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Carbon monoxide (CO) is known as a deathful gas produced by burning of hydrocarbons in a lack of enough oxygen, in which breathing CO leads to serious issues on human life health quality. Therefore, adsorption of CO gas is an essential task for diagnosis or removal of this dreadful gas in environment. To do this, a HEME-like model of iron-nitrogen-doped beryllium oxide (FeNBeO) monolayer was investigated for adsorbing CO gas by performing density functional theory (DFT) calculations. Two models were obtained for this process, in which relaxation of CO with C-head or O-head towards Fe region of monolayer. The results indicated that the formation of FeNBeO-CO model could be achieved more favorable than the formation of FeNBeO-OC model. The obtained optimized geometers and energies all approved this achievement for favorability of FeNBeO-CO model formation. Moreover, molecular orbital based electronic features indicated variations of such features for the models upon adsorption of CO substance, in which the models could be detectable in a sensor function for the existence of CO gas in the environment. As a consequence, the investigated FeNBeO monolayer could be proposed useful for adsorption of CO gas at least for the CO deathful gas diagnosis purposes.

Isothermal oxidation behaviors of Ni–Fe (wt.%) and of the same alloy with additions of 10 and 15%Cr alloys in the air at 800 °C and 900 °C and their anodic behaviors in aluminum electrolysis system at 800 °C were evaluated. The composition morphologies of oxide scales were characterized by XRD, SEM, and EDS. Results show that the scales formed on Ni–Fe alloy at both temperatures consisted of an inner (Ni,Fe)3O4 layer and an outer Fe2O3 layer. For Ni–Fe–10Cr alloy, an external (Ni,Fe)3O4/Fe2O3 layers and an internal oxidation zone were formed at 800 °C, while a continuous Cr2O3 layer forms at the internal oxidation zone/substrate interface at 900 °C. A multilayer structure oxide of Cr2O3/(Ni,Fe,Cr)3O4/(Ni,Fe)3O4/Fe2O3 was formed on Ni–Fe–15Cr alloy at 800 °C, while at 900 °C the Fe2O3 becomes discontinuous disperses in the (Ni,Fe)3O4 layer close to the surface. Increases in oxidation temperature or Cr content for Ni–Fe–Cr alloys promote the growth of the inner Cr2O3 layer and simultaneously reduce Fe2O3 content. After 4 h of electrolysis at an anode current density of 0.25 A cm−2, the oxidation resistance of Ni–Fe–15Cr anode is superior to the Ni–Fe anode.

The demand for a load distributive compression anchor (LDCA) in construction sites has been increasing, owing to its high bearing capacity and removable steel strands. As an LDCA comprises multiple anchor bodies and unbonded steel strands, the load applied to the strands generates a distributive compressive stress in the grout, preventing high concentration of grout–ground shear stress. Unlike in the conventional anchors, in an LDCA, independent load transfer of each anchor body induces interference effect between adjacent anchor bodies. Therefore, for an efficient design of an LDCA, it is necessary to investigate the load transfer mechanism considering the effect of multiple anchor bodies. In this study, a series of anchor pull-out field tests was conducted for LDCAs consisting of a single anchor body, and double and triple anchor bodies spaced by 1, 2, and 3 m. According to the test results, the LDCA showed a stiffer load–displacement behavior with an increase in the number and spacing of the anchor bodies. The multiple anchor bodies of the LDCA generated an overlapping of the grout axial load and induced its rapid dissipation, increasing the grout–ground shear stress. This interference effect was more clearly observed with a decrease in the anchor body spacing.

Ultrastrong nanolayered metallic composites are usually subjected to low ductility due to plastic instability during deformation. Here we investigated the shear instability of a newly designed heterogeneous nanolayered Cu/Zr composites by microindentation. The heterogeneity in size was generated by inserting a few thin Cu-Zr bilayers with an individual layer thickness of 2.5 - 10 nm into the interface region of the Cu/Zr layered composites with an individual layer thickness of 100 nm. The microindentation tests showed that multiple shear bands appeared in the heterogeneous composite with one bilayer, whereas only a single shear band was formed in that with two or three bilayers. Most importantly, the layer strain in the multi-shear band region is much smaller than that in the single-shear band area. For example, the strain of the 100 nm layers within the shear band in the composite with one 10 nm bilayer could reach as low as 2.8, which was less than half of that in the composite with three 10 nm bilayers, i.e., 6.1. These findings demonstrated that strain delocalization can be achieved through shear band multiplication if an appropriate number of thin bilayers were used as interlayers in the 100 nm Cu/Zr composites. Besides, compared with the homogeneous composite with an individual layer thickness of 100 nm and the bimodal composite which is composed of alternating one 100 nm Cu-Zr bilayer and two 10 nm Cu-Zr bilayers, the heterogeneous composite with one bilayer displayed a higher strength (2.15 GPa) and a favorable resistance to strain localization.

With the ever-growing application of lithium-ion batteries (LIBs), their fast-charging technology has attracted great interests of scientists. However, growth of lithium dendrites during fast charge of the batteries with high energy density may pose great threats to the operation and cause serious safety issues. Herein, we prepared a functional separator with an ultra-thin (20 nm) layer of Au nanoparticles deposited by evaporation coating method which could regulate growth direction and morphology of the lithium dendrites, owing to nearly zero overpotential of lithium meal nucleation on lithiated Au. Once the Li dendrites are about to form on the graphite anode during fast charging (or lithiation), they plate predominantly on the Au deposited separator rather than on the graphite. Such selective deposition does not compromise the electrochemical performance of batteries under normal cycling. More importantly, it enables the better cycling stability of batteries at fast charge condition. The Li/Graphite cells with Au nanoparticles coated separator could cycle stably with a high areal capacity retention of 90.5% over 95 cycles at the current density of 0.72 mA cm−2. The functional separator provides an effective strategy to adjust lithium plating position at fast charge to ensure high safety of batteries without a compromise on the energy density of LIBs.

The multilevel storage capability of nonvolatile resistive random access memory (ReRAM) is greatly desired to accomplish high functioning memory density. In this study, Ta2O5 thin film with different thicknesses (2, 4, and 6 nm) was exploited as an appropriate interfacial barrier layer for limiting the formation of the interfacial layer between the 10 nm thick sputtering deposited resistive switching (RS) layer and Ta ohmic electrode to improve the switching cycle endurance and uniformity. Results show that lower forming voltage, narrow distribution of SET-voltages, good dc switching cycles (103), high pulse endurance (106 cycles), long retention time (104 s at room temperature and 100°C), and reliable multilevel resistance states were obtained at an appropriate thickness of ∼2 nm Ta2O5 interfacial barrier layer instead of without Ta2O5 and with ∼4 nm, and ∼6 nm Ta2O5 barrier layer, ZrO2-based memristive devices. Besides, multilevel resistance states have been scientifically investigated via modulating the compliance current (CC) and RESET-stop voltages, which displays that all of the resistance states were distinct and stayed stable without any considerable deprivation over 104 s retention time and 104 pulse endurance cycles. The I-V characteristics of RESET-stop voltage (from −1.7 to −2.3 V) of HRS are found to be a good linear fit with the Schottky equation. It can be seen that Schottky barrier height rises by increasing the stop-voltage during RESET-operation, resulting in enhancing the data storage memory window (on/off ratio). Moreover, RESET-voltage and CC control of HRS and LRS revealed the physical origin of the RS mechanism, which entails the formation and rupture of conducting nanofilaments. It is thoroughly investigated that proper optimization of the barrier layer at the ohmic interface and the switching layer is essential in memristive devices. These results demonstrate that the ZrO2-based memristive device with an optimized ∼2 nm Ta2O5 barrier layer is a promising candidate for multilevel data storage memory applications.

Half-metallic Heusler alloys typically have in-plane magnetic anisotropy, which can be converted to perpendicular by attaching MgO or heavy metal, e.g., Pt, layers as similarly applied for conventional ferromagnets. Recently we have found body-centered cubic (bcc) seed layers, e.g., V and W, to induce perpendicular anisotropy in Heusler-alloy films above, however, they show small giant magnetoresistive (GMR) ratios in spin-valve structures to date. This is partially because of the large resistivity of the seed layer and the nonmagnetic layer in the spin-valve. In this study, we have systematically investigated nonmagnetic overlayers and have found that a Ag layer best maintains the perpendicular anisotropy. The corresponding GMR devices have then been fabricated and characterized, achieving the GMR ratio of ~0.03% at room temperature. Such bcc seed layers can offer an alternative method for perpendicularly magnetized GMR junctions for applications.

In this paper, a Ni coating was deposited on the surface of the A356 aluminum alloy by high velocity oxygen fuel spraying to improve the performance of the AZ91D magnesium/A356 aluminum bimetal prepared by a compound casting. The effects of the Ni coating as well as its thickness on microstructure and mechanical properties of the AZ91D/A356 bimetal were systematically researched for the first time. Results demonstrated that the Ni coating and its thickness had a significant effect on the interfacial phase compositions and mechanical properties of the AZ91D/A356 bimetal. The 10µm's Ni coating cannot prevent the generation of the Al-Mg intermetallic compounds (IMCs) at the interface zone of the AZ91D/A356 bimetal, while the Ni coating with the thickness of 45 µm and 190 µm can avoid the formation of the Al-Mg IMCs. When the Ni coating was 45 µm, the Ni coating disappeared and transformed into Mg-Mg2Ni eutectic structures+Ni2Mg3Al particles at the interface zone. With a thickness of 190µm's Ni coating, part of the Ni coating remained and the interface layer was composed of the Mg-Mg2Ni eutectic structures+ Ni2Mg3Al particles, Mg2Ni layer, Ni solid solution (SS) layer, Al3Ni2 layer, Al3Ni layer and sporadic Al3Ni+Al-Al3Ni eutectic structures from AZ91D side to A356 side in sequence. The interface layer consisting of the Mg-Ni and Al-Ni IMCs obtained with the Ni coating had an obvious lower hardness than the Al-Mg IMCs. The shear strength of the AZ91D/A356 bimetal with a Ni coating of 45 µm thickness enhanced 41.4% in comparison with that of the bimetal without Ni coating, and the fracture of the bimetal with 45µm's Ni coating occurred between the Mg matrix and the interface layer with a mixture of brittle fracture and ductile fracture.

A novel Ni30Cr25Al15Co15Mo5Ti5Y5 high-entropy alloy (HEA) coating was irradiated to optimize its internal structure via laser after supersonic particle deposition (SPD). Owing to the high energy density of the laser and large temperature gradient, the crystallization process of the molecules and atoms in the coating was restrained and supercooling occurred. Experimental results showed that a considerable number of nano-crystal grains precipitated and amorphous structures were formed because of the random orientation of the crystals. The baseline of differential scanning calorimetry scans obtained for the coating started to shift at the Tg of 939.37 ℃ and a step was observed. Multiple dispersion peaks and lattice fringes indicated that the nucleation of the irradiated laser-induced topology optimized (LTO) coating was incomplete. The laser-induced topology optimizing treatment led to quasi-isotropy in the SPD coating. Furthermore, the LTO coating exhibited a residual stress of 18.4 MPa, stress-strain response, and fatigue limit of 265 MPa. Hence, the LTO coating exhibited higher performance than the unirradiated SPD coating. The Nyquist and Bode electrochemical impedance spectra of the LTO coating, including two relaxation processes, indicated that the corrosion process steadily recovered to the equilibrium state. This implies that the uniform oxidation passivation layer on the surface of the LTO coating insulated the material from the corrosive medium, protecting the substrate from further corrosion, thus enhancing the structural security of the material for use in super-intense laser facility applications.

The treatment and repair strategies for reflective and fatigue cracking that initiate at the pavement surface (i.e., top-down cracking) and at the bottom of the asphalt concrete layer (i.e., bottom-up cracking) are noticeably different. However, pavement management engineers are facing difficulties in identifying these cracks in the field because they usually appear in visually identical patterns. The objective of this study was to develop artificial neural network (ANN) and convolutional neural network (CNN) applications to differentiate and classify top-down, bottom-up, and cement-treated reflective cracking in in-service flexible pavements using deep-learning models. The developed CNN model achieved an accuracy of 93.8% in the testing and 91% in the validation phases, and the ANN model showed an overall accuracy of 92%. The ANN classification tool was developed based on variables related to pavement and crack characteristics including pavement age, annual average daily traffic, thickness of the asphalt concrete layer, type of base, crack orientation, and crack location.

Estimation of crack depths and spacing due to desiccation of clayey soils is needed to predict changes in mechanical or hydraulic properties in the cracked layer. These changes affect the infiltration of water, stability, and deformation of a soil mass. Desiccation cracks are associated with increasing suction due to moisture loss accompanied by restrained shrinkage, which results in tensile stresses in near surface soil layers. Cracks propagate when the developed tensile stresses exceed the tensile strength of soil. A simple analytical method is presented to predict crack depths in compacted clayey soil due to changes in matric suction with depth. The model equation is based on the Hookean elastic equation relating incremental strain to incremental stress and incorporates two stress state variables including net normal stress and matric suction. Input to the model equation includes the tensile strength and elastic parameters, and to complete the prediction of crack depth, the suction change profile of interest is needed. The method validity was investigated by comparing predicted crack depths to those observed in soil compacted in a bench scale apparatus for studying desiccation cracking. Tensile strength and elastic properties were determined from tests conducted on soil during desiccation under approximate uniaxial conditions. Predicted crack depths were obtained based on changes in suction interpreted from water content sensors at various depths in the soil bed and compared favorably to observed desiccation crack depths.

This paper presents a method of the formation of composite polymer-containing coatings on a Mg–Mn–Ce magnesium alloy by forming a ceramic-like layer using plasma electrolytic oxidation (PEO) and subsequent spraying superdispersed polytetrafluoroethylene suspension. The coating composition and their morphological features were studied by SEM, EDS, GDOES, and XRD. The presented data confirm the embedding of fluoropolymer in the PEO coating. The evaluation of the corrosion properties of the formed composite polymer-containing coatings indicates a decrease in the corrosion current density by more than 3 orders of magnitude in comparison with the base PEO coating. The incorporation of a fluoropolymer in a PEO layer by more than 32% increases the load value at which abrasion of the coating to the substrate occurs and reduces the wear of the coating by more than 27 fold in comparison with the PEO layer. It has been established that composite coatings possess hydrophobic properties: the value of the contact angle attains 152 °.

Flexible electrodes have attracted the interest of a wide range of people because they can monitor human health signals like ECG, EMG and EEG as wearable devices. However, PDMS-based membrane electrodes have the problem of difficulty in depositing metal layers, while fabric electrodes have high contact impedance. Furthermore, the widely used Ag/AgCl electrodes have the shortcomings of skin inflammation or skin irritation. Therefore, we fabricate a skin-like electrical conductive electrode via electroless silver plating on the surface of regenerated cellulose membrane, in which the cellulose membrane is obtained by the dissolution of cotton fiber with green solvent ionic liquid [Bmim]Cl. The as-prepared biocompatible electrode with low skin-electrode contact impedance can be used as a dry electrode for a long-term period of use. The impedance at 700 Hz is only 8 kΩ/cm2, and the conductivity can reach 252 s/cm. After 5 hours of wear, the skin contact impedance of the electrode was only 10 kΩ/cm2 under 700 Hz(when AgNO3 was used at a concentration of 0.20 mol/L). Importantly, the electrodes not only provide a stable and clear ECG signal, but also offer a high level of comfort and low impedance, when used for long-term health monitoring.

Tantalum oxide film has become an investigation focus for surface modification materials in the biomedical field owing to its outstanding biocompatibility, anti-corrosion, and anti-wear performances. However, tantalum oxide films exhibit poor adhesion because of the mismatch between the properties of the film and the substrate. In this study, a novel multilayer tantalum oxide coating of TamOn/TamOn-TiO2/TiO2/Ti (code M-TamOn) was deposited on Ti6Al4V by magnetron sputtering with TamOn single-layer coating as control. The purpose of this work is to evaluate the influence of the introduced TamOn-TiO2/TiO2/Ti multi-interlayer on the microstructure, adhesive, mechanical, and anti-corrosion properties of reactive sputtered tantalum oxide coatings. The outcomes show that the TamOn-TiO2/TiO2/Ti intermediate layer improves the bonding strength between the TamOn layer and Ti6Al4V matrix from 17.83 N to over 50 N and enables the TamOn coating to have an increased H/E and H3/E2 ratio, decreased friction coefficient and wear rate, raised potential, and reduced corrosion current density. The improved properties of the multilayer system are attributed to the positive effects of the inserted multiple interlayers in reducing the residual stress in the coating, coupling the mechanical performance between the layer and the substrate, blocking the continuous growth of penetrating defects in a film with columnar structure. These experimental results provide a workable route for improving the properties of the tantalum oxide coating on Ti6Al4V alloy for medical applications.

Hypothesis The boundary layer holds the key to solve the puzzle of the unusual stability of the nanobubbles in solution. The quantitative determination on its mechanical and structural properties has not been achieved due to its diffusive and dynamic nature, lack of distinctive interfaces, and difficult differentiation from bulk background. Therefore, it is necessary to investigate this boundary using more sensitive interface analysis technologies to effectively differentiate the water molecules at the interface from those in the bulk. Experiments An in-situ and non-deconstructive method, solvent relaxation nuclear magnetic resonance, was used to investigate the boundary layer on bulk nanobubbles, where the relaxation rate of the water in the layer and its thickness were measured by solvent relaxation NMR and the ratio between the water molecules at the bubble interfaces and those in the bulk and the corresponding boundary layer thickness were determined. Findings The spin-spin relaxation time for the water in the layer (∼101ms) is found to be two orders of magnitude lower than that of the free water (∼103ms). As the first attempt, the determined boundary layer thickness is around 35-45 nanometers and 17.0 %-8.7 % of the effective gaseous size of the nanobubbles, which increases with the decrease of the bubble diameter. As a result, a quantitative measurement model for bubble boundary layer has been established in order to better understand the interfacial properties and stabilization mechanism for bulk nanobubbles.

Electrochemical reduction of CO2 to value-added chemicals using renewable electricity provides a promising strategy to achieve sustainable fuel production and carbon neutrality. Along with the development of electrocatalysts, flow cells with gas-diffusion electrodes (GDEs) have been used to reach commercially viable current densities for CO2 electrolysis, while the local environment and CO2 mass transport in the electrodes remain to be elucidated. In this review article, we highlight some insights into the microenvironment in the catalyst layer for CO2 electrolysis, including typical mass transport models for CO2 reduction in H-type cells and GDE flow cells, the effect of a hydrophobic microenvironment on CO2 mass transport and catalytic performance, and the formation of a gas/liquid balance and solid–liquid–gas interfaces for CO2 electrolysis. The insights and discussions in this article can provide important guidelines on the design of catalysts, electrodes, and electrolyzers for CO2 electrolysis, as well as other gas-involving electrocatalytic reactions.

Quasi-two-dimensional (quasi-2D) perovskites with high stability usually suffers from poor device efficiency. Chemical tuning of the spacer cations has been an effective strategy to achieve efficient and stable quasi-2D perovskite solar cells. Here, we demonstrate that 3-halogon-substituted benzylammonium iodide (3X-BAI, X = F, Cl, Br, I) can significantly affect the orientation of low-dimensional perovskites and charge transport from perovskite to hole extraction layer, as well as device performance. With 3Br-BAI, we achieve the highest device efficiency of 13.21% for quasi-2D perovskites with a nominal n = 3 average composition. Our work provides a facile approach to regulate vertical crystal orientation and charge transport via tuning the molecular structure of organic spacer toward high performance quasi-2D perovskite solar cells.

In this study, a La0.8Ba0.2TiO3−δ (LBT) upper layer was deposited on an yttria-stabilized zirconia (YSZ) thermal barrier coating (TBC) through atmospheric plasma spraying. The thermal cycling behaviors of the YSZ single-ceramic-layer and LBT–YSZ double-ceramic-layer coatings at 1000 °C were investigated through a water quenching method. Moreover, phases, microstructural evolution, and elemental distributions were studied through by X-ray diffraction and scanning electron microscopy–energy-dispersive X-ray spectroscopy. The results showed that the thermal cycling lifetime of the LBT–YSZ coating was 27% higher than that of conventional YSZ coating. The conventional YSZ coating failed after 251 cycles because of the joining of the continuous horizontal and vertical cracks caused by the formation of thermal growth oxides and the bending effect of the single-ceramic-layer structure. The thermal cycling behavior of the LBT–YSZ coating was different from that of the YSZ coating at the edge and center. Although the former was similar to the failure behavior of the YSZ coating, the cracks in the vertical direction were deflected as a result of the bending effect of the double-ceramic-layer structure during quenching. This deflection led to the formation of slope cracks with longer propagation paths and slope spallation zones. The latter showed small-debris spallation on top of the LBT upper layer due to the lower fracture toughness of the LBT, which protected the central coating from the structural damage of the ceramic coating. These two behaviors would either release the thermal stress or increase the crack-propagation energy requirement in the ceramic coating, consequently improving the thermal cycling lifetime of the LBT–YSZ coating. In summary, depositing an LBT upper layer could potentially improve the thermal cycling lifetimes of TBCs.

Anode-free batteries (AFBs) have the potential of ultra-high energy density, but lithium dendrite has largely hindered their practical applications. In this work, an in-situ grown gradient solid electrolyte interface (SEI) layer on pre-designed micro-hole-grid (MHG) Cu reservoir is proposed to guide uniform lithium deposition and propagation, by which the electrode interface is stabilized and the surface stress is considerably decreased endowing the AFBs with outstanding areal capacity and cycling performance. The gradient SEI is confirmed by cryogenic-transmission electron microscopy (Cryo-TEM) and XPS to be composed of (1) an elastic organic top layer to hinder non-Li species migration and withstand volume fluctuation, and (2) a lithophilic LiCl-rich bottom layer to render the rapid lithium supply. Operando electron paramagnetic resonance (EPR) shows a dynamic Li deposition, unambiguously demonstrating a dendrites-free behavior. As a result, the full cells of a gradient SEI modified Cu reservoir paired with a LiFePO4 cathode exhibit high capacity of 95 mAh g–1 and Coulombic efficiency (CE) of 99.5% after 100 cycles, much better than the control cells with planar current collectors (1.6 mAh g–1, 2.6%). These findings are enlightening in engineering better interphases for high energy and safe rechargeable lithium metal batteries.

A novel composite reinforcement with horizontal multilayer "Spider web like" SiC nanowire networks and vertical interconnected "Z-pins like" SiC rods was designed and prepared by facile one-step figuration. The linear ablation rate of "Spider web like" SiC nanowire networks and "Z-pins like" SiC rods collectively reinforced C/C-ZrC-SiC composites at 2610 ± 20 ℃ was 0.4 ± 0.03 μm/s with a 74.19 % reduction. The improved ablation resistance was attributed to a denser gradient oxide layer composed of central ZrO2 layer, transitional ZrO2-SiO2 layer and marginal SiO2 layer generated under the initial sticky net effect from SiCnw networks and subsequent oxide compensation from "Z-pins like" SiC rods.

Layered Ni-rich oxide is a promising cathode material for lithium-ion batteries (LIBs) of high energy density, yet its poor electrochemical stability induced by electrode-electrolyte interfacial degradation has still needed to be addressed. Surface coating is one of the powerful techniques to tackle this issue, nevertheless, it has been extensively used on particle but not electrode regarding a larger area of protection. Herein, we have covered a nano-scaled layer of lithium phosphorus oxynitride (LiPON) on the electrode level of LiNi0.8Co0.1Mn0.1O2 (NCM) surface and found lower impedance, longer cycle life, and better safety for treated battery. Most notably, such an NCM-LiPON based 1.3 Ah pouch cell delivers an energy density of 364.4 Wh kg−1 (based on positive and negative materials), along with the retention of 80.0% over 745 cycles at 0.5 C-rate, which is 1.3 times longer than the bare one. This results from modification of both superficial cathode-electrolyte interphase (CEI) and structure stabilization of general particle surface, therefore, role of conformal coating upon electrode surface should be highlighted.

International audience; Producing ultrathin light absorber layers is attractive towards the integration of lightweight planar components in electronic, photonic, and sensor devices. In this work, we report the experimental demonstration of a thin gold (Au) metallic metasurface with near-perfect visible absorption (~ 95 %). Au nanoresonators possessing heights from 5-15 nm with sub-50 nm diameters were engineered by block copolymer (BCP) templating. The Au nanoresonators were fabricated on an alumina (Al2O3) spacer layer and a reflecting Au mirror, in a film-coupled nanoparticle design. The BCP nanopatterning strategy to produce desired heights of Au nanoresonators was tailored to achieve nearperfect absorption at ≈ 600 nm. The experimental insight described in this work is a step forward towards realizing large area flat optics applications derived from subwavelengththin metasurfaces.

In the last few decades, smart windows made from VO2-based thermochromic films have attracted extensive attention, but their actual commercial applications are limited by low luminous transmittance (Tlum), low solar modulation ability (ΔTsol), high phase transition temperature (Tc), and poor durability. In this study, glass/HfO2/VO2/HfO2 tri-layer films were designed and deposited on glass substrates by pulse laser deposition. Crystal structures, surface morphology, surface roughness, electrical properties, and optical properties of as-prepared sandwich structure films were analyzed. Results showed that both HfO2 buffer layer and antireflection layer (ARL) were monoclinic phase and grew along the (020) and (−111) crystal planes, respectively. HfO2 buffer layer not only reduced Tc of VO2 film by about 20 °C, but also played an important role in regulating crystal quality and surface morphology of VO2 films. More importantly, by covering films with HfO2 ARL, Tlum and ΔTsol of VO2 film were greatly improved. In particular, when the thicknesses of HfO2 buffer layer and ARL were 80 nm and 120 nm, the obtained HfO2/VO2/HfO2 tri-layer film reached a balance between high Tlum (∼47.2%), high ΔTsol (∼9.1%) and low Tc (∼49.1 °C). In addition, after 216 h of boiling water treatment, Tlum and ΔTsol of HfO2/VO2/HfO2 film covered with 120 nm thick ARL still remained at 49.3% and 7.0%, showing excellent durability. This research provides a new strategy for designing VO2-based smart windows with high performance and good durability.

Many highways have been built on the eastern coast of China in the past decades. Recently, some engineering problems have emerged after long-term operation. Due to the different properties between the underlying soil and bridge pile foundations, the problem of bumping at the bridge head is inevitable. To study the potential causes and provide insight for future improvement, the settlement of typical highways in the Hangzhou Bay area, which had been open to traffic for more than 10 years, was investigated. After an analytical calculation with the verification of the numerical method and field data, it was indicated that long-term deformation was mainly caused by the poor properties of the lower of the two layers that make up the underlying soil. The trend of the variation of the lower layer keeps increasing at a slow rate during the construction period, resulting in sustained and rapid changes during the following years. Different kinds of ground improvement such as lightweight materials and soil–cement columns generated by deep mixing or jet grouting methods are discussed. The improvement of the lower layer will be more effective. With the analytical method, it is convenient and efficient to calculate and analyse the settlement at different periods, which is significant for design.

Contaminants on architectural ceramics have become a major problem in people's lives. Interestingly, superhydrophobic surfaces offer a new avenue for anti-fouling applications. In this work, a UV-laser process for constructing groove-like microstructures on architectural ceramics and subsequent fluoridation treatment were used to create superhydrophobic surfaces. After laser processing, nanoporous structures were generated inside the grooves, while the cracked layer was deposited on the non-irradiated area, building up a micro/nanoscale morphology on the ceramic surface. Moreover, the effects of groove pitch and laser scanning cycle on surface morphology and wettability were investigated. Results indicate that the fluoridated groove-like microstructured surface showed good superhydrophobicity based on the Cassie-Baxter model. Dynamic behavior of water droplets impacting on the as-prepared superhydrophobic surface was studied to verify its low adhesion. Additionally, the superhydrophobic surface exhibited remarkable repellency to various stain liquids and outstanding self-cleaning properties. These findings may contribute to developing anti-fouling applications for the architectural ceramics industry.

Ultrasonic fatigue tests are performed on a magnesium alloy with and without ultrasonic peening treatment (UPT). Surface enhancement layer leads to the complete change of crack initiation sites. However, crack initiation mechanism keeps the same and results in a single-faceted morphology at crack initiation site. Microcracks initiate as Mode II crack within the original grain, but deflect to Mode I crack outside of the original cracked grain. A threshold SIF value is proposed to evaluate the retarding effect of grain boundary on microcrack propagation. Outside of the original cracked grain, Mode I crack propagation below the threshold ΔKσ-th is responsible for the formation of fine granular area (FGA, a nanograin layer). Based on the Numerous Cyclic Pressing (NCP) model, it is proposed that crack type should be another necessary condition for the formation of FGA.

Laminated multi-layer graphene/Cu–Al–Mn composites were prepared via packaged hot roll bonding process for the first time. Microscopic observation shows that the grains in the Cu–Al–Mn layers are remarkably refined. Multi-layer graphene films intermittently disperse at the interfaces between Cu–Al–Mn layers. Some small fragments of multi-layer graphene films are squeezed into the Cu–Al–Mn layer, and around them, due to the formation of in-situ Al2O3 phase and nano-twins, multi-stage and multi-phase structures are formed. Performance tests show that the composites have ultrahigh damping capacity. Within a wide temperature range of 25–300 °C, the value of damping plateau is up to 0.1 (about 10 times that of the original Cu–Al–Mn alloy). The composites also have superior tensile mechanical properties. Their tensile strength and elongation are up to 913.3 MPa and 13.4% respectively (2.5 times and 4.1 times that of the original Cu–Al–Mn alloy). Microstructural origins of the excellent comprehensive properties were discussed in detail.

The densification process, microstructure evolution, and final optical quality of the transparent MgO⋅nAl2O3 (n = 1.1 and 1.5) ceramics pre-sintered in air and under vacuum were investigated for the effects of pre-sintering atmosphere. The samples pre-sintered in air exhibited uniform microstructure, which was easier to obtain high optical quality at lower HIP temperatures. However, non-cubic precipitates appeared in the samples with a high Al2O3/MgO ratio after HIP treatment, resulting in the deterioration of transmittance. For the samples pre-sintered under vacuum, a large-grain layer was formed on the sample surface due to accelerated MgO volatilization. However, non-cubic precipitates did not appear due to the generation of oxygen vacancies. The mechanisms of formation of the large-grain layer, non-cubic precipitates were discussed from the viewpoint of MgO vaporization, Al2O3/MgO molar ratio, and oxygen vacancy.

To repair the damaged SiC coated C/C composites, a double-layer system including a Sm-doped borosilicate glass external layer and a Si SiC inner layer was prepared by a slurry-based laser cladding technique. Isothermal oxidation experiment and indirect/direct thermal-radiation measurements were performed. The results showed that the absorbance of borosilicate glass to the laser at 900–1200 nm was improved significantly by Sm-doping. Consequently, the repaired coating with a more compact structure and better oxidation resistance was obtained. After oxidation at 1773 K for 10 h, the mass loss of the damaged sample could be reduced by 74.98% with repairing. By increasing laser-absorption and reducing viscosity, the thermal-radiation property of the repaired coating was enhanced to decrease the surface temperature greatly. A repair system with excellent thermal protection performance was achieved.

All-solid-state lithium batteries (ASSLBs) employ high-capacity lithium (Li) metal as the anode and exhibit a higher energy density than that of conventional Li-ion batteries. However, the problems arose from the Li dendrites induce severely parasitic reaction between Li and electrolytes, leading to low coulombic efficiency (CE) and poor cyclic stability. Herein, a poly(vinylidene-co-hexafluoropropylene)/lithium nitrate (PVDF-HFP/LiNO3, marked as PFH/LN) artificial layer is employed to modified Li and achieve high CE ASSLBs with polyethylene oxide-Li6.4La3Zr1.4Ta0.6O12 (PEO-LLZTO) electrolyte. LN serves as a functionalized additive to facilitate the formation of a robust solid electrolyte interface (SEI), efficiently suppressing the formation of Li dendrites. Additionally, LN as a “binder” effectively links PFH with Li, providing good contact. PFH possesses high mechanical strength and moderate flexibility, which can not only physically inhibit the growth of Li dendrites, but also maintain the structural integrity of artificial layer over long-term cycles. Finally, Li/Li cells with such artificial layer demonstrate ultralong cycle life of 1800 and 1000 h under 0.2 and 0.4 mA cm–1, respectively. Furtherly, high CE can be achieved when applied in both LiFePO4 full cells and Li-Cu half cells. This work offers a facile and efficient strategy to greatly promote CE in PEO-based ASSLBs.

This study has been initiated to form a silver (Ag)-incorporated titanium oxide (TiO2) outermost layer over a medical-grade 316L stainless steel by subsequent applications of cold spray (CS) and thermal oxidation (TO) processes. X-ray diffraction analysis, scanning electron microscopy examination and Raman analysis revealed that TO at 600°C for 60 h in the air formed a 3 μm thick exterior layer composed of the rutile form of titanium oxide and metallic silver over the CS coating fabricated by depositing a mixture of 87 wt.% titanium (Ti), 8 wt.% aluminium (Al) and 5 wt.% silver powder. This exterior layer exhibited superior bioactivity and wear resistance along with a sufficient antibacterial activity, which can further be improved by adjusting the distribution and/or content of silver in its structure.

Lithium (Li) metal is an attractive anode material with high capacity (3860 mAh g−1) and low potential (−3.04 V vs. standard hydrogen electrode) that shows highly promising for applications requiring high energy density. However, the low electrochemical potential of Li metal makes it extremely reactive and inevitably forming a native oxidized layer in the ambient environment and repeatedly being consumed when exposed to liquid electrolytes. It is therefore beneficial to replace the poorly controlled native passivation layer with a tailored artificial SEI to improve interface management between Li and electrolyte and enhance the stability of Li metal battery. Here, we use an integrated glovebox-atomic layer deposition (ALD)- X-ray photoelectron spectroscopy (XPS) setup to in-situ investigating the pristine Li surface and the surface composition after Ar, H2, O2, N2 and NH3 plasma treatment processes. We find that the pristine Li foil is naturally being covered with a native oxidized layer, which is mainly composed of LiOH, Li2O and Li2CO3. These investigated plasmas can efficiently remove the oxidized layer from the Li metal surface, in which metallic Li surface is obtained after Ar or H2 plasma treatments, where Ar plasma is more efficient. While O2 plasma treatment produces a Li2O layer, and N2 or NH3 plasma treatment leads to a Li3N (including a certain amount of LiON) layer on the Li surface. When employing the representative metallic Li (by Ar plasma treatment), Li2O layer coated Li (by O2 plasma treatment) and Li3N layer coated Li (by N2 plasma treatment) foils as electrodes in symmetric Li metal batteries, the Li3N coated Li electrode exhibits much higher stability than that of metallic and Li2O layer coated Li foils. Improved electrochemical performance has also been achieved in LiMn2O4 (LMO)||Li full cells using Li anode with Li3N protective coating layer. Our work reveals the detailed process of surface engineering of Li metal anodes with plasma treatments by in vacuo XPS, which may also be extended to other gas-treatment or plasma-treatment for stabilization of high energy density Li metal anodes and other metal-based anodes.

In this paper, 50 vol% TiCp/Ti6Al4V composites without pores, cracks or poor fusion were fabricated by laser melting deposition (LMD) technology using 500 W laser power (lower power, LP) and 1000 W laser power (higher power, HP). The microstructure of different deposited layers was analyzed and the corresponding microhardness was measured. The results show that the composites are composed of undissolved TiC, in-situ TiC (eutectic TiC and primary TiC), α Ti and β Ti. It is interesting that the microstructure from the bottom layer to the top layer presents a graded distribution when all layers have the same composition. The eutectic TiC is mainly formed in lower layers while the primary TiC is mainly in upper layers. With increasing layer number, the size and number of the primary TiC grains increase and the primary TiC grows gradually from granules into dendrites, however, the number of the undissolved TiC particles decreases along the depositing direction. The simulation results show that the peak temperature of deposited layer increases while the cooling rate decreases with increasing layer number. Different thermal history affects the diffusion of carbon and the evolution of TiC, and then affects the microstructure distribution of the composites. This graded microstructure leads to the graded distribution of microhardness. The microhardness of the LP composite rises from 432.5 HV to 488.1 HV, while the HP composite rises from 435.5 HV to 604.3 HV from the bottom layer to the top layer, respectively.

Two types of Y2O3 partially stabilized ZrO2(YSZ)-based agglomerated powders with and without SiC whiskers were prepared by spray granulation, and the flow ability, apparent density and particle size distribution of them were investigated. The thermal cycling performance and failure mechanism of conventional high temperature sealing coating and modified one with additional layer with whiskers, which were sprayed by air plasma spraying (APS), were comparatively analyzed. The results showed that, compared to the powder without whiskers, the flow ability of that with whiskers reduced by 2.32%, and the apparent density and the proportion of 45–150 μm agglomerated powder increased by 1.53% and 2.29%, respectively. The thermal cycling failure mode of conventional high temperature sealing coating was the overall spalling of ceramic coating, and the spalling position originated from the interface of thermally grown oxide (TGO)/ceramic coating. Microstructure observation indicated that the structure integrity of SiC whiskers in the additional layer sprayed by APS was still retained. The whiskers were uniformly distributed and the interfaces between bonding coating and ceramic coating exhibited excellent bonding. With the additional layer containing whiskers, the thermal cycling life of the coating was increased by 102.53%. In the thermal cycling process, the “bridging” and “pulling-out” effects of whiskers located at the additional layer consumed considerable energy, which could reduce the driving force of crack growth. Besides, a porous structure of the additional layer after thermal cycling was formed due to “bridging” and “pulling-out” of whiskers, further improving the thermal cycling life of coating with the additional layers.

In this study, the effect of the addition of vanadium (V) on the densification, microstructure, and wear behavior of borosintered powder metallurgy steels was investigated. Ball-milled powders containing 0, 1, 5 and 10 wt.% V were cold-compacted under 200 MPa pressure and then subjected to borosintering at 1100°C for 2 h in ambient air. The characterization of the boride layers formed after borosintering was conducted by scanning electron microscopy, X-ray diffraction, microhardness tests, nanoindentation, surface roughness measurements, and ball-on-disk-type wear tests. Wear testing was carried out under 10 N load for a total sliding distance of 250 m in ambient air and in a 3.5% sodium chloride (NaCl) solution. While the thickness of the boride layer decreased with increasing V content, its hardness and modulus of elasticity also increased, owing to the formation of additional vanadium boride (VB) and vanadium carbide (V2C) phases. Wear resistance increased with increasing V content, and the samples tested in 3.5% NaCl displayed lower coefficients of friction and higher wear resistance compared to the samples tested in ambient air. Reduced wear in 3.5% NaCl was attributed to the cooling and lubricant effects provided by the 3.5% NaCl solution.

Although the photovoltaic efficiency of organic solar cells (OSCs) has exceeded 17%, poor lifetime excludes OSCs from practical use. In particular, UV rays in sunlight may cause the decomposition o...

The effect of dip-coating parameters on the coating thickness and uniformity have been investigated for BaCe0.7Zr0.1Y0.16Zn0.04O3-δ (BCZYZ) electrolyte on porous NiO-BCZYZ tubular supports. The calculated thicknesses of electrolyte using both pre-fired and full fired tubes' dimensions and both wet and dry weight gains have been compared to the measured ones using Scanning Electron Microscopy (SEM) analysis after full firing. The calculated thicknesses using pre-fired tubes’ dimensions using both wet and dry weight gains are found in a good agreement with the measured thicknesses. The minimum coating thickness of 20.49 ± 3.36 μ with 16% standard deviation (StDev) is achieved using 1.91 mm·sec−1 (20 steps·sec−1) withdrawal speed and 30 s dwell time. The most uniform coating layer is obtained using that withdrawal speed and 60 s dwell time, leading 23.14 ± 1.69 μ coating thickness and the minimum StDev% of 7%. Using the polynomial fit between StDev% and dwell time, the minimum StDev% can be achieved at that withdrawal speed has been determined as 80 s. The coating parameters have been optimized as 1.91 mm·sec−1 withdrawal speed and 80 s dwell time for BCZYZ electrolyte on porous Ni/NiO-BCZY tubular supports.

This paper proposes a slurryless, highly efficient polishing method called ultrasonic vibration assisted electrochemical mechanical polishing (UAECMP) to realize 4H–SiC wafers with subnanometer surface roughness. UAECMP involves using ultrasonic vibration to simultaneously assist anodic oxidation of the SiC surface and mechanical removal of the generated oxide layer. The performance of UAECMP was evaluated by experiments and theoretical analyses. For a 4H–SiC (0001) surface, UAECMP achieved a material removal rate (MRR) of 14.54 μm/h, which was 4.5 times greater than that of ordinary electrochemical mechanical polishing (ECMP) and 290 times greater than that of mechanical polishing. Ultrasonic vibration increased the anodic oxidation rate by introducing local transient strain to the SiC surface and increasing the temperatures of the polishing area and electrolyte. The effect increased with the amplitude of the ultrasonic vibration. However, increasing the ultrasonic vibration amplitude also increased the surface roughness due to the large fluctuations of polishing marks caused by the grinding stone and SiC surface impact and the increasing residual oxide. Therefore, we propose a high-efficiency and -quality polishing process for SiC wafers that combines UAECMP and ECMP. The proposed polishing process may help simplify the existing manufacturing process for SiC wafers.

The corrosion mechanisms that occurred between the slag-line and mold flux under the applied external electric field are studied. The results show that the slag-line can be effectively protected when the slag-line is connected to the negative electrode, and the graphite as an auxiliary electrode is connected at positive potential. Under the applied negative electric field, a thick protective adhesion layer is formed on the surface of the slag-line due to the electrochemical reactions. Additionally, the slag-line material is further reacted with surface of the formed protective layer and generates another interface reaction layer. Under the effect of double protective layers, the slag-line can be perfectly devoid of corrosion attack under the negative electric field. The performance of the slag-line and the production time of the whole continuous casting can be improved. The external electric field is expected to be a new technical approach to alleviate corrosion of the SEN.

In this work, we studied the effect of Cr element on the corrosion resistance evolution of weathering steel based on corrosion big data technology. It suggested that corrosion big data technology is suitable for evaluation of the effect of microalloying Cr element on the corrosion evolution behavior of weathering steel. New understandings prove that the effect of Cr on the corrosion process is dynamic rather than static, the processes is affected by both of the environmental factors and the electrochemical or chemical reactions in the rust layer. Besides, Cr element has both beneficial effect and detrimental effect on the corrosion resistance of weathering steel. The beneficial effect is that the general corrosion resistance of Cr-additional steel is better than that of Cr-free steel, while the detrimental effect is that localized corrosion is intensified as the increase of Cr content in the Cr-additional steel.

In this work, the corrosion behaviors of as-plasma sprayed Yb2SiO5 and LaMgAl11O19 coatings under an environment with a volumetric ratio of 90% H2O-10% O2 were investigated at 1300 °C. The results showed that Yb2SiO5 and LaMgAl11O19 coatings had good water vapor corrosion resistance. Therefore, Si/Yb2SiO5/LaMgAl11O19 tri-layer EBCs were designed and prepared to completely cover the surface of SiCf/SiC by using atmospheric plasma spraying (APS). The water vapor corrosion behaviors of SiCf/SiC with and without EBCs at 1300 °C were investigated. The results showed that tri-layer coating can provide better corrosion resistance for SiCf/SiC at a high-temperature steam environment at 1300 °C. By comparing the water vapor corrosion behaviors of single-layer coatings and the tri-layer EBCs under same corrosion environment, it was found that the thermal mismatch stress and the formation of TGO is the main causes of tri-layer coating failure.

Three different coatings, namely TiAlN, TiAlN (external)/NbN (internal) and NbN (external)/TiAlN (internal), were deposited on cemented carbides by arc ion plating. The comparative investigation conducted in this study elucidates the effect of the NbN layer and coating systems on the growth, mechanical properties, and tribological performance of the coatings. The results showed that the surface of the TiAlN and TiAlN/NbN coatings was smoother when TiAlN served as the external layer. The NbN/TiAlN coating, wherein NbN formed the external layer, had a much rougher but more symmetrical surface. With the introduction of the NbN layer, the increased micro stress induced a lower adhesion strength in the TiAlN/NbN and NbN/TiAlN coatings. The TiAlN/NbN and NbN/TiAlN coatings exhibited higher hardness and hardness/effective elastic modulus (H/E*). During the friction test, when the temperature was elevated to 700 °C, the tribological performance of the monolayer TiAlN coating was the lowest because of the TiO2-induced breakage of the dense tribo-oxide film. The NbN layer participated in the formation of a NbOx film at elevated temperatures, which was responsible for the high tribological performance of the two bilayer coatings. When the NbN layer was on the outermost layer and in direct contact with the elevated temperature atmosphere, the NbN/TiAlN coating generated a tribo-oxide film with high integrity, and its coefficient of friction decreased by 27% of that at room temperature. Therefore, the NbN/TiAlN coating exhibited the highest wear resistance at 700 °C.

Metallic lithium (Li) is known to consider a critical role in next-generation rechargeable batteries. However, the uncontrolled growth of Li dendrites result in low Coulombic efficiency and safety issues in applications of Li metal batteries. High capacity and stable dense deposits of lithium metal are of great significant for high energy density battery. Herein, we propose a suitable degree of substitution for Carboxymethylcellulose Lithium (CMC-Li) as an artificial SEI layer, which has a high ionic transference number (0.66), high Young's modulus (24.6 GPa) and good lithiophilicity, then it can adapt to the volume changes of the lithium anode, enable superdense lithium deposits on Cu collector. The metallic lithium anode with CMC-Li films (CMC-Li@Li) delivers excellent cycling performance in the symmetrical cell at a large current density of 10 mA cm−2 and an areal capacity of 10 mAh cm−2 for almost 300 h. Moreover, the CMC-Li@Li||NCM613 full cell (N/P=2) delivers an initial specific capacity of 165 mAh g−1 with a high retention of 80% after 200 cycles.

As a high-k material, hafnium oxide (HfO2) has been used in gate dielectrics for decades. Since the discovery of polar phase in Si-doped HfO2 films, chemical doping has been widely demonstrated as an effective approach to stabilize the ferroelectric phase in HfO2 based thin films. However, the extra capping layer deposition, post-growth annealing and wake-up effect are usually required to arouse the ferroelectricity in HfO2 based thin films, resulting in the increase of complexity for sample synthesis and the impediment of device application. In this study, the ferroelectricity is observed in non-capped dopant-free HfO2 thin films prepared by pulsed laser deposition (PLD) without post-growth annealing. By adjusting the deposited temperature, oxygen pressure and thickness, the maximum polarization up to 14.7 μC/cm2 was obtained in 7.4 nm-thick film. The fraction of orthorhombic phase, concentrations of defects and size effects are considered as possible mechanisms for the influences of ferroelectric properties. This study indicates that PLD is an effective technique to fabricate high-quality ferroelectric HfO2 thin films in the absence of chemical doping, capping layer deposition and post-growth annealing, which may boost the process of nonvolatile memory device application.

Antimony sulfide (Sb2S3) is an appealing semiconductor as light absorber for solar cells due to its high absorption coefficient, appropriate band gap (~1.7 eV) and abundance of constituent elements. However, power conversion efficiency (PCE) of Sb2S3-based solar cells still lags much behind the theoretically predicted due to the imperfect energy level alignment at the charge transporting layer/Sb2S3 interfaces and hence severe charge recombination. Herein, we insert a high-temperature sintered magnesium (Mg)-doped tin oxide (SnO2) layer between cadmium sulfide (CdS) and fluorine doped tin oxide to form a cascaded energy level alignment and thus mitigate interfacial charge recombination. Simultaneously, the inserted Mg-doped SnO2 buffer layer facilitates the growth of the neibouring CdS film with orientation followed by Sb2S3 film with larger grains and fewer pinholes. Consequently, the resultant Sb2S3 solar cells with Mg-doped SnO2 deliver a champion PCE of 6.31%, 22.8% higher than those without a buffer layer. Our work demonstrates that deliberate absorber growth as well as efficient hole blocking upon an appropriate buffer layer is viable in obtaining solution-processed Sb2S3 solar cells with high performance.

The behavior of single water drop impacting an oil layer on the deep water pool was recorded by using a high-speed camera. Heptane was used as the target liquid layer on the water pool. A particular phenomenon of double crown can be observed. The formation of double crown is not only related to the impact Weber number of the water droplet, but also the thickness of the oil layer. The critical Weber number for the formation of double crown decreases sharply as the decrease of the oil layer thickness. With the increase of Weber number and the decrease of oil layer thickness, there are four typical phenomena: single crown-jet, single crown-bubble, double crown-bubble and double crown- jet. Moreover, the effects of oil layer thickness and impact Weber number on surface bubble lifetime and the geometry size of crown, crater and jet were quantitatively analyzed.

To enhance the corrosion resistance of an aluminum (Al) 6082 alloy, our research used electroless deposition to coat a trio sequence of Zn-Cu-Sn layers: zinc, copper and tin. To isolate the reactions and micro-mechanisms in the tin coating, the Zn-Cu layering parameters of time, temperature, and bath concentration were held constant while varying those during the Sn electroless deposition. Microstructures and layer thicknesses of the coated samples were studied using both optical and scanning electron microscopy (SEM). Local chemical compositions were analyzed using energy dispersive spectroscopy (EDS). Tin deposition on the Cu layer starts with a displacement reaction formed by the nucleation of discontinuous bulges that gradually grow into inhomogeneous crowns. During Sn deposition, surface Cu consumption and bath composition varies hindering access to displacement reactants, thus curtailing the significance of displacement. However, deposition continues via reduction and disproportionation directly tied to the solution. Peak layer quality was deposited at a temperature of 45 oC with a 1.5 times concentration for 1200 sec. Anti-corrosion behavior of the Sn-coated sample was examined by Electrochemical Impedance Spectroscopy (EIS) to detect notable enhancement.

Lithium (Li) metal batteries have received extensive research focusing on the dendrite growth issue on account of the high chemical activity of Li anode. While, thermal safety, as one of the important security concerns facing the further application, gets little attention. Here, the high-performance polyimide film is successfully developed to enhance the safety margin based on the excellent mechanical strength and heat resistance corresponding to the traditional separator. And, the polyimide film with the MoS2 coating made by spraying method as the composite separator can not only improve the wettability to the electrolyte, but also in-situ form an artificial layer with the low nucleation barrier for the Li ions. When used in both the coin cell and the pouch cell, all achieve the outstanding cycling stability and the coulombic efficiency. Specially, the in-situ Li ions nucleation behaviors are investigated by optical microscopy in the capillary cell. The electric field intensity at the Li anode surface is also simulated by COMSOL Multiphysics to further elucidate the effect of the coating.

Perovskite functional ceramics have been widely applied for thermal protection owing to their unique physical properties. However, formation of oxygen vacancies under external stimuli usually limits their performance in practical applications. Therefore, the mechanism of the effect of oxygen vacancy on the layer structure of perovskite La0.9Sr0.1TiO3+δ was investigated by experiments and first-principles simulations. The experimental results showed that the lattice distortion occurred in oxygen-deficient environment to give a longer c-axis, along with a significant adjustment in the modes of A/B–O bond vibration, resulting in lower reflectivity. Advanced transmission electron microscopy studies revealed that oxygen vacancies induced localized atomic rearrangements via [TiO6] layer movements to adapt to the lattice distortion. This eventually restructured a part of the layer interfaces by expanding the overlapping projection of atoms in the c-axial direction. The specific transformation process was described as a compendious process, while geometric phase analysis effectively clarified how oxygen vacancies can inhibit reflectivity on the layer structure. Thus, this study provides effective approaches for researching the effects of oxygen vacancy on the physical properties of orthorhombic layer perovskite structures, which may facilitate the development of perovskite-based functional devices.

Roll-to-roll (R2R) slot-die coating of polymer electrolyte membrane fuel cell (PEMFC) catalyst layers represents a scalable deposition method for producing 10-20 m2·min-1 of catalyst-coated gas diffusion layers (GDLs). This high-throughput production technique will help lower the cost of PEMFC catalyst layers. The uniformity of the wet layer applied by slot die deposition is affected by process parameters such as substrate speed, vacuum pressure applied at the upstream meniscus, gap between the slot die lips and substrate, ink rheology, and other ink and substrate properties. The set of conditions for producing a defect-free coating with a dilute ink typically requires little to no upstream vacuum pressure, so suitable operating conditions can be found easily through trial and error and operator intuition. However, the higher viscosity of more concentrated inks dramatically shifts the range of settings that result in a homogeneous coating to higher vacuum levels, which are harder to find through hit or miss. A predictive model showing the range of operable conditions decreases material wastage inherent in experimentally searching for suitable parameters. In this study, the defect-free coating parameter window is explored experimentally and theoretically for two concentrations of PEFC cathode inks. Both a full capillary hydrodynamic model and a computationally cheaper viscocapillary model successfully predict the experimentally determined coating window within the experimental and model uncertainty limits for inks with 5.3 wt.% and 12.0 wt.% solids ink while maintaining the 0.1 mgPt·cm-2 Pt areal loading target. This paper demonstrates a viable pathway for meeting the $30/kWnet ultimate cost target of the United States Department of Energy (U.S. DOE) Hydrogen Fuel Cells Technologies Office (HFTO). The concentrated ink lowers the thermal energy and capital expenditure (CapEx) budget of the coating process by decreasing the amount of time, energy, and floorspace required for drying the coating.