Strain-Prompted Giant Flexo-Photovoltaic Effect in Two-Dimensional Violet Phosphorene Nanosheets.

As a second-order nonlinear optical phenomenon, the bulk photovoltaic (BPV) effect is expected to break through the Shockley-Queisser limit of thermodynamic photoelectron conversion and improve the energy conversion efficiency of photovoltaic cells. Here, we have successfully induced a strong flexo-photovoltaic (FPV) effect, a form of BPV effect, in strained violet phosphorene nanosheets (VPNS) by utilizing strain engineering at the h-BN nanoedge, which was first observed in nontransition metal dichalcogenide (TMD) systems. This BPV effect was found to originate from the disruption of inversion symmetry induced by uniaxial strain applied to VPNS at the h-BN nanoedge. We have revealed the intricate relationship between the bulk photovoltaic effect and strain gradients in VPNS through thickness-dependent photovoltaic response experiments. A bulk photovoltaic coefficient of up to 1.3 × 10-3 V-1 and a polarization extinction ratio of 21.6 have been achieved by systematically optimizing the height of the h-BN nanoedge and the thickness of VPNS, surpassing those of reported TMD materials (typically less than 3). Our results have revealed the fundamental relationship between the FPV effect and the strain gradients in low-dimensional materials and inspired further exploration of optoelectronic phenomena in strain-gradient engineered materials.

Bacterial elimination via cell membrane penetration by violet phosphorene peripheral sub-nanoneedles combined with oxidative stress.

The effectiveness of an antibacterial agent is strongly influenced by its antibacterial mechanism, which, in turn, depends on the agent's topological structure. In the natural world, the nanoprotrusions on the surface of insect wings give them excellent antimicrobial properties through physical penetration while being compatible with host cells. Inspired by the novel nanostructure of insect wings, violet phosphorus (VP), a new member of the phosphorus family, has antibacterial potential due to the sub-nanoneedle on its edge. Here, we demonstrate that VP and its exfoliated product, violet phosphorene nanosheets (VPNSs), have superior antibacterial capability against pathogens via cell membrane penetration induced by peripheral sub-nanoneedles combined with oxidative stress. The results show that VPNSs can inactivate more than 99.9% of two common pathogens (Escherichia coli and Staphylococcus aureus) and more than 99.9% of two antibiotic-resistant bacteria (Escherichia coli pUC19 and methicillin-resistant Staphylococcus aureus), while showing almost no toxicity toward normal cells at a high concentration of 2.0 mg mL-1. Moreover, VPNSs can achieve effective treatment of induced skin wound infections and bacterial keratitis (BK) by Staphylococcus aureus and methicillin-resistant Staphylococcus aureus, respectively, showing promising potential for ocular and skin wound infection theragnostics.

Dynamics of an Excess Electron in Molten LiF, KF, MgF2, and BeF2.

Ab initio molecular dynamics simulations suggest that the dynamics of an excess electron in different types of molten salts are not always the same. In molten LiF, KF, and MgF2, the excess electron localizes in the cavity as a solvated electron for 10 ps, which agrees with the widely accepted theory of Pikaev. In molten BeF2, the excess electron shows a different localization pattern: it mostly exists in localized states but also occurs in many delocalized states. This "localize-delocalize" pattern originates from the high viscosity of BeF2 (16 000 cP at 900 °C), which will lead to slow ionic motion and finally result in slow solvent relaxation. Besides, the species formed by the localization of the excess electron in these four melts are also different. The spectral feature (broad peak in the vis-IR region) of the localized electron in molten alkaline halides was also observed in LiF, KF, MgF2, and BeF2. Both an excess electron and electrons in the bulk liquid could contribute to the spectra, but the excitation of the excess electron makes a bigger contribution to the broad vis-IR peak. Our predicted spectrum of molten LiF/KF qualitatively reproduces the major feature of the experimental spectrum, which partially validates our simulations.

P-N Bonds-Mediated Atomic-Level Charge-Transfer Channel Fabricated between Violet Phosphorus and Carbon Nitride Favors Charge Separation and Water Splitting.

Heterostructures are widely employed in photocatalysis to promote charge separation and photocatalytic activity. However, their benefits are limited by the linkages and contact environment at the interface. Herein, violet phosphorus quantum dots (VPQDs) and graphitic carbon nitride (g-C3 N4 ) are employed as model materials to form VPQDs/g-C3 N4 heterostructures by a simple ultrasonic pulse excitation method. The heterostructure contains strong interfacial P-N bonds that mitigate interfacial charge-separation issues. P-P bond breakage occurs in the distinctive cage-like [P9] VPQD units during longitudinal disruption, thereby exposing numerous active P sites that bond with N atoms in g-C3 N4 under ultrasonic pulse excitation. The atomic-level interfacial P-N bonds of the Z-scheme VPQDs/g-C3 N4 heterostructure serve as photogenerated charge-transfer channels for improved electron-hole separation efficiency. This results in excellent photocatalytic performance with a hydrogen evolution rate of 7.70 mmol g-1  h-1 (over 9.2 and 8.5 times greater than those of pure g-C3 N4 and VPQDs, respectively) and apparent quantum yield of 11.68% at 400 nm. Using atomic-level chemical bonds to promote interfacial charge separation in phosphorene heterostructures is a feasible and effective design strategy for photocatalytic water-splitting materials.

Peritendinous adhesion: Therapeutic targets and progress of drug therapy.

Peritendinous adhesion (PA) is one of the most common complications following hand surgery and characterized with abnormal hyperplasia of connective tissue and excessive deposition of extracellular matrix. Subsequently, various clinical symptoms such as chronic pain, limb dyskinesia and even joint stiffness occur and patients are always involved in the vicious cycle of "adhesion - release - re-adhesion", which seriously compromise the quality of life. Until present, the underlying mechanism remains controversial and lack of specific treatment, with symptomatic treatment being the only option to relieve symptoms, but not contributing no more to the fundamentally rehabilitation of basic structure and function. Recently, novel strategies have been proposed to inhibit the formation of adhesion tissues including implantation of anti-adhesion barriers, anti-inflammation, restraint of myofibroblast transformation and regulation of collagen overproduction. Furthermore, gene therapy has also been considered as a promising anti-adhesion treatment. In this review, we provide an overview of anti-adhesion targets and relevant drugs to summarize the potential pharmacological roles and present subsequent challenges and prospects of anti-adhesion drugs.

Synthesis of violet phosphorus with large lateral sizes to facilitate nano-device fabrications.

Violet phosphorus has been proven to be the most stable phosphorus allotrope and has attracted much attention recently. The growth of violet phosphorus with large lateral sizes is crucial to obtain good quality violet phosphorene for nanodevice fabrication. Herein, a large number of violet phosphorus plates have been produced from molten lead using an optimized method to achieve red bronze luster. The crystal structure of the as-produced violet phosphorus was determined by single-crystal X-ray diffraction to be monoclinic with the space group P2/n (13) (CSD-2160375), identical to the one from the chemical vapor transport method (CSD-1935087). The as-produced violet phosphorus plates were found to have lateral sizes of 1.30 ± 0.41 mm2. The violet phosphorus plates were easily exfoliated and directly transferred to silicon substrates to facilitate building of a back-gate field-effect transistor. A hole mobility of 2.308 cm2 V-1 s-1 was obtained from a violet phosphorus nanosheet with a thickness of 52 nm under ambient conditions. The absolute responsivity of 130 mA W-1 with a fast response time of 27 ms was also obtained under the irradiation of a 530 nm laser.

Violet Antimony Phosphorus with Enhanced Photocatalytic Hydrogen Evolution.

Violet phosphorus (VP), a recently confirmed layered elemental structure, is demonstrated to have unique photoelectric, mechanical, and photocatalytic properties. Element substitution plays a significant role in modifying the physical/chemical properties of semiconducting materials. Herein, antimony is adopted to substitute some phosphorus atoms in VP crystals to tune their physical and chemical properties, resulting in a significantly enhanced photocatalytic hydrogen evolution performance. The antimony-substituted violet phosphorus single crystal (VP-Sb) is synthesized and characterized by single crystal X-ray diffraction (CSD-2214937). The bandgap of VP-Sb has been found to be lowered from that of VP by UV/vis diffuse reflectance spectroscopy and density-functional theory (DFT) calculation, enhancing the optical absorption during photocatalytic reaction. The conducting band minimum of VP-Sb is found to be upshifted from that of VP from measurements and calculation, enhancing its hydrogen reduction activity. The valance band maximum is found to be lowered to weaken its oxidation activity. The edge of VP-Sb is calculated to have an excellent H* adsorption-desorption performance and superior H2 generation kinetics. The H2 evolution rate of VP-Sb is demonstrated to be significantly enhanced to be 1473 µmol h-1 g-1 , about five times of that of pristine VP (299 µmol h-1 g-1 ) under the same experimental conditions.

SARS-CoV-2 and gastrointestinal diseases.

Background: Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) is the causative agent of the novel coronavirus disease (COVID-19) pandemic, which has caused serious challenges for public health systems worldwide. Literature review: SARS-CoV-2 invades not only the respiratory system, but also the digestive system, causing a variety of gastrointestinal diseases. Significance: Understanding the gastrointestinal diseases caused by SARS-CoV-2, and the damage mechanisms of SARS-CoV-2 to the gastrointestinal tracts and gastrointestinal glands are crucial to treating the gastrointestinal diseases caused by SARS-CoV-2. Conclusion: This review summarizes the gastrointestinal diseases caused by SARS-CoV-2, including gastrointestinal inflammatory disorders, gastrointestinal ulcer diseases, gastrointestinal bleeding, and gastrointestinal thrombotic diseases, etc. Furthermore, the mechanisms of gastrointestinal injury induced by SARS-COV-2 were analyzed and summarized, and the suggestions for drug prevention and treatment were put forward for the reference of clinical workers.

A Review of Phosphorus Structures as CO2 Reduction Photocatalysts.

Effective photocatalytic carbon dioxide (CO2 ) reduction into high-value-added chemicals is promising to mitigate current energy crisis and global warming issues. Finding effective photocatalysts is crucial for photocatalytic CO2 reduction. Currently, metal-based semiconductors for photocatalytic CO2 reduction have been well reviewed, while review of nonmetal-based semiconductors is almost limited to carbon nitrides. Phosphorus is a promising nonmetal photocatalysts with various allotropes and tunable band gaps, which has been demonstrated to be promising non-metallic photocatalysts. However, no systematic review about phosphorus structures for photocatalytic CO2 reduction reactions has been reported. Herein, the progresses of phosphorus structures as photocatalysts for CO2 reduction are reviewed. The fundamentals of photocatalytic CO2 reduction, corresponding properties of phosphorus allotropes, photocatalysts with phosphorus doping or phosphorus-containing ligands, research progress of phosphorus allotropes as photocatalysts for CO2 reduction have been reviewed in this paper. The future research and perspective of phosphorus structures for photocatalytic CO2 reduction are also presented.

Transcription Factor IAA27 Positively Regulates P Uptake through Promoted Adventitious Root Development in Apple Plants.

Phosphate (P) deficiency severely limits the growth and production of plants. Adventitious root development plays an essential role in responding to low phosphorus stress for apple plants. However, the molecular mechanisms regulating adventitious root growth and development in response to low phosphorus stress have remained elusive. In this study, a mutation (C-T) in the coding region of the apple AUXIN/INDOLE-3-ACETIC ACID 27 (IAA27) gene was identified. MdIAA27T-overexpressing transgenic apple improved the tolerance to phosphorus deficiency, which grew longer and denser adventitious roots and presented higher phosphorous content than the control plants under low phosphorus conditions, while the overexpression of MdIAA27C displayed the opposite trend. Moreover, the heterologous overexpression of MdIAA27 in tobacco yielded the same results, supporting the aforementioned findings. In vitro and in vivo assays showed that MdIAA27 directly interacted with AUXIN RESPONSE FACTOR (ARF8), ARF26 and ARF27, which regulated Small Auxin-Up RNA 76 (MdSAUR76) and lateral organ boundaries domain 16 (MdLBD16) transcription. The mutation in IAA27 resulted in altered interaction modes, which in turn promoted the release of positive ARFs to upregulate SAUR76 and LBD16 expression in low phosphorus conditions. Altogether, our studies provide insights into how the allelic variation of IAA27 affects adventitious root development in response to low phosphorus stress.

Violet phosphorus: an effective metal-free elemental photocatalyst for hydrogen evolution.

Violet phosphorus, a non-metallic elemental layered structure, has not been reported as a photocatalyst due to the lack of its resources. An excellent photocatalytic H2 evolution rate of 675 ± 109 µmol h-1 g-1 with high stability has been achieved by the violet phosphorus simply dispersed in deionized water with addition of 1.0 wt% of co-catalyst Pt, which is much higher than that obtained from black phosphorus. The H2 evolution rate was observed to reach values as high as 553 µmol h-1 g-1 with addition of 0.5 wt% co-catalyst Pt.

Wide Bandgap Tuning of Violet Phosphorus Quantum Dots by Functionalization.

Violet phosphorus quantum dots (VPQDs) are promising structures for bioimaging, solar cells, LEDs, diode lasers, and transistors due to the quantum confinement effects. Bandgap tuning is important for QDs to adjust their emissions for various applications. Nevertheless, no bandgap tuning of VPQDs has been investigated, since the violet phosphorus has just recently been successfully produced and confirmed. In this work, the bandgap of VPQDs has been demonstrated to be effectively tuned from 2.3 to 3.1 eV by a facile solvothermal path in different solvents to introduce different functional groups. The HOMO-LUMO gaps of VPQDs from different functionalizations have also been calculated by density functional theory to be 2.73, 2.77, 2.74, 2.80, 2.51, and 2.56 eV, respectively, which are well-consistent with the experimental results. Our results provide a simple pathway for bandgap tuning of VPQDs, which can be used for future optoelectronic applications.

Preparation of Few-Layer Porous Graphene by a Soft Mechanical Method with a Short Rolling Transfer Process.

Few-layer porous graphene is a promising material for a variety of fields. However, the synthesis of few-layer porous graphene is a great challenge. Here we report a feasible green path to produce few-layer porous graphene, which was exfoliated from high-pressure graphite balls onto microspheres with rough surfaces by a mild rolling transfer process. Ordinary ball milling equipment was adopted for the low-speed (100 rpm) ball-microsphere rolling transfer process. The rolling time (<10 min) was controlled to obtain porous graphene instead of graphene. The porous graphene on the exfoliating microspheres was then easily dispersed in solution by bath sonication. The product contains very few impure functional groups. The hole size and layer distribution of the few-layer porous graphene have been demonstrated to be 2.37±1.17 nm and 2.4±0.7 layers, respectively, and can be adjusted by redesigning the surface of the microspheres.

Dynamic Changes of Phenolic Compounds and Their Associated Gene Expression Profiles Occurring during Fruit Development and Ripening of the Donghong Kiwifruit.

The newly released Donghong kiwifruit is a promising commercial cultivar. The dynamic changes of major phenolic compounds (flavonols, flavanols, phenolic acids, and anthocyanins) during the representative stages of fruit development and ripening of the Donghong kiwifruit were determined by high-performance liquid chromatography. The corresponding time-course transcriptional changes were evaluated using the combined analysis of RNA-Seq and qRT-PCR. The most predominant phenolic compound in the Donghong kiwifruit was epicatechin. Cyanidin 3-O-[2-O-(ß-xylosyl)-ß-galactoside] and cyanidin 3-O-ß-galactoside were two essential anthocyanins detected. Candidate genes and pathways involved in phenolic compounds biosynthesis were highlighted. The structural genes (AcLDOX2, Ac5GGT1, and Ac5AT2) and the transcription factor (bHLH74-2) were strongly associated with anthocyanin biosynthesis. AcMYB4-1 may be a novel transcription factor that reduces anthocyanin accumulation. Results from the study may be a very useful supplement to current knowledge of molecular mechanisms to elucidate coloration in the red-fleshed kiwifruit and could help breeders modify the kiwifruit germplasm.

Structure and Properties of Violet Phosphorus and Its Phosphorene Exfoliation.

Black phosphorene has attracted much attention as a semiconducting two-dimensional material. Violet phosphorus is another layered semiconducting phosphorus allotrope with unique electronic and optoelectronic properties. However, no confirmed violet crystals or reliable lattice structure of violet phosphorus had been obtained. Now, violet phosphorus single crystals were produced and the lattice structure has been obtained by single-crystal x-ray diffraction to be monoclinic with space group of P2/n (13) (a=9.210, b=9.128, c=21.893 Å, ß=97.776°). The lattice structure obtained was confirmed to be reliable and stable. The optical band gap of violet phosphorus is around 1.7 eV, which is slightly larger than the calculated value. The thermal decomposition temperature was 52 °C higher than its black phosphorus counterpart, which was assumed to be the most stable form. Violet phosphorene was easily obtained by both mechanical and solution exfoliation under ambient conditions.

A Facile Path to Graphene-Wrapped Polydopamine-Entwined Silicon Nanoparticles with High Electrochemical Performance.

Graphene-coated silicon nanoparticles with polydopamine buffers have been designed and successfully fabricated as anodes for lithium ion batteries, where the polydopamine was grown on the silicon nanoparticles and then coated with graphene layers. The expansion cavities for silicon nanoparticles during charging and discharging process are provided by the polydopamine buffer layers. The outermost graphene coating layers not only keep the pulverized silicon particles together without disintegration, but also improve the electric conductivity of silicon nanoparticles. Silicon nanoparticles of an industrial product level with different size distributions and oxidation layers were used in this work. High electrochemical performances with specific capacities of 1100 mAh g-1 were achieved by the designed silicon composites with polydopamine and graphene after 550 cycles at a current rate of 200 mA g-1 .

Controlling of smart home system based on brain-computer interface.

BACKGROUND: Brain computer interface (BCI) technology is a communication and control approach. Up to now many studies have attempted to develop an EEG-based BCI system to improve the quality of life of people with severe disabilities, such as amyotrophic lateral sclerosis (ALS), paralysis, brain stroke and so on. The proposed BCIBSHS could help to provide a new way for supporting life of paralyzed people and elderly people. OBJECTIVE: The goal of this paper is to explore how to set up a cost-effective and safe-to-use online BCIBSHS to recognize multi-commands and control smart devices based on SSVEP. METHODS: The portable EEG acquisition device (Emotiv EPOC) was used to collect EEG signals. The raw signals were denoised by discrete wavelet transform (DWT) method, and then the canonical correlation analysis (CCA) method was used for feature extraction and classification. Another part is the control of smart home devices. The classification results of SSVEP can be translated into commands to control several devices for the smart home. RESULTS: Here, the Power over Ethernet (PoE) technology was utilized to provide electrical energy and communication for those devices. During online experiments, four different control commands have been achieved to control four smart home devices (lamp, web camera, guardianship telephone and intelligent blinds). Experimental results showed that the online BCIBSHS obtained 86.88 ± 5.30% average classification accuracy rate. CONCLUSION: The BCI and PoE technology, combined with smart home system, overcoming the shortcomings of traditional systems and achieving home applications management rely on EEG signal. In this paper, we proposed an online steady-state visual evoked potential (SSVEP) based BCI system on controlling several smart home devices.

Enhanced Interfacial Adhesion by Reactive Carbon Nanotubes: New Route to High-Performance Immiscible Polymer Blend Nanocomposites with Simultaneously Enhanced Toughness, Tensile Strength, and Electrical Conductivity.

Physically anchoring carbon nanotubes (CNTs) onto the interface of immiscible polymer blends has been extensively reported; however, enhancement of physical properties of the blends has seldom been achieved. Herein, we used CNTs with reactive epoxide groups and long poly(methyl methacrylate) (PMMA) tails as a thermodynamic compatibilizer for immiscible poly vinylidene fluoride/poly l-lactide (PVDF/PLLA) blends. The CNTs acted as an efficient compatibilizer and bridged the two phases through physical entanglement and chemical reaction. The sea-island structure of the blend transformed into a bicontinuous structure for CNT contents greater than 3 wt %. The mechanical properties, including ductility and tensile strength, thermal properties, and electrical conductivities were all enhanced by the CNTs compatibilizer. This strategy thermodynamically compatibilized by reactive nanofillers paves the way for advanced blend nanocomposites.

Reactive Nanoparticles Compatibilized Immiscible Polymer Blends: Synthesis of Reactive SiO2 with Long Poly(methyl methacrylate) Chains and the in Situ Formation of Janus SiO2 Nanoparticles Anchored Exclusively at the Interface.

The exclusive location of compatibilizers at the interface of immiscible binary polymer blends to bridge the neighboring phases is the most important issue for fabricating desirable materials with synergistic properties. However, the positional stability of the compatibilizers at the interface remains a challenge in both scientific and technical points of view due to the intrinsic flexibility of compatibilizer molecules against aggressive processing conditions. Herein, taking the typical immiscible poly vinylidene fluoride (PVDF)/polylactic acid (PLLA) blend as an example, we demonstrate a novel approach, termed as the interfacial nanoparticle compatibilization (IPC) mechanism, to overcome the challenges by packing nanoparticles thermodynamically at the interface through melt reactive blending. Specifically, we have first synthesized nanosilica with both reactive epoxide groups and long poly(methyl methacrylate) (PMMA) tails, called reactive PMMA-graft-SiO2 (Epoxy-MSiO2), and then incorporated the Epoxy-MSiO2 into the PVDF/PLLA (50/50, w/w) blends by melt blending. PLLA was in situ grafted onto SiO2 by the reaction of the carboxylic acid groups with epoxide groups on the surface of SiO2. Therefore, the reacted SiO2 particles were exclusively located at the interface by the formation of the Janus-faced silica hybrid nanoparticles (JSNp) with pregrafted PMMA tails entangled with PVDF molecular chains in the PVDF phase and the in situ grafted PLLA chains embedded in the PLLA phase. Such JSNp with a distinct hemisphere, functioning as compatibilizer, can not only suppress coalescence of PVDF domains by its steric repulsion but also enhance interfacial adhesion via the selective interactions with the corresponding miscible phase. The interfacial location of JSNp is very stable even under the severe shear field and annealing in the melt. This IPC mechanism paves a new possibility to use the various types of nanoparticles as both effective compatibilizers and functional fillers for immiscible polymer blends.