Sheet Surface Research Articles

Hole Polaron-Mediated Suppression of Electron-Hole Recombination Triggers Efficient Photocatalytic Nitrogen Fixation.

In the pursuit of successful photocatalytic transformations, challenges persist due to limitations in charge carrier utilization and transfer efficiency, which stemming from rapid recombination. Overcoming these limitations necessitates the exploration of novel mechanisms that enhance the effective separation of photogenerated electron-hole pairs. Herein, deviating from the conventional approach of enhancing carrier migration to separate photogenerated charges and extend their lifetime, the proposal is to directly prevent the recombination of photogenerated electrons and holes by forming hole polarons. Specifically, disordered pores are introduced on the surface of KTaO3 ultrathin sheets, and the clear-cut evidences in electron paramagnetic resonance, photoluminescence, and ultrafast spectroscopy unambiguously confirm the enhanced carrier-phonon coupling, which results in the formation of hole polarons to impede the recombination of photogenerated electron-hole pairs. Taking the challenging nitrogen oxidation reaction as an example, it is found that the hole polarons in atomic-disordered pore KTaO3 ultrathin nanosheets trigger outstanding photo-oxidation performance of nitrogen (N2)to nitrate, with a nitrate-producing rate of 2.1 mg g-1 h-1. This scenario is undoubtedly applicable to a wide variety of photocatalytic reactions due to the common challenge of charge carrier recombination in all photocatalytic processes, manifesting broad implications for promoting photocatalysis performance.

Corrosion shielding effect of polyaluminium sulphate on metallic aluminium during the solidification of radioactive incineration bottom ash by low alkalinity cement

Radioactive incineration bottom ash containing metallic Al is difficult to be directly solidified in the cement matrix due to the generation of hydrogen gas during the reaction of aluminium with alkali pore solution of cement paste. In this study, the simulated incineration bottom ash (SIBA) containing metallic Al was successfully and directly solidified by polyaluminium sulphate (PAS)-modified low alkalinity cement (LAC), and the mechanism of the corrosion shielding effect of PAS on metallic Al was characterized by a range of analytical techniques. The results indicate that the cement waste form containing 29.56 wt% SIBA achieved a compressive strength of 16.6 MPa at 28 days of hydration, which increased by 13.3 % and 36.1 % after freeze-thawing test and immersion test, respectively. The 42d cumulative fraction leached of Nd3+ and Ce3+ were 1.74×10−7 cm and 3.40×10−7 cm, respectively. The corrosion degree and corrosion rate of Al sheets in LAC with PAS addition was much lower than that without PAS at early and late age hydration, by transforming thick porous corrosion layer to thin dense one. The mineral phase of corrosion product remained as bayerite (Al(OH)3), regardless of whether PAS was added. The addition of PAS reduced the hydrogen gas generation and prevented the dissolution of Al(OH)4- from metallic Al sheet. The hydrolysis of PAS produced a large amount of Al(OH)4- in pore solution, which extended the pH range for Al(OH)3 passivation by preventing the transformation of Al(OH)3 protection layer on the Al sheet surface to Al(OH)4- in the pore solution, and accelerated the formation of ettringite to decrease the pH of pore solution. This study cast the light on the direct solidification of metallic-aluminium-containing incineration bottom ash or Al bulks by cement-based materials without the need for complex pretreatment processes.

The Effects of Botulinum Toxin Type A on the Biological Behavior of Fibroblasts on Silicone Implants.

Capsular contracture is one of the most severe complications following breast augmentation surgery. It has been reported that botulinum toxin Type A (BTX-A) can inhibit capsular contracture, but the exact mechanisms remain unclear. Therefore, this study aims to explore the potential mechanisms behind BTX-A's inhibition of capsular contracture by observing its effects on the biological behavior of fibroblasts and its impact on the TGF-β/Smad signaling pathway. In vitro experiments involved culturing fibroblasts on PDMS surfaces, subsequently treating them with various concentrations of BTX-A. Fibroblast proliferation activity was assessed using the CCK-8 assay, while the migration and cytoskeletal morphology of the fibroblasts were meticulously examined. ELISA was utilized to quantify the expression of fibrosis-related cytokines. Gene and protein expressions related to the TGF-β/Smad pathway were analyzed through real-time PCR and Western blotting techniques. BTX-A moderately enhanced the early proliferation and migration of fibroblasts on the surface of PDMS silicone sheets and reduced the synthesis of collagen types I and III. Furthermore, under the influence of BTX-A, the expression of TGF-βR2 and α-SMA in the TGF-β/Smad pathway was significantly inhibited. This study demonstrates that BTX-A can inhibit fibroblast differentiation by downregulating the expression of TGF-βR2, thereby suppressing the TGF-β/Smad pathway. This suggests a possible mechanism through which BTX-A mitigates capsular contracture. This journal requires that authors assign a level of evidence to each submission to which Evidence-Based Medicine rankings are applicable. This excludes Review Articles, Book Reviews, and manuscripts that concern Basic Science, Animal Studies, Cadaver Studies, and Experimental Studies. For a full description of these Evidence-Based Medicine ratings, please refer to the Table of Contents or the online Instructions to Authors www.springer.com/00266 .

Superhydrophobic coatings prepared by spraying method with corrosion resistance and flame-retardant properties

In this study, aluminum tripolyphosphate (ATP) and silicon dioxide (SiO2) composites were introduced on the surface of copper sheets by spraying technique to prepare coating with flame retardant, superhydrophobic and corrosion resistant properties (ATP@SiO2). The coating not only exhibits excellent water repellency, but also has remarkable mechanical stability, with the corrosion current density reduced by an order of magnitude in electrochemical tests and the corrosion inhibition rate of 99.17 %. In flame retardant tests, the burning time of cotton fabrics coated with sprayed ATP@SiO2was extended by 38 s, with no smoldering observed. This study provides insights into the development of novel superhydrophobic materials with enhanced corrosion protection and flame-retardant properties.

The Effect of Artificial Ageing on the Changes in Selected Properties of Organic Coated Sheets.

This contribution presents the results of research focused on changes in selected properties of organic-coated steel sheets in a corrosive environment of salt mist. The aim of this study was to characterise coated sheets and to analyse the influence of elevated temperature on changes in their selected properties. The methodology and experiments were chosen to simulate the accelerated ageing and to evaluate the surface of organic-coated steel sheets. During the research, the effect of artificial ageing due to increased temperature on changes in mechanical properties of coated sheets was monitored, which were determined by tensile testing according to STN EN 10002-1. The fracture surface of the test samples was analysed using a SEM. The following observations were made for the evaluation of coating by cross-cut tests according to EN ISO 2409. Corrosion tests were carried out by conducting salt spray corrosion tests according to EN ISO 9227. The test specimens were artificially sectioned using a laser beam. The results of the research experiments confirmed the assumption that the utilisation of the laser beam was convenient for the creation cross-cut test of the material. After the ageing test, only small significant changes in the basic mechanical properties of the tested materials were observed. It is necessary to take into account that there were changes in the appearance of the coating. The cross-cut test confirmed the results that the plastic-coated sheets could be utilised in salt corrosion environments.

Synthesis and characterization of zinc ferrite nanoparticles@GO for the photocatalytic degradation of Methylene Blue dye under visible light

Due to rising environmental pollution, there has been a growing focus on photo degradation catalysts for pollution removal. Under visible light irradiation, methylene blue dye (MB) photocatalytic degradation has been studied using Zinc ferrite nanoparticles (ZnFe2O4 NPs) and Zinc ferrite nanoparticles/graphene oxide (ZnFe2O4/GO). Methylene blue dye is a carcinogenic pollutant that poses risks to both humans and marine life. The synthesis of ZnFe2O4/GO was achieved by the biotemplating method. Synthesized nanoparticles were loaded on graphene oxide (GO) in different ratios (Zn1:GO1, Zn1:GO3, and Zn1:GO5). Nanocomposite characterization was done utilizing Raman Spectroscopy analysis, FT–IR, XRD, BET, FE-SEM–EDX, XPS, and TEM. The confirmation of the cubic spinel structure of ZnFe2O4 NPs has been validated uniformly distributed on the surface of the GO sheets. The vigorous interaction between ZnFe2O4 NPs and graphene sheets facilitates rapid electron mobility, enhancing electron separation and holes in photocatalytic applications. The aforementioned parameters are crucial in MB’s photocatalytic degradation performance. Photocatalytic degradation processes depend on pH solution, initial dye concentration, and catalyst dosage. The outcomes demonstrated that augmenting the proportion of graphene oxide amplified MB photo degradation. Under the optimum conditions of 1 g/L dose, pH 8, 10 mg/L initial dye concentration, and 180-min irradiation time, the degradation ratio increased to 51.17 %, 59.70 %, 89.49 %, and 97.38 % using ZnFe2O4, Zn1:GO1, Zn1:GO3, and Zn1:GO5, respectively. Based on the photo degradation process, GO exhibited superior photocatalytic performance at the highest concentration. The kinetics data showed that the photo degradation reaction adheres to the pseudo-second-order. The study indicated that the eco-friendly, non-toxic photocatalyst ZnFe2O4/GO can be used as an effective potential substance for water treatment as well as the elimination of hazardous organic dyes from aqueous solutions.

A strain acceleration method to identify the onset of diffuse necking

This paper presents an innovative ‘strain acceleration method’ for determining the onset of diffuse necking in sheet forming tests using data obtained from digital image correlation (DIC). The method identifies the onset time of diffuse necking and provides the corresponding in-plane principal strain values by detecting a local extreme in the second derivative of the minor principal in-plane strain with respect to time at the edges of the sheet surface region where diffuse necking occurs. Results obtained from applying the method to tensile testing on two different materials and comparisons with available methods based on force-time or principal strain rate evolutions confirm its accuracy and validity. The new method was implemented in a computer software to be used for research and education that also enables determination of localized necking and fracture and plotting the strain loading paths in principal strain space.

Synthesis and Performance Evaluation of High-Temperature-Resistant Extreme-Pressure Lubricants for a Water-Based Drilling Fluid Gel System.

Addressing the high friction and torque challenges encountered in drilling processes for high-displacement wells, horizontal wells, and directional wells, we successfully synthesized OAG, a high-temperature and high-salinity drilling fluid lubricant, using materials such as oleic acid and glycerol. OAG was characterized through Fourier-transform infrared (FTIR) spectroscopy and thermogravimetric analysis (TGA). The research findings demonstrate the excellent lubricating performance of OAG under high-temperature and high-salinity conditions. After adding 1.0% OAG to a 4% freshwater-based slurry, the adhesion coefficient of the mud cake decreased to 0.0437, and at a dosage of 1.5%, the lubrication coefficient was 0.032, resulting in a reduction rate of 94.1% in the lubrication coefficient. After heating at 200 °C for 16 h, the reduction rate of the lubrication coefficient reached 93.6%. Even under 35% NaCl conditions, the reduction rate of the lubrication coefficient remained at 80.3%, indicating excellent lubrication retention performance. The lubricant OAG exhibits good compatibility with high-density drilling fluid gel systems, maintaining their rheological properties after heating at 200 °C and reducing filtration loss. The lubrication mechanism analysis indicates that OAG can effectively adsorb onto the surface of N80 steel sheets. The contact angle of the steel sheets increased from 41.9° to 83.3° before and after hot rolling, indicating a significant enhancement in hydrophobicity. This enhancement is primarily attributed to the formation of an extreme-pressure lubricating film through chemical reactions of OAG on the metal surface. Consequently, this film markedly reduces the friction between the drilling tools and the wellbore rocks, thereby enhancing lubrication performance and providing valuable guidance for constructing high-density water-based drilling fluid gel systems.

P-doped MoS2 nanosheets embedded in 3D porous carbon for electrocatalytic hydrogen evolution reaction

Due to its inherent electrochemical catalytic activity, molybdenum sulfide (MoS2) is a potential electrocatalyst for hydrogen evolution reaction (HER). However, the limited exposure of its active sites resulting from the easy stacking of nanosheets and inert basal plane hampered its optimal catalytic activity. Herein, we developed a novel facile hydrothermal method to prepare phosphorus-doped MoS2 nanosheets anchored on agar-derived 3D nitrogen-doped porous carbon (P-MoS2/NC). The synthesized P-MoS2/NC electrocatalyst possesses high HER catalytic activity with a low overpotential of 167 mV at 10 mA cm−2 and a small Tafel slope of 45 mV dec−1. The excellent performance is attributed to the unique 3D network carbon structure, which avoids the stacking of the MoS2 sheets resulting in more exposed active sites. Additionally, the P atom introduced on the surface of MoS2 sheets successfully activated the in-plane inertness. This work provides an efficient strategy for designing and preparing high-quality catalysts with enhanced electrocatalytic HER activity.

Enhanced Fenton Degradation of Tetracycline over Cerium-Doped MIL88-A/g-C3N4: Catalytic Performance and Mechanism.

Since enormous amounts of antibiotics are consumed daily by millions of patients all over the world, tons of pharmaceutical residuals reach aquatic bodies. Accordingly, our study adopted the Fenton catalytic degradation approach to conquer such detrimental pollutants. (Ce0.33Fe) MIL-88A was fabricated by the hydrothermal method; then, it was supported on the surface of g-C3N4 sheets using the post-synthetic approach to yield a heterogeneous Fenton-like (Ce0.33Fe) MIL-88A/10%g-C3N4 catalyst for degrading the tetracycline hydrochloride drug. The physicochemical characteristics of the catalyst were analyzed using FT-IR, SEM-EDX, XRD, BET, SEM, and XPS. The pH level, the H2O2 concentration, the reaction temperature, the catalyst dose, and the initial TC concentration were all examined as influencing factors of TC degradation efficiency. Approximately 92.44% of the TC was degraded within 100 min under optimal conditions: pH = 7, catalyst dosage = 0.01 g, H2O2 concentration = 100 mg/L, temperature = 25 °C, and TC concentration = 50 mg/L. It is noteworthy that the practical outcomes revealed how the Fenton-like process and adsorption work together. The degradation data were well-inspected by first-order and second-order models to define the reaction rate. The synergistic interaction between the (Ce0.33Fe) MIL-88A/10%g-C3N4 components produces a continuous redox cycle of two active metal species and the electron-rich source of g-C3N4. The quenching test demonstrates that •OH is the primary active species for degrading TC in the H2O2-(Ce0.33Fe) MIL-88A/10%g-C3N4 system. The GC-MS spectrum elucidates the yielded intermediates from degrading the TC molecules.

CRYOGELS TO INCREASE THE SERVICE LIFE OF WINTER ROADS

The work proposes a method for forming a composite cryotron material based on an aqueous solution of polyvinyl alcohol for application to the surface of a snow-ice sheet. Freezing an aqueous solution of polyvinyl alcohol at a negative temperature and subsequent thawing at a temperature above zero leads to the formation of elastic cryogels. The introduction of boric acid into a polymer solution leads to chemical cross-linking of kinetically individual macromolecules of polyvinyl alcohol into spatial networks that have elastic properties. The practical interest in using materials based on cryogels is due to environmental safety, high physicochemical and thermophysical properties, a simple method for their preparation and low cost. When studying the kinetics of gelation of multicomponent systems, it was observed that the formation of a gel at a temperature of 5 °C occurs after approximately 13 hours. It has been established that with increasing temperature control time of the gel at a temperature of 5 °C, the elastic modulus of samples obtained as a result of a chemical reaction increases by 2 times in approximately 120 h. It has been shown that after cryostructuring of multicomponent solutions, the elastic modulus increases 9 times. The presence of sand in a structured system significantly increases the elastic properties of the gel and cryogel. It should be noted that the thermal conductivity coefficient of cryogels is almost 2 times less than that of water, and the melting point is more than 60 °C. The results of practical experiments show that coating a snow-ice surface with cryogel reduces the rate of its melting and, therefore, compositions based on cryogels can be used to extend the life of safe operation of winter roads. For citation: Fufaeva M.S., Altunina L.K. Cryogels to increase the service life of winter roads. ChemChemTech [Izv. Vyssh. Uchebn. Zaved. Khim. Khim. Tekhnol.]. 2024. V. 67. N 8. P. 29-35. DOI: 10.6060/ivkkt.20246708.13t.

Damage evolution and ductile fracture of commercially-pure titanium sheets subjected to simple tension and cyclic bending under tension

This paper describes a study into the evolution of damage in commercial-purity titanium (CP–Ti) sheets subjected to cyclic bending under tension (CBT) and uniaxial tension (simple tension, ST). Sections were taken from sheets that were strained to various levels under both methods and were imaged using X-ray computed tomography (XCT) to reveal insights into the size, density, and distribution of microvoids in the sheets. Digital image correlation (DIC) was also used to observe the surface strain of CBT and ST sheets during testing. These results showed that elongation to failure (ETF) for CBT deformation is about 2.5× higher than for ST, local longitudinal strains in the bulk of the CBT sample are around 1.3× higher than the peak strain in the ST necked region, and 1.7× higher in the localized region of CBT failure. It was found that the volume-density of voids in both sheets followed a similar exponential increase with strain, reaching nearly 45× higher in the CBT than the ST sheets before the onset of failure, mainly due to the higher strain levels achieved. A higher volume density of voids developed in the center of sheets at high levels of strain, for both processes, with the density in the sheet center becoming approximately double that found near the edges. Scanning electron microscopy (SEM) was used to examine the fracture surface of CBT and ST sheets after failure. The observations are presented and discussed highlighting the CBT process as effective to delay ductile fracture of the CP-Ti sheets.

Effect of Countersample Coatings on the Friction Behaviour of DC01 Steel Sheets in Bending-under-Tension Friction Tests.

The aim of this article is to provide an analysis of the influence of the type of hard anti-wear coatings on the friction behaviour of DC01 deep-drawing steel sheets. DC01 steel sheets exhibit high formability, and they are widely used in sheet metal forming operations. The tribological properties of the tool surface, especially the coating used, determine the friction conditions in sheet metal forming. In order to carry out the research, this study developed and manufactured a special bending-under-tension (BUT) friction tribometer that models the friction phenomenon on the rounded edges of tools in the deep-drawing process. The rationale for building the tribotester was that there are no commercial tribotesters available that can be used to model the phenomenon of friction on the rounded edges of tools in sheet forming processes. The influence of the type of coating and sheet deformation on the coefficient of friction (CoF) and the change in the topography of the sheet surface were analysed. Countersamples with surfaces prepared using titanium + nitrogen ion implantation, nitrogen ion implantation and electron beam remelting were tested. The tests were carried out in conditions of dry friction and lubrication with oils with different kinematic viscosities. Under dry friction conditions, a clear increase in the CoF value, with the elongation of the samples for all analysed types of countersamples, was observed. Under lubricated conditions, the uncoated countersample showed the most favourable friction conditions. Furthermore, oil with a lower viscosity provided more favourable conditions for reducing the coefficient of friction. Within the entire range of sample elongation, the most favourable conditions for reducing the CoF were provided by uncoated samples and lubrication with S100+ oil. During the friction process, the average roughness decreased as a result of flattening the phenomenon. Under dry friction conditions, the value of the Sa parameter during the BUT test decreased by 20.3-30.2%, depending on the type of countersample. As a result of the friction process, the kurtosis and skewness increased and decreased, respectively, compared to as-received sheet metal.

Fabrication of SrTiO3 anchored rGO/g-C3N4 photocatalyst for the removal of mixed dye from wastewater: dual photocatalytic mechanism

A metal-free combination of rGO/g-C3N4-coupled SrTiO3 (SRN) ternary nanocomposite prepared via a wet impregnation method for UV–Vis light photocatalytic applications. Various physicochemical properties of the samples were investigated by several spectroscopic techniques including X-ray diffraction (XRD), FT-IR, Raman, field emission scanning electron microscopy with energy dispersive X-ray spectroscopy (FE-SEM-EDX), high-resolution transmission electron microscopy (HR-TEM), UV–Vis, photoluminescence (PL), X-ray photoelectron spectroscopy (XPS) and Brunauer–Emmett–Teller (BET) surface area analysis. The data suggest agglomerated SRT nanoparticles are dispersed and distributed throughout the surface of the rGO sheets and GCN nanostructures. The photocatalytic performance of the SRN towards combined mixed dye and its degradation activities were evaluated towards the most common industrial effluents, Rhodamine B (RhB) and Methylene blue (MB), under UV–Vis light illumination. The results revealed that the degradation efficiency of the SRN photocatalyst shows excellent performance compared with that of the binary composition and the pure SrTiO3 (SRT) sample. The reaction rate constant for RhB was estimated to be 0.0039 min−1 and for MB to be 0.0316 min−1, which are 3.26 (RhB) and 4.21 (MB) times faster than the pure SRT sample. The enhanced degradation efficiency was attained not only by interfacial formation but also by the speedy transportation of electrons across the heterojunction. After 5 runs of the photocatalytic recylic process, the SRN photocatalyst exhibited ultimate stability without structural changes, and no noticeable degradation was observed. The outcomes of the ternary SRN nanocomposite manifest a dual photocatalytic scheme, the photocatalytic enrichment could be caused by the Z-scheme charge transfer process between GCN, SRT, and rGO nanocomposite, which helps effectual charge separation and keeps a high redox potential. From the results, SRN sample provides insight into the integration of an effective and potential photocatalyst for wastewater treatment toward real-time environmental remediation applications.

Reforming toolpath effect on deformation mechanics in double-sided incremental forming

Incremental sheet metal forming is a die-less process known for its high flexibility, making it a suitable choice for fabricating low-batch, highly customized complex parts. In this paper, the deformation mechanism of double-sided incremental forming (DSIF) with single pass or reforming toolpaths and its effect on the deformation-induced martensite transformation kinetics are investigated by experiments and finite element (FE) simulations for a truncated pyramid part geometry for the first time. An FE model accounting for tool deflection is developed, considering the change in tools' position caused by the forces applied at the contact with the blank. This is done to enhance the simulation accuracy in comparison to experimental results. A comprehensive analysis is conducted with respect to the stress state change and strain accumulation during DSIF with the single pass and reforming toolpaths. The findings reveal that material points along the pyramid wall primarily deform by a combination of plane strain tension, plane strain compression, and shear, depending on the tools’ locations on the sheet surfaces in relation to the material point of interest. The reversal of the forming direction in the reforming toolpath causes material points to experience different stress states and more strain accumulation than the single pass case. Under the same forming temperature, this phenomenon results in a higher and closer martensite transformation on both forming and supporting surfaces of the final part when employing the reforming toolpath as opposed to the single pass case.

Design and fabrication of reduced graphene oxide (RGO) incorporated NiCo2S4 hybrid composites as electrode materials for high performance supercapacitors

One of the most promising bimetallic sulphides for use in energy-storage systems is NiCo2S4, but further research is required to give it a high reversibility and electrochemical reaction capacity. In this study, we show the rational materials design of an ideal NiCo2S4 nanoparticle as a NiCo2S4/RGO nanocomposite, embedded in a reduced graphene oxide (RGO) matrix. NiCo2S4 nanoparticles, which ranged in size from 20 to 25 nm and were firmly fixed on the surface of RGO sheets, made up the produced composite. As predicted, the produced nanocomposite displayed a high specific surface area, a mesoporous structure, and high conductivity, resulting in a large electroactive area and rapid electron and ion motion. Additionally, we present the advancements in material science, showcasing the NiCo2S4/RGO nanocomposite electrode, which has a long cycle life of 5000 cycles, a high capacitance retention of 85.6 %, and an exceptional specific capacitance of 1505 Fg-1 at 1 Ag-1. A high active-material loading asymmetric supercapacitor serves as an example of the real-world use. The NiCo2S4/RGO nanocomposite exhibits an exceptional 48 Whkg-1 energy density at a power density of 985 Whkg-1, while maintaining a high power density of 7227 Wkg-1 density of 25 Whkg-1. The exceptional stability and electrochemical efficiency of the NiCo2S4/RGO nanocomposite validate that our methodical materials science and technology optimisation in the areas of active substance synthesis, electrode expansion, and device design/fabrication will help advance the development of high-performance supercapacitors in future years.

Green Sonochemical Synthesis of rGO Nanosheets‐Decorated by SnO2 Nanoparticles for Nitrogen Gas‐Sensing Applications

In recent years, the development of efficient and environmentally friendly synthesis methods for nanomaterials has gained significant attention in various research fields, particularly in gas‐sensing applications. Among these methods, ultrasonic synthesis stands out for its simplicity, cost‐effectiveness, and ecofriendly nature. Herein, a simple and green ultrasonic synthesis process is used to synthesize the SnO2 nanoparticles‐decorated rGO nanosheets. The obtained X‐ray diffraction reveals the tetragonal rutile‐type crystal structure. The transmission electron microscopy images reveal the decoration of SnO2 nanoparticles on the surfaces of the rGO sheets. SnO2 nanoparticles of size 4–8 nm are identified on the surfaces of the rGO sheets. Furthermore, the optical absorbance and photoluminescence spectra of the nanocomposites validate charge migrations occurring at the interface of SnO2 and the rGO sheets. Compared to the pristine SnO2 nanoparticles, the green ultrasonically synthesized SnO2 nanoparticles‐decorated SnO2/rGO nanocomposite exhibits better sensing performance against NO2 gas and shows selectivity for NO2 gas at 200 °C. The SnO2/rGO nanocomposite demonstrates high NO2 sensing with appealing sensing properties such as excellent responsiveness (67% at 400 °C), rapid reaction time (18 s), and short recovery time (25 s).

Assessment of various microwave brightness temperature products and methods for surface melt detection over Greenland ice sheet

Microwave brightness temperature have widely been used for the detection of the ice sheet's surface melt conditions and understanding their spatio-temporal variability. In this study, we investigated the sensitivity of microwave brightness temperature products from three different sensors, namely, Advanced Microwave Scanning Radiometer-2 (AMSR2), Special Sensor Microwave Imager/Sounder (SSMIS) and Indian scatterometer satellite (SCATSAT-1) for surface melt detection over the Greenland ice sheet (GrIS). In-situ air temperature measurements from GC-Net AWSs were used for sensitivity and inter-comparison analysis. Our findings show that brightness temperature (Tb) from SSMIS better correlates (Pcoef = 0.81 for 19 GHz) with air temperature measurements in comparison to AMSR2 (Pcoef = 0.7 for 18 GHz) and SCATSAT-1 (Pcoef = 0.67). However, interestingly, AMSR2 and SCATSAT-1 uniquely discriminated the surface conditions during pre- and post-melt period, due to their heterogeneity in Tb values during the two period. Error analysis with respect to AWS melt days shows that SSMIS 19 GHz Tb (Tb/SSMIS/19H) products with TED method giving the most promising observations. A wide variability in Tb values is observed during the melt season across the various AWS sites depending upon the elevation, location and frequency. During our study period, using Tb/SSMIS/19H for TED method, we observed the highest melt extent area for the extreme melt event in year 2019 (∼1.12 million km2), followed by another melt event year 2021 when it went as high as ∼1.02 million km2.

The effect of surface modification strategies on biological activity of titanium implant

The surface morphology of titanium metal is an important factor affecting its hydrophilicity and biocompatibility, and exploring the surface treatment strategy of titanium metal is an important way to improve its biocompatibility . In this study , titanium (TA4) was firstly treated by large particle sand blasting and acid etching (SLA) technology, and then the obtained SLA-TA4 was treated by single surface treatments such as alkali-heat, ultraviolet light and plasma bombardment. According to the experimental results, alkali-heat treatment is the best treatment method to improve and maintain surface hydrophilicity of titanium. Then, the nanowire network morphology of titanium surface and its biological property, formed by further surface treatments on the basis of alkali-heat treatment, were investigated. Through the cell adhesion experiment of mouse embryonic osteoblast cells (MC3T3-E1), the ability of titanium material to support cell adhesion and cell spreading was investigated after different surface treatments. The mechanism of biological activity difference of titanium surface formed by different surface treatments was investigated according to the contact angle, pit depth and roughness of the titanium sheet surface. The results showed that the SLA-TA4 titanium sheet after a treatment of alkali heat for 10 h and ultraviolet irradiation for 1 h has the best biological activity and stability. From the perspective of improving surface bioactivity of medical devices, this study has important reference value for relevant researches on surface treatment of titanium implantable medical devices.

Selective removal of single-layer graphene over double-layer graphene on SiO2 by remote oxygen plasma irradiation

Graphene sheet transferred onto the SiO2 substrate has various types at different regions such as single-layer graphene (SLG), double-layer graphene (DLG), and multi-layer graphene (MLG). These layers were identified by Raman analysis of 2D band position around 2700 cm−1 and full width at half maximum (FWHM). The transferred graphene sheets on SiO2 were remotely irradiated by oxygen plasma without energetic ions at a room temperature. At the beginning of the oxygen plasma irradiation, the carbons on the surface of the graphene sheets were oxidized and the 2D-FWHMs were broadened due to an increase of defects on the basal plane. By controlling the plasma irradiation time up to 120 min, selectively stripping away the SLG regions on the SiO2 surface was observed while leaving the other DLG and MLG regions. The difference in attractive forces resulted in favorable desorption of carbon atoms occurred in the oxidized SLG regions on SiO2 surface by the remote oxygen plasma irradiation.