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Boosting organic room-temperature phosphorescence performance through luminescence sensitization involving multi-step energy transfer.

The price of mammalian milk from different animal species varies greatly due to differences in their yield and nutritional value. Therefore, the authenticity of dairy products has become a hotspot issue in the market due to the replacement or partial admixture of high-cost milk with its low-cost analog. Herein, four common commercial varieties of milk, including goat milk, buffalo milk, Holstein cow milk, and Jersey cow milk, were successfully profiled and differentiated from each other by rapid evaporative ionization mass spectrometry (REIMS) combined with chemometric analysis. This method was developed as a real-time lipid fingerprinting technique. Moreover, the established chemometric algorithms based on multivariate statistical methods mainly involved principal component analysis, orthogonal partial least squares-discriminant analysis, and linear discriminant analysis as the screening and verifying tools to provide insights into the distinctive molecules constituting the four varieties of milk. The ions with

Understanding the dynamic process of epitaxial microstructure forming in laser additive manufacturing is very important for achieving products with a single crystalline texture. Here, we perform in situ, real-time synchrotron Laue diffraction experiments to capture the microstructural evolution of nickel-based single-crystal superalloys during the rapid laser remelting process. In situ synchrotron radiation Laue diffraction characterises the crystal rotation behaviour and stray grain formation process. With a complementary thermomechanical coupled finite element simulation and molecular dynamics simulation, we identify that the crystal rotation is governed by the localised heating/cooling heterogeneity-induced deformation gradient and recognise that the sub-grain rotation caused by rapid dislocation movement could be the origin of granular stray grains at the bottom of the melt pool.

A number of studies have focused on the effects of rare earth elements (REEs) on crop plants, while little attention has been paid on how tolerant plant species respond to increasing mixed REE concentrations. In this study, ramie (Boehmeria nivea L.) was exposed to a series of REE concentrations prepared with equimolar mixtures of 16 REEs (i.e. 0, 1.6, 8, 16, 80, 160, 400, 800 μmol/L) in order to explore REE accumulation and fractionation characteristics in ramie and the responses of this plant to mixed REEs. Results show that ramie root and shoot biomasses are unaffected under lower REE concentrations (1.6–80 μmol/L), while the growth of ramie and the uptake of nutrients especially Ca and Mn are largely inhibited under higher REE concentrations (160–800 μmol/L). The P and Mo concentrations in the roots increase with the increasing REE concentrations in the solution, suggestive of an involvement of P and Mo in dealing with the high concentrations of REEs in this plant. The preferential uptake of Ce and heavy REEs (HREEs) and the preferential transport of HREEs within the plant lead to a positive Ce anomaly and a HREE enrichment in ramie leaves. Our study suggests that ramie could be a good candidate for the phytoremediation of heavily REE-contaminated soils (e.g., REE mine tailings in southern China). Our results also shed light on points of taking into account phytoremediation management strategies of REE-contaminated soils (e.g., P and Mo fertilization).

Cadmium (Cd) is one of the most toxic heavy metal elements to the environment, which seriously threatens the safe production of food crops. In this study, we identified a novel function of the cytomembrane TaSFT2L protein in wheat (

A robust Zn(ii) MOF with good chemical and thermal stability, was prepared as an effective fluorescent probe for 2,4,6-trinitrophenol (TNP), levofloxacin (LVX) and l-cystine (l-Cys) with recyclability.

High-performance water-responsive OURTP polymers with simultaneously elongated lifetimes and improved efficiency were achieved by harmonizing cluster-triggered emission and conjugated luminance.

As a novel driving concept, the liquid metal motor (LMM) has been regarded as a promising actuator due to its unique traits, such as infinitely variable speed, lack of transmission chain, convenient maintenance, and silence. However, at present, driving devices based on this material are still in the preliminary and rudimentary stage, and representative application examples are scarce. Therefore, an 8-shaped tripodal wheeled mobile robot (WMR) completely driven by a LMM is designed in this study to further prove the practicability of this material. Through combining the Marangoni surface flow on a liquid metal droplet (LMD) caused by an electrochemical reaction and the eccentric torque generated by the change in droplet shape and position, the two independently driven wheels of the mobile robot are actuated at differential moving speeds. Additionally, a matching control module, a cell phone application, and a battery have been developed and added for wireless control of three types of driving functions (moving forward, steering, and stopping). It is expected that this work could further advance the development and application of LMMs and bring new ideas to the design of WMRs.

Silicon phthalocyanines as ternary additives are a promising way to increase the performance of organic photovoltaics. The miscibility of the additive and the donor polymer plays a significant role in the enhancement of the device performance, therefore, ternary additives can be designed to better interact with the conjugated polymer. We synthesized

The heart beating phenomenon of room temperature liquid metal (LM) mercury has attracted much attention in the past years, but its research and application are limited because of the low vapor pressure and high toxicity. Here, a fundamental scientific finding is reported that the non-toxic eutectic gallium indium (EGaIn) alloy droplets beat periodically at a certain frequency based on a floating electrode under the stimulation of the direct current (DC) field. The essential characteristics of heart beating are the displacement and the projected area change of the LM droplet. The mechanism of this phenomenon is the self-regulation of interfacial tension caused by chemical oxidation, chemical corrosion, and continuous electrowetting. In this article, a series of experiments are also carried out to examine the effects of different factors on the heartbeat, such as voltage, the volume of the droplet, the droplet immersion depth, the electrolyte solution concentration, the distance of electrodes, and the type of floating electrode. Finally, the heartbeat state and application boundary of the LM droplet under different conditions are summarized by imitating the human life process. The periodic changes of the LM droplet under an external DC electric field provide a new method to simulate the beating of the heart artificially, and can be applied to the research of organ chip fluid pumping in the future.

High-efficiency narrowband emission is always in the central role of organic optoelectronic display applications. However, the development of organic afterglow materials with sufficient color purity and high quantum efficiency for hyperafterglow is still great challenging due to the large structural relaxation and severe non-radiative decay of triplet excitons. Here we demonstrate a simple yet efficient strategy to achieve hyperafterglow emission through sensitizing and stabilizing isolated fluorescence chromophores by integrating multi-resonance fluorescence chromophores into afterglow host in a single-component copolymer. Bright multicolor hyperafterglow with maximum photoluminescent efficiencies of 88.9%, minimum full-width at half-maximums (FWHMs) of 38 nm and ultralong lifetimes of 1.64 s under ambient conditions are achieved. With this facilely designed polymer, a large-area hyperafterglow display panel was fabricated. By virtue of narrow emission band and high luminescent efficiency, the hyperafterglow presents a significant technological advance in developing highly efficient organic afterglow materials and extends the domain to new applications.

Rare earth elements (REEs) are critical for numerous modern technologies, and demand is increasing globally; however,production steps are resource-intensive and environmentally damaging.Some plant species are able to hyper accumulate REEs, and understanding the biology behind this phenomenon could play a pivotal role in developing more environmentally friendly REE recovery technologies. Here, we identified a REE transporter NRAMP REE Transporter 1 (NREET1)from the REE hyper accumulator fern Dicranopteris linearis. AlthoughNREET1 belongs to the natural resistance-associated macrophage protein(NRAMP) family, it shares a low similarity with other NRAMP members.When expressed in yeast, NREET1 exhibited REE transport capacity, but itcould not transport divalent metals, such as zinc, nickel, manganese, or iron.NREET1 is mainly expressed in D. linearis roots and predominantly localized in the plasma membrane. Expression studies in Arabidopsis thaliana revealed that NREET1 functions as a transporter mediating REE uptake and transfer from root cell walls into the cytoplasm. Moreover, NREET1 has a higher affinity for transporting light REEs compared to heavy REEs, which is consistent to the preferential enrichment of light REEs in field-grown D. linearis. We therefore conclude that NREET1 may play an important role in the uptake and consequently hyper accumulation of REEs in D.linearis. These findings lay the foundation for the use of synthetic biology techniques to design and produce sustainable, plant-based REE recovery systems.

Electrokinetic sample manipulation is a key step for many kinds of microfluidic chips to achieve various functions, such as particle focusing and separation, fluid pumping and material synthesis. But these microfluidic experiments usually rely on large-scale signal generators for power supply, microscopes for imaging and other instruments for analysis, which hampers the portable process of microfluidic technology. Inspired by this situation, we herein designed a portable general microfluidic device (PGMD) with complex electric field regulation functions, which can accurately regulate static or continuous fluid samples. Through the graphical user interface (GUI) and modular design, the PGMD can generate multiple different electrical signals, and the micro-flow of fluid can be pumped through the built-in micropump, which can meet the requirements of most microfluidic experiments. Photos or videos of the microfluidic chip captured by the built-in microscope are received and displayed by a smartphone. We carried out a variety of microfluidic experiments such as induced-charge electroosmosis (ICEO), particle beam exit switching, thermal buoyancy flow and dielectrophoresis (DEP) on the PGMD. In addition, the PGMD can perform rapid microalgae concentration estimation in an outdoor environment, which can be used to guide microalgae cultivation, further demonstrating the development potential of this device in the field of microbial applications. Numerous results show that the PGMD has a high degree of integration and strong reliability, which expands the application of microfluidic electrokinetic experiments and provides technical support for the integration and portability of microfluidic experimental devices.

The excellent motion performance of gallium-based liquid metals (LMs) upon the application of a modest electric field has provided a new opportunity for the development of autonomous soft robots. However, the locomotion of LMs often appears in an alkaline solution, which hampers the application under other different conditions. In this work, a novel robot arm is designed to transfer the motion of the LM from an alkaline solution in a synchronous drive mode. The liquid metal droplet (LMD) at the bottom of the robot arm is actuated using a DC voltage to provide the driving force for the system. By introducing an end effector at the center of the robot arm, the synchronous motion of the system is replicated and can be applied to different situations. The theoretical understanding of continuous electrowetting (CEW) at the LM interface is explained, and then the motion performance of the robot arm against the function of the applied voltage and driving direction is investigated. Moreover, several applications using this robot arm, such as pattern drawing, cargo transportation, and drug concentration detection, are demonstrated. The presented robot arm has the potential to observably expand the application fields of the LM.

This study aimed to investigate the therapeutic effect of black ginseng (BG) on non-alcoholic fatty liver disease (NAFLD) using network pharmacology combined with the molecular docking strategy. The saponin composition of BG was analyzed by liquid chromatography-mass spectrometry (LC/MS) instrument. Then the network pharmacology was applied to explore the potential targets and related mechanisms of BG in the treatment of NAFLD. After screening out key targets, molecular docking was used to predict the binding modes between ginsenoside and target. Finally, a methionine and choline deficiency (MCD) diet-induced NAFLD mice model was established to further confirm the therapeutic effect of BG on NAFLD. Twenty-four ginsenosides were annotated based on the MS and tandem MS information. Ten proteins were screened out as key targets closely related to BG treatment of NAFLD. The molecular docking showed that most of the ginsenosides had good binding affinities with AKT1. The validation experiment revealed that BG administration could reduce serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels and improve the MCD diet-induced histological changes in liver tissue. Moreover, BG could upregulate the phosphorylation level of AKT in the liver of NAFLD mice, thereby exerting the therapeutic effect on NAFLD. Further studies on the active ginsenosides as well as their synergistic action on NAFLD will be required to reveal the underlying mechanisms in-depth. This study demonstrates that network pharmacological prediction in conjunction with molecular docking is a viable technique for screening the active chemicals and related targets of BG, which can be applied to other herbal medicines.

The increasing demand for rare earth elements (REEs) motivates the development of novel strategies for cost-effective REE recovery from secondary sources, especially rare earth tailings. The biggest challenges in recovering REEs from ion-adsorption rare earth tailings are incomplete extraction of cerium (Ce) and the coleaching of iron (Fe) and manganese (Mn). Here, a synergistic process between reduction and stabilization was proposed by innovatively using elemental sulfur (S) as reductant for converting insoluble CeO2 into soluble Ce2(SO4)3 and transforming Fe and Mn oxides into inert FeFe2O4 and MnFe2O4 spinel minerals. After the calcination at 400 °C, 97.0% of Ce can be dissolved using a diluted sulfuric acid, along with only 3.67% of Fe and 23.3% of Mn leached out. Thermodynamic analysis reveals that CeO2 was indirectly reduced by the intermediates MnSO4 and FeS in the system. Density functional theory calculations indicated that Fe(II) and Mn(II) shared similar outer electron arrangements and coordination environments, favoring Mn(II) over Ce(III) as a replacement for Fe(II) in the FeO6 octahedral structure of FeFe2O4. Further investigation on the leaching process suggested that 0.5 mol L-1 H2SO4 is sufficient for the recovery of REEs (97.0%). This research provides a promising strategy to selectively recover REEs from mining tailings or secondary sources via controlling the mineral phase transformation.

While aerosol pH is among the most important parameters in atmospheric chemistry, it can be challenging to have a priori knowledge of the factors that are most strongly influencing the pH in a specific environment. In this study, we present a calculation method to more intuitively quantify the relationship between aerosol pH and its influencing factors, including gaseous NH3 concentration, particle properties, relative humidity, temperature, and nonvolatile cations, based on the NHx phase-partitioning equilibrium used in the E-AIM thermodynamic model. The applications of this calculation framework include (1) expressing the pH values directly as the function of influencing factors, (2) quantitatively studying the contribution of different factors to pH value changes, and (3) decomposing the standard deviation of pH values to find the dominant influencing factors on total pH fluctuations. This calculation framework provides a direct, quantitative, and intuitive approach to interpret pH values and differences. The relationship derived from pH and phase partitioning of semivolatile NHx can be extended to other phase-partitioning pairs as well. Our method provides a new way to quantitatively study pH and allows the pH studies conducted in different locations and meteorological conditions to be more easily compared and interpreted.

The outbreak of coronavirus disease 2019 (COVID-19) is a global health emergency. Various omics results have been reported for COVID-19, but the molecular hallmarks of COVID-19, especially in those patients without comorbidities, have not been fully investigated. Here we collect blood samples from 231 COVID-19 patients, prefiltered to exclude those with selected comorbidities, yet with symptoms ranging from asymptomatic to critically ill. Using integrative analysis of genomic, transcriptomic, proteomic, metabolomic and lipidomic profiles, we report a trans-omics landscape for COVID-19. Our analyses find neutrophils heterogeneity between asymptomatic and critically ill patients. Meanwhile, neutrophils over-activation, arginine depletion and tryptophan metabolites accumulation correlate with T cell dysfunction in critical patients. Our multi-omics data and characterization of peripheral blood from COVID-19 patients may thus help provide clues regarding pathophysiology of and potential therapeutic strategies for COVID-19., COVID-19 is a critical public health threat, but molecular characterizations of patients’ immunity is still lacking. Here the authors collected blood from patients with various disease severity, and prefiltered to exclude selected comorbidity, to obtain genomic, transcriptomic, proteomic, metabolomic and lipidomic profiles to report a trans-omics landscape.

Nitrogen oxides (NOx) play a key role in regulating the oxidizing capacity of the atmosphere through controlling the abundance of O3, OH, and other important gas and particle species. Some recent studies have suggested that particulate nitrate, which is conventionally considered as the ultimate oxidation product of NOx, can undergo "renoxification" via photolysis, recycling NOx and HONO back to the gas phase. However, there are large discrepancies in estimates of the importance of this channel, with reported renoxification rate constants spanning three orders of magnitude. In addition, previous laboratory studies derived the rate constant using bulk particle samples collected on substrates instead of suspended particles. In this work, we study renoxification of suspended submicron particulate sodium and ammonium nitrate through controlled laboratory photolysis experiments using an environmental chamber. We find that, under atmospherically relevant wavelengths and relative humidities, particulate inorganic nitrate releases NOx and HONO less than 10 times as rapidly as gaseous nitric acid, putting our measurements on the low end of recently reported renoxification rate constants. To the extent that our laboratory conditions are representative of the real atmosphere, renoxification from the photolysis of inorganic particulate nitrate appears to play a limited role in contributing to the NOx and OH budgets in remote environments. These results are based on simplified model systems; future studies should investigate renoxification of more complex aerosol mixtures that represent a broader spectrum of aerosol properties to better constrain the photolysis of ambient aerosols.

Continuous medium exchange within a microchannel represents a highly sought-after technique in functionalizing micro-objects with coating layers, enabling a myriad of applications ranging from biomedical engineering to materials science. Herein, we introduce a unique medium exchange approach, namely, tilted-angle dielectrophoresis, to accomplish layer-by-layer (LbL) coating on droplets in a wide microchannel. Pairs of adjacent tilted parallel electrodes arranged in a zigzag fashion are exploited to consecutively and repeatedly guide particles/droplets travelling through three parallel laminar streams comprising two reagents and a washing buffer. The performance of medium exchange is demonstrated using PS microparticles and oil droplets. We show that multi-cycle medium exchange, droplet transfer accompanied with purification, and multi-mode medium exchange around different micro-objects are achieved by conveniently regulating the applied voltage and the inlet flow rate, indicating a flexible, versatile and label-free alternative for characterizing and handling colloidal particles. Furthermore, LbL coating on droplets utilizing the presented strategy is implemented in the parallel coating-chemical and washing streams to obtain multiple layers of microcapsules. The linearly increasing fluorescence intensity of the coated droplets with each subsequent fluorescent coating demonstrates the capability of the tilted-angle dielectrophoretic medium exchanger for on-chip generation of LbL microcapsules on demand. The presented medium exchange strategy, together with its unique features of simple geometric configuration, facile control and multifunctionality, can provide a refined alternative for further expanding the utility scope in functional particles and cells.

An unprecedented [Mn18(CO3)9] inorganic core and [Mn20] metal–organic periphery composed the largest homometallic single-valence {MnII38} aggregate with a four-shells matryoshka doll that displays a significant magnetocaloric effect (MCE).

Gallium-based liquid metal droplets (LMDs) from micro-electromechanical systems (MEMS) have gained much attention due to their precise and sensitive controllability under an electric field. Considerable research progress has been made in the field of actuators by taking advantage of the continuous electrowetting (CEW) present within the solution. However, the motion generated is confined within the specific liquid environment and is lacking a way to transmit its motion outwardly, which undoubtedly serves as the greatest obstacle restricting any further development. Therefore, a driving module is proposed to generate rotational motion outside the solution for universality. Its performance can be easily tuned by adjusting the applied voltage. As an example of further application, the module is designed in the form of a pump that realizes the continuous/intermittent propulsion to mimic the veins/arteries of the human body without the problem in the previous LMD-based pumps. The feasibility of this pump in the on-chip in vitro analysis is proved by preparing a dynamic cell culture to simulate the movement of biofluids within human bodies. This study proposes an optional solution with an LMD-based motor for generating rotational motion and to expand current research on soft materials in actuators.

Using the pyridine–triazole based ligand of bis(3-(pyridin-2-yl)-1,2,4-triazol-5-yl)methane (H2L), two hexanuclear dysprosium(III) complexes, [Dy6(μ4-NO3)2 (OAc)6(L)4(DMF)2]·2NO3 (1) and [Dy6(μ3-OH)4(μ2-OH)2(OAc)4(L)4(EtOH)4]·2H2O (2), have been successfully obtained by hydrothermal reaction in different solvents. The crystal structure analysis reveals that the {Dy6} core in 1 is connected by two μ4-NO3− ions, whereas by four μ3-OH− and two μ2-OH− ions in 2. The HRESI-MS (high-resolution electrospray ionization mass spectrum) measurement of 1–2 was recorded. The presence of prominent peaks for the {Dy6} fragment in 1 (m/z, 1354–1380) at different ion-source voltages showed the higher solution stability and structural integrity of the {Dy6} cluster in 1, compared with that in 2. Temperature- and frequency-dependent alternating current (AC) susceptibility measurements of 1–2 in a zero direct current field display only a characteristic feature of single-molecule magnet (SMM) behavior for 2, indicating different magnetic behavior.

Design of high-performance red thermally activated delayed fluorescence (TADF) materials remains a great challenge owing to their small energy bandgaps with severe nonradiative decay for low luminous efficiency. Introducing rigid and fused moieties is an effective way to enhance the luminescence of red emitters, but the solubility is also significantly reduced, prohibiting inevitably their applications in solution-processed TADF organic light-emitting diodes (OLEDs). Herein, we propose an intermolecular locking strategy to improve both the solution processibility and photoluminescence efficiency of red TADF emitters by using a highly-soluble flexible difluoroboron β-diketonate unit with exposed and easily reachable fluorines that can form hydrogen bonds to induce strong intermolecular locking in the solid state for high luminescent efficiency. The thus designed emitters show excellent device performance in solution-processed TADF OLEDs with a low turn-on voltage of 4.4 V, red electroluminescence around 600 nm, a high external quantum efficiency up to 8.2% and a small efficiency roll-off of 9.0% at 1000 cd m−2, which are among the best results of solution-processed red OLEDs. These results demonstrate that the intermolecular locking strategy by directly addressing the internal conflicts between solubility and luminescent efficiency provides important clues in developing highly efficient and solution-processible red emitters for high-performance OLEDs.

Cell/particle concentration inside droplets holds great potential in extending lab-in-a-droplet applications, typically ranging from biological and chemical assays. Herein, we present a universal, massive and versatile technique, namely, alternating current electrothermal-flow field-effect transistor (ACET-FFET) to accomplish in-droplet cell/synthetic particle concentration on demand. Three parallel planar electrodes are utilized to generate an artificially reorderable electric field inside droplets by tuning the gate voltage through field-effect control, which results in a reshapable ACET-based microvortices pattern for in-droplet concentration. A downstream Y-shaped junction promotes the mother droplet splitting into two daughter droplets containing highly and poorly concentrated cells/particles, respectively. Fluorescent polystyrene (PS) nanoparticles are used to characterize the variations of ACET-microvortices flow pattern formation within droplets. Moreover, the concentration performance is demonstrated using PS microparticles and Neurospora crassa cells. We show that particles/cells can flexibly accumulate into any daughter droplet or be equally concentrated in both daughter droplets by conveniently regulating the gate voltage. The highly concentrated cells at the entrance of the concentrator show an instantaneous response performance to the external electric field. Further, online simultaneous particle synthesis and concentration inside droplets are proposed and implemented for the first time, demonstrated by efficient in-droplet micromixing and Prussian blue (PB) reaction. The accompanying synthetic PB particles are highly concentrated into either daughter droplet, thereby extending the versatility of the platform. The presented in-droplet concentration strategy, together with its unique features of simple geometric configuration, facile operation and broad applicability can broaden utility in droplet microfluidics.

High portability and miniaturization are two of the most important objectives pursued by microfluidic methods. However, there remain many challenges for the design of portable and visual microfluidic devices (

Organic ultralong room temperature phosphorescence (OURTP) materials having stimuli-responsive attributes have attracted great attention due to their great potential in a wide variety of advanced applications. It is of fundamental importance but challengeable to develop stimuli-responsive OURTP materials, especially such materials with modulated optoelectronic properties in a controlled manner probably due to the lack of an authentic construction approach. Here, we propose an effective strategy for OURTP materials with controllably regulated stimuli-responsive properties by engineering the resonance linkage between flexible chain and phosphor units. A quantitative parameter to demonstrate the stimuli-responsive capacity is also established by the responsivity rate constant. The designed OURTP materials demonstrate efficient photoactivated OURTP with lifetimes up to 724 ms and tunable responsivity rate constants ranging from 0.132 to 0.308 min

n-Butyl acetate is an important food additive commonly produced via concentrated sulfuric acid catalysis or immobilized lipase catalysis of butanol and acetic acid. Compared with chemical methods, ...

Multiple micromixing in a controlled sequence is an essential process for complex chemical synthesis of functional nanoparticles with desired physicochemical properties. Herein, we developed a uniq...

Harvesting solar energy for catalytic conversion of CO2 into valuable chemical fuels/feedstocks is an attractive yet challenging strategy to realize a sustainable carbon-cycle utilization. Homogene...

Purely organic materials showing room temperature phosphorescence (RTP) and ultralong RTP (OURTP) have recently attracted much attention. However, it is challenging to integrate circularly polarized luminescence (CPL) into RTP/OURTP. Here, we show a strategy to realize CPL-active OURTP (CP-OURTP) by binding an achiral phosphor group directly to the chiral center of an ester chain. Engineering of this flexible chiral chain enables efficient chirality transfer to carbazole aggregates, resulting in strong CP-OURTP with a lifetime of over 0.6 s and dissymmetry factor of 2.3×10-3 after the conformation regulation upon photo-activation. The realized CP-OURTP is thus stable at room temperature but can be deactivated quickly at 50 °C to CP-RTP with high CPL stability during the photo-activation/thermal-deactivation cycles. Based on this extraordinary photo/thermal-responsive and highly reversible CP-OURTP/RTP, a CPL-featured lifetime-encrypted combinational logic device has been successfully established.

The inferior stability of perovskite solar cells (PSCs) under ultraviolet (UV) irradiation has been a bottleneck for their further commercialization. Herein, we report a simple strategy to enhance the UV stability of PSCs by using an alkaloid 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) doped C60 electron transport layer (ETL). By improving the electron mobility of ETLs to 2 cm2 V−1 s−1 and optimizing the conduction band position to 4.2 eV, the DBU-doped C60 (DBU-C60) ETLs enable the rigid and flexible planner n-i-p PSCs to exhibit PCEs of 20% and 16%, respectively. Most importantly, the devices based on the DBU-C60 ETLs retain over 80% of their initial efficiency after storage either under UV irradiation for 336 h or light socking for 1000 h in an ambient environment. These results indicate that the optimized C60 is a promising electron transport material to stabilize the PSCs under UV light illumination without the cost of efficiency loss.

Here, we demonstrate use of a Mg2+-dependent, site-specific DNA enzyme (DNAzyme) to cleave oligos from polyacrylamide gel beads, which is suitable for use in drop-based assays. We show that cleavage efficiency is improved by use of a tandem-repeat cleavage site. We further demonstrate that DNAzyme-released oligos function as primers in reverse transcription of cell-released mRNA.

The rapid improvements in the performance of organic–inorganic perovskite solar cells have been astonishing but their commercialized production requires further achievements on device stability and efficiency. Herein, we introduce a bifunctional additive, biuret, with multiple Lewis base groups to regulate the crystallization process of perovskite crystals and passivate the defects at grain boundaries. Compared with the control, methylammonium lead iodide (MAPbI3), films processed with biuret exhibit increased grain size, reduced trap state density, and more uniform local photoluminescence. The addition of biuret leads to suppressed trap-assisted nonradiative recombination and an efficiency improvement from 18.26% to 21.16%, which is among the highest efficiency for MAPbI3 solar cells with the mesoscopic structure. Meanwhile, as biuret interacts with uncoordinated Pb2+ and iodide from the iodoplumbate complex on two adjacent perovskite grains, the thermal durability of the MAPbI3 film is enhanced due to the crosslink through chemical bonding. Under 85 °C annealing in nitrogen, the biuret-modified device retains 94% of its initial efficiency after 12 days while the control cells lose more than half the efficiency.

Circularly polarized organic afterglow (CPOA) with both long-lived room-temperature phosphorescence (RTP) and circularly polarized luminescence (CPL) is currently attracting great interest, but the development of multicolor-tunable CPOA in a single-component material remains a formidable challenge. Here, we report an efficient strategy to achieve multicolor CPOA molecules through chiral clusterization by implanting chirality center into non-conjugated organic cluster. Owing to excitation-dependent emission of clusters, highly efficient and significantly tuned CPOA emissions from blue to yellowish-green with dissymmetry factor over 2.3 × 10−3 and lifetime up to 587 ms are observed under different excitation wavelengths. With the distinguished color-tunable CPOA, the multicolor CPL displays and visual RTP detection of ultraviolent light wavelength are successfully constructed. These results not only provide a new paradigm for realization of multicolor-tunable CPOA materials in single-component molecular systems, but also offer new opportunities for expanding the applicability of CPL and RTP materials for diversified applications., Circularly polarized organic afterglow (CPOA) with both long-lived room-temperature phosphorescence and circularly polarized luminescence is attracting great interest, but the development of multicolor-tunable CPOA in a single-component material remains challenging. Here, the authors report a strategy to achieve multicolor CPOA through chiral clusterization by inserting a chirality center into a non-conjugated organic cluster.

Nonmetallic particles from waste-printed circuit boards are toxic pollutants due to their brominated flame-retardant content. Developing green technology for the disposal of nonmetallic particles i...