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The torque acting on cognate 'ternary complex' consisting of elongation factor-Tu, guanosine-5'-triphosphate GTP and aminoacyl-transfer RNA due to induced wrapping of the 30S subunit of the ribosome and the speed with which the ternary complex samples the space allowed by diffusion is analyzed. The magnesium binding sites are predicted in the ternary complex at low magnesium concentration and have disclosed the nature of the interaction energy of magnesium with site-specific tRNA bases.

High entropy oxides (HEOs) represent a class of solid solutions comprising multiple elements, offering significant scientific potential. Due to the enormous combination types of elements, the design of HEOs with desirable properties within high-dimensional composition spaces has traditionally relied heavily on knowledge and intuition. In this study, we present an active learning (AL) strategy tailored to efficiently explore the vast compositional space of HEOs. Our approach operates as a closed-loop system, iteratively cycling through "Training, Prediction, and Experiment" stages. Across multiple AL iterations, we have successfully identified four novel HEOs from a vast array of potential compositions. These newly discovered materials exhibit exceptional stability and demonstrate outstanding performance in H 2 evolution rate (251 μmol g cat -1 min -1 ) during the water-gas shift reaction, surpassing benchmarks set by established catalysts such as Pt/γ-Al 2 O 3 (135 μmol g cat -1 min -1 ) and Cu/ZnO/Al 2 O 3 (81 μmol g cat -1 min -1 ). X-ray photoelectron spectroscopy and density functional theory calculations revealed a loss of elemental identity in the selected HEOs. This catalyst discovery process underscores the efficacy of Machine Learning in accelerating the identification of HEOs with unique characteristics by effectively leveraging insights from limited experimental data.

Kiwifruit, renowned for its antioxidant properties and nutritional richness, faces challenges in maintaining quality during transportation, often leading to suboptimal products reaching the market. To address this issue, a wireless transmission flexible ethylene monitoring device (WFEMD) was developed. This device comprises a flexible ethylene gas sensor and a signal transmission processing unit integrated with electronic components, enabling real-time monitoring capabilities. In this study, the catalytic activity of Pd and Pd/Ti heterojunctions was leveraged to enhance the ethylene gas sensing. The impact of Ti 3 C 2 T x modified with varying masses of Pd nanoparticles on ethylene gas response levels was investigated. The signal transmission processing unit, fabricated by using the laser direct-writing method, was optimized to collect signals from the flexible ethylene gas sensor, convert them into corresponding ethylene concentrations, and transmit data via an antenna. By introducing a random forest (RF) classification algorithm, a remarkable 97.5% accuracy in predicting kiwifruit ripeness grades was achieved. The algorithm facilitated precise classification by collecting key parameters such as ethylene and CO 2 during transportation. The WFEMD enables real-time acquisition of kiwifruit ethylene gas information, which is transmitted wirelessly for data visualization and traceability via mobile terminals. This empowers managers with timely insights into ethylene emissions and ripeness predictions, facilitating informed decision-making processes.

The lattice parameter of platinum-based intermetallic compounds (IMCs), which correlates with the intrinsic activity of the oxygen reduction reaction (ORR), can be modulated by crystal phase engineering. However, the controlled preparation of IMCs with unconventional crystal structures remains highly challenging. Here, we demonstrate the synthesis of carbon-supported PtCu-based IMC catalysts with an unconventional L1 0 structure by a composition-regulated strategy. Experiment and machine learning reveal that the thermodynamically favorable structure changes from L1 1 to L1 0 when slight Cu atoms are substituted with Co. Benefiting from crystal-phase-induced strain enhancement, the prepared L1 0 -type PtCu 0.8 Co 0.2 catalyst exhibits much-enhanced mass and specific activities of 1.82 A mg Pt -1 and 3.27 mA cm Pt -2 , which are 1.91 and 1.73 times higher than those of the L1 1 -type PtCu catalyst, respectively. Our work highlights the important role of crystal phase in determining the surface strain of IMCs, and opens a promising avenue for the rational preparation of IMCs with different crystal phases by doping.

Organic materials have attracted extensive attention for potassium-ion batteries due to their flexible structure designability and environmental friendliness. However, organic materials generally suffer from unavoidable dissolution in aprotic electrolytes, causing an unsatisfactory electrochemical performance. Herein, we designed a weakly solvating electrolyte to boost the potassium storage performance of perylene-3,4,9,10-tetracarboxylic dianhydride (PTCDA). The electrolyte induces an in situ morphology evolution and achieves a nanowire structure. The weakly dissolving capability of ethylene glycol diethyl ether-based electrolyte and unique nanowire structure effectively avoid the dissolution of PTCDA. As a result, PTCDA shows excellent cycling stability (a capacity retention of 89.1% after 2000 cycles) and good rate performance (70.3 mAh g -1 at 50C). In addition, experimental detail discloses that the sulfonyl group plays a key role in inducing morphology evolution during the charge/discharge process. This work opens up new opportunities in electrolyte design for organic electrodes and illuminates further developments of potassium-ion batteries.

Twinning is an important deformation mode of face-centered-cubic (FCC) medium- and high-entropy alloys, especially under extreme loading conditions. However, the twinning mechanism in these alloys that have a low or even negative stacking fault energy remains debated. Here, we report atomic-scale in situ observations of the deformation process of a prototypical CrCoNi medium-entropy alloy under tension. We found that the parent FCC phase first transforms into a hexagonal close-packed (HCP) phase through Shockley partial dislocations slipping on the alternate {111} planes. Subsequently, the HCP phase rapidly changes to an FCC twin band. Such reversible phase transformation assisted twinning is greatly promoted by external tensile loads, as elucidated by geometric phase analysis. These results indicate the previously underestimated role of the metastable HCP phase in nanotwin nucleation and early plastic deformations of CrCoNi alloys and shed light on microstructure regulation of medium-entropy alloys with enhanced mechanical properties.

Plasmon-induced hot-electron transfer at the metallic nanoparticle/semiconductor interface is the basis of plasmon-enhanced photocatalysis and energy harvesting. However, limited by the nanoscale size of hot spots and femtosecond time scale of hot-electron transfer, direct observation is still challenging. Herein, by using spatiotemporal-resolved photoemission electron microscopy with a two-color pump-probe beamline, we directly observed such a process with a concise system, the Au nanoparticle/monolayer transition-metal dichalcogenide (TMD) interface. The ultrafast hot-electron transfer from Au nanoparticles to monolayer TMDs and the plasmon-enhanced transfer process were directly measured and verified through an in situ comparison with the Au film/TMD interface and free TMDs. The lifetime at the Au nanoparticle/MoSe 2 interface decreased from 410 to 42 fs, while the photoemission intensities exhibited a 27-fold increase compared to free MoSe 2 . We also measured the evolution of hot electrons in the energy distributions, indicating the hot-electron injection and decay happened in an ultrafast time scale of ∼50 fs without observable electron cooling.

Electrocatalytic carbon dioxide reduction reaction (CO 2 RR) toward value-added chemicals/fuels has offered a sustainable strategy to achieve a carbon-neutral energy cycle. However, it remains a great challenge to controllably and precisely regulate the coordination environment of active sites in catalysts for efficient generation of targeted products, especially the multicarbon (C 2+ ) products. Herein we report the coordination environment engineering of metal centers in coordination polymers for efficient electroreduction of CO 2 to C 2+ products under neutral conditions. Significantly, the Cu coordination polymer with Cu-N 2 S 2 coordination configuration (Cu-N-S) demonstrates superior Faradaic efficiencies of 61.2% and 82.2% for ethylene and C 2+ products, respectively, compared to the selective formic acid generation on an analogous polymer with the Cu-I 2 S 2 coordination mode (Cu-I-S). In situ studies reveal the balanced formation of atop and bridge *CO intermediates on Cu-N-S, promoting C-C coupling for C 2+ production. Theoretical calculations suggest that coordination environment engineering can induce electronic modulations in Cu active sites, where the d-band center of Cu is upshifted in Cu-N-S with stronger selectivity to the C 2+ products. Consequently, Cu-N-S displays a stronger reaction trend toward the generation of C 2+ products, while Cu-I-S favors the formation of formic acid due to the suppression of C-C couplings for C 2+ pathways with large energy barriers.

Correlating the microscopic structural characteristics with the macroscopic electrochemical performance in electrode materials is critical for developing excellent-performance lithium-ion batteries, which however remains largely unexplored. Here, we show that the Zn 2 SnO 4 (ZTO) nanowires (NWs) with smaller diameters ( d < 5 nm) exhibit slower capacity fade rate and better cycling stability, as compared with the NWs with larger diameters ranging from tens to hundreds of nanometers. By applying in situ transmission electron microscopy (TEM), we discover a strong correlation of cracking behavior with the NW diameter. Upon the first lithiation, there exists a critical diameter of ∼80 nm, below which the NWs neither crack nor fracture, and above which the cracks could easily nucleate and propagate along the specific planes, resulting in the deteriorated cycling stability in larger sized electrodes. Further theoretical calculations based on the finite element model and the climbing image nudged elastic band method faithfully predict the size-dependent cracking behaviors, which may result from the synergistic effect of axial stress evolution as well as preferential Li-ion migration directions during the first lithiation. This work provides a real-time tracking of the tempo-spatial structural evolution of a single ZTO NW, which facilitates a fundamental understanding of how the sample size affects the electrochemical behavior and thus offers a reference for future battery design and application strategy.

Although various oxidase mimetic or peroxidase (POD) mimetic nanozymes have been extensively studied, their poor substrate selectivity significantly inhibits their practical applications. Nanozymes with specific biomolecules as substrates, especially ascorbic acid oxidase (AAO) mimetic nanozymes with ascorbic acid (AA) as a substrate, have scarcely been studied. Herein, inspired by the multi-Cu atom sites and the redox electron transfer pathway of Cu 2+ /Cu + in the natural AAO, atomically dispersed Cu sites immobilized on N-doped porous carbon (Cu-N/C) are artificially designed to simulate the function of natural AAO. Compared with their natural counterparts, the Cu-N/C catalysts exhibited higher catalytic efficiency and superior stability. Combined theoretical calculation and experimental characterizations reveal that the Cu-N/C nanozymes could catalyze the AA oxidation through a 2e - oxygen reduction pathway with H 2 O 2 as the product. Moreover, the Cu-N/C nanozymes also possess high POD activity. As a proof-of-concept application, Cu-N/C can simultaneously realize AA detection in fluorescent mode based on its AAO activity and total antioxidant capacity detection in colorimetric mode utilizing its POD activity.

Layered oxides are widely accepted to be promising cathode candidate materials for K-ion batteries (KIBs) in terms of their rich raw materials and low price, while their further applications are restricted by sluggish kinetics and poor structural stability. Here, the high-entropy design concept is introduced into layered KIB cathodes to address the above issues, and an example of high-entropy layered K 0.45 Mn 0.60 Ni 0.075 Fe 0.075 Co 0.075 Ti 0.10 Cu 0.05 Mg 0.025 O 2 (HE-KMO) is successfully prepared. Benefiting from the high-entropy oxide with multielement doping, the developed HE-KMO exhibits half-metallic oxide features with a narrow bandgap of 0.19 eV. Increased entropy can also reduce the surface energy of the {010} active facets, resulting in about 2.6 times more exposure of the {010} active facets of HE-KMO than the low-entropy K 0.45 MnO 2 (KMO). Both can effectively improve the kinetics in terms of electron conduction and K + diffusion. Furthermore, high entropy can inhibit space charge ordering during K + (de)insertion, and the transition metal-oxygen covalent interaction of HE-KMO is also enhanced, leading to suppressed phase transition of HE-KMO in 1.5-4.2 V and better electrochemical stability of HE-KMO (average capacity drop of 0.20%, 200 cycles) than the low-entropy KMO (average capacity drop of 0.41%, 200 cycles) in the wide voltage window.

This study aims to investigate the effect and molecular mechanism of the interaction between circRNA circ&#95;0088300 and the RNA binding protein (RBP) BOLL on the growth and metastasis of gastric cancer. A prognostic risk model was established by screening differentially expressed RBP genes from the TCGA database, and BOLL was identified as a critical RBP. Gene Set Enrichment analysis (GSEA) showed that BOLL was associated with mitochondrial function. The upregulation fold change of circ&#95;0088300 was the highest in the GSE93541 data set, and the RPISeq database confirmed its binding relationship with BOLL. In vitro experiments showed that BOLL regulates mitochondrial metabolism and cancer cell function and circ&#95;0088300 upregulates the expression level of BOLL. In vivo experiments demonstrated that knocking down circ&#95;0088300 can inhibit tumor growth and metastasis, whereas overexpression of BOLL can reverse this effect. In conclusion, we have reached a preliminary conclusion that upregulation of BOLL by circ&#95;0088300 promotes gastric cancer growth and metastasis by promoting mitochondrial metabolic reprogramming.

In harsh environments, it is crucial to design personal protective materials that possess both puncture/cut resistance and chemical resistance. In order to fulfill these requirements, this study introduces an innovative approach that combines hydrophobically modified rigid nanoparticles with thermoplastic polyurethane elastomers. These materials are then laminated with high-performance aramid fabrics through a scraping process, resulting in a multifunctional composite with puncture/cut resistance, superhydrophobicity, self-cleaning properties, and acid/alkali resistance. The quasi-static puncture tests conducted reveal the remarkable performance of the composite. The maximum spike puncture resistance reaches 267.62 N, which is 17.14 times higher than that of the pure fabric (15.61 N). Similarly, the maximum knife puncture resistance reaches 115.02 N, exhibiting a 5.01 times increase compared to that of the pure aramid fabric (22.97 N). Furthermore, the results obtained from the yarn pull-out, fabric burst strength, and tearing experiments demonstrate that the incorporation of rigid nanoparticles significantly enhances the friction between the yarns, enabling a greater number of yarns to participate in the dissipation of impact energy. As a result, the puncture resistance of the fabric is greatly improved. Significantly, the composite exhibits sustained superhydrophobicity even after exposure to harsh chemicals such as concentrated sulfuric acid and sodium hydroxide as well as undergoing cyclic mechanical wear. These findings highlight the composite's exceptional durability and resistance to corrosion. Overall, this study offers insights and methods for the development of multifunctional flexible puncture-resistant equipment for individuals.

Redox flow batteries (RFBs) as promising technologies for energy storage have attracted burgeoning efforts and have achieved many advances in the past decades. However, for practical applications, the exploration of high-performance RFB systems is still of significance. In this work, inspired by the high solubility and low cost of both polysulfides and permanganates, the S/Mn RFBs with S 4 /S 2- /S 2 2- and MnO 4 - /MnO 4 as the redox-active molecule in the catholyte. The resulting S/Mn RFB cells show outstanding cell performance, such as high energy density (67.8 Wh L 2- as negative and positive redox pairs are demonstrated. Moreover, to solve the poor cycling performance caused by the sluggish kinetics of polysulfide-involved redox reactions and instability of the carbon felt (CF) electrode in the strong oxidative and corrosive catholyte, both the anode and cathode are designed to obtain high performance. Herein, the NiS x /Ni foam exhibiting electrocatalysis activity toward polysulfide ions is prepared and works as the anode while the graphene-modified carbon felt (G/CF) with high stability is fabricated and utilized as the cathode. Additionally, NaMnO 4 ). Moreover, a three-cell stack shows good cycling stability over 100 cycles (226.8 h) with high performance, verifying the good scalability of the proposed S/Mn RFB system. Therefore, the present strategy provides a reliable candidate for stable, energy-dense, and cost-effective devices for future energy storage applications.4 as the redox-active molecule in the catholyte. The resulting S/Mn RFB cells show outstanding cell performance, such as high energy density (67.8 Wh L -1 ), long cycling lifetime with a temporal capacity fade of 0.025% h -1 , and low chemical cost of electrolytes (17.31 $ kWh -1 ). Moreover, a three-cell stack shows good cycling stability over 100 cycles (226.8 h) with high performance, verifying the good scalability of the proposed S/Mn RFB system. Therefore, the present strategy provides a reliable candidate for stable, energy-dense, and cost-effective devices for future energy storage applications.

Hard carbons (HCs) have gained much attention for next-generation high energy density lithium-ion battery (LIB) anode candidates. However, voltage hysteresis, low rate capability, and large initial irreversible capacity severely affect their booming application. Herein, a general strategy is reported to fabricate heterogeneous atom (N/S/P/Se)-doped HC anodes with superb rate capability and cyclic stability based on a three-dimensional (3D) framework and a hierarchical porous structure. The obtained N-doped hard carbon (NHC) exhibits an excellent rate capability of 315 mA h g -1 at 10.0 A g -1 and a long-term cyclic stability of 90.3% capacity retention after 1000 cycles at 3 A g -1 . Moreover, the as-constructed pouch cell delivers a high energy density of 483.8 W h kg -1 and fast charging capability. The underlying mechanisms of lithium storage are illustrated by electrochemical kinetic analysis and theoretical calculations. It is demonstrated that heteroatom doping imposes significant effects on adsorption and diffusion for Li + . The versatile strategy in this work opens an avenue for rational design of advanced carbonaceous materials with high performance for LIB applications.

Identifying the impact of water on iodoplumbate complexes in various solutions is essential for linking the coordination environment of the perovskite precursor to its final perovskite solar cell (PSC) properties. In this study, we propose a digital twin approach based on X-ray absorption fine structure and molecular dynamic simulation to investigate the structure evolution of iodoplumbate complexes in precursor solutions as a function of storage time under a constant humidity environment. A full picture about what water does in the perovskite formation process is brought out, and the "making and breaking" role of water molecules is uncovered to link the structure of iodoplumbate complexes to its final properties. This study sheds light on a full picture about what water does in the perovskite formation process and the role of water, which will lead to developing water-involved strategies for consistent PSC fabrication under ambient conditions.

Single-molecule localization microscopy (SMLM) has been widely used in biological imaging due to its ultrahigh spatial resolution. However, due to the strategy of reducing photodamage to living cells, the fluorescence signals of emitters are usually weak and the detector noises become non-negligible, which leads to localization misalignments and signal losses, thus deteriorating the imaging capability of SMLM. Here, we propose an active modulation method to control the fluorescence of the probe emitters. It actually marks the emitters with artificial blinking character, which directly distinguishes weak signals from multiple detector noises. We demonstrated from simulations and experiments that this method improves the signal-to-noise ratio by about 10 dB over the non-modulated method and boosts the sensitivity of single-molecule localization down to -4 dB, which significantly reduces localization misalignments and signal losses in SMLM. This signal-noise decoupling strategy is generally applicable to the super-resolution system with versatile labeled probes to improve their imaging capability. We also showed its application to the densely labeled sample, showing its flexibility in super-resolution nanoscopy.

Rechargeable aqueous zinc (Zn) batteries are promising for large-energy storage because of their low cost, high safety, and environmental compatibility, but their implementation is hindered by the severe irreversibility of Zn metal anodes as exemplified by water-induced side reactions (H 2 evolution and Zn corrosion) and dendrite growth. Here, we find that the introduction of a hydrophobic carbonate cosolvent into a dilute aqueous electrolyte exhibits a much stronger ability to address the reversible issues facing Zn anodes than that with hydrophilic ones. Among the typical carbonates (ethylene carbonate, propylene carbonate, dimethyl carbonate, and diethyl carbonate (DEC)), DEC as the most hydrophobic additive enables the strongest breaking of water's H-bond network and replaces the solvating H 2 O in a Zn 2+ -solvation sheath, which significantly reduces the water activity and its decomposition. Additionally, DEC molecules preferentially adsorb onto the Zn surface to create an H 2 O-poor electrical double layer and render a dendrite-free Zn 2+ -plating behavior. The formulated hybrid 2 m Zn(OTf) 2 + 7 m DEC electrolyte endows the Zn electrode with an ability to achieve high cycling stability (over 3500 h at 5 mA cm -2 with 2.5 mA h cm -2 ) and supports the stable operation of Zn||V 2 O 5 · n H 2 O full battery. This efficient strategy with hydrophobic cosolvent suggests a promising direction for designing aqueous battery chemistries.

The identification of synergistic effect of Pt-based alloys on hydrogen evolution reaction (HER) requires a combination of experimental studies and theoretical calculations. Here, we present the construction of uniform PtCo nanoparticles grown on N-doped carbon frameworks via pyrolyzing Pt and Co ions adsorbed polyaniline, whereby the nanostructure of the nanoalloys can be effectively tuned by controlling the calcination temperature. As-prepared PtCo@NC-900 shows the optimal HER performance in 0.5 M H 2 SO 4 , resulting in a high mass activity of 4.31 A mg Pt -1 and excellent operation durability, which far exceeds that of commercial 20 wt % Pt/C (0.30 A mg Pt -1 ). Density functional theory calculations further reveal that the improved HER activity on PtCo(111) is originated from the strong electronic interaction between Pt and Co with favorable electron transfer, allowing for a more suitable binding strength for hydrogen (i.e., Δ G *H = -0.164 eV) compared with that of pristine Pt(111) (-0.287 eV).

Upconverting nanoparticles (UCNPs) are an emerging platform for mechanical force sensing at the nanometer scale. An outstanding challenge in realizing nanometer-scale mechano-sensitive UCNPs is maintaining a high mechanical force responsivity in conjunction with bright optical emission. This Letter reports mechano-sensing UCNPs based on the lanthanide dopants Yb 3+ and Er 3+ , which exhibit a strong ratiometric change in emission spectra and bright emission under applied pressure. We synthesize and analyze the pressure response of five different types of nanoparticles, including cubic NaYF 4 host nanoparticles and alkaline-earth host materials CaLuF, SrLuF, SrYbF, and BaLuF, all with lengths of 15 nm or less. By combining optical spectroscopy in a diamond anvil cell with single-particle brightness, we determine the noise equivalent sensitivity (GPa/√Hz) of these particles. The SrYb 0.72 Er 0.28 F@SrLuF particles exhibit an optimum noise equivalent sensitivity of 0.26 ± 0.04 GPa/√Hz. These particles present the possibility of robust nanometer-scale mechano-sensing.

First, a range of experiments using a stainless steel shallow plate in a thermostatic oscillator were carried out to simulate evaporation weathering of oil spills under different temperatures, wind velocities, oil film thicknesses, and wave conditions. The information on influencing factors of evaporation weathering could be obtained. Then, evaporation experiments of four oil samples with three emulsification states were conducted, and the effect of emulsification on evaporation of oil spills was investigated. The characteristics of each operation were described, mass loss characteristics of oil spills with time were plotted, and the effects of evaporative weathering processes under different conditions were quantitatively compared. A high-precision visualization system was utilized to simulate experimentally oil spill emulsification processes, and the effect of evaporative weathering on emulsification weathering of oil spills was investigated. The results of evaporation experiments showed that the increase of temperature could promote the evaporative weathering. The thin film thickness was beneficial to evaporation of oil spills. The increment of the wind speed could promote evaporation behavior when the wind velocity was small, but the increase of velocity had little effect on oil evaporation when the wind speed was large. Wave conditions had little effect on oil evaporation under the conditions of this experiment. The effect of different emulsification states on oil evaporation was not consistent. Unstable or semistable water-in-oil emulsions inhibited oil evaporation at the initial stage of evaporation, but water evaporation would increase oil-phase evaporation with the destruction of the emulsion structure. Stable water-in-oil emulsions inhibited evaporation weathering. The evaporation weathering of oil was conducive to the emulsification of oil., Competing Interests: The authors declare no competing financial interest., (© 2021 The Authors. Published by American Chemical Society.)

The self-assembly system of the rod-shaped tobacco mosaic virus (TMV) has been studied extensively for nanoscale applications. TMV coat protein assembly is modulated by intersubunit carboxylate groups whose electrostatic repulsion limits the assembly of virus rods without incorporating genomic RNA. To engineer assembly control into this system, we reprogrammed intersubunit carboxylate interactions to produce self-assembling coat proteins in the absence of RNA and in response to unique pH and ionic environmental conditions. Specifically, engineering a charge attraction at the intersubunit E50-D77 carboxylate group through a D77K substitution stabilized the coat proteins assembly into virus-like rods. In contrast, the reciprocal E50K modification alone did not confer virus-like rod assembly. However, a combination of R46G/E50K/E97G substitutions enabled virus-like rod assembly. Interestingly, the D77K substitution displays a unique pH-dependent assembly-disassembly profile, while the R46G/E50K/E97G substitutions confer a novel salt concentration dependency for assembly control. In addition, these unique environmentally controlled coat proteins allow for the directed assembly and disassembly of chimeric virus-like rods both in solution and on substrate-attached seed rods. Combined, these findings provide a controllable means to assemble functionally discrete virus-like rods for use in nanotechnology applications.

The global COVID-19 pandemic has changed many aspects of daily lives. Wearing personal protective equipment, especially respirators (face masks), has become common for both the public and medical professionals, proving to be effective in preventing spread of the virus. Nevertheless, a detailed understanding of respirator filtration-layer internal structures and their physical configurations is lacking. Here, we report three-dimensional (3D) internal analysis of N95 filtration layers via X-ray tomography. Using deep learning methods, we uncover how the distribution and diameters of fibers within these layers directly affect contaminant particle filtration. The average porosity of the filter layers is found to be 89.1%. Contaminants are more efficiently captured by denser fiber regions, with fibers <1.8 μm in diameter being particularly effective, presumably because of the stronger electric field gradient on smaller diameter fibers. This study provides critical information for further development of N95-type respirators that combine high efficiency with good breathability.

In March of 2020, the World Health Organization declared a pandemic of coronavirus disease 2019 (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The pandemic led to a shortage of N95-grade filtering facepiece respirators (FFRs), especially surgical-grade N95 FFRs for protection of healthcare professionals against airborne transmission of SARS-CoV-2. We and others have previously reported promising decontamination methods that may be applied to the recycling and reuse of FFRs. In this study we tested disinfection of three viruses, including SARS-CoV-2, dried on a piece of meltblown fabric, the principal component responsible for filtering of fine particles in N95-level FFRs, under a range of temperatures (60-95 °C) at ambient or 100% relative humidity (RH) in conjunction with filtration efficiency testing. We found that heat treatments of 75 °C for 30 min or 85 °C for 20 min at 100% RH resulted in efficient decontamination from the fabric of SARS-CoV-2, human coronavirus NL63 (HCoV-NL63), and another enveloped RNA virus, chikungunya virus vaccine strain 181/25 (CHIKV-181/25), without lowering the meltblown fabric's filtration efficiency.

Layered oxides acting as sodium hosts have attracted extensive attention due to their structural flexibility and large theoretical capacity. However, the diffusion of Na ions always presents sluggish kinetics due to the larger ionic radius sand mass of Na compared to Li. Herein, we report a P2-type layered cathode material, namely, Na 0.75 Ni 1/3 Ru 1/6 Mn 1/2 O 2 with superfast ion transport, where the Na + diffusion coefficient is calculated mainly in the region of 10 -10 to 10 -11 cm 2 s -1 during the charge and discharge process. The electrochemical tests also show that this cathode material exhibits a high capacity of 161.5 mAh g -1 , excellent rate performance (when the rate increases from 0.2C-10C, the capacity retention is 74%), and outstanding cyclic performance (maintaining 79.5% for 500 cycles even at a high rate of 10C). Our findings provide new insights for the design of the open framework for fast transport of Na and promote the high-power performance of sodium-ion batteries (SIBs).

The COVID-19 pandemic is currently causing a severe disruption and shortage in the global supply chain of necessary personal protective equipment (e.g., N95 respirators). The U.S. CDC has recommended use of household cloth by the general public to make cloth face coverings as a method of source control. We evaluated the filtration properties of natural and synthetic materials using a modified procedure for N95 respirator approval. Common fabrics of cotton, polyester, nylon, and silk had filtration efficiency of 5-25%, polypropylene spunbond had filtration efficiency 6-10%, and paper-based products had filtration efficiency of 10-20%. An advantage of polypropylene spunbond is that it can be simply triboelectrically charged to enhance the filtration efficiency (from 6 to >10%) without any increase in pressure (stable overnight and in humid environments). Using the filtration quality factor, fabric microstructure, and charging ability, we are able to provide an assessment of suggested fabric materials for homemade facial coverings.

Few studies have considered the effect of co-occurring heavy metals on plant accumulation of hydrophobic organic compounds (HOCs), and less is known about the role of intermolecular interactions. This study investigated the molecular mechanisms of Cu/Zn effects on hydroponic uptake of four deuterated polycyclic aromatic hydrocarbons (PAHs- d 10 ) by spinach ( Spinacia oleracea L.). Both solubility enhancement experiment and quantum mechanical calculations demonstrated the existence of [PAH-Cu(H 2 O) 0-4 ] 2+ and [2·PAH-Cu(H 2 O) 0-2 ] 2+ via cation-π interactions when Cu 2+ concentration was ≤100 μmol/L. Notably, PAH- d 10 concentrations in both roots and shoots increased significantly with Cu 2+ concentration. This was because the formation of phytoavailable PAH-Cu 2+ complexes decreased PAH- d 10 hydrophobicity and consequently decreased their sorption onto dissolved organic carbon (DOC, i.e., root exudates), thereby increasing phytoavailable concentrations and uptake of PAHs- d 10 . X-ray absorption near-edge structure analysis showed that PAH-Cu 2+ complexes could enter defective spinach roots via apoplastic pathway. However, Zn 2+ and PAHs- d 10 cannot form the cation-π interactions because of the high desolvation penalty of Zn 2+ . Actually, Zn 2+ decreased the spinach uptake of PAHs- d 10 due to the increase of DOC induced by Zn. This work provides molecular insights into how metals could selectively affect the plant uptake of HOCs and highlights the importance of considering the HOC phytoavailability with coexisting metals.

The coronavirus disease 2019 (COVID-19) pandemic has led to a major shortage of N95 respirators, which are essential for protecting healthcare professionals and the general public who may come into contact with the virus. Thus, it is essential to determine how we can reuse respirators and other personal protective equipment in these urgent times. We investigated multiple commonly used disinfection schemes on media with particle filtration efficiency of 95%. Heating was recently found to inactivate the virus in solution within 5 min at 70 °C and is among the most scalable, user-friendly methods for viral disinfection. We found that heat (≤85 °C) under various humidities (≤100% relative humidity, RH) was the most promising, nondestructive method for the preservation of filtration properties in meltblown fabrics as well as N95-grade respirators. At 85 °C, 30% RH, we were able to perform 50 cycles of heat treatment without significant changes in the filtration efficiency. At low humidity or dry conditions, temperatures up to 100 °C were not found to alter the filtration efficiency significantly within 20 cycles of treatment. Ultraviolet (UV) irradiation was a secondary choice, which was able to withstand 10 cycles of treatment and showed small degradation by 20 cycles. However, UV can potentially impact the material strength and subsequent sealing of respirators. Finally, treatments involving liquids and vapors require caution, as steam, alcohol, and household bleach all may lead to degradation of the filtration efficiency, leaving the user vulnerable to the viral aerosols.

Random lasing is a lasing phenomenon realized in random media, and it has attracted a great deal of attention in recent years. An essential requirement for strong random lasing is to achieve strong and recurrent scattering among grain boundaries of a disordered structure. Herein, we report a random laser (RL) based on individual polycrystalline GaTe microflakes (MFs) with a lasing threshold of 4.15 kW cm -2 , about 1-2 orders of magnitude lower than that of the reported single GaN microwire random laser. The strongly enhanced light scattering and trapping benefit from the reduced grain size in the polycrystalline GaTe MF, resulting in a ultralow threshold. We also investigate the dependence of spatially localized cavities' dimension on the pumping intensity profile and temperature. The findings provide a feasible route to realize RL with a low threshold and small size, opening up a new avenue in fulfilling many potential optoelectronic applications of RL.

Ingestible electronic systems that are capable of embedded sensing, particularly within the gastrointestinal (GI) tract and its accessory organs, have the potential to screen for diseases that are difficult if not impossible to detect at an early stage using other means. Furthermore, these devices have the potential to (1) reduce labor and facility costs for a variety of procedures, (2) promote research for discovering new biomarker targets for associated pathologies, (3) promote the development of autonomous or semiautonomous diagnostic aids for consumers, and (4) provide a foundation for epithelially targeted therapeutic interventions. These technological advances have the potential to make disease surveillance and treatment far more effective for a variety of conditions, allowing patients to lead longer and more productive lives. This review will examine the conventional techniques, as well as ingestible sensors and sensing systems that are currently under development for use in disease screening and diagnosis for GI disorders. Design considerations, fabrication, and applications will be discussed.

To discover the nonlinear optical (NLO) materials with strong second harmonic generation (SHG), the design of NLO-active molecular units with large polarization is considered as a common strategy. Herein, we propose that the local structural distortion induced with vacancies, apart from the NLO-active units, can be employed to improve the NLO effect in solids as well. Accordingly, a new tungsten bronze (TB) oxide, Pb 2 (Pb 0.15 Li 0.7 □ 0.15 )Nb 5 O 15 (□ representing vacancies), is successfully designed and prepared, which exhibits a strong SHG response of 39 times that of KH 2 PO 4 . The detailed analysis reveals that the local structural distortions enhanced by the vacancies in PLN strengthen the local dipole moments of neighboring NbO 6 octahedra, and thus significantly prompt the SHG effect. Moreover, a series of new TB compounds with large NLO effects are discovered by this molecular design strategy, which are perspectives for new NLO materials synthesis.

Instrument-free, portable, and direct read-out mini-devices have wider application prospects in various fields, especially for real-time/on-site sensing. Herein, combined with a paper strip, a smartphone sensing platform integrated with a UV lamp and dark cavity by 3D-printing technology has been developed for the rapid, sensitive, instrument-free, and visual quantitative analysis in real-time/on-site conditions. The platform proved the feasibility for visual quantitative detection of pesticide via a fluorescence "on-off-on" response with a single dual-emissive ratiometric paper strip. Red-emitting CdTe quantum dots (rQDs) were embedded into the silica nanoparticles (SiO 2 NPs) as an internal reference, while blue-emitting carbon dots (bCDs) as a signal report unit were covalently linked to the outer surface of SiO 2 NPs. The blue fluorescence could be quenched by gold nanoparticles (Au NPs) and then recovered with pesticide. The red (R), green (G), and blue (B) channel values of the generated images were determined by a color recognizer application (APP) installed in the smartphone, and the R/B values could be used for pesticide quantification with a sensitive detection limit (LOD) of 59 nM. The smartphone sensing platform based on 3D printing might provide a general strategy for visual quantitative detection in a variety of fields including environments, diagnosis, and safety monitoring.

Understanding the formation and evolution of bicontinuous nanoporous structure during dealloying has been one of the most challenging subjects of dealloying research. However, previous in situ investigations either suffer from insufficient spatial resolution (e.g., X-ray tomography) or lack morphology visualization and mass information (e.g., scanning tunneling microscopy). In this work, we report the kinetics of the whole course of dealloying by utilizing liquid-cell aberration-corrected scanning transmission electron microscopy. With Z -contrast imaging analysis, the in situ sub-nanoscale characterization reveals two new phenomena, an initial period of dealloying indicative of an initial length scale for bulk dealloying and a large volume shrinkage in a nanoscale alloy precursor. We explain the particle-size-dependent volume shrinkage with the formation of a dense shell and quantify the dependence with a simple geometric model. These insights into the mechanisms of dealloying will enable deliberate designs of nanoporous structures.

Flexible, stretchable, and wearable electrically conductive elements were prepared by coating partially oxidized liquid metals (POLMs) on cloth material, i.e., nylon lycra fabric (NLF, see details in the Supporting Information), which were achieved by filling POLMs in fiber networks. The products show good and stable electrically conductive properties upon strong twisting and stretching. A wearable electrical heating function is then demonstrated as a direct application. The infrared thermal images of the POLM conducting wires indicate that the distribution of POLMs in NLF is uniform. Time-dependent heating temperature versus different stretching demonstrates that the POLMs/NLF heating element is highly reliable and endurable. Moreover, the electrical resistance remains unchanged after 1000 cycles of bending and twisting. These characterization methods prove that POLMs can be applied to clothes and enable ultrathin, comfortable electronic applications.

Developing highly efficient non-precious-metal catalysts for electrochemical reduction reaction is vital for artificial nitrogen fixation under ambient conditions. Herein, we report a bioinspired Fe 3 C@C composite as an efficient electrocatalyst for nitrogen reduction. The composite based on a leaf skeleton successfully replicates the natural vein structure with multichannels. The Fe 3 C@C core-shell structure as the real active center contributes to selective electrocatalytic synthesis of ammonia from nitrogen with Faraday efficiency of 9.15% and production rate of 8.53 μg/(h mg cat ) or 12.80 μg/(h cm 2 ) at a low potential of -0.2 V versus reversible hydrogen electrode (vs RHE), which is better than that of recently reported carbon- and iron-based materials, even comparable with that of noble-metal-based catalyst. Experiments with density functional theory calculations reveal that graphene-encapsulated Fe 3 C nanoparticles can improve charge transfer due to core-shell interaction, beneficial for inducing active sites for N 2 adsorption and activation and thereby facilitate ammonia synthesis.

Upconverting nanoparticles provide valuable benefits as optical probes for bioimaging and Förster resonant energy transfer (FRET) due to their high signal-to-noise ratio, photostability, and biocompatibility; yet, making nanoparticles small yields a significant decay in brightness due to increased surface quenching. Approaches to improve the brightness of UCNPs exist but often require increased nanoparticle size. Here we present a unique core-shell-shell nanoparticle architecture for small (sub-20 nm), bright upconversion with several key features: (1) maximal sensitizer concentration in the core for high near-infrared absorption, (2) efficient energy transfer between core and interior shell for strong emission, and (3) emitter localization near the nanoparticle surface for efficient FRET. This architecture consists of β-NaYbF 4 (core) @NaY 0.8- x Er x Gd 0.2 F 4 (interior shell) @NaY 0.8 Gd 0.2 F 4 (exterior shell), where sensitizer and emitter ions are partitioned into core and interior shell, respectively. Emitter concentration is varied ( x = 1, 2, 5, 10, 20, 50, and 80%) to investigate influence on single particle brightness, upconversion quantum yield, decay lifetimes, and FRET coupling. We compare these seven samples with the field-standard core-shell architecture of β-NaY 0.58 Gd 0.2 Yb 0.2 Er 0.02 F 4 (core) @NaY 0.8 Gd 0.2 F 4 (shell), with sensitizer and emitter ions codoped in the core. At a single particle level, the core-shell-shell design was up to 2-fold brighter than the standard core-shell design. Further, by coupling a fluorescent dye to the surface of the two different architectures, we demonstrated up to 8-fold improved emission enhancement with the core-shell-shell compared to the core-shell design. We show how, given proper consideration for emitter concentration, we can design a unique nanoparticle architecture to yield comparable or improved brightness and FRET coupling within a small volume.

Milk contains a number of beneficial fatty acids including short and medium chain and unsaturated conjugated and nonconjugated fatty acids. In this study, microRNA sequencing of mammary tissue collected in early-, peak-, mid-, and late-lactation periods was performed to determine the miRNA expression profiles. miR-16a was one of the differentially expressed miRNA and was selected for in-depth functional studies pertaining to fatty acid metabolism. The mimic of miR-16a impaired fat metabolism [triacylglycerol (TAG) and cholesterol] while knock-down of miR-16a promoted fat metabolism in vitro in bovine mammary epithelial cells (BMECs). In addition, the in vitro work with BMECs also revealed that miR-16a had a negative effect on the cellular concentration of cis 9-C18:1, total C18:1, C20:1, and C22:1 and long-chain polyunsaturated fatty acids. Therefore, these data suggesting a negative effect on fatty acid metabolism extend the discovery of the key role of miR-16a in mediating adipocyte differentiation. Through a combination of bioinformatics analysis, target gene 3' UTR luciferase reporter assays, and western blotting, we identified large tumor suppressor kinase 1 ( LATS1 ) as a target of miR-16a. Transfection of siRNA- LATS1 into BMECs led to increases in TAG, cholesterol, and cellular fatty acid concentrations, suggesting a positive role of LATS1 in mammary cell fatty acid metabolism. In summary, data suggest that miR-16a regulates biological processes associated with intracellular TAG, cholesterol, and unsaturated fatty acid synthesis through LATS1 . These data provide a theoretical and experimental framework for further clarifying the regulation of lipid metabolism in mammary cells of dairy cows.

One-step single-spinneret electrospinning synthesis of 1D fibrous hierarchical structure can not only prevent the agglomeration or restacking of fibers or particles and enlarge surface active area but also promote the directional migration of electrons in materials and achieve effective regulation of resistances. Herein, tunable SnO 2 and SnO 2 /ZnO fibrous hierarchical structures with in situ growth of monodisperse spherical-like particles on surface provide a new sight for adjusting component distribution, surface absorption and chemical reaction, electronic transmission path, and electron transfer efficiency. Compared with SnO 2 porous fibers and SnO 2 hierarchical structures, the optimal SnO 2 /ZnO sensors exhibit superior gas-sensing response value of 366-100 ppm ethanol at 260 °C as well as excellent gas selectivity and long-term stability, in which the enhanced gas-sensing mechanism is primarily derived from multilevel effective heterojunctions with unique interface electronic effects. Especially, these SnO 2 -based sensors can achieve favorable linear relationship of the response and gas concentration for sensitive trace detection in cosmetics for the first time, providing a new strategy to design composite materials for quantitative analysis of volatiles in the cosmetics evaluation process.

With the great success of organic light-emitting diodes (OLEDs) based on thermal evaporation techniques, the development of printable materials for inkjet-printing high-performance OLEDs is particularly attractive yet challenging. In this paper, a set of printable Ir(III)-complexed polydendrimers, poly[bis[2-(2,4-difluorophenyl)-4-(4-((2-ethylhexyl)oxy)phenyl)pyridine][1-ethyl-5-phenyl-3-propyl-1 H -1,2,4-triazole] iridium(III)] ( PIr-D1 ) and poly[bis[2-(2,4-difluorophenyl)-4-(4-((2-ethylhexyl)oxy)-2,6-dimethylphenyl)pyridine][1-methyl-5-phenyl-3-propyl-1 H -1,2,4-triazole] iridium(III)] ( PIr-D2 ), were designed and synthesized via ring-opening metathesis polymerization (ROMP). As a comparison, the iridium precursor complexes bis[2-(2,4-difluorophenyl)-4-(4-((2-ethylhexyl)oxy)phenyl)pyridine][1-methyl-5-phenyl-3-propyl-1 H -1,2,4-triazole]iridium(III) ( Ir-D1 ) and bis[2-(2,4-difluorophenyl)-4-(4-((2-ethylhexyl)oxy)-2,6-dimethylphenyl)pyridine][1-methyl-5-phenyl-3-propyl-1 H -1,2,4-triazole] iridium(III) ( Ir-D2 ) and the core structure bis[2-(2,4-difluorophenyl)pyridine] [1-methyl-5-phenyl-3-propyl-1 H -1,2,4-triazole] iridium(III) ( Ir-D0 ) were also synthesized and the corresponding OLEDs were fabricated. Compared with the dendritic iridium complexes Ir-D1 and Ir-D2 , the resulting polydendrimers PIr-D2 and PIr-D2 showed enhanced film-forming properties, good thermal stability, and attractive ink rheological characteristics with a suitable viscosity for inkjet-printing. Promising device performance has been achieved for the resulting polydendrimers by both spin-coating and inkjet-printing, showing low driving voltages and relatively high current efficiencies and brightnesses. The results suggest that the construction of polydendritic Ir(III) complexes is an attractive design strategy for exploring efficient printable light-emitting materials for inkjet-printing high-performance OLEDs.

Multimodality imaging involves the use of more imaging modes to image the same living subjects and is now generally preferred in clinics for cancer imaging. Here we present multimodality-Magnetic Particle Imaging (MPI), Magnetic Resonance Imaging (MRI), Photoacoustic, Fluorescent-nanoparticles (termed MMPF NPs) for imaging tumor xenografts in living mice. MMPF NPs provide long-term (more than 2 months), dynamic, and accurate quantification, in vivo , of NPs and in real time by MPI. Moreover, MMPF NPs offer ultrasensitive MPI imaging of tumors (the tumor ROI increased by 30.6 times over that of preinjection). Moreover, the nanoparticle possessed a long-term blood circulation time (half-life at 49 h) and high tumor uptake (18% ID/g). MMPF NPs have been demonstrated for imaging breast and brain tumor xenografts in both subcutaneous and orthotopic models in mice via simultaneous MPI, MRI, fluorescence, and photoacoustic imaging with excellent tumor contrast to normal tissues.

Oxygen evolution reaction (OER) is a key step in many energy conversion and storage processes. Here, by rationally adding an appropriate amount of Mn into the lattice of a layered Na x CoO 2 parent oxide, high solubility of iron into the Na x CoO 2 oxide lattice is realized without the use of an extremely air-sensitive Na 2 O 2 raw material, and the synergy created between the Co and Fe can boost the catalytic activity of the layered oxide for OER. Moreover, the water intercalation capability of the layered oxides can be utilized to make the oxide resemble mixed metal hydroxides, which will also bring a beneficial effect for OER. As a result, the as-developed Na 0.67 Mn 0.5 Co 0.3 Fe 0.2 O 2 (CF-32) layered oxide with an optimal Co/Fe ratio and water intercalation shows high OER performance in alkaline media, overperforming the benchmark IrO 2 catalyst. In 0.1 M KOH solution, the novel catalyst shows 0.39 V overpotential at 10 mA cm -2 and favorable stability. The excellent OER performance of CF-32 is due to the synergistic effect of transition-metal elements (Co and Fe) and water intercalation, leading to little charge transfer resistance, large amounts of exposed catalytic active sites, plenty of surface high oxidation state O 2 2- /O - oxygen species, and hydroxide-rich surface. The facile synthesis and high OER performance of CF-32 enriches the non-noble metal family of OER catalysts and boosts the practical application of non-noble metal catalysts.

A simple, instrument-free, paper-based analytical device with dual-emission carbon dots (CDs) (blue CDs and red CDs) was developed for the semiquantitative, visual, and sensitive speciation analysis of lead ions in a real sample with a sensitive detection limit of 2.89 nM. When a paper strip was immersed into the sample solution, the blue fluorescence was quenched by Pb 2+ in solution, while the red fluorescence served as a background reference without color change, and significant color evolutions from blue to red were observed under the ultraviolet lamp, resulting in a semiquantitative visual detection. Furthermore, a smartphone was used in the visual detection of lead ions by identifying the RGB value of the fluorescent probe solution and corresponding paper strip. The application of smartphones and fluorescent paper strips has greatly shortened the detection time and reduced the cost of detection, providing a new strategy for the on-site and semiquantitative detection of heavy-metal ions in water samples.

Research on the mechanisms that regulate milk fat synthesis in dairy cows is essential to identify potential molecular targets that in the long term can help develop appropriate molecular breeding programs. Although some studies have revealed that microRNA (miRNA) affect lipid metabolism by targeting specific genes, joint analysis of miRNA and target mRNA data from bovine mammary tissue has revealed few clues regarding the underlying mechanisms controlling milk fat synthesis. The objective of the present study was to use high-throughput sequencing and bioinformatics analysis to identify miRNA and mRNA pairs and explore further their potential roles in regulating milk fat synthesis. A total of 233 pairs of negatively associated miRNA and mRNA pairs were detected. Among those, there were 162 pairs in which the miRNAs were down-regulated and the target mRNAs were up-regulated. Among the identified miRNA, miR-106b can bind the 3'-UTR of the ATP binding cassette subfamily A member 1 ( ABCA1), a gene previously identified as having a positive association with bovine milk fat synthesis. The overexpression of miR-106b in bovine mammary epithelial cells caused a decrease in triglyceride and cholesterol content while the inhibition of miR-106b increased triglyceride and cholesterol content, confirming its role in lipid metabolism. The present study allowed for the construction of a miR-106b- ABCA1 regulatory network map, thus providing a theoretical basis to target this gene in the molecular breeding of dairy cows.

Ovarian granulosa cell tumors (GCTs) are hormonally active cancers characterized by indolent growth and late, invasive relapse. No therapies have yet proven to be efficacious. We previously reported that the inhibition of the antiapoptotic X-linked inhibitor of apoptosis protein (XIAP) removes transrepression of the pro-proliferative nuclear receptor, peroxisome proliferator-activated receptor (PPAR)-γ, in a GCT-derived cell line, KGN. Both PPARγ and XIAP are overexpressed in human GCT. The inhibition of XIAP with the restoration of PPARγ signaling using a SMAC-mimetic (Compound A (CmpdA)) and rosiglitazone (RGZ)/retinoic acid (RA), respectively, reduced cell proliferation and induced apoptosis in the KGN cells. Utilizing stable isotope labeling with amino acids in cell culture, we identified 32 differentially expressed proteins in the KGN cells following the CmpdA/RGZ/RA-treatment, 22 of which were upregulated by ≥1.5 fold. Of these, stearoyl-CoA desaturase (SCD; 4.5-fold induction) was examined for putative binding sites for PPARγ using in silico screening. Chromatin immunoprecipitation confirmed the direct binding of PPARγ on the promoter region of SCD, with increased binding in the CmpdA/RGZ/RA-treated KGN cells. Because PPARγ plays a pivotal role in lipid and glucose metabolism, the upregulation of proteins associated with metabolic processes such as SCD is consistent with the restoration of PPARγ activity.

As a highly toxic heavy metal ion, divalent mercuric ion (Hg 2+ ) is one of the most widely diffused and hazardous environmental pollutants. In this work, a simple, portable, and inexpensive fiber-optic sensor based on surface plasmon resonance (SPR) effect was developed for Hg 2+ detection, which takes advantage of 4-mercaptopyridine (4-MPY)-functionalized Au nanoparticles (Au NPs/4-MPY) as a signal amplification tag. Based on the coordination between Hg 2+ and nitrogen in the pyridine moiety, we developed the sensor by self-assembling 4-MPY on Au film surfaces to capture Hg 2+ and then introducing Au NPs/4-MPY to generate a plasmonic coupling structure with the configuration of nanoparticle-on-mirror. The coupling between localized SPR increased changes in SPR wavelength, which allowed highly sensitive Hg 2+ sensing in aqueous solution. The sensor exhibited superior selectivity for Hg 2+ detection compared with other common metal ions in water. The sensor's Hg 2+ detection limit is 8 nM under optimal conditions. Furthermore, we validated the sensor's practicality for Hg 2+ detection in tap water samples and demonstrated its potential application for environmental water on-site monitoring.

Morphology-tunable C-N/SnO 2 -based hierarchical microspheres with good gas sensitivity for triethylamine (TEA) have been fabricated via facile electrospinning and a subsequent calcination process. The reaction temperature and modifying calcining technology played a dominant role for the morphological evolution from precursor fibers to microspherical shapes and the formation of C-N-decorated SnO 2 phase composition. C-N/SnO 2 /ZnO composites with tunable crystallinity, microstructure, and gas-sensing performance were strictly dependent on the added amount of Zn element. Fascinatingly, the constructed C-N/SnO 2 /ZnO/Au composites can not only precisely regulate the crystal size, dispersion status, loading position, and content of Au nanoparticles but also display excellent gas-sensing properties with ultrasensitivity and high selectivity under various temperature detections. The response of C-N/SnO 2 /ZnO/Au composites can reach up to approximately 1970, calculated to be 121.6 and 23.6 times for 50 ppm TEA molecules at optimal conditions compared with C-N/SnO 2 and C-N/SnO 2 /ZnO microspheres, respectively, actually representing the highest response value at high temperatures reported to date. The superior long-aging stability of sensing behaviors and phase structures can be also observed after 1 month. More importantly, novel C-N/SnO 2 /ZnO/Au sensors were employed for availably detecting low-concentration volatiles released from the storage procedure of fishes at 80 °C, indicating the practical application in chemical detectors and biosensors at low temperature. The novel gas-sensing mechanisms derived primarily from the combination of phase compositions, morphologies, and unique surface/interface transfer processes of C-N/SnO 2 /ZnO/Au composites are presented and investigated in detail, which will contribute to the design and development of other semiconductor-based composite sensors.