Surface Structure Research Articles

High-Quality Thiophene-Based Two-Dimensional Perovskite Films Prepared with Dual Additives and Their Application in Solar Cells.

This study explores the optimization of (TMA)2MA4Pb5I16 perovskite films by regulating the film quality through the addition of MACl and MAAc additives. We found that adding MACl resulted in a film of larger grains with a power conversion efficiency (PCE) of 5.34%, while excessive MACl led to the formation of low-dimensional phases. Adding 7.5% MAAc improved the film quality with a PCE of 5.64%, although excessive MAAc induces pores and smaller grains. To address these issues, we proposed the combined use of MACl and MAAc additives, resulting in films with a larger grain size, smoother surface, and denser structure. Remarkably, the addition of MAAc + MACl achieved a champion PCE of 8.86% with good reproducibility. Mechanism studies revealed that TMA and MAAc formed a stable complex with PbI2 in solution, disrupting nucleation laws and promoting the formation of nuclei, leading to denser films with smaller grains. Additionally, the MACl treatment effectively promoted grain growth, resulting in high-quality films. This study presents novel insights into dual additive usage and their role in film crystallization, offering valuable guidance for the preparation of high-performance perovskite films.

Cultural adaptation of an internet-based self-help app for grieving Syrian refugees in Switzerland.

Loss and grief pose significant challenges for victims of armed conflicts, such as Syrian refugees. Internet-based interventions (IBIs) present a promising solution to address this treatment gap and provide adequate support. However, research on grief, grief support, and IBIs remain largely limited to Western cultural contexts, and culturally adapted IBIs for grief are needed. Following the Reporting Cultural Adaptation in Psychological Trials (RECAPT) framework, this study aimed to develop and further adapt a culturally sensitive IBI for bereaved Syrian refugees in Switzerland. The study employed qualitative methods. Initially, formative research was conducted to create a first version of the intervention, including semi-structured interviews with 10 experts to identify necessary cultural adaptations. The preliminary version of the intervention was then presented to six potential users and three experts to gather feedback on additional cultural adaptations through two iterative feedback rounds. The first round involved semi-structured interviews using a "paper version" of the intervention, followed by a second round with a walk-through think-aloud protocol with a beta version. Data were analyzed using framework analysis. The input from various key informants at different stages of development provided valuable feedback on surface and deep structure adaptation, which may enhance treatment adherence, acceptance, and motivation. These findings provide important insights and recommendations for the cultural adaptation of interventions and may help address the treatment gap for bereaved Syrian refugees.

Polymicrobial interactions between Staphylococcus aureus and Pseudomonas aeruginosa promote biofilm formation and persistence in chronic wound infections.

Chronic, non-healing wounds are a leading cause of prolonged patient morbidity and mortality due to biofilm-associated, polymicrobial infections. Staphylococcus aureus and Pseudomonas aeruginosa are the most frequently co-isolated pathogens from chronic wound infections. Competitive interactions between these pathogens contribute to enhanced virulence, persistence, and antimicrobial tolerance. P. aeruginosa utilizes the extracellular proteases LasB, LasA, and AprA to degrade S. aureus surface structures, disrupt cellular physiology, and induce cell lysis, gaining a competitive advantage during co-infection. S. aureus evades P. aeruginosa by employing aggregation mechanisms to form biofilms. The cell wall protein SasG is implicated in S. aureus biofilm formation by facilitating intercellular aggregation upon cleavage by an extracellular protease. We have previously shown that proteolysis by a host protease can induce aggregation. In this study, we report that P. aeruginosa proteases LasA, LasB, and AprA cleave SasG to induce S. aureus aggregation. We demonstrate that SasG contributes to S. aureus biofilm formation in response to interactions with P. aeruginosa proteases by quantifying aggregation, SasG degradation, and proteolytic kinetics. Additionally, we assess the role of SasG in influencing S. aureus biofilm architecture during co-infection in vivo, chronic wound co-infections. This work provides further knowledge of some of the principal interactions that contribute to S. aureus persistence within chronic wounds co-infected with P. aeruginosa, and their impact on healing and infection outcomes.

One-Step Carbonization Synthesis of N, S Co-Doped Carbon Materials Derived from Agricultural Waste Peanut Shells for High-Performance Symmetric Supercapacitors.

Biomass carbon has the advantages of wide source, low cost and environmental protection, and has been widely used in the field of electrochemical energy storage. In this work, N and S co-doped carbon materials were prepared by using peanut shell as carbon source and thiourea as activator. When the peanut shell and activator were 2 g and 4 g, respectively, the prepared NSPC-4 had the largest specific surface area and special pore structure. Elemental analysis showed that the activator introduced more N, S and O atoms to the carbon material, and more heteroatoms helped to improve the surface structure of the carbon material and provide additional pseudocapacitance. In addition, NSPC-4 contains a short-range ordered graphite structure, which can provide excellent electrical conductivity. The electrochemical test results show that NSPC-4 has the largest specific capacitance. When the mass of the activator is higher than or below 4 g, the electrochemical performance of the carbon material will be reduced. The symmetric supercapacitor (SSC) assembled by NSPC-4 has an energy density of 8.3 Wh kg-1 when the power density is 350 W kg-1. The synthesis method is not only simple, green and economical, but also has important application value.

Low-Cost and Contactless Survey Technique for Rapid Pavement Texture Assessment Using Mobile Phone Imagery

Collecting pavement texture information is crucial to understand the characteristics of a road surface and to have essential data to support road maintenance. Traditional texture assessment techniques often require expensive equipment and complex operations. To ensure cost sustainability and reduce traffic closure times, this study proposes a rapid, cost-effective, and non-invasive surface texture assessment technique. This technology consists of capturing a set of images of a road surface with a mobile phone; then, the images are used to reconstruct the 3D surface with photogrammetric processing and derive the roughness parameters to assess the pavement texture. The results indicate that pavement images taken by a mobile phone can reconstruct the 3D surface and extract texture features with accuracy, meeting the requirements of a time-effective documentation. To validate the effectiveness of this technique, the surface structure of the pavement was analyzed in situ using a 3D structured light projection scanner and rigorous photogrammetry with a high-end reflex camera. The results demonstrated that increasing the point cloud density can enhance the detail level of the real surface 3D representation, but it leads to variations in road surface roughness parameters. Therefore, appropriate density should be chosen when performing three-dimensional reconstruction using mobile phone images. Mobile phone photogrammetry technology performs well in detecting shallow road surface textures but has certain limitations in capturing deeper textures. The texture parameters and the Abbott curve obtained using all three methods are comparable and fall within the same range of acceptability. This finding demonstrates the feasibility of using a mobile phone for pavement texture assessments with appropriate settings.

Welding Pollen-Based Solar Evaporator for Clean Water Production.

The world faces a trade-off between water availability and food supply, as agricultural irrigation consumes the largest freshwater globally. Inspired by inherent water transport channels in plants, a cost-effective welding pollen-based solar evaporator (PSE) is developed to obtain clean water from seawater desalination. Based on the convex and folded surface structure of natural pollen (Helianthus annuus) and the porous structure of welding pollen evaporator interconnection, the PSE reveals an efficient evaporation rate of 1.86kg m-2 h-1 under one-sun illumination and further exhibits excellent cycling performance for 10 cycles tested in 7.0 wt.% saline water without salt accumulation. In addition, PSE has superior mechanical stability (3.44MPa) and remains stable after being immersed in pH 1 and 14 solutions for 24 h without sacrificing mechanical properties. Importantly, the work has demonstrated the success of the freshwater collected from the evaporation process, which can effectively facilitate the cultivation of lettuce, rice, and wheat. These findings highlight the practical application of pollen as a low-cost, eco-friendly natural resource in interfacial solar evaporation. Furthermore, they inspire addressing current global water scarcity and promoting sustainable agriculture.

3D morphometry of Martian craters from HRSC DEMs using a multi-scale semantic segmentation network and morphological analysis

The morphology of impact craters reveals the structure and composition of the Martian surface, especially the subsurface conditions and Martian geological history, which have increasing importance in Mars exploration missions. This work presents a 3D morphometric method for detecting and delineating Martian craters, and a 3D morphological analysis was conducted. Specifically, this work first focused on the segmentation of Martian craters. Based on the segmentation results, clustering of crater instances was then carried out. Finally, with the individual craters that were extracted, a morphological analysis involving the measurements of their diameter, depth, area, RMS height, rim height, circularity, and the statistics thereof was performed. Unlike previous studies, which have mainly used optical images and object detection approaches, this work regards crater extraction as a semantic segmentation task instead of an object detection task to better delineate the precise shape and boundary information. Digital elevation model (DEM) was utilized as primary data to directly obtain 3D information, which was converted into 3D point cloud format and fed to a multi-scale semantic segmentation network. The semantic segmentation results achieved an overall accuracy of 0.932 and mIOU of 0.871 on the test data. We automatically counted 63 craters in Noachis Terra and 40 craters in Terra Cimmeria. The 3D morphological measurements showed that 66% of the impact craters in the first region were larger than 10 km in diameter, while 50% of the impact craters in the second region were larger than 10 km. In both areas, craters could reach a maximum depth of 2000 m. With the proposed method, we can automatically conduct 3D morphological measurements of Martian craters with high efficiency that is improved by 15 times compared with that of manual crater analysis tools. The achieved 3D morphometric results can provide a reference and support for future research on Martian landforms.

Influence of Detonation Spraying Parameters on the Microstructure and Mechanical Properties of Hydroxyapatite Coatings.

The process of osteointegration depends significantly on the surface roughness, structure, chemical composition, and mechanical characteristics of the coating. In this regard, an important direction in the development of medical materials is the development of new techniques of surface modification and the creation of bioactive ceramic coatings. Calcium-phosphate materials based on hydroxyapatite have been proposed as bioactive ceramic coatings on titanium implants for the effective acceleration of bone tissue healing. To obtain bioactive ceramic coatings, pulse power sources are best suited, namely detonation spraying, in which the energy of the explosion of gas mixtures is used as a source of pulse action. The pulse mode of operation in the detonation spraying method is preferable for the formation of bioactive ceramic coatings. It provides a high velocity of hydroxyapatite particles, which promotes their effective fixation on the titanium substrate, while minimizing the heating of the material. This approach preserves the substrate structure and improves the coating adhesion. Four different types of coatings with varying O2/C2H2 molar ratios, ranging from 2.6 to 3.7, were obtained using detonation spraying. Powders and obtained coatings of hydroxyapatite were studied by Raman spectroscopy and XRD structural analysis. The results of XRD phase analysis showed the partial conversion of the hydroxyapatite phase to the α-tricalcium phosphate (α-TCP) phase during the detonation spraying process. The results obtained by Raman spectroscopy indicate that hydroxyapatite is the main phase in coatings. All hydroxyapatite-based coatings exhibited hydrophobic properties, which was confirmed by contact-angle values above 90° in wettability tests, characteristic of hydrophobic surfaces. The adhesive strength of the coatings was measured by the scratch test method. Tribological tests were conducted using the ball-on-disk method under both dry conditions and in Ringer's solution. This approach enabled the evaluation of wear resistance and friction coefficient of the coatings in different environments, simulating both lubrication-free conditions and those resembling physiological environments.

Self-consistent quasiparticle GW and hybrid functional calculations for Al/InAs/Al heterojunctions: Band offset and spin-orbit coupling effects

The electronic structure of surfaces and interfaces plays a key role in the properties of quantum devices. Here, we study the electronic structure of realistic Al/InAs/Al heterojunctions using a combination of density functional theory with hybrid functionals and state-of-the-art quasiparticle GW (QSGW) calculations. We find a good agreement between QSGW calculations and hybrid functional calculations, which themselves compare favorably well with angle-resolved photoemission spectroscopy experiments. Our paper confirms the need for well-controlled quality of the interfaces to obtain the needed properties of InAs/Al heterojunctions. A detailed analysis of the effects of spin-orbit coupling on the spin splitting of the electronic states shows a linear scaling in k space, related to the two-dimensional nature of some interface states. The good agreement by QSGW and hybrid functional calculations opens the door towards trustable use of an effective approximation to QSGW for studying very large heterojunctions. Published by the American Physical Society 2024

Development of waterborne epoxy-based resin incorporated with modified natural rubber latex for coating application

Water-based coating has gained much attention globally due to environmental issues. This work aims to develop a waterborne epoxy coating incorporated with modified natural rubber (NR) latex for improved performance. For this purpose, the NR latex was modified into three types of low molecular weight epoxidized natural rubber (LENR) latex. The waterborne epoxy resin was prepared by simply mixing the epoxy resin with an amine curing agent in water and various LENR latex contents (10 to 50 wt%). The waterborne epoxy/LENR blend was coated on a tin substrate and the cured coating demonstrated better adhesion and bending properties than the neat epoxy. Phase morphological properties displayed a rough surface with a heterogeneous surface structure of the dispersed rubber and epoxy matrix. Two glass transition temperatures were observed, corresponding to the rubber modifier and the epoxy matrix. The mechanical properties of the thermosetting epoxy/LENR blends were assessed, revealing a maximum increment in elongation ability by approximately 370% for adding 50 wt% LENR, compared to the neat epoxy. These results hold the potential avenue for utilizing NR-based material in the waterborne epoxy-based resin for coating applications. Furthermore, it contributes to the NR, a renewable and eco-friendly material, in the coating technology, embracing a sustainable future.

Potential-Dependent ATR-SEIRAS and EQCM-D Analysis of Interphase Formation in Zinc Battery Electrolytes.

With the heightening interest in bivalent battery technology, there arises a necessity for a thorough investigation into zinc-ion battery (ZIB) electrolytes, accommodating their chemical attributes and potential-dependent structural dynamics. While the phenomenon of in situ solid electrolyte interphase formation is extensively documented in lithium-ion batteries, its analogous occurrences in ZIBs remain limited. Herein is a comparative study of three zinc electrolytes of interest: ZnSO4, ZnOTF, and Zn(TFSI)2/LiTFSI hybrid water-in-salt electrolyte. Additionally, the impact of an acetonitrile additive is scrutinized, with a comparative assessment of the interfacial behavior in aqueous solutions. Utilizing ATR-SEIRAS, potential-dependent alterations in the composition of the electrolyte/electrode interface were monitored, while EQCM-D facilitated a comprehensive understanding of variations in the mass and structural properties of the adsorbed layer. Aqueous ZnSO4 demonstrated the accumulation of porous Zn4SO4(OH)6·xH2O at negative potentials, leading to a mass of 1.47 μg cm-2 after five cycles. Bisulfate formation was observed at positive potentials. SEIRAS measurements for ZnOTF demonstrated reorientation and surface adsorption of CF3SO3- to favor CF3 at the surface for positive potentials, and acetonitrile showed increased stability for the electrode at negative potentials. The additive was also reported to lead to the accumulation of a substantial passivation layer with viscoelastic properties. The zinc water-in-salt showed exceptional surface stability at negative potentials and a widened potential window. A thin rigid zinc SEI layer is reported with a mass of 0.7 μg cm-2. The compositional intricacies of these surface structures are discussed in relation to their solvent conditions. This investigation not only sheds light on the initial charge/discharge cycles in ZIBs but also underscores their pivotal role in instigating enduring transformations that can significantly influence their long-term cycling performance.

Laser power modulation between disturbed and undisturbed material removal regime in laser chemical processing

Laser chemical machining (LCM) is a method for removing material by thermally induced chemical dissolution of self-passivating metals. However, the process window is limited by disrupted material removal due to gas bubble formation and metallic salts and oxides deposition at higher energy input. Since the temperature increases, and therefore gas bubble growth takes time, it is hypothesized that the temporal modulation of laser power can remove the metal homogeneously, i.e., without disrupted material removal, while achieving a higher removal rate. Based on this, the dynamic process behavior of material removal is investigated for the LCM of titanium in phosphoric acid, using a rectangular modulation of the laser power with varying irradiation durations. As a result, however, high-speed videos show that gas bubbles are consistently generated, regardless of the applied laser power and power modulation, although the quantity of bubbles varies with different parameters. Even with short power durations (10 ms), the material deposition occurs after multiple irradiations. When the duration is longer, the material deposition increases in height along the laser scan direction. For the studied process parameters, a Fourier analysis in the spatial domain further indicates the correlation between the material removal frequencies and the modulation frequencies. In conclusion, the laser power modulation cannot prevent the disturbed material removal at high laser powers. Nevertheless, the material deposition can be utilized to generate periodic surface structures with a depth below and above the initial surface.

Glycation of sunnhemp protein with dextran via dry heating: Thermal, micro-structural characterization, and amino acid profiling.

This study aims to obtain sunnhemp protein isolate (SHPI) and dextran conjugates by dry heating method of Maillard conjugation. The effects of different incubation time (0, 1, 3, 5, 7, and 9 days) on the molecular flexibility, available lysine content, antioxidant properties, molecular structure, and thermal and micro-structural properties of conjugates were compared with SHPI (no conjugation) at 60°C and 79% relative humidity. The results indicated the formation of SHPI-dextran conjugates as confirmed by the change in molecular flexibility, lysine content, antioxidant activities, color, and water activity values. The molecular structure revealed the confirmation of covalent bonding between SHPI and dextran. Differential scanning calorimetry and thermo-gravimetric analysis results exhibited improvement in the thermal stability of SHPI when conjugated with dextran. The microstructural characterization showed that Maillard conjugation changed the surface structure of SHPI. The analysis of amino acid composition displayed that lysine, arginine, and phenylalanine were the dominant Maillard reaction sites of SHPI and dextran. Among all the conjugated samples, 5 days of incubation time was selected as an optimum condition for the development of SHPI-dextran conjugates on the basis of the aforementioned characterization. Overall, it was concluded that Maillard conjugation of sunnhemp protein with dextran via dry-heating technique could modify and improve its various attributes. PRACTICAL APPLICATION: The conjugation of plant proteins with polysaccharide through the Maillard reaction under dry heating conditions represents a natural and green technique for improving the techno-functional properties of proteins. The study has the potential to establish framework for the utilization of Sunnhemp protein isolate-dextran conjugates. This approach offers the potential for cost-effective production of emulsifiers and development of effective encapsulating matrices. The investigation expands on an underutilized plant protein source facilitating an alternative to animal-based proteins and contributing to the development of a sustainable circular bioeconomy.

Morphological, physicochemical, and pasting properties of pre-gelatinized starch prepared by high-pressure homogenizer: A comparative study on starches from different resources

Pre-gelatinized starch, a physically modified starch known for its ability to swell in cold water, has wide applications across various industries. This study assesses the feasibility of high-pressure homogenization (HPH) in producing pre-gelatinized starches and compares their morphological, physicochemical, and pasting properties from different sources. Starches from eleven sources, including mung bean, pea, wheat, sweet potato, cassava, corn, non-waxy rice, waxy rice, chickpea, lentil, and chestnut, were processed using HPH at 150 MPa for three cycles. The resulting pre-gelatinized starch granules exhibited disrupted surface structures, increased water absorption and solubility, decreased crystallinity, and altered gelatinization temperatures. Results showed that waxy rice pre-gelatinized starch had the highest degree of pre-gelatinization (90.27%) and water absorption index (61.95%), while chestnut pre-gelatinized starch had the highest water solubility index (21.58%) and lentil pre-gelatinized starch demonstrated the highest gel strength (2178.00 g). X-ray diffraction analysis revealed a significant reduction in crystallinity, with values ranging from 13.96% to 18.29%. Additionally, the study observed variations in pasting properties, with cassava pre-gelatinized starch exhibiting the highest peak viscosity (5458 cP), trough viscosity (3864 cP), and final viscosity (6536 cP). These findings indicate that HPH is an effective method for producing pre-gelatinized starch with enhanced functional properties, enriching the scientific understanding of pre-gelatinized starches from different sources and promoting their application in the food industry and other sectors.

Computer-aiding evaluation of north wall effects of a solar greenhouse: Multiphysics modelling of the indoor environment

The north wall (NW) of a solar greenhouse (SG), oriented away from direct sunlight, plays a crucial role in thermal insulation; however, impacts of the NW internal surface structure (ISS) on the SG indoor environment remains underexplored. Driven by in situ measurements, the temperature (Ti) and relative humidity (RHi) of a SG are evaluated for three typical NW designs: flat wall (FW), striped wall (SW) and alveolate/honeycombed wall (AW). In both sunny and cloudy scenarios, the AW setup ensures a more favourable thermal environment, well aligned with the power spectral analysis indicating enhanced thermal energy capture. The time-lagged cross correlation highlights solar radiation as the primary driver of SG internal thermal variability, with outdoor temperature being of secondary relevance. Additionally, the AW setup consistently maintains the lowest RHi on sunny days, promoting optimal conditions for plant growth, and ensures more stable humidity levels during cloudy nights. The revealed response of SG internal environments to modified NW ISS should offer some insights into SG design, particularly in optimising conditions for plant growth through modifications to the NW structure.

On the Relationship between Water Adsorption and Surface Chemistry in Soda-lime Silicate Glasses.

Understanding how the surface structure affects the bioactivity and degradation rate of the glass is one of the primary challenges in developing new bioactive materials. Here, classical and reactive molecular dynamics simulations are used to investigate the relationship between local surface chemistry and local adsorption energies of water on three soda-lime silicate glasses. The compositions of the glasses, (SiO2)65-x(CaO)35(Na2O)x with x=5, 10, and 15, were chosen for their bioactive properties. Analysis of the glass surface structure, compared to the bulk structure, showed that the surface is rich in modifiers and non-bridging oxygen atoms, which were correlated with local adsorption energies. The reactivity of the glasses is found to increase with higher Na2O content, attributed to elevated Na cations and undercoordinated species at the glass surfaces. The current work provides insights into the relationship between the surface structure, chemistry, and properties in these bioactive glasses and offers a step toward their rational design.

Dopant effects on the environment-dependent chemical properties of NiO(100) surfaces

NiO is a promising material for applications such as electronic devices and catalysts due to its low cost, environmental friendliness, and optimal chemical and electronic properties. Inclusion of a dopant element into the NiO near surface structure can further tune material properties. Despite extensive studies on doped NiO (M−NiO) materials, there remains a lack of knowledge regarding the connection between dopant, environment-dependent dominant near surface structures, and overall chemical properties. Here, the dopant effects on the near surface structure and electronic properties on M−NiO(100) are systematically examined using a combination of density functional theory (DFT) and ab initio phase diagrams. The simultaneous factors tested include dopant element (Al, Mo, Nb, Sn, Ti, V, W, or Zr), dopant placement (surface or subsurface), Ni/O vacancies (surface or subsurface), and oxygen species (O* or O2*) adsorption. The results reveal the dominant structures and compositions of M−NiO(100) under a wide range of environmental conditions (i.e. varying temperature and pressure). Subsequent electronic analyses of the dominant M−NiO(100) structures show non-uniform changes in charge redistribution, band gap, work function, and d-band center with dopant and near surface structure, emphasizing the role of dopants in tuning M−NiO(100) both geometric and electronic properties. Overall, these multiscale modeling results enable a rapid, effective, and a priori prediction of dominant M−NiO(100) structures with distinct chemical properties, crucial for guiding NiO-based materials design with enhanced performance for advanced electronics, energy storage, and catalytic systems.

Estimation, tuning, and evaluation of propagation direction behavior in superimposed orthogonal two-dimensional structure-borne traveling waves

Abstract Structure-borne traveling waves (SBTW) are observed in nature as a means for propulsion and locomotion of creatures on land and in the ocean. Recently, various approaches have been investigated to replicate this phenomenon. Previous studies have successfully generated SBTWs suitable for propulsion applications and particle motion on active surfaces. Much recent literature has focused on generating traveling waves that propagate only along a single axis for 1D and 2D structures. This limits their potential and does not take advantage of the full potential of 2D structures.
This study examines the potential of employing superposition to control the propagation direction of 2D SBTW. This is investigated numerically using an experimentally validated Finite Element model of a 2D plate with piezoelectric actuators. The individual SBTWs are superimposed by simultaneously exciting two pairs of actuators that are aligned orthogonally on the surface of a plate. Traveling waves are excited in the plate using two-mode excitation. Structural intensity is utilized to develop quantifiable metrics to describe the overall propagation direction and uniformity, which are necessary for describing the complex propagation patterns encountered with 2D SBTW. The potential of the proposed approach along with developed tuning and evaluation methods are demonstrated through case studies of two plates, one square and one rectangular. For both cases, the overall direction of the SBTW is tuned to propagate for any direction between the individual SBTW. This was achieved while maintaining a high-quality overall SBTW. With this approach, 2D SBTW can be steered for wave-driven motion applications such as propulsion of the structure itself or conveying particles in any direction along the structure's surface without compromising the quality of the overall traveling wave.

Surface structure reconstruction to suppress heterogeneous phase transformation for air-stable single crystalline O3-type sodium oxide

O3-type layered oxide cathode material for sodium-ion batteries (SIBs) has attracted much attention as one of the most viable candidates due to its high specific capacity and mature synthesis process, while the moisture sensitivity and harmful phase transformation lead to poor processing properties and unsatisfactory life-span, hindering its large-scale and commercial application. Herein, single crystallization strategy is adopted to enhance air stability and processing performance, and surface structure reconstruction for single crystalline cathode material O3-NaNi1/3Fe1/3Mn1/3O2 by ammonium tetraborate pretreatment is employed to further remove residual alkali and improve sodium ions diffusion dynamics and suppress heterogeneous phase transformation, achieving superior structure stability. Surface residual alkali is in-situ converted into a protective coating layer of Na2B4O7 and meanwhile partial B atoms enter into the interstitial site of sub-surface or near surface, which accelerates sodium ions transport as well as enhances TM-O bonding and hybridization of surface O (2p)-Fe (3d-t2g) orbital, inhibits TMO6 slabs gliding and strengthens structure on the surface and near surface. Additionally, the formed boron-rich surface exhibits high stability, effectively alleviating structural degradation from surface to bulk and enhancing air stability. Benefiting from the reconstructed surface structure, the modified single crystalline oxides (NFM@B) exhibit distinguished processing performance and electrochemical properties.

Sintering Behavior of Molybdenite Concentrate During Oxidation Roasting Process in Air Atmosphere: Influences of Roasting Temperature and K Content.

Sintering is a common phenomenon, which often takes place during the oxidation roasting process of molybdenite concentrate in multiple-hearth furnaces. The occurrence of sintering phenomena has detrimental effects on the product quality and the service life of the furnace. In this work, the influence of two key factors (roasting temperature and K content) on the sintering behavior is investigated using molybdenite concentrate as the raw material. Different technologies such as XRD, FESEM-EDS, and phase diagrams are adopted to analyze the experimental data. The results show that the higher the roasting temperature is, the greater the mass loss and the more serious the sintering degree will be. The results also show that with the increase in K content, the mass loss of the raw material is first increased and then decreased, while its sintering degree is still gradually increased. The sintering products obtained during the oxidation roasting process are often tightly combined with the bottom of the used crucible with a smooth and dense surface structure, while their internal microstructures are very complicated, which not only includes numerous MoO3 species, but also unoxidized MoS2, Mo sub-oxide, SiO2, and a variety of molybdates. Among them, both MoO3 and molybdates can be easily dissolved into the ammonia solution, leading to a residue mainly composed of SiO2 and CaMoO4. This study also finds that the sintering phenomenon is caused by the increase in local temperature and the formation of various low-melting-point eutectics. It is suggested that decreasing the roasting temperature and K content, especially the K content, are effective methods for reducing the sintering degree of molybdenite concentrate during the oxidation roasting process.