Homeopathic Medicines in Third (Omicron) Wave of COVID-19: Prognostic Factor Research.

BACKGROUND: With the emergence of new variants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus, such as the Omicron variant, during the third wave of the coronavirus disease 2019 (COVID-19) pandemic, there was a need to identify useful homeopathic medicines. This study aimed to identify such medicines and their indications using prognostic factor research (PFR). METHODS: This was an open-label, multi-centred observational study conducted in January 2022, on confirmed COVID-19 cases. The data were collected from integrated COVID Care Centres in Delhi, India, where homeopathic medicines were prescribed along with conventional treatment. Only those cases that met a set of selection criteria were considered for analysis. The likelihood ratio (LR) was calculated for the frequently occurring symptoms of the frequently prescribed medicines. An LR of 1.3 or greater was considered meaningful. RESULTS: Out of the 362 COVID-19 cases, 263 cases were selected for analysis after applying selection criteria. Common symptoms included fatigue, cough, sore throat, myalgia and headache. Twenty-one medicines were prescribed, of which nine medicines - Gelsemium sempervirens, Bryonia alba, Hepar sulphuris, Rhus toxicodendron, Pulsatilla nigricans, Arsenicum album, Belladonna, Nux vomica and Phosphorus - were frequently used. By calculating LRs, the study identified meaningful indications for these medicines. CONCLUSION: Homeopathic medicines have shown promising results in the third wave of COVID-19 as an adjunct therapy. The medicines that were used in the first and second waves were found useful in the third wave also, and their indications were analogous to those found in the earlier waves. Certain new indications of some medicines were elicited in this wave, which warrant further research. However, it is important not to restrict to these medicines only and to continue data collection on COVID-19 in future waves for the improvement of the COVID-19 mini-repertory.

Atomic-layered V2C MXene containing bismuth elements: 2D/0D and 2D/2D nanoarchitectonics for hydrogen evolution and nitrogen reduction reaction.

The exploitation of two-dimensional (2D) vanadium carbide (V2CTx, denoted as V2C) in electrocatalytic hydrogen evolution reaction (HER) and nitrogen reduction reaction (NRR) is still in the stage of theoretical study with limited experimental exploration. Here, we present the experimental studies of V2C MXene-based materials containing two different bismuth compounds to confirm the possibility of using V2C as a potential electrocatalyst for HER and NRR. In this context, for the first time, we employed two different methods to synthesize 2D/0D and 2D/2D nanostructures. The 2D/2D V2C/BVO consisted of BiVO4 (denoted BVO) nanosheets wrapped in layers of V2C which were synthesized by a facile hydrothermal method, whereas the 2D/0D V2C/Bi consisted of spherical particles of Bi (Bi NPs) anchored on V2C MXenes using the solid-state annealing method. The resultant V2C/BVO catalyst was proven to be beneficial for HER in 0.5 M H2SO4 compared to pristine V2C. We demonstrated that the 2D/2D V2C/BVO structure can favor the higher specific surface area, exposure of more accessible catalytic active sites, and promote electron transfer which can be responsible for optimizing the HER activity. Moreover, V2C/BVO has superior stability in an acidic environment. Whilst we observed that the 2D/0D V2C/Bi could be highly efficient for electrocatalytic NRR purposes. Our results show that the ammonia (NH3) production and faradaic efficiency (FE) of V2C/Bi can reach 88.6 µg h-1 cm-2 and 8% at -0.5 V vs. RHE, respectively. Also V2C/Bi exhibited excellent long-term stability. These achievements present a high performance in terms of the highest generated NH3 compared to recent investigations of MXenes-based electrocatalysts. Such excellent NRR of V2C/Bi activity can be attributed to the effective suppression of HER which is the main competitive reaction of the NRR.

Hydrogen-Terminated Two-Dimensional Germanane/Silicane Alloys as Self-Powered Photodetectors and Sensors.

2D monoelemental materials, particularly germanene and silicene (the single layer of germanium and silicon), which are the base materials for modern electronic devices demonstrated tremendous attraction for their 2D layer structure along with the tuneable electronics and optical band gap. The major shortcoming of synthesized thermodynamically very unstable layered germanene and silicene with their inclination toward oxidation was overcome by topochemical deintercalation of a Zintl phase (CaGe2, CaGe1.5Si0.5, and CaGeSi) in a protic environment. The exfoliated Ge-H, Ge0.75Si0.25H, and Ge0.5Si0.5H were successfully synthesized and employed as the active layer for photoelectrochemical photodetectors, which showed broad response (420-940 nm), unprecedented responsivity, and detectivity on the order of 168 µA W-1 and 3.45 × 108 cm Hz1/2 W-1, respectively. The sensing capability of exfoliated germanane and silicane composites was explored using electrochemical impedance spectroscopy with ultrafast response and recovery time of less than 1 s. These positive findings serve as the application of exfoliated germanene and silicene composites and can pave a new path to practical applications in efficient future devices.

One-Step Electrochemical Synthesis of AlO x -Passivated Twisted-Phosphorene Nanosheets for Potentially Stable Energy Storage Devices.

Black phosphorus (BP), a promising 2D material for electronics, energy storage, catalysis, and sensing, has sparked a research boom. However, exfoliated thin-layered BP is unstable and can easily be degraded under environmental conditions, severely limiting its practical applications. In this context, a simple and cost-effective method has been proposed that involves electrochemically exfoliating BP and simultaneously electrochemically depositing aluminum oxide (AlO x ) for passivation of the exfoliated BP. The ambient stability of the exfoliated BP is studied using a time-dependent atomic force microscope (AFM). The AlO x capping layer significantly improves the environmental stability of BP compared to uncapped BP. The thermal stability of the resulting BP is evaluated using power-dependent Raman spectroscopy. The results show that the AlO x -passivated BP has increased thermal stability, with only a slight shift in peak position toward higher Raman power intensity. These properties can make the material suitable for stable energy storage devices. Interestingly, the electrochemical exfoliation and passivation processes resulted in the BP with a twist angle (9.86°), which is expected to exhibit unique electronic properties similar to those of graphene with a twist angle.

Chalcogen (S, Se, and Te) decorated few-layered Ti3C2Tx MXene hybrids: modulation of properties through covalent bonding.

2D carbides and nitrides of transition metals (MXenes) have shown great promise in a variety of energy storage and energy conversion applications. The extraordinary properties of MXenes are because of their excellent conductivity, large carrier concentration, vast specific surface area, superior hydrophilicity, high volumetric capacitance, and rich surface chemistry. However, it is still desired to synthesize MXenes with specific functional groups that deliver the required characteristics. This is due to the fact that a considerable amount of metal atoms is exposed on the surface of MXenes during their synthesis through an etching procedure; hence, other anions and cations are uncontrollably implanted on their surfaces. Because of this situation, the first invented Ti3C2Tx MXene suffers from low photoresponsivity and detectivity, large overpotential, and small sensitivity in photoelectrochemical (PEC) photodetectors, hydrogen evolution reaction (HER), and sensing applications. Therefore, surface modification of the MXene structure is required to develop the device's performance. On the other hand, there is still a lack of understanding of the MXene mechanism in such cutting-edge applications. Thus, the manipulations of MXenes are highly dependent on understanding the device mechanism, suitable modification elements, and modification methods. This study for the first time reveals the conjugation effect of pre-selected S, Se, and Te chalcogen elements on a few-layered Ti3C2Tx MXene to synthesize new composites for PEC photodetector, HER, and vapor sensor applications. Also, the mechanism of the chalcogen decorated few-layered Ti3C2Tx MXene composites for each application is discussed. The selection of a few-layered Ti3C2Tx MXene is due to its fascinating characteristics which make it capable to be considered as an appropriate substrate and incorporating chalcogen atoms. The Te-decorated few-layered Ti3C2Tx MXene composite provides better performances in PEC photodetector and vapor sensing applications. Although the potential value of the Se-decorated few-layered Ti3C2Tx composite is slightly lower than that of the Te-decorated sample in HER application, its overpotential is still greater than that of the Te-decorated sample. The acquired results show that the S-decorated few-layered Ti3C2Tx composite demonstrates the lowest performance in all three examined applications in comparison with the other two samples.

Synthesis and characterization of titanium-substituted nanocrystalline Co2-Y hexaferrite: magnetically retrievable photocatalyst for treatment of methyl orange contaminated wastewater.

Rapid industrial growth causes considerable environmental havoc, adversely affecting human and aqueous life. It becomes a significant concern to deal with adequate wastewater treatment strategies by converging on water scarcity. This research work explored the synthesis of titanium-substituted Y-type barium hexaferrite (Co2-Y), having a general formula of Ba2Co2Fe12-xTixO22 (x = 0.0, 0.1, 0.2, 0.3, 0.4, and 0.5), using a facile nitrate-based sol-gel auto-combustion route and its suitability was investigated as a heterogeneous catalyst within the photo-Fenton-based degradation of methyl orange (MO), one of the significant pollutants generated from textile industries. Developing a thermochemically stable and magnetically separable heterogeneous catalyst for photocatalytic decomposition of nonbiodegradable organic dye from wastewater was also emphasized. The as-prepared nanocrystalline Co2-Y powders were analyzed using XRD, FTIR, DLS, UV-visible spectroscopy, SEM, VSM, and XPS. Furthermore, the photocatalytic degradation performance of pristine and titanium substituted Ba2Co2Fe11.6Ti0.4O22 ferrite, having the lowest bandgap value among all samples, was quantified and compared in terms of apparent rate constant (karc) value and turnover frequency values. The enriched photocatalytic performance was correlated with the existence of multi-valance states of transition metal cations and the availability of oxygen vacancy, confirmed by the surface chemistry using the XPS analysis. The modified (enhanced thermal and chemical stability) hexaferrite catalyst was magnetically separable and reusable without significant losses to its catalytic performance. This promising catalyst may be considered as a replacement for soft ferrite materials to catalyze the degradation of several other nonbiodegradable organic pollutants from wastewater in large-scale industries.

A New, Thorough Look on Unusual and Neglected Group III-VI Compounds Toward Novel Perusals.

The attention on group III-VI compounds in the last decades has been centered on the optoelectronic properties of indium and gallium chalcogenides. These outstanding properties are leading to novel advancements in terms of fundamental and applied science. One of the advantages of these compounds is to present laminated structures, which can be exfoliated down to monolayers. Despite the large knowledge gathered toward indium and gallium chalcogenides, the family of the group III-VI compounds embraces several other noncommon compounds formed by the other group III elements. These compounds present various crystal lattices, among which a great deal is offered from layered structures. Studies on aluminium chalcogenides show interesting potential as anodes in batteries and as semiconductors. Thallium (Tl), which is commonly present in the +1 oxidation state, is one of the key components in ternary chalcogenides. However, binary Tl-Q (Q = S, Se, Te) systems and derived films are still studied for their semiconducting and thermoelectric properties. This review aims to summarize the biggest features of these unusual materials and to shed some new light on them with the perspective that in the future, novel studies can revive these compounds in order to give rise to a new generation of technology.

2D Few-Layered PdPS: Toward High-Efficient Self-Powered Broadband Photodetector and Sensors.

Photodetectors and sensors have a prominent role in our lives and cover a wide range of applications, including intelligent systems and the detection of harmful and toxic elements. Although there have been several studies in this direction, their practical applications have been hindered by slow response and low responsiveness. To overcome these problems, we have presented here a self-powered (photoelectrochemical, PEC), ultrasensitive, and ultrafast photodetector platform. For this purpose, a novel few-layered palladium-phosphorus-sulfur (PdPS) was fabricated by shear exfoliation for effective photodetection as a practical assessment. The characterization of this self-powered broadband photodetector demonstrated superior responsivity and specific detectivity in the order of 33 mA W-1 and 9.87 × 1010 cm Hz1/2 W-1, respectively. The PEC photodetector also exhibits a broadband photodetection capability ranging from UV to IR spectrum, with the ultrafast response (∼40 ms) and recovery time (∼50 ms). In addition, the novel few-layered PdPS showed superior sensing ability to organic vapors with ultrafast response and a recovery time of less than 1 s. Finally, the photocatalytic activity in the form of hydrogen evolution reaction was explored due to the suitable band alignment and pronounced light absorption capability. The self-powered sensing platforms and superior catalytic activity will pave the way for practical applications in efficient future devices.

Self-Powered Broadband Photodetector and Sensor Based on Novel Few-Layered Pd3(PS4)2 Nanosheets.

Optoelectronics and sensing devices are of enormous importance in our modern lives, which has propelled the scientific community to explore new two-dimensional (2D) nanomaterials to meet the requirements of future devices. Herein, we present the exfoliation of palladium thiophosphate (Pd3(PS4)2) by mechanical shear force exfoliation. The Pd3(PS4)2-based photoelectrochemical (PEC) device demonstrated self-powered broadband photodetection in the range of 385-940 nm with an unprecedented responsivity of 2 A W-1 and a specific detectivity of about 8.67 × 1011 cm Hz1/2 W-1 under the illumination of 420 nm LED light. The crucial parameters such as photoresponsivity, response, and recovery time of the device can be controlled by an externally applied voltage and the analyte concentration. Moreover, Pd3(PS4)2-based vapor-sensing devices exhibited frequency-dependent selective acetone sensing in the presence of other organic vapors with an ultrafast response and a recovery time of less than 1 s. Finally, the photocatalytic activity of Pd3(PS4)2 was revealed, which can be attributed to the presence of an appropriate band alignment with the catalytic activity of Pd. This novel material with the aforementioned fascinating phenomenon will pave the way toward practical future applications in optoelectronics and sensing.

Single-Step Synthesis of Platinoid-Decorated Phosphorene: Perspectives for Catalysis, Gas Sensing, and Energy Storage.

The originality of phosphorene is suppressed by its structural defects, irreproducibility, and sensitivity to the ambient environment. To preserve phosphorene's essential characteristics, for example, influencing the charge redistribution and generating the formation of active centers, noble-metal decoration is found to be an efficient approach. Herein, we demonstrate a single-step electrochemical synthesis of platinoid-decorated few-layer phosphorene (FP). The material's structure and effects of metal (Ru, Rh, and Pd) deposition on the FP nanosheets were first explored by numerous analytical techniques and theoretical calculations. Platinoid-decorated FPs demonstrate high quality and consist of one to five layers modified with round- and heptagon-shaped metal nanoparticles with the most intense distribution of Pd. The high-rate Rh deposition provides the enhanced electrocatalytic efficiency for hydrogen evolution (79 mV·dec-1-Tafel slope) and almost 20 times increased capacity for the Li-ion batteries in comparison to bare and Ru-decorated FP. The chemosensing of platinoid-decorated FP indicates a response to methanol plus ethanol and shows inertness to acetone. The incorporation of Ru and Rh nanoparticles increases FP's selectivity toward methanol. This research provides a new approach for the in situ FP functionalization during top-down synthesis and thus broadens the material's feasibility for advanced nanotechnology.

Unprecedented random lasing in 2D organolead halide single-crystalline perovskite microrods.

Three-dimensional organic-inorganic hybrid halide perovskites have been demonstrated as great materials for applications in optoelectronics and photonics. However, their inherent instabilities in the presence of moisture, light, and heat may hinder their commercialization. Alternatively, emerging two-dimensional (2D) organic-inorganic hybrid perovskites have recently attracted increasing attention owing to their great environmental stability and inherent natural quantum-well structure. In this work, we have synthesized a high-quality long-chain organic diammonium spacer assisted 2D hybrid perovskite FA-(N-MPDA)PbBr4 (FA = formamidinium and N-MPDA = N-methylpropane-1,3-diammonium) by the slow evaporation at constant temperature method. The millimeter-sized single-crystalline microrods demonstrate low threshold random lasing behavior at room temperature. The single-crystalline 2D hybrid perovskite random laser achieved a very narrow linewidth (∼0.1 nm) with a low threshold (∼0.5 µJ cm-2) and a high quality factor (∼5350). Furthermore, the 2D hybrid microrod laser shows stable lasing emission with no measurable degradation after at least 2 h under continuous illumination, which substantially proves the stability of 2D perovskites. Our results demonstrate the promise of 2D organic-inorganic microrod-shaped perovskites and provide an important step toward the realization of high-performance optoelectronic devices.

Ultralow Threshold Cavity-Free Laser Induced by Total Internal Reflection.

Total internal reflection is one of the most important phenomena when a propagated wave strikes a medium boundary, which possesses a wide range of applications spanning from optical communication to a fluorescence microscope. It has also been widely used to demonstrate conventional laser actions with resonant cavities. Recently, cavity-free stimulated emission of radiation has attracted great attention in disordered media because of several exciting physical phenomena, ranging from Anderson localization of light to speckle-free imaging. However, unlike conventional laser systems, the total internal reflection has never been implemented in the study of laser actions derived from randomly distributed media. Herein, we demonstrate an ultra-low threshold cavity-free laser system using air bubbles as scattering centers in which the total internal reflection from the surface of air bubbles can greatly reduce the leakage of the scattered beam energy and then enhance light amplification within a coherent closed loop. Our approach provides an excellent alternative for the manipulation of optical energy flow to achieve ultra-low threshold cavity-free laser systems, which should be very useful for the development of high performance optoelectronic devices.

Emerging pnictogen-based 2D semiconductors: sensing and electronic devices.

Pnictogens are an intensively studied group of monoelemental two-dimensional materials. This group of elements consists of phosphorus, arsenic, antimony, and bismuth. In this group, the elements adopt two different layered structural allotropes, orthorhombic structure with true van der Waals layered interactions and rhombohedral structure, where covalent interactions between layers are also present. The orthorhombic structure is well known for phosphorus and arsenic, and the rhombohedral structure is the most thermodynamically stable allotropic modification of arsenic, antimony, and bismuth. Due to the electronic structure of pnictogen layers and their semiconducting character, these materials have huge application potential for electronic devices such as transistors and sensors including photosensitive devices as well as gas and electrochemical sensors. While photodetection and gas sensing applications are often related to lithography processed materials, chemical sensing proceeds in a liquid environment (either aqueous or non-aqueous) and can be influenced by surface oxidation of these materials. In this review, we explore the current state of pnictogen applications in sensing and electronic devices including transistors, photodetectors, gas sensors, and chemical/electrochemical sensors.

Microplasma-Enabled Graphene Quantum Dot-Wrapped Gold Nanoparticles with Synergistic Enhancement for Broad Band Photodetection.

Plasmonic nanostructure/semiconductor nanohybrids offer many opportunities for emerging electronic and optoelectronic device applications because of their unique geometries in the nanometer scale and material properties. However, the development of a simple and scalable synthesis of plasmonic nanostructure/semiconductor nanohybrids is still lacking. Here, we report a direct synthesis of colloidal gold nanoparticle/graphene quantum dot (Au@GQD) nanohybrids under ambient conditions using microplasmas and their application as photoabsorbers for broad band photodetectors (PDs). Due to the unique AuNP core and graphene shell nanostructures in the synthesized Au@GQD nanohybrids, the plasmonic absorption of the AuNP core extends the usable spectral range of the photodetectors. It is demonstrated that the Au@GQD-based visible light photodetector simultaneously possesses an extraordinary photoresponsivity of ∼103 A/W, ultrahigh detectivity of 1013 Jones, and fast response time in the millisecond scale (65 ms rise time and 53 ms fall time). We suggest that the synergistic effect can be attributed to the strong fluorescence quenching in Au@GQD coupled with the two-dimensional graphene layer in the device. This work provides knowledge of tailoring the optical absorption in GQDs with plasmonic AuNPs and the corresponding photophysics for broad band response in PD-related devices.

Graphene Sandwich Stable Perovskite Quantum-Dot Light-Emissive Ultrasensitive and Ultrafast Broadband Vertical Phototransistors.

Dual-functional devices that can simultaneously detect light and emit light have a tremendous appeal for multiple applications, including displays, sensors, defense, and high-speed optical communication. Despite the tremendous efforts of scientists, the progress of integration of a phototransistor, where the built-in electric field separates the photogenerated excitons, and a light-emitting diode, where the radiative recombination can be enhanced by band offset, into a single device remains a challenge. Combining the superior properties of perovskite quantum dots (PQDs) and graphene, here we report a light-emissive, ultrasensitive, ultrafast, and broadband vertical phototransistor that can simultaneously act as an efficient photodetector and light emitter within a single device. The estimated value of the external quantum efficiency of the vertical phototransistor is ∼1.2 × 1010% with a photoresponsivity of >109 A W-1 and a response time of <50 µs, which exceed all the presently reported vertical phototransistor devices. We also demonstrate that the modulation of the Dirac point of graphene efficiently tunes both amplitude and polarity of the photocurrent. The device exhibits a green emission having a quantum efficiency of 5.6%. The moisture-insensitive and environmentally stable, light-emissive, ultrafast, and ultrasensitive broadband phototransistor creates a useful route for dual-functional optoelectronic devices.

Gold coated Cicada wings: Anti-reflective micro-environment for plasmonic enhancement of fluorescence from upconversion nanoparticles.

We demonstrate that the upconversion nanoparticles (UCNPs) fluoresce 50 times more on a gold (Au) coated Cicada wing. UCNPs are attractive bioimaging, and therapeutic materials as it is excited in the infrared, limited only by the low fluorescence quantum yield. Here, a plasmonic effect, coupled with an anti-reflecting (AR) Cicada wing substrate coated with Au is demonstrated to enhance the fluorescence of the UCNPs. Silica (SiO2) coated Erbium doped green emitting core-shell UCNPs (NaYF4: Yb3+, Er3+@SiO2) show conventional metal enhanced fluorescence. The AR property of the Cicada wing (R ~0.2% @ 1000 nm) contributes >6-fold enhancement as compared to flat (silicon, and quartz) substrates (R~10-30% @ 1000 nm). Upon plasmon coupling, with an optimally sputtered Au coating, an unprecedented enhancement of >50-fold for the 520, and 655 nm emission was obtained on the Au coated Cicada wings, vis-à-vis planar uncoated (silicon, and quartz) substrates. The enhancement was also confirmed by direct fluorescence imaging of the photonic substrates used. The fluorescence lifetime of the core, and the core-shell UCNPs (~300 µs) decreased by ~30-40%, and 10-30%, respectively, when placed on Au coated substrates.

Ultrasensitive Gas Sensors Based on Vertical Graphene Nanowalls/SiC/Si Heterostructure.

Gas sensors, which play an important role in the safety of human life, cover a wide range of applications including intelligent systems and detection of harmful and toxic gases. It is known that graphene is an ideal and attractive candidate for gas sensing due to its high surface area and excellent mechanical, electrical, optical, and thermal properties. However, in order to fully realize its potential as a commercial gas sensor, demand for a graphene-based device of low-limit detection, high sensitivity, and fast response time needs to be met. Here, we demonstrate a metal/insulator/semiconductor (MIS) based gas sensor consisting of as-grown epitaxial graphene nanowalls (EGNWs)/silicon carbide (SiC)/silicon (Si) structure. The unique edge dominant three-dimensional (3D) EGNWs based MIS device achieved an extraordinarily low limit of detection (0.5 ppm) and unprecedented sensitivity (82 µA/ppm/cm2 for H2) with a fast response of shorter than 500 ms. These unique properties of our MIS device are attributed to the abundance of vertically oriented nanographitic edges and structural defects that act as extra-favorable adsorption sites and exhibit fast electron-transfer kinetics through the edges. Our experimental findings can pave the way for the realization of high-performance 3D graphene-based gas sensor devices.

Nanoscale Core-Shell Hyperbolic Structures for Ultralow Threshold Laser Action: An Efficient Platform for the Enhancement of Optical Manipulation.

Plasmonic material has emerged with multifunctionalities for its remarkable tailoring light emission, reshaping density of states (DOS), and focusing subwavelength light. However, restricted by its propagation loss and narrowband resonance in nature, it is a challenge for plasmonic material to provide a broadband DOS to advance its application. Here, we develop a novel nanoscale core-shell hyperbolic structure that possesses a remarkable coupling effect inside the multishell nanoscale composite owing to a higher DOS and a longer time of collective oscillations of the electrons than the plasmonic-based pure-metal nanoparticles. Subsequently, a giant localized electromagnetic wave of surface plasmon resonance is formed at the surface, causing pronounced out-coupling effect. Specifically, the nanoscale core-shell hyperbolic structure confines the energy well without being decayed, reducing the propagation loss and then achieving an unprecedented stimulated emission (random lasing action by dye molecule) with a record ultralow threshold (∼30 µJ/cm2). Besides, owing to the radial symmetry of the nanoscale core-shell hyperbolic structure, the excitation of high wavevector modes and induced additional DOS are easily accessible. We believe that the nanoscale core-shell hyperbolic structure paves a way to enlarge the development of plasmonic-based applications, such as high optoelectronic conversion efficiency of solar cells, great power extraction of light-emitting diodes, wide spectra photodetectors, carrying the emitter inside the core part as quantitative fluorescence microscopy and bioluminescence imaging system for in vivo and in vitro research on human body.

A Highly-Efficient Single Segment White Random Laser.

Production of multicolor or multiple wavelength lasers over the full visible-color spectrum from a single chip device has widespread applications, such as superbright solid-state lighting, color laser displays, light-based version of Wi-Fi (Li-Fi), and bioimaging, etc. However, designing such lasing devices remains a challenging issue owing to the material requirements for producing multicolor emissions and sophisticated design for producing laser action. Here we demonstrate a simple design and highly efficient single segment white random laser based on solution-processed NaYF4:Yb/Er/Tm@NaYF4:Eu core-shell nanoparticles assisted by Au/MoO3 multilayer hyperbolic meta-materials. The multicolor lasing emitted from core-shell nanoparticles covering the red, green, and blue, simultaneously, can be greatly enhanced by the high photonic density of states with a suitable design of hyperbolic meta-materials, which enables decreasing the energy consumption of photon propagation. As a result, the energy upconversion emission is enhanced by ∼50 times with a drastic reduction of the lasing threshold. The multiple scatterings arising from the inherent nature of the disordered nanoparticle matrix provide a convenient way for the formation of closed feedback loops, which is beneficial for the coherent laser action. The experimental results were supported by the electromagnetic simulations derived from the finite-difference time-domain (FDTD) method. The approach shown here can greatly simplify the design of laser structures with color-tunable emissions, which can be extended to many other material systems. Together with the characteristics of angle free laser action, our device provides a promising solution toward the realization of many laser-based practical applications.

Wrinkled 2D Materials: A Versatile Platform for Low-Threshold Stretchable Random Lasers.

A stretchable, flexible, and bendable random laser system capable of lasing in a wide range of spectrum will have many potential applications in next- generation technologies, such as visible-spectrum communication, superbright solid-state lighting, biomedical studies, fluorescence, etc. However, producing an appropriate cavity for such a wide spectral range remains a challenge owing to the rigidity of the resonator for the generation of coherent loops. 2D materials with wrinkled structures exhibit superior advantages of high stretchability and a suitable matrix for photon trapping in between the hill and valley geometries compared to their flat counterparts. Here, the intriguing functionalities of wrinkled reduced graphene oxide, single-layer graphene, and few-layer hexagonal boron nitride, respectively, are utilized to design highly stretchable and wearable random laser devices with ultralow threshold. Using methyl-ammonium lead bromide perovskite nanocrystals (PNC) to illustrate the working principle, the lasing threshold is found to be ≈10 µJ cm-2 , about two times less than the lowest value ever reported. In addition to PNC, it is demonstrated that the output lasing wavelength can be tuned using different active materials such as semiconductor quantum dots. Thus, this study is very useful for the future development of high-performance wearable optoelectronic devices.