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As an essential part in the toolbox of super-resolution microscopy, stimulated emission depletion (STED) nanoscopy has been widely explored in revealing the substructure and bioactivities in fluorescence imaging. Among the applied STED fluorophores, silicon-substituted rhodamines (SiRs) belong to one of the most extensively employed fluorophores. The carboxy-SiR was favored in STED bioimaging with many advantages, including reliable photostability, cell permeability, tunable fluorogenicity, feasible structural decoration and so on. We reviewed the research of carboxy-SiR in the STED nanoscopy and hopefully this can inspire more efforts in the design and application of STED fluorophores.

The responses of Al/PTFE reactive materials (RMs) under shock compression were investigated by a single-stage gas gun. A 3D mesoscale-model was established based on micro-computed tomography (micro-CT) slice images and confirmed with experimental results. In the high-pressure stage, the composites reacted partially, whereas there were no deviations between the partially reacted Hugoniot and the inert simulation results. The simulation reveals that the Teflon matrix melting on the high shock pressure. Melts and decomposition of the PTFE accelerated the diffusion of the atoms. Thus, the reactions of the Al/PTFE composites are more like a combustion rather than a detonation.

We report the fabrication and measurement of an ab -plane Josephson junction created in an 80-nm thick thin-film-like exfoliated Bi $_{2}$ Sr $_{2}$ CaCu $_{2}$ O $_{8+x}$ single crystal flake. The junctions are formed using ion irradiation from a focused helium ion beam which locally converts the material from a superconductor to an insulator. Current-voltage characteristics show the device to be a weak link with I $_\text{C}$ R $_\text{N}$ product of 40 $\mu$ A. The critical current exhibits a well-behaved Fraunhofer pattern with magnetic field applied perpendicular to the film confirming the DC Josephson effect. Simulations reveal a large amount of ion straggle deep into the film which is likely influencing the electrical properties. Combination of these devices with the intrinsic junctions could provide a method for multi-dimensional Josephson devices.

Electron beam welding experiments of TZM alloy and 30CrMnSiA steel butt joints were carried out with different beam currents. Microstructures and chemical compositions of typical zones were analyzed by optical microscopy, scanning electron microscopy and X-ray diffraction. The mechanical properties of the joints were evaluated by tensile strength tests. Besides, nanoindentation tests were carried out to compare the brittleness of the reaction layer and other typical microstructures. The results illustrated that the reaction layer at the interface between fusion zone (FZ) and TZM alloy was the weak position of the joint, which was divided into Fe2Mo layer and a mixture layer of Fe2Mo and α-Fe phases. As the beam current increased, the thickness of the Fe2Mo layer decreased, which resulted in the increasing of the tensile strength of the joints. When the beam current exceeded 24 mA, the formation of the joint was poor with a low tensile strength. When the beam current was 24 mA, the joint presented the highest strength of 191.3 MPa and the joint fractured along the Fe2Mo layer near the TZM alloy side with a brittle fracture mode.

The promising photocatalytic conversion of CO2 into valuable fuel promotes the development of photocatalyst through various methods. In this work, TiO2 nanoparticle was composited with covalent porphyrin polymers (COP-Ps) to fabricate composite photocatalysts. The resultant COP-Ps/TiO2 composites by in situ hydrothermal method exhibit much improved photocatalytic activity for the conversion of CO2 into CO relative to two components, and it is attributable to improved charge transfer between two moieties led by strong interaction. Especially, TiO2 is composited more evenly with the sulfonated hollow COP-P (sh-COP-P). The resultant composite sh-COP-P/TiO2 performs best with a CO production rate of 5.70 μmol·g−1·h−1, which is approximately 20.4 times as high as that of pure TiO2 and 2.3 times of sh-COP-P polymer. For comparison, the simple physical mixture of sh-COP-P and TiO2 (sm-sh-COP-P/TiO2) was fabricated, and it performs more badly due to poor mixing uniformity. A Z-scheme photocatalytic mechanism was proposed for sh-COP-P/TiO2 composite on the basis of energy band analysis and hydroxyl radical test. This study provides a new in situ strategy to fabricate organic polymer/metal oxide composites of high photocatalytic activity for CO2 reduction.

The solid-state cultivation of Acaulium sp. H-JQSF isolated from Armadillidium vulgare produces acautalides A-C (1-3) as skeletally unprecedented Diels-Alder adducts of a 14-membered macrodiolide to an octadeca-9,11,13-trienoic acid. The acautalide structures, along with the intramolecular transesterifications of 1-acylglycerols, were elucidated by mass spectrometry, nuclear magnetic resonance, chemical transformation, and single-crystal X-ray diffraction. Compounds 1-3 were found to be neuroprotective with antiparkinsonic potential in the 1-methyl-4-phenylpyridinium-challenged nematode model, with the magnitude impacted by the glycerol esterification.

A styrene-butadiene-styrene triblock copolymer (SBS) was grafted with an unsaturated polar monomer (monomer A) composed of maleic anhydride (MAH) and methoxy polyethylene (MPEG) via a ring-opening reaction after epoxidizing styrene-butadiene-styrene triblock copolymer (ESBS). The microscopic changes of SBS before and after grafting has been characterized with Fourier transform infrared spectrum (FT-IR), X-ray photoelectron spectroscopy (XPS) and gel permeation chromatography (GPC). The results revealed that the monomer A was successfully grafted on SBS backbone, and the maximum graft ratio (GR) was 20.32%. To verify the compatibility between SBS and asphalt, solubility parameters and surface free energy (SFE) of SBS, grafted SBS and asphalt were measured. It was found that the solubility parameter and SFE of grafted SBS were closer to asphalt compared with SBS. It also has been confirmed from storage stability that the temperature susceptibility of grafted SBS modified asphalt was reduced in compare with SBS modified asphalt binder. As consequence, the use of grafted copolymer can be considered a suitable alternative for modification of asphalt binder in pavement.

We demonstrate a versatile nanoparticle with imaging-guided chemo-photothermal synergistic therapy and EpCAM-targeted delivery of liver tumor cells. EpCAM antibody (anti-EpCAM) and Pt(IV) were grafted onto the polydopamine carbon dots (PDA-CDs) by the amidation reaction. The EpCAM antibody of particles enables the targeted interaction with liver progenitor cells due to their overexpressed EpCAM protein. The tetravalent platinum prodrug [Pt(IV)] induces apoptosis with minimum toxic side effects through the interaction between cisplatin and tumor cell DNA. The nanoparticles displayed stable photothermal property and considerable anti-tumor therapeutic effect in vivo. Coupling with cellular imaging due to their fluorescence property, anti-EpCAM@PDA-CDs@Pt(IV) offers a convenient and effective platform for imaging-guided chemo-photothermal synergistic therapy toward liver cancers in the near future.

Two new cycloartane triterpenoids, (24 R)-cycloartane-3β,24,25,30-tetrol (1) and (24 R)-24,25,30-trihydroxy-9,19-cycloartane-3-one (2), along with three known compounds (3-5) were isolated from leaves and twigs of Aphanamixis polystachya. The new compounds were elucidated based on comprehensive spectroscopic analysis, including 1 D, 2 D NMR and HREIMS. The in vitro cytotoxic activities evaluation of five human cancer cell lines revealed that compound 1 exhibited cytotoxic activity on all of tested human cancer cell lines, while compound 2 only had specific activity on SMMC-7721 cell line.

Due to the poor permeability across Gram-negative bacterial membranes and the troublesome bacterial efflux mechanism, only a few GyrB/ParE inhibitors with potent activity against Gram-negative pathogens have been reported. Among them, pyrimido[4,5-b]indole derivatives represented by GP-1 demonstrated excellent broad-spectrum antibacterial activity against both Gram-positive and Gram-negative bacteria but were limited by hERG inhibition and poor pharmacokinetics profile. To improve their drug-like properties, we designed a series of novel pyrimido[4,5-b]indole derivatives based on the tricyclic scaffold of GP-1 and the C-7 moiety of acorafloxacin. These efforts have culminated in the discovery of a promising compound 18r with reduced hERG liability and an improved PK profile. Compound 18r exhibited superior broad-spectrum in vitro antibacterial activity compared to GP-1, including a variety of clinical multidrug G- pathogens, especially Acinetobacter baumannii, and the in vivo efficacy was also demonstrated in a neutropenic mouse thigh model of infection with multidrug-resistant A. baumannii.

The development of new techniques and materials that can separate ethylene from ethane is highly relevant in modern applications. Although adsorption-based separation techniques using metal-organic frameworks (MOFs) have gained increasing attention, the relatively low stability (especially water resistance) and unscalable synthesis of MOFs severely limit their application in real industrial scenarios. Addressing these challenges, we rationally designed and synthesized two new C2H6-selective MOF adsorbents (NKMOF-8-Br and -Me) with ultrahigh chemical and thermal stability, including water resistance. Attributed to the nonpolar/hydrophobic pore environments and appropriate pore apertures, the MOFs can capture C2 hydrocarbon gases at ambient conditions even in high humidity. The single-crystal structures of gas@NKMOF-8 realized the direct visualization of adsorption sites of the gases. Both the single-crystal data and simulated data elucidate the mechanism of selective adsorption. Moreover, the NKMOF-8 possesses high C2H6 adsorption capacity and high selectivity, allowing for efficient C2H6/C2H4 separation, as verified by experimental breakthrough tests. Most importantly, NKMOF-8-Br and -Me can be scalably synthesized through stirring at room temperature in minutes, which confers them with great potential for industrial application. This work offers new adsorbents that can address major chemical industrial challenges and provides an in-depth understanding of the gas binding sites in a visual manner.

A new porous copper-organic framework assembled from 12-nuclear [Cu12] nanocages {[Cu2(L4-)(H2O)2]·4DMA·2H2O}n (1) (H4L = 5,5'-(butane-1,4-diyl)-bis(oxy)-diisophthalic acid) was successfully prepared and structurally characterized. Compound 1 feathering of a 3D framework with two types of 1D nanotubular channels and a large specific surface area can effectively enrich various harmful dyes. Additionally, due to the carbon dioxide (CO2) interactions with open Cu(II) sites and the electron-rich ether oxygen atoms of ligand in 1, it exhibits a highly selective CO2 uptake. Interestingly, 1 can effectively catalyze the cycloaddition reaction of CO2 with various epoxides under mild conditions, which is ascribed to the Lewis acid Cu(II) sites in the framework of 1. Importantly, 1 acting as a heterogeneous catalyst can be recycled at least 10 times without an obvious loss of catalytic activity, and the CO2 cycloaddition mechanism was further uncovered by density functional theory (DFT) calculations. This study can greatly enrich the MOF catalysts system of CO2 conversion and also provide a valuable guidance for the design of efficient MOFs catalysts.

Forest management practices play an important role in regulating the soil water-holding capacity of plantation. However, most studies focus on soil water dynamics present during large-scale forest loss and afforestation events, while little is known about how soil water under different forest management practices responds to rainfall events and which factors mainly regulate soil water-holding capacity. In this study, a stable hydrogen isotope was used to explore the contribution of three natural rainfall events (8.9, 13.3 and 67.7 mm) to soil water (CRSW) in a Pinus massoniana plantation under four forest management practices (no thinning (NTN), understory removal (USR), light-intensity thinning (LIT) and heavy-intensity thinning (HIT)) in the Three Gorges Reservoir Area of the Yangtze River Basin in China. Furthermore, a structural equation model was employed to determine the effects of vegetation biomass and soil properties on the CRSW. The results showed that plantation soil under different forest management practices exhibited different water-holding capacities. Following light (8.9 mm) and moderate (13.3 mm) rainfall events, the CRSW in the HIT stand was slightly higher than that in the other stands. Following heavy (66.7 mm) rainfall event, the CRSW of most layers in USR stand was not different from the other three stands, while the CRSW in the LIT and NTN stands was significantly higher than that in the HIT stand in the 0–100 cm soil layers, suggesting that soil in the LIT and NTN stands had a greater water-holding capacity than that in the HIT stand. In addition, soil properties were the main factors directly affecting the CRSW, explaining 60% and 37% of the variation in the CRSW on the first and seventh days after heavy rainfall, respectively. Overall, compared to the HIT stand, the LIT and NTN stands showed greater capacity in retaining rainwater. Therefore, under expected global changes with frequent occurrences of extreme precipitation events, methods involving light-intensity and no thinning should be employed to build up soil and water conservation functions, which will be critical for keeping water-holding capacity and moderating floods.

A new intercalation-type anode material is reported herein to improve the lithium storage kinetics for high-rate lithium ion capacitors. The crystal structure of orthorhombic NaNbO3 indicates two possible tunnels for lithium ions insertion into NaNbO3 host along the and directions. Moreover, in situ XRD is conducted to investigate the lithium storage mechanism and structural evolution of the NaNbO3 anode, demonstrating its intercalation behavior through (101) and (141) planes. Furthermore, the rGO nanosheets are introduced to facilitate the charge transfer, which also effectively prevent the aggregation of NaNbO3 nanocubes. As expected, the NaNbO3/rGO nanocomposites possess remarkable reversible capacity (465 mA h g−1 at 0.1 A g−1), superior rate capability (325 mA h g−1 at 1.0 A g−1) and cycling stability, attributed to their synergistic effect and high Li+ diffusion coefficient DLi [D(NaNbO3/rGO)/D(NaNbO3) ≈ 31.54]. Remarkably, the NaNbO3/rGO-based LIC delivers a high energy density of 166.7 W h kg−1 at 112.4 W kg−1 and remains 24.1 W h kg−1 at an ultrahigh power density of 26621.2 W kg−1, with an outstanding cycling durability (90% retention over 3000 cycles at 1.0 A g−1). This study provides new insights on novel intercalation-type anode material to enrich the materials system of LICs. This work was supported by the Natural Science Foundation of Jiangsu Province (No. BK20170549), the National Natural Science Foundation of China (No. 21706103) and Postdoctoral Science Foundation of Jiangsu Province (No. 2019K295).

Photocatalytic selective oxidation of alcohols into high value-added carbonyl compounds accompanied by producing hydrogen peroxide (H2O2) is undoubtedly a more efficient solar energy conversion strategy with high atom economy. Herein, we have developed an efficient photocatalyst of bismuth-molybdate (Bi2MoO6) hierarchical hollow microspheres with tunable surface oxygen vacancies (OVs) for promoting the photocatalytic selective alcohol oxidation with H2O2 production. The effect of surface OVs on the photocatalytic efficiency is studied systematically by comparing the performance of different photocatalysts. The benzaldehyde and H2O2 production rates over the OV-rich Bi2MoO6 photocatalyst reach up to 1310 and 67.2 μmol g−1 h−1, respectively, which are 2.3 and 4.0 times those generated from the OV-poor Bi2MoO6 hollow microspheres. The roles of various active radicals in the photocatalytic reaction are probed by a series of controlled experiments and in situ ESR measurements, revealing that both superoxide radical (• O 2 - ) and carbon-centered radical are the key active intermediates. The introduction of surface OVs on Bi2MoO6 hollow microspheres accelerates the separation and transfer of photo-generated charge carriers as well as enhances the adsorption and activation of reactant molecules, thereby greatly promoting the photocatalytic selective oxidation of alcohols along with H2O2 production. This work not only demonstrates a facile strategy for the preparation of high-efficiency photocatalysts by simultaneous modulations of morphology and surface defects, but also offers insight into developing the dual-functional photocatalytic reactions for the full utilizations of photoinduced electrons and holes.

High-performance AlGaN/GaN lateral Schottky barrier diodes (SBDs) with recess structure and dual metal nitride anodes were demonstrated. With high work-function and nonrecess structure, a NiN anode enhances the breakdown voltage (BV), while a TiN anode reduces the turn-on voltage ( ${V}_{ \mathrm{\scriptscriptstyle ON}}$ ) due to its low work-function and contact to the two-dimensional electron gas (2DEG) layer directly on a recess structure. As the length of the NiN anode ( ${L}_{r}$ ) on the nonrecess region decreases from 75 to 3 $\mu \text{m}$ , ${V}_{ \mathrm{\scriptscriptstyle ON}}$ is reduced from 0.56 to 0.30 V, while the reverse leakage current slightly increases from ${3} \times {10}^{-{4}}$ to ${2} \times {10}^{-{3}}$ A/cm2 at the bias of −10 V. The lateral AlGaN/GaN SBD with a ${L}_{r}$ of 3 $\mu \text{m}$ at a distance of cathode–anode ( ${L}_{\text {AC}}$ ) of 20 $\mu \text{m}$ achieves a high BV of 1.62 kV, an ultralow ${V}_{ \mathrm{\scriptscriptstyle ON}}$ of 0.30 V and a small capacitance of 6.0 pF at zero bias with little degradation on ON-resistance, indicating superior potential application in high-frequency and high-power devices.

Anderson-type polyoxometalate containing Fe3+ and Mo6+, (NH4)3[H6Fe(III)Mo6O24] (FeMo6), was found to work as an oxidase-mimicking nanoenzyme for the first time, exhibiting the ability of catalytic oxidation of o-phenylenediamine (OPD), 2,2′-azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) (ABTs), and 3,3′,5,5′-tetramethylbenzidine (TMB), which features easy synthesis, low cost, simple operation, and low consumption. Attributed to the nature of FeMo6 and Fenton-like effect, a novel sensor based on two consecutive “turn on” fluorescence was developed for detecting dopamine (DA) by employing the FeMo6-OPD system, and the linear range was from 1 to 100 μM with the detection limit 0.0227 μM (3σ/s). Moreover, to increase oxidase-mimic activity of FeMo6, reduced graphene oxide (rGO) loading FeMo6 composites (FeMo6@rGO (n), n = 5%, 10%, 15%) was fabricated, and results show that oxidase-like activities of FeMo6@rGO (n) are dependent on the mass ratio of FeMo6/rGO, and FeMo6@rGO (10%) exhibits the highest oxidase-mimic activity and the fastest respond time (4 min) among all reported oxidase mimic of DA to date.

Effects of welding parameters on the microstructure and mechanical properties of Ti/Cu/Ni joint welded by electron beam were investigated. High welding heat input increased the melting quantity of Ti60 titanium alloy and promoted the formation of Ti–Cu intermetallic compounds (IMC) such as Ti2Cu and Ti3Cu4, increasing the brittleness of the joints. Low welding heat input was not conducive to the complete melting of the copper interlayer, and the unmelted copper reduced the performance of the joints. Under the optimal welding parameters, Ti–Ni IMCs in the weld would be replaced by (Cu, Ni) solid solutions ((Cu, Ni)ss). However, Ti–Cu IMC layers cannot be eliminated entirely by changing the welding parameters. The maximum tensile strength of the joints was 201 MPa. The fracture of the joints occurred at the Ti–Cu IMC layer, which was a typical brittle fracture.

Electrocatalytic N2 reduction is deemed as a prospective strategy toward low-carbon and environmentally friendly NH3 production under mild conditions, but its further application is still plagued by low NH3 yield and poor faradaic efficiency (FE). Thus, electrocatalysts endowing with high activity and satisfying selectivity are highly needed. Herein, Bi nanoparticles in situ confined in carbon rods (Bi NPs@CRs) are reported, which are fabricated via thermal annealing of a Bi-MOF precursor as a high-efficiency electrocatalyst for artificial NH3 synthesis with favorable selectivity. Such an electrocatalyst conducted in 0.1 M HCl achieves a high FE of 11.50% and a large NH3 yield of 20.80 μg h-1 mg-1cat. at -0.55 and -0.60 V versus reversible hydrogen electrode, respectively, which also possesses high electrochemical durability.

The importance of self-association and desolvation in the process of crystal nucleation is emphasized; the rearrangement of supramolecular structures also has a non-negligible effect on the nucleation kinetics., As the first step in the crystallization process, nucleation has been studied by many researchers. In this work, phenacetin (PHEN) was selected as a model compound to investigate the relationship between the solvent and nucleation kinetics. Induction times at different supersaturation in six solvents were measured. FTIR and NMR spectroscopy were employed to explore the solvent–solute interactions and the self-association properties in solution. Density functional theory (DFT) was adopted to evaluate the strength of solute–solvent interactions and the molecular conformations in different solvents. Based on these spectroscopy data, molecular simulation and nucleation kinetic results, a comprehensive understanding of the relationship between molecular structure, crystal structure, solution chemistry and nucleation dynamics is discussed. Both the solute–solvent interaction strength and the supramolecular structure formed by the self-association of solute molecules affect the nucleation rate. The findings reported here shed new light on the molecular mechanism of nucleation in solution.

Lactobacillus kefiranofaciens contains two types of β-galactosidase, LacLM and LacZ, belonging to different glycoside hydrolase families. The difference in function between them has been unclear so far for practical application. In this study, LacLM and LacZ from L. kefiranofaciens ATCC51647 were cloned into constitutive lactobacillal expression vector pMG36e, respectively. Furtherly, pMG36n-lacs was constructed from pMG36e-lacs by replacing erythromycin with nisin as selective marker for food-grade expressing systems in Lactobacillus plantarum WCFS1, designated recombinant LacLM and LacZ respectively. The results from hydrolysis of o-nitrophenyl-β-galactopyranoside (ONPG) showed that the β-galactosidases activity of the recombinant LacLM and LacZ was 1460% and 670% higher than that of the original L. kefiranofaciens. Moreover, the lactose hydrolytic activity of recombinant LacLM was higher than that of LacZ in milk. Nevertheless, compare to LacZ, in 25% lactose solution the galacto-oligosaccharides (GOS) production of recombinant LacLM was lower. Therefore, two β-galactopyranosides could play different roles in carbohydrate metabolism of L. kefiranofaciens. In addition, maximal growths rate of two recombinant strains were evaluated with different temperature level and nisin concentration in fermentations assay for practical purpose. The results displayed that 37 °C and 20-40 U/ mL nisin were the optimal fermentation conditions for the growth of recombinant β-galactosidase strains. Altogether the food-grade Expression system of recombinant β-galactosidase was feasible for applications in the food and dairy industry.

A series of Ag/Au clusters have been synthesized by reacting the π-acidic cyclic trinuclear Ag(I) pyrazolate and its Au(I) analogue with 3-substituted phenylacetylene. Single-crystal X-ray studies ...

Both afterglow-catalysis and photoluminescence (PL) self-reporting of pollutant degradation are achieved by persistent luminescent ethylenediaminetetraacetic acid disodium (EDTA)-etched Cr3+-doped ...

Water-bearing porous rocks can be greatly strengthened by freezing; its microscopic mechanisms lie in how subzero temperature modifies pore structure but have not yet been clearly defined. In this study, we link the mechanical properties of frozen sandstone to phase composition of pore water (i.e., relative amount of unfrozen water and ice). Both the strength (uniaxial compressive strength and tensile strength) and the phase composition of pore water (tested through the nuclear magnetic resonance (NMR) method) of frozen sandstone at nine subzero temperatures were measured. The results showed the following: (1) subzero temperature strengthened saturated sandstone significantly, both the strengths increased in a three-stage mode and each stage showed an approximately linear trend as temperature decreased from 0 to – 20 °C; and (2) change of phase composition with freezing displayed two distinct stages: the rapid decreasing stage of unfrozen water content (0 to – 4 °C), when bulk water and capillary water froze almost completely, and the slow decreasing stage (− 4 to – 20 °C), when adsorbed water froze partially. Based on direct observations on microscopic pore structure of sandstone and detailed discussion on the mechanical interactions between water, ice, and pore wall, phase composition may modify the mechanical properties of frozen rocks through the following effects: the supporting effect of ice under compression, the crack-filling effect of ice, the cementing effect of unfrozen water film under tension or under shearing load, and the frost damage effect. The former three are strengthening effects, while the latter one is weakening effect.

The utilization of thermal energy from different sources is an important development direction for conserving energy. With the development of technology, refined and rapid utilization of thermal energy is required. Traditional thermal conductive materials cannot meet the growing needs of human beings. Therefore, people pay attention to two-dimensional graphene film materials for their thermal conductivity. This review collects current modeling group of thermal transport on graphene, including non-equilibrium Green function (NEGF) theory, molecular dynamics (MD) simulations modeling and Boltzmann transport equation method. These models can well explain several phenomena of phonon transport in graphene. Further, structural defects were discussed and expounded the effect for graphene thermal conductivity, including doping, grain boundary and defects. Deeply understanding of defects on graphene, we can better grasp the thermal conductivity of graphene from the microscopic point of view.

Recently, lightweight has gradually become the most concerned property for a practical microwave absorber in the frequency range of 2–18 GHz. In this work, using commercial carbon fiber (CF) as matrix, the hybrid nanocomposites constructed by CF core, polyaniline (PANI) coating and dispersed Fe3O4 nanoparticles (NPs) were successfully synthesized by the electrodeposition and subsequent hydrothermal process. The systematic characterization results revealed that both PANI and Fe3O4 exerted positive roles in enhancing the microwave absorption properties of bare CF. Under the combined action of various components, the desired products (CF@PANI@Fe3O4 hybrid nanocomposites) exhibited remarkable microwave absorption performances, and the minimal reflection loss (RL) was −46.86 dB at a filler content of 10 wt% and a matching thickness of 2.7 mm. Moreover, a synergistic mechanism was proposed according to multiple reflection/scattering, dipole polarization, interface polarization, eddy current and magnetic resonance, so as to demonstrate the multi-attenuation approaches of the incident electromagnetic wave.

PurposeThis study focused on how to realize automatic recognition of young women's neck-shoulder shape based on the front and side images.Design/methodology/approachThe reverse engineering software was used to measure the body sizes of the neck-shoulder part based on the young women's three-dimensional (3D) point cloud data, and the important parameters closely related to the neck-shoulder shape were determined. The neck-shoulder shape of the subjects was classified to establish the classification rules. Then, based on the front and side images, the human body contour was extracted by Matlab, and the data required for neck-shoulder shape classification were obtained by identifying the feature points.FindingsThrough the cluster analysis based on the shoulder angle, back angle, shoulder depth/width ratio and armpit depth/width ratio, young women's neck-shoulder shape was divided into four categories, namely round wide shoulder, flat narrow shoulder, round drop shoulder and hunchback flat shoulder. The neck-shoulder shape could be automatically recognized based on the established classification rules and two-dimensional (2D) body measurement method, with an accuracy rate of 90%. The neck-shoulder shape automatic recognition system constructed based on this method is effective.Originality/valueThis study proposed a simple neck-shoulder automatic recognition method based on the 2D body images. This approach can be extended to other group of human body or other parts of the body.

Zn-ion energy storage devices employing hydrogel electrolytes are considered as promising candidates for flexible and wearable electronics applications. This is because of their safe nature, low cost, and good mechanical characteristics. However, conventional hydrogel electrolytes face limitation at subzero temperatures. Herein, we report an antifreezing, safe, and nontoxic gel electrolyte based on the poly(vinyl alcohol) (PVA)/Zn/ethylene glycol system. The optimal gel electrolyte membrane exhibits a high ionic conductivity (15.03 mS cm-1 at room temperature) and promising antifreezing performance (9.05 mS cm-1 at -20 °C and 3.53 mS cm-1 at -40 °C). Moreover, the antifreezing gel electrolyte can suppress the growth of Zn dendrites to display a uniform Zn plating/stripping behavior. Also, a flexible antifreezing Zn-ion hybrid supercapacitor fabricated with the optimum antifreezing gel electrolyte membrane exhibits excellent electrochemical properties. The supercapacitor possesses a high specific capacity of 247.7 F g-1 at room temperature under a high working voltage of 2 V. It also displays an outstanding cyclic stability at room temperature. Moreover, the supercapacitor shows an extraordinary electrochemical behavior and cyclic stability over up to 30 000 cycles at -20 °C under a current load of 5 A g-1, demonstrating its outstanding low-temperature electrochemical performance. Besides, the antifreezing supercapacitor device also offers high flexibility under different deformation conditions. Therefore, it is believed that this work provides a simplistic method of realizing the application of flexible antifreezing Zn-ion energy storage devices in a subzero-temperature environment.

The establishment of a heterojunction is a crucial strategy to design highly effective nonnoble metal nanocatalysts for the photocatalytic nitrogen reduction reaction (PNRR). Heteropoly blues (r-POMs) can act as electron-transfer mediators in PNRR, but its agglomeration limits the further promotion of PNRR productivity. In this work, we construct a protonation-modified surface of N-vacancy

Crystal growth, which is one of the fundamental steps in the crystallization process, can affect the morphology of crystals which will further affect physicochemical properties of products and down...

Development of tunable-emission solid fluorescent materials remains a challenge due to tedious synthesis strategies. Polymorphism plays a critical role in tuning solid state photophysical propertie...

Nitrated aromatic compounds (NACs) are a group of key chromophores for brown carbon (light-absorbing organic carbon, i.e., BrC) aerosol, which affects radiative forcing. The chemical composition and sources of NACs and their contributions to BrC absorption, however, are still not well understood. In this study, PM 2.5 -bound NACs in Xi'an, Northwest China, were investigated for 112 daily PM 2.5 filter samples from 2015 to 2016. Both the total concentrations and contributions from individual species of NACs show distinct seasonal variations. The seasonally averaged concentrations of NACs are 2.1 (spring), 1.1 (summer), 12.9 (fall), and 56 ng m −3 (winter). Thereinto, 4-nitrophenol is the major NAC component in spring (58 %). The concentrations of 5-nitrosalicylic acid and 4-nitrophenol dominate in summer (70 %), and the concentrations of 4-nitrocatechol and 4-nitrophenol dominate in fall (58 %) and winter (55 %). The NAC species show different seasonal patterns in concentrations, indicating differences in emissions and formation pathways. Source apportionment results using positive matrix factorization (PMF) further show large seasonal differences in the sources of NACs. Specifically, in summer, NACs were highly influenced by secondary formation and vehicle emissions ( ∼ 80 %), while in winter, biomass burning and coal combustion contributed the most ( ∼ 75 %). Furthermore, the light absorption contributions of NACs to BrC are wavelength-dependent and vary greatly by season, with maximum contributions at ∼ 330 nm in winter and fall and ∼ 320 nm in summer and spring. The differences in the contribution to light absorption are associated with the higher mass fractions of 4-nitrocatechol ( λ max⁡ = 345 nm) and 4-nitrophenol ( λ max⁡ = 310 nm) in fall and winter, 4-nitrophenol in spring, and 5-nitrosalicylic acid ( λ max⁡ = 315 nm) and 4-nitrophenol in summer. The mean contributions of NACs to BrC light absorption at a wavelength of 365 nm in different seasons are 0.14 % (spring), 0.09 % (summer), 0.36 % (fall), and 0.91 % (winter), which are about 6–9 times higher than their mass fractional contributions of carbon in total organic carbon. Our results indicate that the composition and sources of NACs have profound impacts on the BrC light absorption.

Conversion of syngas into aromatics via the Fischer–Tropsch (FT) route provides a promising way to supply the value-added chemicals. However, it is still a great challenge to achieve controllable a...

Understanding the presence and dynamics of chemical pollutants in individual cells is fundamentally important for their trafficking, fate, and toxicity in humans. The presence of molecular components (i.e., proteins and mRNA) in individual cells of higher organisms is considered a stochastic event. The characteristics of chemical pollutants, as extrinsic compounds, in subpopulation of human cells on single-cell basis have not been explored yet. Here, we demonstrated the lead (Pb) content in individual mature erythrocytes (m-erythrocytes) of Pb-intoxicated patients, and healthy subjects exhibited a unified pattern in probability distribution (gamma distribution) and dynamics, despite being highly heterogeneous. The Pb content in individual m-erythrocytes decreased with the lifetime of m-erythrocytes. Meanwhile, the distribution and dynamics were found to be highly related to the Pb content in m-erythrocytes and was independent of patients and their status. This is the first study to analyze the distribution pattern of chemical pollutants at a single-cell level in higher organisms. This study sheds light on the molecular mechanism of Pb trafficking and fate in humans and the search for an efficient strategy to improve Pb excretion during Pb treatment.

AlGaN/gallium nitride (GaN) ion-sensitive field-effect transistors (ISFETs) were fabricated as pH sensors. The sensitivity of the AlGaN/GaN ISFETs was evolved with gate recess process and ammonium hydroxide (NH4OH) treatment. By performing the gate recess process, the threshold voltage ( ${V}_{\text {T}}$ ) of the ISFET increased from −3.33 to −0.31 V and the maximum conductance ( ${G}_{\text {M}}$ ) of the ISFET increased from 0.8 to 2 mS, with the current sensitivity of the pH sensor improving from 52.25 to $78.86~\mu \text{A}$ /pH. Further, after performing the ammonium hydroxide treatment, the ${V}_{\text {T}}$ of the ISFET increased from −0.33 to −0.14 V, with the current sensitivity of the pH sensor improving from 78.86 to $84.39~\mu \text{A}$ /pH. To characterize the surface conditions the X-ray photoelectron spectroscopy (XPS) was deployed. The results indicated that many nitrogen vacancies ( ${V}_{\text {N}}$ ) were introduced during the recess process, leading to a negative ${V}_{\text {T}}$ shift and a smaller potential sensitivity ( ${S}_{V}$ ), which can be improved by ammonium hydroxide treatment.

Di-galacturonic acid (Di-GalA) and tri-galacturonic acid (tri-GalA) are emerging as new prebiotics. A novel biorefining strategy was established to prepare di-GalA and tri-GalA (oligogalacturonic acids) from commercial pectin, which utilized a two-stage process consisting of a hydrothermal pretreatment of low-esterification pectin (LP) followed by enzymatic hydrolysis with endo-polygalacturonase. Hydrothermal pretreatment at 140 °C for 35 min significantly decreased molecular weight, esterification degree and viscosity of LP. The pretreatment process was found to greatly enhance subsequent enzymatic hydrolysis by increasing the accessibility of substrate to enzyme and weakening the steric hindrance effect of enzymatic hydrolysis. The oligogalacturonic acids yield of 75.3 % and 84.8 % of the selectivity of endo-polygalacturonase to oligogalacturonic acids after enzymatic hydrolysis of hydrothermal pretreated LP at enzyme loading of 10 U/g pectin for 24 h were obtained.

Chloroplast genome sequences have been used to understand evolutionary events and to infer efficiently phylogenetic relationships. Callitropsis funebris (Cupressaceae) is an endemic species in China. Its phylogenetic position is controversial due to morphological characters similar to those of Cupressus, Callitropsis, and Chamaecyparis. This study used next‐generation sequencing technology to sequence the complete chloroplast genome of Ca. funebris and then constructed the phylogenetic relationship between Ca. funebris and its related species based on a variety of data sets and methods. Simple sequence repeats (SSRs) and adaptive evolution analysis were also conducted. Our results showed that the monophyletic branch consisting of Ca. funebris and Cupressus tonkinensis is a sister to Cupressus, while Callitropsis is not monophyletic; Ca. nootkatensis and Ca. vietnamensis are nested in turn at the base of the monophyletic group Hesperocyparis. The statistical results of SSRs supported the closest relationship between Ca. funebris and Cupressus. By performing adaptive evolution analysis under the phylogenetic background of Cupressales, the Branch model detected three genes and the Site model detected 10 genes under positive selection; and the Branch‐Site model uncovered that rpoA has experienced positive selection in the Ca. funebries branch. Molecular analysis from the chloroplast genome highly supported that Ca. funebris is at the base of Cupressus. Of note, SSR features were found to be able to shed some light on phylogenetic relationships. In short, this chloroplast genomic study has provided new insights into the phylogeny of Ca. funebris and revealed multiple chloroplast genes possibly undergoing adaptive evolution., The complete chloroplast genome sequence of Callitropsis funebris was obtained for the first time. Phylogenetic tree construction based on various methods and simple sequence repeat characteristic analysis showed that Ca. funebri s was located at the base of Cupressus. In the process of Cupressales evolution, positive selection branches were detected in 3 genes, positive selection sites were detected in 10 genes, and positive selection sites were detected in rpoA gene in Ca. funebris.

Perovskite materials have received extensive attention as optical gain media. However, it is tough to realize lasing using such materials on account of the unstable structure of MAPbI3/CsPbI3 nanocrystals (NCs), and the propensity for mixed-halogen perovskites to undergo phase decomposition into bromine-rich and iodide-rich regions under intense laser irradiation. To solve this issue, we fabricated CsPbX3 (X = Br, I) NCs, which were embedded into a glassy matrix with high stability. In addition, by doping Br− ions into the CsPbI3 NCs to partially replace I− ions, the optical efficiency and the optical gain properties were found to be significantly improved. Here, under 800 nm pulse laser excitation, red random lasing was realized with the assistance of such anion modulation. Moreover, we demonstrate that the perovskite NCs glasses (PNG) show strong water stability after immersion in water for one week, seeding a promise for application in high-definition (HD) displays and photonic devices.

Inspired by the diversity created by nature, organic chemists have been using a divergent strategy to improve the synthetic efficiency of diverse molecules. Transition-metal-catalyzed C-H functionalization has become one of the most straightforward, powerful, and atom-economical methods to construct complex scaffolds. However, C-H activation initiated divergent transformation to prepare diverse molecules is still limited. To address this challenge, we herein developed Rh(III)-catalyzed C-H olefination/annulation reaction cascades to divergently construct diverse polyheterocycles by tuning manipulations of directing groups (DGs). Up to 9 distinct scaffolds were creatively synthesized under simple conditions with good functional group tolerance, chemo-, and regioselectivity. Such a versatile strategy and its extension may encourage researchers to discover more promising manipulations of DGs for transition-metal-catalyzed C-H bond activation, making diverse available targets and materials that would have been previously out of range.

Invasive species face new selective pressures and low genetic variation caused by genetic bottlenecks and founder effects when they are introduced into novel environments. Epigenetic variation may help them to cope with these problems. Mile-a-minute (Mikania micrantha Kunth) is a highly invasive exotic weed that has seriously damaged biodiversity and agricultural ecosystems. We first adopted methylation-sensitive amplified polymorphism (MSAP) markers to investigate epigenetic variation of 21 M. micrantha populations in southern China, and further explored the effects of environmental factors on population epigenetic differentiation by correlating epigenetic and climate and soil data. Adaptive epiloci positively correlated with climate/soil variables were identified. Minimum temperature of the coldest month and mean temperature of the coldest quarter were considered as decisive factors for its distribution. Climate is presumed to play a relatively more important role than soil in shaping the adaptive epigenetic differentiation in M. micrantha. Under ongoing global warming, populations of M. micrantha are predicted to expand northward. In addition, the weed also presented higher epigenetic variation compared with genetic variation. Leaf shape variation was detected related to methylation-state change at the population level.

Summary Cutaneous treatment possesses advantages, including the decrease of transient drug overdosage or systematic side effects. The evolution of biomedical materials with multifunctionalities to overcome the limitations of existing materials can bring revolutionary development in this field. A promising solution can turn to the emerging materials known as metal-organic frameworks (MOFs), featuring high porosity, easy modification, and multifunctionality. The work herein developed a systemic assay package to seek suitable MOFs for cutaneous applications. Versatile platforms based on MOFs were built, which integrated superb functions and features, including biocompatibilities, sebum adsorbability, selective adsorption, antimicrobial activity, controlled release, and skin permeability promotion. Such features endow MOFs as high-performance matrixes for cutaneous applications. This study paves a new avenue for the reformation of cosmetic and biomedicinal materials. Moreover, this comprehensive MOF screening system can be broadly applied for material evaluation in this field, which also provides valuable guidance for the design of advanced biomedical materials.

Interstitial flows in breakwater cores and seabeds are a key consideration in coastal and marine engineering designs and have a direct impact on their structural safety. In this paper, a unified fully coupled model for wave-permeable breakwater-porous seabed interactions is built based on an improved N-S equation. A numerical wave flume is constructed, and numerical studies are carried out by applying the finite difference method. In combination with a physical model test, the accuracy of the numerical simulation results is verified by comparing the calculated and measured values of wave height at measurement points and the seepage pressure within the breakwater and seabed. On this basis, the characteristics of the surrounding wave field and the internal flow field of the pore structure, as well as the evolution process of the fluctuating pore water pressure inside the breakwater and seabed, are further analyzed. The spatial distribution of the maximum fluctuating pore water pressure in the breakwater is compared between two cases by considering whether the seabed is permeable, and then the effect of seabed permeability on the dynamic pore water pressure in the breakwater is clarified. This study attempts to provide a reference for breakwater design and the protection of nearby seabeds.

The design and construction of advanced electrode materials is important to the development of high-performance electrochemical energy storage devices. In this paper, V-doped 1T MoS2 nanosheets with a large layer spacing are grown on carbon cloth (CC) via a one-step hydrothermal method. The resulting material features abundant edge sites and active centers, and its large layer spacing facilitates the interlayer shuttle of Na+. Doping with V buffers the volume change and maintains the integrity of MoS2. The layered structure of the composite featuring CC as a conductive substrate effectively prevents the agglomeration of MoS2 during the electrochemical process. When used as an anode material for a Na+ battery, the material displays a high first-cycle irreversible discharge specific capacity of 1234.9 mAh g−1. A specific capacity of 453.2 mAh g−1 is obtained after 100 cycles at a current density of 200 mA g−1. This work provides an effective and eco-friendly route toward obtaining superior MoS2 electrodes for high-performance Na+ storage.

With the emerging trend of big data and internet-of-things, sensors with compact size, low cost and robust performance are highly desirable. Spectral imaging and spectral LIDAR systems enable measurement of spectral and 3D information of the ambient environment. These systems have been widely applied in different areas including environmental monitoring, autonomous driving, biomedical imaging, biometric identification, archaeology and art conservation. In this review, modern applications of state-of-the-art spectral imaging and spectral LIDAR systems in the past decade have been summarized and presented. Furthermore, the progress in the development of compact spectral imaging and LIDAR sensing systems has also been reviewed. These systems are based on the nanophotonics technology. The most updated research works on subwavelength scale nanostructure-based functional devices for spectral imaging and optical frequency comb-based LIDAR sensing works have been reviewed. These compact systems will drive the translation of spectral imaging and LIDAR sensing from table-top toward portable solutions for consumer electronics applications. In addition, the future perspectives on nanophotonics-based spectral imaging and LIDAR sensing are also presented.

The ground motion response in a moderately stiff soil in seismic events has been traditionally studied based on the actual field records which, however, have yet to offer consistent results regarding the amplification effect of the ground motion. In the present study, a centrifuge model of the moderately stiff soil field is designed to study the amplification effect of the ground motion in response to seismic loads. Four El Centro waves of different strengths are used as the input wave at the base under a gravitational field of 75 g. Ground motion data at different depths are collected via a number of sensors to study the acceleration peak, time history, and response spectrum of the ground motion. The measured amplitude and energy of seismic waves are found to gradually increase from the bottom to the surface during the propagation of seismic waves, and the peak acceleration at the surface is significantly magnified. The response spectrum analysis shows that the acceleration response spectrum gradually moves to the high-frequency direction from the base to the surface and the value of the response spectrum decreases with the increase of the depth in the present study.

Elucidating hydrogen oxidation reaction (HOR) mechanisms in alkaline conditions is vital for understanding and improving the efficiency of anion-exchange-membrane fuel cells. However, uncertainty remains around the alkaline HOR mechanism owing to a lack of direct in situ evidence of intermediates. In this study, in situ electrochemical surface-enhanced Raman spectroscopy (SERS) and DFT were used to study HOR processes on PtNi alloy and Pt surfaces, respectively. Spectroscopic evidence indicates that adsorbed hydroxy species (OHad ) were directly involved in HOR processes in alkaline conditions on the PtNi alloy surface. However, OHad species were not observed on the Pt surface during the HOR. We show that Ni doping promoted hydroxy adsorption on the platinum-alloy catalytic surface, improving the HOR activity. DFT calculations also suggest that the free energy was decreased by hydroxy adsorption. Consequently, tuning OH adsorption by designing bifunctional catalysts is an efficient method for promoting HOR activity.

PtNi alloy catalysts have excellent catalytic activity and are considered some of the most promising electrocatalysts capable of replacing pure Pt for the oxygen reduction reaction (ORR). For PtNi alloys, Ni-doping can improve performance by changing the electronic and structural properties of the catalyst surface and its interaction with reaction intermediates. However, to date there is no direct spectral evidence detecting or identifying the effect of Ni on the ORR in PtNi alloy catalysts. Herein, we introduce a surface-enhanced Raman spectroscopic (SERS) "borrowing" strategy for investigating ORR processes catalyzed by Au@PtNi nanoparticles (NPs). The bond vibration of adsorbed peroxide intermediate species (*OOH) was obtained, and the effect of Ni on the interaction between surface Pt and *OOH was studied by varying the Ni content in the alloy. The frequency of the *OOH spectral band has an obvious red-shift with increasing Ni content. Combined with density functional theory (DFT) calculations, we show that Ni-doping can optimize *OOH surface binding on the Pt surface, achieving more efficient electron transfer, thus improving the ORR rate. Notably, these results evidence the SERS borrowing strategy as an effective technique for in situ observations of catalytic processes.

A multidimension source model for generating broadband ground motions with deterministic 3D numerical simulations is proposed in this article. In this model, the source is composed of several superimposed layers, and the total seismic moment is assigned to these layers in different proportions. Each layer exactly fills up the seismic fault and is uniformly divided into subsources with size decreased progressively to reflect different levels of rupture details. Hence, the proposed multidimension source model may consider the realistic rupture process of an earthquake, that is, the spatial and temporal heterogeneity of source parameters, and generate broadband ground motions. To verify this source model, the 1994 Northridge earthquake is simulated with four multidimension source models, based on different source inversion results. The amplitudes, durations, and spectral characteristics of the observed ground motions of the 1994 Northridge earthquake are respectably reproduced in a range of frequencies up to 5 Hz. In addition, a scenario earthquake is also simulated with four multidimension source models, with different synthetic rupture process. The simulated ground motions of the scenario earthquake are generally in good agreement with the Next Generation Attenuation-West 2 ground-motion prediction equations. This demonstrates that it is promising to simulate realistic broadband ground motions of strong earthquakes with a proper source description and realistic Earth models.