Pure toroidal dipole in a single dielectric disk.

The toroidal dipole is a peculiar electromagnetic excitation and has attracted increasing interests because of unusual radiation characteristics. However, the realization of toroidal moment requires complicated structure and are often disturbed by the conventional electric and magnetic multipoles. In this paper, we explore the electromagnetic properties of a simple dielectric disk illuminated by a focused radially polarized beam and demonstrate a pure toroidal dipolar response. A comprehensive approach is proposed to suppress other undesirable electromagnetic multipolar resonances step by step. The disk with optimized geometry is employed to construct an all-dielectric electric mirror dominated by toroidal dipolar resonance. And two kinds of anapole modes with total suppression of far-field radiation are investigated, which proves electric and magnetic non-radiating sources, respectively. Besides, by simultaneously introducing the asymmetry in both structure and incidence, a transformation from Mie-type mode to trapped mode is observed. Our study provides an opportunity to realize a unique pure toroidal dipole and may boost the relevant light-matter interaction.

Tunable anisotropic parameters realized by metal-dielectric hybrid meta-atoms.

Rational design of the structure enables metamaterials to go beyond the ingredients and achieve unprecedented material properties. However, the realization of complicated and anisotropic electromagnetic parameters relies on the elaborate design of building blocks, and the mutual coupling between the anisotropic responses makes precise control of material parameters even more difficult. Here, we propose a metal-dielectric hybrid metamaterial, not only realizing the decoupling between anisotropic electromagnetic responses, but also establishing a one-to-one correspondence between independent geometric dimensions and anisotropic parameter components. Moreover, a tuning theoretical paradigm applied to an anisotropic and resonant system is further suggested, which proves that the operating frequency of this hybrid metamaterial can be easily adjusted by changing external fields. As prototypes, two typical and tunable microwave meta-devices, a transformation-optics cloak and a frequency splitter, are constructed with Ba-Sm-La-Ti ferroelectric ceramic and flexible printed circuit board, which successfully demonstrate our proposed design theory. This work provides a simple strategy for the design and fabrication of tunable anisotropic metamaterials, and boost the development of meta-devices toward practical application.

Excitation and manipulation of both magnetic and electric surface plasmons.

Surface plasmons (SPs) is the cornerstone in terahertz (THz) near-field photonics, which play crucial roles in the miniaturization and integration of functional devices. The excitation and manipulation of SPs, however, is currently restricted to electric SPs paradigm, while magnetic SPs receive less attention despite the importance of magnetic light-matter interactions. Here, a scheme is proposed to simultaneously convert the propagating waves in free space into magnetic and electric SPs using a single ultracompact device. First, a plasmonic structure composed of connected slit rings is designed and demonstrated to support both electric and magnetic SPs, which is ascribed to the two distinct eigenmodes of oscillating electrons and vortex currents, respectively. Second, with the assistance of an anisotropic and gradient metasurface, orthogonal linear polarized components of incident THz beams are coupled into different electric and magnetic SP channels with little crosstalk. Furthermore, by encoding two distinct polarization-dependent phase profile into the metasurface, it is shown that the resulting meta-device can individually tailor the wavefronts of magnetic and electric SPs, thus simultaneously engineering magnetic and electric near-field distributions. This work can pave the road to realize bi-channel and on-chip devices, and inspire more integrated functionalities especially related to near-field manipulations of magnetic SPs.

Light-Controlled Friction by Carboxylic Azobenzene Molecular Self-Assembly Layers.

Nowadays, reversible friction regulation has become the focus of scientists in terms of the flexible regulatory structure of photosensitive materials and theories since this facilitates rapid development in this field. Meanwhile, as an external stimulus, light possesses great potential and advantages in spatiotemporal control and remote triggering. In this work, we demonstrated two photo-isomerized organic molecular layers, tetra-carboxylic azobenzene (NN4A) and dicarboxylic azobenzene (NN2A), which were selected to construct template networks on the surface of the highly oriented pyrolytic graphite (HOPG) to study the friction properties, corresponding to the arrangement structure of self-assembled layers under light regulation. First of all, the morphology of the self-assembled layers were characterized by a scanning tunneling microscope (STM), then the nanotribological properties of the template networks were measured by atomic force microscope (AFM). Their friction coefficients are respectively changed by about 0.6 and 2.3 times under light control. The density functional theory (DFT) method was used to calculate the relationship between the force intensity and the friction characteristics of the self-assembled systems under light regulation. Herein, the use of external light stimulus plays a significant role in regulating the friction properties of the interface of the nanometer, hopefully serving as a fundamental basis for further light-controlling research for the future fabrication of advanced on-surface devices.

Insight into the Lubrication Behavior of Phospholipids Pre-adsorbed on Silica Surfaces at Different Adsorption Temperatures.

Phospholipids, as essential components in joint synovial fluid, play a dominant role in joint lubrication. In this study, atomic force microscopy was used to evaluate the normal and shear forces between two surfaces bearing three types of phospholipids with different acyl chain lengths, which were pre-adsorbed onto silica surfaces at different temperatures (25, 45, and 60 °C). When the pre-adsorption temperature was below the phospholipid phase transition temperature (Tm), a super-low friction coefficient [1,2-distearoyl-sn-glycero-3-phosphocholine (DSPC): 0.002; 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC): 0.007] between two opposing silica surfaces in water was achieved because of the super-low shear strength of the hydration shell and robustness of the vesicle when the load was less than the critical value (DSPC: 500 nN; DPPC: 85 nN). However, when the pre-adsorption temperature exceeded Tm, the silica surface was covered by a bilayer structure with many defects, which exhibited poor adsorption density and low bearing capacity, resulting in a relatively high friction coefficient. This study gains insights into the influence of structure and temperature on the lubrication mechanism of phospholipids as biolubricants, providing guidance for the application of artificial joint synovial fluid.

Ice-Inspired Superlubricated Electrospun Nanofibrous Membrane for Preventing Tissue Adhesion.

Inspired by the superlubricated surface (SLS) of ice, which consists of an ultrathin and contiguous layer of surface-bound water, we built a SLS on the polycaprolactone (PCL)/poly(2-methacryloxyethylphosphorylcholine) (PMPC) composite nanofibrous membrane via electrospinning under controlled relative humidity (RH). The zwitterionic PMPC on the nanofiber provided a surface layer of bound water, thus generating a hydration lubrication surface. Prepared under 20% RH, electrospun PCL/PMPC nanofibers reached a minimum coefficient of friction (COF) of about 0.12 when the weight ratio of PMPC to PCL was 0.1. At a higher RH, a SLS with an ultralow COF of less than 0.05 was formed on the composite nanofibers. The high stability of the SLS hydration layer on the engineered nanofibrous membrane effectively inhibited fibroblast adhesion and markedly reduced tissue adhesion during tendon repair in vivo. This work demonstrates the great potential of this ice-inspired SLS approach in tissue adhesion-prevention applications.

Hydration-Enhanced Lubricating Electrospun Nanofibrous Membranes Prevent Tissue Adhesion.

Lubrication is the key to efficient function of human tissues and has significant impact on the comfort level. However, the construction of a lubricating nanofibrous membrane has not been reported as yet, especially using a one-step surface modification method. Here, bioinspired by the superlubrication mechanism of articular cartilage, we successfully construct hydration-enhanced lubricating nanofibers via one-step in situ grafting of a copolymer synthesized by dopamine methacrylamide (DMA) and 2-methacryloyloxyethyl phosphorylcholine (MPC) onto electrospun polycaprolactone (PCL) nanofibers. The zwitterionic MPC structure provides the nanofiber surface with hydration lubrication behavior. The coefficient of friction (COF) of the lubricating nanofibrous membrane decreases significantly and is approximately 65% less than that of pure PCL nanofibers, which are easily worn out under friction regardless of hydration. The lubricating nanofibers, however, show favorable wear-resistance performance. Besides, they possess a strong antiadhesion ability of fibroblasts compared with pure PCL nanofibers. The cell density decreases approximately 9-fold, and the cell area decreases approximately 12 times on day 7. Furthermore, the in vivo antitendon adhesion data reveals that the lubricating nanofiber group has a significantly lower adhesion score and a better antitissue adhesion. Altogether, our developed hydration-enhanced lubricating nanofibers show promising applications in the biomedical field such as antiadhesive membranes.

An in situ shearing x-ray measurement system for exploring structures and dynamics at the solid-liquid interface.

Revealing interfacial structure and dynamics has been one of the essential thematic topics in material science and condensed matter physics. Synchrotron-based x-ray scattering techniques can deliver unique and insightful probing of interfacial structures and dynamics, in particular, in reflection geometries with higher surface and interfacial sensitivity than transmission geometries. We demonstrate the design and implementation of an in situ shearing x-ray measurement system, equipped with both inline parallel-plate and cone-and-plate shearing setups and operated at the advanced photon source at Argonne National Laboratory, to investigate the structures and dynamics of end-tethered polymers at the solid-liquid interface. With a precise lifting motor, a micrometer-scale gap can be produced by aligning two surfaces of a rotating upper shaft and a lower sample substrate. A torsional shear flow forms in the gap and applies tangential shear forces on the sample surface. The technical combination with nanoscale rheology and the utilization of in situ x-ray scattering allow us to gain fundamental insights into the complex dynamics in soft interfaces under shearing. In this work, we demonstrate the technical scope and experimental capability of the in situ shearing x-ray system through the measurements of charged polymers at both flat and curved interfaces upon shearing. Through the in situ shearing x-ray scattering experiments integrated with theoretical simulations, we aim to develop a detailed understanding of the short-range molecular structure and mesoscale ionic aggregate morphology, as well as ion transport and dynamics in soft interfaces, thereby providing fundamental insight into a long-standing challenge in ionic polymer brushes with a significant technological impact.

Tribo-Induced Near-Infrared Light Emission between Metal and Quartz.

Triboluminescence (TL) refers to the luminescence phenomenon at the material surface under the action of pressure or shear. This fascinating phenomenon can directly convert mechanical energy into light emission without the need for other auxiliary components; therefore, it attracts more and more researchers to conduct research in different wavelength ranges, such as X-ray, ultraviolet, visible light, and terahertz. However, there have been few reports on the study of the near-infrared (NIR) range, which is very important in the integrity of the triboluminescence research. In this research, we found that NIR light with a wavelength ranging from 800 to 1000 nm was generated by friction between solid metals and a quartz crystal. Analysis of the cross section of the quartz disk after friction revealed that the TL phenomenon had a strong relationship with the doping of metal grains into the silica. Density functional theory (DFT) and X-ray photoelectron spectroscopy were also conducted to further identify the results. We infer that such light emission arises from the implantation of metal grains into the surface of the quartz, which forms a metal-insulator junction with amorphous silica. Moreover, electron transition between the metal and the insulator, followed by a transition at the center of the defects, causes near-infrared light emission. Our research reveals the infrared luminescence behavior from a different perspective, the transfer of materials, and perhaps deepens the understanding of the near-infrared emission mechanism.

Super-Slippery Degraded Black Phosphorus/Silicon Dioxide Interface.

The interfaces between two-dimensional (2D) materials and the silicon dioxide (SiO2)/silicon (Si) substrate, generally considered as a solid-solid mechanical contact, have been especially emphasized for the structure design and the property optimization in microsystems and nanoengineering. The basic understanding of the interfacial structure and dynamics for 2D material-based systems still remains one of the inevitable challenges ahead. Here, an interfacial mobile water layer is indicated to insert into the interface of the degraded black phosphorus (BP) flake and the SiO2/Si substrate owing to the induced hydroxyl groups during the ambient degradation. A super-slippery degraded BP/SiO2 interface was observed with the interfacial shear stress (ISS) experimentally evaluated as low as 0.029 ± 0.004 MPa, being comparable to the ISS values of incommensurate rigid crystalline contacts. In-depth investigation of the interfacial structure through nuclear magnetic resonance spectroscopy and in situ X-ray photoelectron spectroscopy depth profiling revealed that the interfacial liquid water was responsible for the super-slippery BP/SiO2 interface with extremely low shear stress. This finding clarifies the strong interactions between degraded BP and water molecules, which supports the potential wider applications of the few-layer BP nanomaterial in biological lubrication.

Electrical friction modulation on MoS2 using electron beam radiation without electrostatic interactions.

Nanoscale friction under different electronic states and the corresponding friction controlling methods are both scientifically interesting and technologically important. However, friction measurements under electrical modulation are severely hampered by electrostatic forces induced by the charge-trapping effect. Therefore, in this study, we developed a new modulation method free from the charge-trapping effect through electron beam radiation; this method successfully modulated the friction between few-layer MoS2 and the silicon tip on atomic force microscopy. Friction on monolayer MoS2 increased under electron beam radiation. Strong correlations between the accelerating voltage, beam current, and friction force were found, and constant adhesion force demonstrate that the influence of static electricity was eliminated in this method. Excited electron states caused by electron injection could be possible mechanisms for friction modulation. However, the electron beam radiation had a negligible influence on the friction of bilayer MoS2. This study is the first of its kind, revealing the effect of electron beam radiation and electronic states on friction, which is important for the development of tribological theories and nanoelectromechanical systems, and offers a new electrical modulation method for friction tuning.

Core-shell nanospheres to achieve ultralow friction polymer nanocomposites with superior mechanical properties.

Core-shell nanospheres have been widely used in catalysis, batteries, medicine, etc. owing to their unique structural characteristics, which exhibit optimal performance and integrated functions of both the core and shell materials. To simultaneously achieve outstanding mechanical properties and remarkable lubrication properties in desirable polymer composites, core-shell nanospheres with polytetrafluoroethylene (PTFE) as the core and poly methyl methacrylate (PMMA) as the shell have been adopted as structural units to form bulk nanocomposites. We demonstrated that the mechanical and lubrication properties of the nanocomposites prepared using core-shell nanospheres as the continuous matrix were dramatically improved. Specifically, when compared with that of pure PTFE, the compressive strength of the PTFE@PMMA nanocomposite obviously increased up to one order of magnitude (from ∼9 to ∼90 MPa), the friction coefficient reduced to 25% (the lowest value was 0.03), and the wear rate decreased up to two orders of magnitude. Moreover, the mechanical and lubrication properties of the nanocomposites could be adjusted by changing the core-shell ratio, and an appropriate core-shell ratio was beneficial for achieving the desired comprehensive properties. It has been proposed that the properties, such as the confinement effect, improved dispersion capacity, etc., imparted by the core-shell structure effectively lead to high dispersion of the reinforcement phase, improvement of the binding force of the transfer film to the friction surface, and interruption of the wear process of the polymer composite.

Supramolecular-based nanofibers.

Supramolecular-based nanofibers, which successfully combine the unique properties of supramolecular interactions with the advantages of nanofibrous structure, are widely used in a variety of biomedical applications such as controlled drug delivery. Compared with traditional polymer nanofibers, supramolecular-based nanofibers can overcome the bottleneck of sensitivity because of the non-covalent binding modes, and therefore match the requirements of rapid and reversible response to the external stimuli. In addition, supramolecular-based nanofibers can achieve extra controllable and dynamic responsive (e.g. pH, temperature) functions in different environments. In this review, we retrospected and summarized the recent development of supramolecular-based nanofibers, focusing particularly on electrospun supramolecular nanofibers, while also touching on the advances of directly self-assembled supramolecular nanofibers without the use of electrospinning. Furthermore, we discussed the potential biomedical applications of supramolecular nanofibers. Finally, this review was concluded by elaborating upon individual reflection on the current situation, forecasting the future trend of this promising material.

AFM Study on Superlubricity between Ti6Al4V/Polymer Surfaces Achieved with Liposomes.

Liposomes have been considered as the boundary lubricant in natural joints. They are also the main component of bionic lubricant. In this study, the tribological properties of liposomes on Ti6Al4V/polymer surface were studied by atomic force microscope (AFM) at the nanoscale. The superlubricity with a friction coefficient of 0.007 was achieved under the maximal pressure of 15 MPa, consisting with the lubrication condition of natural joints. Especially, when the AFM probe was hydrophilically modified and preadsorbed, the friction coefficient and load bearing capacity could be further improved. In addition, the probe with a large radius could maintain the stable lubrication of liposomes in the contact zone. Finally, an optimal lubrication model of liposomes was established and the critical force for superlubricity was also proposed. It was the boundary between elastic deformation and plastic deformation for vesicles. It was also the indicator of the plough effect appearing on the adsorbed layer. This work reveals the interfacial behavior of liposomes and realizes the controllable superlubricity system, providing more guidance for clinical application.

Dual functional electrospun core-shell nanofibers for anti-infective guided bone regeneration membranes.

In clinic infection is the paramount cause for failure of guided bone regeneration (GBR) membranes. Therefore, it is crucial to develop anti-infective GBR membranes for clinical bone repair application. In this research, we successfully prepared electrospun core-shell nanofibers loaded with metronidazole (MNA) and nano-hydroxyapatites (nHA), which could be employed for anti-infective GBR membranes due to the achievement of dual functions with enhanced osteogenesis and slow MNA release. The nanofiber shell was composed of polycaprolactone and nHA, whilst the nanofiber core was gelatin and MNA. The MNA release and cell proliferation experiments showed that compared with directly MNA-loaded nanofibers, the core-shell nanofibers possessed slower MNA release profile, which resulted in the decrease in cytotoxicity of MNA to bone mesenchymal stem cells. The osteogenic measurements demonstrated that the core-shell nanofibers could enhance bone formation. Additionally, the anti-bacterial experiments indicated that the core-shell nanofibers could prevent colonization of anaerobic bacteria. In summary, the results in the present study revealed the potential of the core-shell electrospun nanofibers with dual functions of enhanced osteogenesis and anti-infection for optimal clinical application as GBR membranes.

Bone remodeling-inspired dual delivery electrospun nanofibers for promoting bone regeneration.

Developing a highly bioactive bone tissue engineering scaffold that can modulate the bone remodeling process for promoting bone regeneration is a great challenge. In order to tackle this issue, inspired by the balance between bone resorption and formation in the bone remodeling process, here we developed a mesoporous silicate nanoparticle (MSN)-based electrospun polycaprolactone (PCL)/gelatin nanofibrous scaffold to achieve dual delivery of alendronate (ALN) and silicate for a synergetic effect in modulating bone remodeling, where ALN inhibited the bone-resorbing process via preventing guanosine triphosphate-related protein expression, and silicate promoted the bone-forming process via improving vascularization and bone calcification. The scaffold was successfully prepared by encapsulation of ALN into MSNs (ALN@MSNs) and co-electrospinning of an acetic acid-mediated PCL/gelatin homogeneous solution with well-dispersed ALN@MSNs. The results of ALN and Si element release profiles indicated that the ALN@MSN-loaded nanofibers achieved dual release of ALN and silicate (produced due to the hydrolysis of MSNs) simultaneously. The bone repair data from a rat critical-sized cranial defect model revealed that the developed strategy accelerated the healing time from 12 weeks to 4 weeks, almost three times faster, while the other nanofiber groups only had limited bone regeneration at 4 weeks. In addition, we used interactive double-factor analysis of variance for the data of bone volume and maturity to evaluate the synergetic effect of ALN and silicate in promoting bone regeneration, and the result clearly proved our original design and hypothesis. In summary, the presented bone remodeling-inspired electrospun nanofibers with dual delivery of ALN and silicate may be highly promising for bone repair in the clinic.

Electrospun nanosilicates-based organic/inorganic nanofibers for potential bone tissue engineering.

Although growth factors and drugs (BMP-2, dexamethasone, etc.) have been widely used for bone tissue engineering, they have unignored limits such as adverse effects at high concentrations and easy inactivation in vivo. Accordingly, more osteoinductive supplements without side effects should be considered as alternatives in the design of bone tissue engineering scaffolds. Nanosilicate is a bioactive inorganic nanomaterial consisting of hydrous sodium lithium magnesium silicate, which is recently found to be safe and effective for bone induction. In this study, a range of organic/inorganic nanofibrous scaffolds with varied nanosilicate concentrations (0%, 1%, 5%, and 10% w/w to PCL matrix) were successfully fabricated via electrospinning. The tensile properties of the nanofibers were enhanced at low nanosilicate concentrations, and the incorporation of nanosilicates had no influence on cytocompatibility. Besides, in vitro osteogenesis experiments showed that nanosilicates-doped nanofibers were capable of inducing bone formation better than pure PCL nanofiber samples. More importantly, the results of histological and immunohistochemical assessments further revealed that the nanosilicates-enriched nanofibers had a significant potential of ectopic bone formation in vivo, while the pure PCL samples only induced limited osteogenic cues. All these results indicate that the nanosilicates-based organic/inorganic nanofibers may be potentially efficient for bone tissue engineering.

Black Phosphorus: Degradation Favors Lubrication.

Due to its innate instability, the degradation of black phosphorus (BP) with oxygen and moisture was considered the obstacle for its application in ambient conditions. Here, a friction force reduced by about 50% at the degraded area of the BP nanosheets was expressly observed using atomic force microscopy due to the produced phosphorus oxides during degradation. Energy-dispersive spectrometer mapping analyses corroborated the localized concentration of oxygen on the degraded BP flake surface where friction reduction was observed. Water absorption was discovered to be essential for the degraded characteristic as well as the friction reduction behavior of BP sheets. The combination of water molecules as well as the resulting chemical groups (P-OH bonds) that are formed on the oxidized surface may account for the friction reduction of degraded BP flakes. It is indicated that, besides its layered structure, the ambient degradation of BP significantly favors its lubrication behavior.

Investigation on the Nanomechanics of Liposome Adsorption on Titanium Alloys: Temperature and Loading Effects.

The mechanical properties of liposomes, determined by the lipid phase state at ambient temperature, have a close relationship with their physiological activities. Here, atomic force microscopy (AFM) was used to produce images and perform force measurements on titanium alloys at two adsorbed temperatures. The mechanical properties were evaluated under repeated loading and unloading, suggesting a better reversibility and resistance of gel phase liposomes. The liquid phase liposomes were irreversibly damaged during the first approach while the gel phase liposomes could bear more iterations, resulting from water flow reversibly going across the membranes. The statistical data offered strong evidence that the lipid membranes in the gel phase are robust enough to resist the tip penetration, mainly due to their orderly organization and strong hydrophobic interactions between lipid molecules. This work regarding the mechanical properties of liposomes with different phases provides guidance for future clinical applications, such as artificial joints.

Detection of depth-depend changes in porcine cartilage after wear test using Raman spectroscopy.

Cartilage damage and wear can lead to severe diseases, such as osteoarthritis, thus, many studies on the cartilage wear process have already been performed to better understand the cartilage wear mechanism. However, most characterization methods focus on the cartilage surface or the total wear extent. With the advantages of high spatial resolution and easy characterization, Raman microspectroscopy was employed for the first time to characterize full-depth changes in the cartilage extracellular matrix (ECM) after wear test. Sections from the cartilage samples after wear were compared with sections from the control group. Univariate and multivariate analyses both indicated that collagen content loss at certain depths (20%-30% relative to the cartilage surface) is possibly the dominating alteration during wear rather than changes in collagen fiber orientation or proteoglycan content. These findings are consistent with the observations obtained by scanning electron microscopy and histological staining. This study successfully used Raman microspectroscopy efficiently assess full-depth changes in cartilage ECM after wear test, thus providing new insight into cartilage damage and wear.