decomposition of CoOOH decreased DAP level, causing IFE being restrained. The concentration of GA indicates an excellent linear relationship with fluorescence ratio (F443/F556) in range of 0.4–12 μM (R2 = 0.9937) with 0.16 μM detection limit. This nanoprobe is applied to GA detection in water, tea leaves, fruits and nut fruits, which would be expected to act as a portable device for complex substances analysis.

Multi-color emission composites of white carbon dots and dyes through inner filter effect

A series of multi-color carbon dot composites were obtained by transforming white carbon dots (WCDs) into three primary colors using the dyes' inner filter effect (IFE). WCDs were combined with three distinct dyes (methyl red, bromocresol green, and methylene blue), and three fluorescence colors (red, yellow, and blue) were obtained. The colors of the emitting light excited by the same UV light were similar to the colors of the respective dyes, and have a large Stokes shift. The presence of the IFE between WCDs and dyes was proved through a variety of methods, the analysis of the relationship between the UV of dyes and fluorescence spectra of WCDs, the excitation-emission matrix, as well as the comparison PL decay profiles of WCDs before and after dye addition. The Stern-Volmer quenching constant KSV exhibited no temperature dependence during the IFE process with increasing concentrations of dyes. The UV spectra of the mixture of WCDs and dyes were simply the sum of two individual components, which implies that there is no chemical interaction between WCDs and dyes. Since methyl red and bromocresol green are acid-base indicators, the fluorescence color of the carbon dot composite also changed continuously during the dilute NaOH solution titration process. In furtherment, distributing the binary system of “WCDs + dye” within poly (vinyl alcohol) (PVA), three colors fluorescent composite films of “WCDs / Dye / PVA” were produced successfully.

Nitrogen-doped carbon quantum dots (NCQDs) detected to mercury ions in food monitoring

Using 2,3-diaminopyridine and citric acid as precursors, blue fluorescent nitrogen-doped carbon quantum dots (NCQDs) with a narrow size distribution (∼7.2 nm) were prepared and applied in the following assay for mercury ion detection at a weight ratio of 2,3-diaminopyridine:citric acid = 1:1 (0.2 g: 0.2 g, 20 mL for H2O), 220 °C, and 10 h. NCQDs was characterized by TEM, FT-IR, XPS, UV–Vis and EDS, and the prepared NCQDs display excitation-independent behavior due to less surface defects and uniform size. The optimal excitation and emission wavelengths of the NCQDs were 380 nm and 430 nm, respectively. Interestingly, the fluorescence of the NCQDs could be rapidly and selectively quenched by Hg2+ within 9 min at room temperature without further modification. Under optimal conditions, the limit of detection (LOD) was measured to be at the nanomolar level (42.4 nmol/L) with a linear range of 0–5.0 μmol/L, and fluorescence analysis of NCQDs was successfully used for the qualitative and quantitative analysis of mercury ions in food samples. Furthermore, our results revealed that fluorescence quenching occurred under the common fluences of the inner filter effect, and the static quenching effect was authenticated in the process in which Hg2+ coordinates with the NCQDs to form nonfluorescent complexes.

Smart sensing property of Eu3+-induced polyelectrolyte nanoaggregates on nitrofuran antibiotics in aqueous environments

Pollution of water with antibiotics is a very serious global issue. So, simple, fast, and ecofriendly detection of such pollutants in aqueous environments has aroused great attention. Several intriguing properties such as narrow emission band, large stokes shift, long luminescence decay time and resistance to photobleaching distinguishes europium-based materials from commonly used fluorophores in biology as a superior optical smart material for applications in diverse fields. Herein, strongly luminescent Eu3+-induced polyelectrolyte nanoaggregates (EINAP) were synthesized and successfully characterized. The biocompatible polysaccharides hyaluronic acid and chitosan are used to disperse organic europium complexes resulting in formation of hybrid nanoaggregates. As synthesized EINAP demonstrated excellent quantum yield (89.29 %) and luminescence lifetime (656 µs). The EINAP also have high sensitivity and low limit of detection with good analytical precision for nitrofuran antibiotics in aqueous environments. The luminescent nano sensor developed in this work could be a novel tool for assessment of antibiotic pollution in the environment. The overall sensing mechanisms for detection of nitrofurans in aqueous environments were found to be the combination of inner filter effect and photoinduced electron transfer respectively.

Tetralactam macrocycle based aggregation-induced emission dots for selective detection of Fe3+ in water and drugs

Iron ion (Fe3+) is crucial for both biological organisms and the environment, and iron dyshomeostasis can lead to a variety of diseases and environmental issues. Therefore, the detection of Fe3+ is of significant importance across various fields. For this purpose, through the co-assembly of water-soluble tetralactam macrocycle H and 1,1,2,2-tetraphenylethylene (TPE), we prepared a new type of tetralactam macrocycle based aggregation-induced emission dots (AIE-dots), namely TPE@H. TPE@H exhibitted good water-solubility and allowed the water-insoluble TPE to aggregate and exhibit strong fluorescence emission in water. Furthermore, the fluorescence of TPE@H could be quenched by Fe3+ through the inner filter effect, making TPE@H a potential “turn-off” fluorescent probe for Fe3+ detection. TPE@H exhibited a limit of detection as low as 1 μM with high selectivity, and also retained good detection performance in domestic water, human serum, and even drugs, indicating its great potential for biological and environmental monitoring of Fe3+. This study not only provides a green and efficient method for detecting Fe3+, but also expands the approach for application of water-insoluble dyes in the aqueous environment.

A LMOF/MIP paper-based chip and analysis of tetracycline in foodstuff with sample-to-answer performance

The development of high-performance specific sensors is promising for the rapid detection of harmful residues in animal-derived foods. Recently, luminescent metal-organic framework/molecularly imprinted polymer (LMOF/MIP) materials have been developed as ideal candidates for the analysis of harmful residues. Here, we reported a simple fabrication protocol of paper-based chip through in-situ growth of LMOF on a negatively charged modified filter paper, a paper-based molecularly imprinting layer (FP@BA-Eu@MIP) was thereafter successfully prepared via the boronate affinity-based controllable oriented surface imprinting strategy. The paper-based chips obtained were used to construct a rapid test strip of tetracycline (TC). After addition of TC, significant fluorescence changes on the surface of the FP@BA-Eu@MIP paper-based chip could be observed from blue to red via inner filter effect and photo-induced electron transfer under the excitation of 360 nm. The adsorption kinetics was explored in detail. The presented strip exhibited satisfied selectiveness and sensitivity with a limit of detection of 8.47 μg L−1 for TC. It was confirmed that LMOF/MIP as a biomimetic recognition module can play a crucial role in enrichment and fluorescence response. This study provided a real application case for an in-situ fabricated fluorescence paper-based chip in rapidly detecting harmful residues.

Dual-State Red-Emitting Zinc-Based MOF Accompanied by Dual-Mode and Dual-State Detection: Color Tonality Visual Mode for the Detection of Tetracycline.

Red-emitting metal-organic frameworks (MOFs) are still mostly based on the use of lanthanides or functionalization with red fluorophores. However, production of transition-metal-based MOFs with red-emitting is scarce. This work reports on the synthesis of a novel dual-state red-emitting Zn-based MOF (denoted as UoZ-7) with the capability to detect target molecules in dual state, in solution, and as solid on paper. UoZ-7 gives strong red emission when excited in the solution and in the solid state with 365 nm ultraviolet (UV) lamp irradiation. Coordination-induced emission is the mechanism for the red emission enhancement in the MOF as a restriction of intramolecular rotation occurred to the ligand within the framework structure. UoZ-7 was successfully used for tetracycline (TC) using dual-mode detection, fluorescence-based ratiometry, and color tonality, in the dual state, in solution, and on the paper. TC molecules adsorb on the red-emitting UoZ-7 surface, and a yellow-greenish color emerges due to aggregation-induced emission between TC and UoZ-7. Concurrently, the inner filter effect diminishes the red emission of UoZ-7. The dual-mode or dual-state detection platform provides a simple and reliable fast method for the detection of TC on-site in various environmental and biomedical applications. Moreover, red-emitting UoZ-7 will have further luminescence-based biomedical applications.

Carbon Dots Employed for the Detection of Ranitidine and Elaborating the Detecting Mechanism.

Carbon dots (CDs) has been widely utilized in multiple fields, especially towards kinds of drug analyses, owing to its superior optical properties and satisfactory stability. Herein, we rapidly synthesized one kind of soluble bright-blue fluorescent CDs through a facile microwave method, while disodium ethylenediaminetetraacetic acid and phosphoric acid served as the raw materials. Importantly, introducing ranitidine into these CDs resulted in its decreased fluorescence, and thus an innovative method of detecting ranitidine was successfully established, which showed the favorable selectivity and anti-interference ability. With the optimal conditions, the standard curve diagram of F0/F against concentration of ranitidine was linear in the range of 6-2000 µM with a correlation coefficient of 0.9833, and the limit of detection (LOD) was calculated to be 4.2 µM. Meanwhile, we also explored the detecting mechanism of ranitidine by CDs, and elaborated that as the internal filtration effect. Consequently, we may broaden the avenues of detecting ranitidine on the basis of CDs.

Variability of Bile Baseline Excitation-emission Fluorescence of Two Tropical Freshwater Fish Species.

The quantification of pollutant metabolites in fish bile is an efficient approach to xenobiotic pollution monitoring in freshwaters since these measurements directly address exposure. Fluorescence excitation-emission matrix spectroscopy (EEMS) has demonstrated to be a highly specific and cost-effective technique for polycyclic aromatic hydrocarbon (PAH) and PAH-metabolite identification and quantification. EEMS ability to quantify these compounds strongly depends on the intensity and variability of the bile baseline fluorescence (BBF). We found large differences in BBF among Aequidens metae (AME) individuals and of these with Piaractus orinoquensis (PIO). Moreover, BBF was large enough that solvent dilutions of over 1:400 were needed to avoid inner filter effects. We used parallel factor analysis (PARAFAC) to model the intra- and inter-species BBF variability. PARAFAC successfully decomposed the EEMS set into three fluorophores present in all samples, although in concentrations spreading over ~ 3 orders of magnitude. One of the factors was identified as tryptophan. Tryptophan and Factor 2 were covariant and much more abundant in AME than in PIO, while Factor 3 was ~ 6 times more abundant in PIO than in AME. Also, tryptophan was ~ 10x more abundant in AME specimens immediately caught in rivers than in their laboratory-adapted peers. The PARAFAC decomposition effectiveness was confirmed by the positive proportionality of scores to dilution ratios. A large inner filter indicates that Factor 2 is as strong a light absorber as tryptophan. Our results stress the need to include bile matrix variable components for the detection and quantification of pollutant metabolites using PARAFAC.

The effect of sunglass filters on contrast sensitivity, monocular eye closure, and blinking rate in people with intermittent exotropia

ABSTRACT Clinical relevance Transient monocular eye closure and photosensitivity under bright light have been reported in people with intermittent exotropia (IXT). The exact mechanism of these symptoms has not been established. Background This study examines the effect of sunglass filters on contrast sensitivity (CS), transient monocular eye closure, and blinking rate under bright light in people with IXT. Methods Forty participants with IXT and complaints of photosensitivity were included in the study. The binocular CS test was performed under mesopic and photopic conditions with and without glare, and with and without two filters with different grades of light transmission (filter 1: 44–80%; filter 2: 20–43% light transmittance). The effect of two filters on transient eye closure, contrast sensitivity, and blinking rate was assessed under bright light. Also, participants were divided into 3 groups based on their degree of control of fusion (good, fair, and poor control). Results The mean age of the participants was 12.0 years ± 8.0 (standard deviation) (range: 7–40 years). There was no significant difference between the age (p = 0.139), stereopsis (p = 0.134), as well as the near and far degree of deviation (p = 0.516, and p = 0.237) between the three groups of fusion control. Under mesopic conditions with glare, mean binocular CS was significantly higher with filters (p < 0.001). Without filters, 57.5% of the participants exhibited monocular eye closure under a photopic setting with additional glare. No participant showed eye closure using filter 2. People in the poor control group showed exodeviation before monocular eye closure (62.5% without filter and 12.5% with filter 1, p = 0.01). The blinking rate decreased from 36.0 ± 4.0 blinks per minute without filter to 21.0 ± 3.0 using filter 1, and 20.0 ± 3.0 with filter 2. Conclusion In people with IXT, wearing sunglass filters of different transmittance reduces monocular eye closure and blinking rate under bright light. To improve these symptoms, sunglasses can be considered for IXT.

A europium (III) functionalized hydrogen-bonded organic framework for sensitively ratiometric fluorescent sensing of tetracycline.

As a kind of antibiotic, tetracycline (TC) might remain in animal blood and milk products during use, which poses a risk to humans after consumption. Therefore, a ratiometric fluorescence probe was proposed for the detection of TC, which was based on anEu3+ functionalized hydrogen-bonded organic framework (HOF). Since there are alarge number of N and O atoms in the skeleton of HOF, more Eu3+ could be loaded onto HOF by forming coordinate bonds, while preserving the fluorescence of luminol monomer in HOF. In the presence of TC, the fluorescence of luminol monomer was attenuated at 425nm due to inner filter effect (IFE), while TC selectively enhanced the fluorescence peak at 617nm of Eu3+ under the influence of antenna effect (AE). This highly sensitive probe could detect TC in the range of0.1-60μM and had a low limit ofdetection of 8.51nM. Besides, the HOF@Eu probe was able to detect TC in actual samples (milk and tap water) with good recoveries (95.09%-111.51%) and precision (R < 4.78%), indicating this probe has great application potential forthe detection of TC in food.

Carbon dots-based dual-mode sensor for highly selective detection of nitrite in food substrates through diazo coupling reaction

As an antioxidant and preservative agent, nitrite (NO2−) plays an essential role in the food industry to maintain freshness or inhibit microbial growth. However, excessive addition of NO2− is detrimental to health, so accurate and portable detection of NO2− is critical for food quality control. Notably, the selectivity of most carbon dots (CDs)-based fluorescence sensors was not enough due to the nonspecific interaction mechanism of hydrogen bond, electrostatic interaction and inner filter effect etc. Herein, a novel fluorescence/UV–vis absorption (FL/UV–vis) dual-mode sensor was developed on basis of mC-CDs, which were prepared by simple solvothermal treatment of m-Phenylenediamine (m-PDA) and cyanidin cation (CC). The fluorescence of these mC-CDs could be selectively responded by NO2− through the specific diazo coupling reaction between NO2− and amino groups on the surface of mC-CDs, thus effectively improving the selectivity of NO2− detection. The CDs-based fluorescence sensor possessed a low detection limit of 0.091 μM and 0.143 μM for FL and UV–vis methods and the excellent linear range of 0.0–60.0 μM. Furthermore, the mC-CDs sensor was employed to detect NO2− in real samples with a recovery rate of 97.11 %–104.15 % for quantitative addition. Moreover, the smartphone-assisted fluorescence sensing platform developed could identify the subtle color changes that could not be distinguished by the naked eye, and had the advantages of fast detection speed and intelligence. More importantly, the portable solid phase sensor based on mC-CDs had been successfully applied to the specific fluorescence identification and concentration monitoring of NO2−. Accordingly, the designed sensor provided a new strategy for the highly selective and convenient sensing of NO2− in food substrates, and paved the way for the wide application of CDs-based nanomaterials in the detection of food safety.

Synergistic strategy via modulated energy filtering and hierarchical defects evolution for high performance GeTe thermoelectrics

GeTe thermoelectric materials are very promising for sustainable waste-heat harvesting, while optimizations have been focusing on lowering lattice thermal conductivity or decreasing carrier concentration. As a long-pursued strategy to improve electronic transport properties, the full realization of effective energy filtering has been hindered by the mismatch between the energy barriers introduced and the intrinsic Fermi level of the matrix material. In this work, a synergistic strategy combining modulated energy filtering effect and hierarchical defect evolution engineering leads to ultrahigh performance GeTe-based thermoelectric materials. Very effective energy filtering is achieved by incorporating carbon fibers, which increases the overall energy of charge carriers. This greatly enhances Seebeck coefficient to over 230 μVK-1 with minor reduction in electrical conductivity which simultaneously decreases electronic thermal conductivity. Furthermore, the inclusion of carbon fibers modulates the microstructure of GeTe and facilitates the evolution of point defects to higher dimensional defects for broadband phonon scattering, greatly suppressing the lattice thermal conductivity to 0.3 Wm-1K-1. This strategy yields a prominent thermoelectric figure of merit ZTmax ∼ 2.3 and an exceptional quality factor Bmax ∼ 2.24 for Ge0.97Bi0.07Te with 0.9 wt% carbon fibers. This study demonstrates a promising strategy to modulate the convoluted thermoelectric properties for ultrahigh performance thermoelectric materials.

Pseudospin-filter tunneling of massless Dirac fermions

Abstract The tunneling of the massless Dirac fermions through a vector potential barrier are theoretically investigated, where the vector potential can be introduced by the very high and very thin (δ-function) magnetic potential barriers. We show that, distinct from the previously studied electric barrier tunneling, the vector potential barriers are more transparent for pseudospin-1/2 Dirac fermions but more obstructive for pseudospin-1 Dirac fermions. By tuning the height of the vector potential barrier, the pseudospin-1/2 Dirac fermions remain transmitted, whereas the transmission of the pseudospin-1 Dirac fermions is forbidden, leading to a pseudospin filtering effect for massless Dirac fermions.

Enhanced Sensitivity and Accuracy of Tb3+-Functionalized Zirconium-Based Bimetallic MOF for Visual Detection of Malachite Green in Fish.

The ratiometric fluorescent probe UiO-OH@Tb, a zirconium-based MOF functionalized with Tb3+, was synthesized using a hydrothermal method. This probe employs the fluorescence resonance energy transfer (FRET) mechanism between Tb3+ and malachite green (MG) for the double-inverse signal ratiometric fluorescence detection of MG. The probe's color shifts from lime green to blue with an increasing concentration of MG. In contrast, the monometallic MOFs' (UiO-OH) probe shows only blue fluorescence quenching due to the inner filter effect (IFE) after interacting with MG. Additionally, the composite fluorescent probe (UiO-OH@Tb) exhibits superior sensitivity, with a detection limit (LOD) of 0.19 μM, which is significantly lower than that of the monometallic MOFs (25 μM). Moreover, the content of MG can be detected on-site (LOD = 0.94 μM) using the RGB function of smartphones. Hence, the UiO-OH@Tb probe is proven to be an ideal material for MG detection, demonstrating significant practical value in real-world applications.

Ultra high-speed 3D shape measurement technology for specular surfaces based on μPMD

Phase measuring deflectometry (PMD) has been extensively applied to measure specular surfaces due to its non-contact, high-precision, full-field measurement capabilities. Liquid crystal display (LCD) screen is the most common structured light source in PMD. However, the response time of liquid crystal molecules limits its frame rate to around 100 frames per second (fps). Therefore, it is quite difficult for traditional PMD to measure rapidly moving surfaces. This paper proposes a 3D dynamic sensing technique, microsecond-PMD (µPMD) based on the high-frame-rate sinusoidal fringe display (HSFD). In the proposed method, the switching time for each fringe pattern display is at a sub-microsecond level, enabling high-speed fringe acquisition with kHz-level area array detection or 100kHz-level line array scanning. The HSFD method uses a specially designed LED array and two-step optical expansion. The high-speed switching characteristic of LED sources is utilized to allow a superfast display rate. Moreover, the superior sinusoidal property can be achieved by the combination of the specially designed discrete sinusoidal LED array, the light-diffracting effect of orthogonal gratings, and the filtering effect of the light diffuser. The mechanism and analytic model of fringe generation are thoroughly analyzed and discussed in this work. Furthermore, the swarm optimization algorithm and corresponding weighted fringe quality evaluation function are presented to obtain the optimal fringes. To the best of our knowledge, the proposed µPMD, for the first time, achieved a superfast fringe acquisition rate of 4000fps with sub-micrometer precision in three-dimensional (3D) reconstruction for specular surfaces. We envision this proposal to be broadly implemented for real-time monitoring in manufacturing.

What sizes of droplets contribute to long-range airborne transmission?

The size range of respiratory droplets contributing to long-range airborne transmission of infections determines the targeted intervention methods. However, the exact size range remains unknown, and the influencing parameters are also undetermined. Here, we investigated the size-resolved transport and fate of respiratory droplets in four reported venues of COVID-19 outbreaks. We utilised a transient number balance model, a set of expired droplet size distributions, existing formulas for size-resolved settling rates and filtration efficiencies, and a deposition model from the International Commission on Radiological Protection. This enabled us to obtain the size-resolved concentrations of exhaled droplets in indoor air, the size-resolved number of droplet nuclei in the inhaled air, and the number of droplets deposited throughout the respiratory tract. The newly defined airborne transmission size range of expired droplets depends on the effective dilution flow rate of the infection venue under consideration. Three criteria were proposed for determining the sizes of droplets involved in long-range airborne transmission. The airborne transmission droplets typically featured an initial diameter of 0.1–4–6 µm, with an hourly volume generation rate of 0.38–0.42 nL/h per index case in the four venues. This newly estimated volume of airborne transmission droplets provides an essential input into the viral load method for estimating the infectious quanta generation rate. Practical significanceOur size-resolved estimation reveals that only a tiny fraction of expired infectious droplets within an airborne transmission size range survives after the removal effects of ventilation, settling, deactivation, and filtration, as well as the transient dilution effect. These droplets remain in indoor air, potentially contributing to long-range airborne transmission. The airborne transmission size range depends on the size-dependent dilution capacity of a room.