X-ray Photoelectron Spectroscopy Results Research Articles

Efficient Sb(Ⅲ) removal from printing and dyeing wastewater using TiCl4 as a potential coagulant instead of polyferric sulfate

With increasing health concerns and the tightening of discharge standards, there is growing demand for more efficient Sb(Ⅲ) removal from printing and dyeing wastewater (PDW). Currently, the most common coagulant used in Sb removal in industry is polyferric sulfate (PFS). However, the residual Fe ions in the effluent cause colorimetric problems and irreversibly damage the membrane components during the subsequent reverse osmosis treatment process. Therefore, identifying novel coagulants to replace PFS in the removal of Sb(Ⅲ) is necessary. In this study, TiCl4 was employed for in-situ hydrolysis to produce flocs for Sb(Ⅲ) removal in simulated and real PDW. TiCl4 exhibited an excellent performance compared to PFS in terms of dosage, turbidity, application pH, and anti-interference properties. Sb(Ⅲ) removal of 97.3 % was realized at a dosage of 30 mg/L and a final pH of 5.0 in slightly contaminated PDW, whereas PFS required a higher dosage, resulting in higher disposal costs. Furthermore, the application of TiCl4 led to lower turbidity and reduced secondary contamination. An investigation of the co-existing ions revealed that TiCl4 was considerably more tolerant than PFS toward PO43–, humic acid, and silicate at a lower concentration. Simultaneously, Sb(Ⅲ) was partially oxidised to Sb(Ⅴ) during removal, but TiCl4 exhibited lower oxidative properties. The results of PDW treatment indicated that TiCl4 could realize 85.6 % Sb(Ⅲ) removal at a dosage of 30 mg/L, and the pre-reduction of Sb(Ⅴ) to Sb(Ⅲ) was a safe, effective treatment. The results of zeta potential measurements and X-ray photoelectron spectroscopy revealed that Sb(Ⅲ) removal was mainly realised via chemical adsorption. Overall, this study provides a promising alternative material for use in practical Sb(Ⅲ) removal from PDW, particularly for reducing coagulation sludge, operational costs, and damage during the possible subsequent reverse osmosis process.

Pullulan Polysaccharide as an Eco-Friendly Depressant for Flotation Separation of Chalcopyrite and Molybdenite.

It is difficult to separate molybdenite and chalcopyrite by froth flotation due to the good floatability of the two minerals. In this paper, the separation of copper-molybdenum sulfide minerals was realized by using pullulan polysaccharide (PU) as the depressant. The flotation test results showed that the copper concentrate grade increased from 16.24 to 29.86%, and the copper concentrate recovery reached 83.55% under low alkali conditions. The selective separation mechanism of the two minerals by PU was revealed through contact angle measurements, ζ-potential measurements, Fourier transform infrared (FTIR) spectroscopy analyses, and X-ray photoelectron spectroscopy (XPS) analyses. The ζ-potential and contact angle results showed that PU is more easily adsorbed on molybdenite to strengthen the hydrophilicity of molybdenite. The FTIR and XPS results showed that PU is adsorbed on molybdenite by physical interactions, and hydrophobic interactions and hydrogen bonding play a major role.

Visible light- and dark-driven degradation of palm oil mill effluent (POME) over g-C3N4 and photo-rechargeable WO3.

The investigations of real industrial wastewater, such as palm oil mill effluent (POME), as a recalcitrant pollutant remain a subject of global water pollution concern. Thus, this work introduced the preparation and modification of g-C3N4 and WO3 at optimum calcination temperature, where they were used as potent visible light-driven photocatalysts in the degradation of POME under visible light irradiation. Herein, g-C3N4-derived melamine and WO3 photocatalyst were obtained at different calcination temperatures in order to tune their light absorption ability and optoelectronics properties. Both photocatalysts were proven to have their distinct phases, crystallinity levels, and elements with increasing temperature, as demonstrated by the ultraviolet-visible spectroscopy (UV-Vis), X-ray diffraction analysis (XRD), thermogravimetric analysis (TGA), Fourier-transform infrared spectroscopy (FTIR), Brunauer-Emmett-Teller (BET), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS) results. Significantly, g-C3N4 (580°C) and WO3 (450°C) unitary photocatalysts exhibited the highest removal efficiency of POME without dilution due to good crystallinity, extended light absorption, high separation, and less recombination efficiency of electron-hole pairs. Furthermore, surprisingly, the superior energy storage photocatalytic performance with outstanding stability by WO3 achieved an approximately 10% increment during darkness, compared with g-C3N4 under visible light irradiation. Moreover, it has been proven that the WO3 and g-C3N4 photocatalysts are desirable photocatalysts for various pollutant degradations, with excellent visible-light utilization and favorable energy storage application.

Efficient Sb(Ⅲ) removal from printing and dyeing wastewater using TiCl4 as a potential coagulant instead of polyferric sulfate

With increasing health concerns and the tightening of discharge standards, there is growing demand for more efficient Sb(Ⅲ) removal from printing and dyeing wastewater (PDW). Currently, the most common coagulant used in Sb removal in industry is polyferric sulfate (PFS). However, the residual Fe ions in the effluent cause colorimetric problems and irreversibly damage the membrane components during the subsequent reverse osmosis treatment process. Therefore, identifying novel coagulants to replace PFS in the removal of Sb(Ⅲ) is necessary. In this study, TiCl4 was employed for in-situ hydrolysis to produce flocs for Sb(Ⅲ) removal in simulated and real PDW. TiCl4 exhibited an excellent performance compared to PFS in terms of dosage, turbidity, application pH, and anti-interference properties. Sb(Ⅲ) removal of 97.3% was realized at a dosage of 30mg/L and a final pH of 5.0 in slightly contaminated PDW, whereas PFS required a higher dosage, resulting in higher disposal costs. Furthermore, the application of TiCl4 led to lower turbidity and reduced secondary contamination. An investigation of the co-existing ions revealed that TiCl4 was considerably more tolerant than PFS toward PO43–, humic acid, and silicate at a lower concentration. Simultaneously, Sb(Ⅲ) was partially oxidised to Sb(Ⅴ) during removal, but TiCl4 exhibited lower oxidative properties. The results of PDW treatment indicated that TiCl4 could realize 85.6% Sb(Ⅲ) removal at a dosage of 30mg/L, and the pre-reduction of Sb(Ⅴ) to Sb(Ⅲ) was a safe, effective treatment. The results of zeta potential measurements and X-ray photoelectron spectroscopy revealed that Sb(Ⅲ) removal was mainly realised via chemical adsorption. Overall, this study provides a promising alternative material for use in practical Sb(Ⅲ) removal from PDW, particularly for reducing coagulation sludge, operational costs, and damage during the possible subsequent reverse osmosis process.

Fabrication of Zn-doped Cu2O for auxiliary graphdiyne to enhance photocatalytic H2 evolution performance

Graphdiyne (GDY) is widely used in photocatalysis due to its large specific surface area, high porosity and good stability. In this study, GDY was prepared by ball-milling-assisted alkyne-negative method, and GDY/Zn-Cu2O S-scheme heterojunction catalysts were constructed by introducing Zn-doped Cu2O into it through low-temperature mixing. The modified composite catalysts showed hydrogen evolution performance reached 213.65 μmol after 5 h of visible light irradiation, which was 142.4, 82.2 and 8.1 times than that of Cu2O, Zn-Cu2O and GDY, respectively. The large specific surface area of GDY provided abundant active sites to promote surface kinetics. Zinc doping adjusted the energy band structure of Cu2O and improved the light absorption efficiency of the catalysts. The S-scheme heterojunction established between Zn-Cu2O and GDY greatly facilitated the separation and transport of photogenerated carriers, which was the dominant factor for the improvement of hydrogen evolution performance. A possible mechanism is proposed and analyzed by combining ultraviolet photoelectron spectroscopy (UPS), valence band XPS (VB-XPS), in-situ irradiated X-ray photoelectron spectroscopy (In-situ XPS) and density functional theory (DFT) results. This work provides a new insight into the doping and construction strategies of GDY-based S-scheme heterojunction.

Fabrication of Zn-doped Cu2O for auxiliary graphdiyne to enhance photocatalytic H2 evolution performance

Graphdiyne (GDY) is widely used in photocatalysis due to its large specific surface area, high porosity and good stability. In this study, GDY was prepared by ball-milling-assisted alkyne-negative method, and GDY/Zn-Cu2O S-scheme heterojunction catalysts were constructed by introducing Zn-doped Cu2O into it through low-temperature mixing. The modified composite catalysts showed hydrogen evolution performance reached 213.65 μmol after 5h of visible light irradiation, which was 142.4, 82.2 and 8.1 times than that of Cu2O, Zn-Cu2O and GDY, respectively. The large specific surface area of GDY provided abundant active sites to promote surface kinetics. Zinc doping adjusted the energy band structure of Cu2O and improved the light absorption efficiency of the catalysts. The S-scheme heterojunction established between Zn-Cu2O and GDY greatly facilitated the separation and transport of photogenerated carriers, which was the dominant factor for the improvement of hydrogen evolution performance. A possible mechanism is proposed and analyzed by combining ultraviolet photoelectron spectroscopy (UPS), valence band XPS (VB-XPS), in-situ irradiated X-ray photoelectron spectroscopy (ISI-XPS) and density functional theory (DFT) results. This work provides a new insight into the doping and construction strategies of GDY-based S-scheme heterojunction.

Preparation, electronic structure and thermal properties of Zn-doped LaMgAl11O19 materials

LaMgAl11O19 (LMA) with magnetoplumbite structure is a promising thermal barrier material due to its excellent thermal properties. In this work, Zn-doped LMA materials were studied in order to improve the thermal performance, and LaZnxMg1-xAl11O19 (x = 0, 0.1, 0.3, 0.5, 0.7, 1.0) were prepared by sol-gel method. The as-synthesized powder materials possess pure LMA phase and show the morphology of hexagonal plates. X-ray photoelectron spectroscopy result shows that there are AlO4 tetrahedra and AlO6 octahedra units in the target materials, and Zn2+ ions replace Mg2+ ions to occupy the tetrahedral position of magnetoplumbite structure. The composition LaZn0.3Mg0.7Al11O19 material exhibits the lowest thermal conductivity of 0.38 W/(m·K) at 1000oC while maintaining a high coefficient of thermal expansion (10.86×10-6 K-1). Therefore, the thermal properties of LMA materials can be improved by adding an appropriate amount of Zn ions.

Graphitic carbon nitride sheets sandwiched metal oxides: A novel platform for S-Scheme heterojunction generation for efficient photodegradation of volatile organics

This study reports the preparation of new kind of S-Scheme heterojunction (SSHJ) photocatalyst by distributing two semiconducting metal oxides (titanium dioxide and ZnO) onto the surface of graphitic carbon nitride (G-CN) two dimensional (2D) sheets. The composite photocatalysts, designated as T/Z@ GCN SSHJ, were prepared with different mass ratios of T,Z and G-CN.X-ray diffraction (XRD) analysis, transmission electron microscopy (TEM), field emission scanning electron microscopy, X-ray photoelectron spectroscopy (XPS), UV-Vis diffuse reflectance spectroscopy (DRS), photoluminescence (PL) spectroscopy were used to characterize the microstructure, morphology, chemical composition, electronic states, and optical properties of the T/Z@ GCN SSHJ composite. TEM image of the typical T/Z@ GCN SSHJ composite shows the presence of distribution of particles with sizes in the range 40–80 nm on the lamellar surface of G-CN inferring the formation of a heterostructure Z(0 D) /G-CN(2D)/T(0D) SSHJ composite. The comparison of the core level XPS spectrum of Ti 2p, Zn 2p, C1s, O1s and N1s of T/Z@ GCNSSHJ composite with the binary composites (T+G-CN and Z+G-CN) and pristine components clearly suggests that that Z, T and G-CN are kept together through van der Walls interactions. The T/Z@ GCN SSHJ composite photocatalyst with T: Z: G-CN mass ratio of 1.0: 0.80: 0.12 exhibited enhanced photocatalytic degradation (%) over binary and pristine single components for all the tested volatile organic compounds (VOCs), namely, acetaldehyde (ACD), ethyl acetate (EA), toluene (T) and benzaldehyde (BA). On comparing the % removal of VOCs after 20 minute of light irradiation, BA showed the highest removal % (94.3 %) and the others take the following order: ACD (70.9 %) >EA (56.45 %)> TL (40.12 %). The study explains the enhanced performance of T/Z@ G-CN HJ composite towards VOC photodegradation in terms of S-Scheme based charge transfer and internal electric field driven efficient charge separation. The charge transfer process of T/Z@ GCN HJ composite photocatalysts is discussed through S-Scheme HJ formation and supported with electronic states and band energy levels of the constituent components derived through the results of XPS and DRS analysis. This study gives insight into the design for regulating the hetero-interfaces for enhancing the photocatalysis and expected to further understand into charge transfer mechanism at multi-junction-based photocatalysts.

Effect of tin doping on the structural, optical, and dielectric properties of unintentionally β-Ga2O3 single crystal

This paper studied the structural, optical, electrical, and dielectric properties of the undoped and 0.05 mol% Sn-doped β-Ga2O3 single crystals through comprehensive characterizations by x-ray diffraction (XRD), Raman scattering, Optical transmittance spectroscopy, x-ray photoelectron spectroscopy (XPS), Ultraviolet photoelectron (UPS) spectroscopy, and dielectric measurements. The optical bandgap decreases as Sn content increases. The results of XPS showed that Sn atoms were successfully added to the host β-Ga2O3 crystal. The position of the Fermi level of 0.05 mol% Sn-doped β-Ga2O3 is calculated to be 2.56 eV above the valence band and 1.85 eV beneath the conduction band. Also, the computed value of the work function of 0.05% mole Sn-doped β-Ga2O3 is 4.53 eV. AC conductivity increases, while dielectric loss and dielectric constant decrease with increasing frequency.

The Surface Chemistry of Methanol on Pd(111) and H-Pd(111) Surfaces: C-O Bond Cleavage and the Effects of Metal Hydride Formation.

Palladium catalysts are frequently employed in processes where methanol is an energy vector or carrier, being useful for the synthesis of methanol from mixtures of carbon dioxide and hydrogen (CO2/H2) or its steam reforming on demand. Results of synchrotron-based ambient pressure X-ray photoelectron spectroscopy for the adsorption of methanol on a Pd(111) model catalyst show a rich surface chemistry and complex phenomena that strongly depend on pressure and temperature. At low pressures (<10-6 Torr) and temperatures (<300 K), CO is the dominant decomposition product. As the pressure increases, cleavage of C-H, O-H, and C-O bonds is observed, and at elevated temperatures (400-600 K) the formation of CO and CHx/C fragments compete on the surface. Thus, existing reaction networks for methanol decomposition must be modified. Furthermore, surface and subsurface hydrogen (coming from PdHx) play a significant role in the stability and removal of CHx and C species.

Praseodymium orthovanadate-waste PET bottle derived sulfur doped carbon for efficient Z-scheme photocatalytic CO2 reduction

Escalating amounts of carbon dioxide (CO2) in the Earth's atmosphere are a major cause of climate change and its negative consequences, making it a global concern. The present work highlights the intersection of waste management, resource utilization, and climate change mitigation, showcasing the potential for an additional sustainable and circular economy. Synthesizing carbon from waste polyethylene terephthalate (PET) bottles is an eco-friendly approach. X-ray diffraction, Raman spectroscopic, scanning electron microscopic, tunnelling electron microscopic, infrared fourier transform spectroscopy (FTIR) and X-ray photoelectron spectroscopic results indicate the effective extraction of carbon doped with sulfur (S@C) and the successive formation of nanocomposite with PrVO4 (PrV/S@C). Superior photocatalytic activity was observed under visible light compared to UV light. PrV/S@C showed enhanced light-driven CO2 reduction compared to pristine materials and was found to evolve 39, 56, and 98 µmol h−1 g−1 of H2, CH4 and CO, respectively. The effect of reaction temperature was examined and optimized at 100 °C. The enhanced activity in PrV/S@C compared to PrV and S@C probably due to the increased surface area, conductivity and synergy. In-Situ Diffused reflectance (DRIFT-IR) and liquid chromatography mass spectroscopy (LC-MS) confirm the evolution of CO and CH4. The optical, photo/electrochemical, Scavenger studies, Electron spin resonance (ESR) and Mott-Schottky studies suggest the formation of a direct Z-scheme photoredox reaction in the presence of PrV/S@C and sacrificial gent. The reusability studies for 5 cycles indicate good stability with a slight deviation in structure and morphology of PrV/S@C, as observed in XRD and SEM. Tackling plastic pollution and generating value-added carbonaceous products through CO2 reduction is the twin application of the present work that has piqued the interest of several researchers in environmental remediation.

Molten glass-mediated conditional CVD growth of MoS2 monolayers and effect of surface treatment on their optical properties

In the rapidly developing field of optoelectronics, the utilization of transition-metal dichalcogenides with adjustable band gaps holds great promise. MoS2, in particular, has garnered considerable attention owing to its versatility. However, a persistent challenge is to establish a simple, reliable and scalable method for large-scale synthesis of continuous monolayer films. In this study, we report the growth of continuous large-area monolayer MoS2 films using a glass-assisted chemical vapor deposition (CVD) process. High-quality monolayer films were achieved by precisely controlling carrier gas flow and sulfur vaporization with a customized CVD system. Additionally, we explored the impact of chemical treatment using lithium bistrifluoromethylsulfonylamine (Li-TFSI) salt on the optical properties of monolayer MoS2 crystals. To investigate the evolution of excitonic characteristics, we conditionally grew monolayer MoS2 flakes by controlling sulfur evaporation. We reported two scenarios on MoS2 films and flakes based on substrate-related strain and defect density. Our findings revealed that high-quality monolayer MoS2 films exhibited lower treatment efficiency due to substrate-induced surface strain. whereas defective monolayer MoS2 flakes demonstrated a higher treatment sensitivity due to the p-doping effect. The Li-TFSI-induced changes in exciton density were elucidated through photoluminescence, Raman, and x-ray photoelectron spectroscopy results. Furthermore, we demonstrated treatment-related healing in flakes under variable laser excitation power. The advancements highlighted in our study carry significant implications for the scalable fabrication of diverse optoelectronic devices, potentially paving the way for widespread real-world applications.

Carbon nanotube reinforced FeMoO4 nanorods as a high-performance anode for sodium-ion batteries

Iron molybdate (FeMoO4) nanostructures show great promise as a superior anode for sodium-ion batteries. However, its use in practical application is hampered by its poor electronic conductivity, large volume changes and sluggish reaction kinetics. Herein, we have developed an interconnected network of multiwall carbon nanotube (CNT) and FeMoO4 (FMO) by a simple one-step hydrothermal method. As well as providing efficient channels for charge transfer and diffusion, highly conductive CNTs also have a degree of volume elasticity and excellent electrical conductivity to ensure migration of sodium ions, enabling both fast kinetics and long-term stability. As a result, the FMO@CNT anode delivers a high reversible capacity of 485 mA h g−1 at 0.05 A/g and very long cycling stability with a capacity of 75 mA h g−1 after 1000 cycles at 1 A/g. Furthermore, by combining the ex-situ X-ray diffraction, ex situ X-ray photoelectron spectroscopy and cyclic voltammetry results, sodium ion storage mechanism of the FMO@CNT electrode obeys a conversion mechanism. The results of this work provide a better understanding on the sodium ion storage mechanism of binary metal oxides.

Effects of dissolved organic matter from sludge pyrolysis biochar on the triclosan removal from contaminated soil

When sludge biochar (SC) prepared from sewage sludge was used to remove triclosan (TCS) from both aqueous solution and soil, the adsorption capacity increased with increasing pyrolysis temperature, while the degradation rate showed a different pattern, namely, SC-500 > SC-800 > SC-600 > SC-700. TCS degradation rate achieved nearly 100 % at 2 h with SC-500 used as a Fenton catalyst. Aromaticity of dissolved organic matter (DOM) was positively correlated with the degradation of TCS and adding homologous DOM solution shortened the equilibrium time of TCS degradation, while removing DOM from SC prolonged, compared to the original SC. The results of X-ray photoelectron spectroscopy (XPS) and electron paramagnetic resonance spectrometer (EPR) characterization indicated that SC-500 performed a stronger catalytic degradation ability due to the relatively high Fe2+ content to produce more ∙OH and SC-derived DOM act as an electron shuttle to promote other reactive oxidative species generation through two free radical pathways in the activation of H2O2 by Fe2+, which in turn promoted the degradation of TCS.

From Bulk to Interface: Solvent Exchange Dynamics and Their Role in Ion Transport and the Interfacial Model of Rechargeable Magnesium Batteries.

Multivalent battery chemistries have been explored in response to the increasing demand for high-energy rechargeable batteries utilizing sustainable resources. Solvation structures of working cations have been recognized as a key component in the design of electrolytes; however, most structure-property correlations of metal ions in organic electrolytes usually build upon favorable static solvation structures, often overlooking solvent exchange dynamics. We here report the ion solvation structures and solvent exchange rates of magnesium electrolytes in various solvents by using multimodal nuclear magnetic resonance (NMR) analysis and molecular dynamics/density functional theory (MD/DFT) calculations. These magnesium solvation structures and solvent exchange dynamics are correlated to the combined effects of several physicochemical properties of the solvents. Moreover, Mg2+ transport and interfacial charge transfer efficiency are found to be closely correlated to the solvent exchange rate in the binary electrolytes where the solvent exchange is tunable by the fraction of diluent solvents. Our primary findings are (1) most battery-related solvents undergo ultraslow solvent exchange coordinating to Mg2+ (with time scales ranging from 0.5 μs to 5 ms), (2) the cation transport mechanism is a mixture of vehicular and structural diffusion even at the ultraslow exchange limit (with faster solvent exchange leading to faster cation transport), and (3) an interfacial model wherein organic-rich regions facilitate desolvation and inorganic regions promote Mg2+ transport is consistent with our NMR, electrochemistry, and cryogenic X-ray photoelectron spectroscopy (cryo-XPS) results. This observed ultraslow solvent exchange and its importance for ion transport and interfacial properties necessitate the judicious selection of solvents and informed design of electrolyte blends for multivalent electrolytes.

A Solid-State Reaction in a Vapor Chamber: Synthesis of Bi2(MoO4)3 Nanorods as High-Capacity Anode for Lithium-Ion Batteries

Conversion- and alloying-type materials have been investigated as alternatives to intercalating graphite anodes of lithium-ion batteries for recent decades. However, the electrochemical pulverization and limitations in large-scale production of metal oxides prohibit them from practical applications. This work provided an ambient solid-state reaction accelerated by water vapor for synthesizing Bi2(MoO4)3 nanorods combined with carbon under mild-condition ball-milling for composite fabrication. The obtained composite performs superior electrochemical performance: a delivered capacity of 802.2 mAh·g−1 after 300 cycles at a specific current of 500 mA·g−1 with a retention of 82.3%. This improvement was ascribed to the better accommodation to volume variation and reinforced physical contact raised by one-dimensional morphology and ball-milling treatment. The complex conversion-intercalation-alloying mechanism of the lithium-ion storage in Bi2(MoO4)3 anode was also clarified using cyclic voltammetry and ex situ X-ray photoelectron spectroscopy results.

NASICON-structure Na3+xMnVxTi1-x(PO4)3/C cathode for sodium-ion battery with excellent cycling performance and high specific capacity

The recently discovered Na3MnTi(PO4)3 cathode material has an extremely high theoretical capacity, but its poor cycling performance makes it challenging to apply. In this work, a series of NASICON-type Na3+xMnVxTi1-x(PO4)3/C (x = 0, 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.8, 1) cathode materials were prepared by sol-gel method for sodium-ion batteries. X-ray diffraction (XRD) indicates that vanadium doping has increased the cell spacing within the material and the cell volume. From the results of X-ray photoelectron spectroscopy (XPS) and Energy dispersive X-ray spectroscopy (EDS) mapping images, it is shown that vanadium has been successfully doped into the material. Among them, the Na3·3MnV0·3Ti0·7(PO4)3/C delivers an outstanding specific capacity (121.7 mAh g−1 at 0.1C, C = 135 mA g−1) and Na3·4MnV0·4Ti0·6(PO4)3/C shows an excellent capacity retention (80.88 % after 1500 cycles at 1C). Notably, the coulombic efficiency of both materials during cycling is close to 100 %, indicating that these materials have great practical application value.

New spin-electronics compositions: Large ferromagnetic order of BaSn0.98-xFe0.02CuxO3 (x = 0.02, 0.04, 0.06) semiconductor

Inducing robust ferromagnetic order in dilute magnetic semiconductor materials is an essential topic for spin-based electronics devices. Herein, the escalating concentration of nonmagnetic Cu ions was employed to strongly reinforce the room temperature ferromagnetism of 2% Fe doped BaSnO3 structure. BaSn0.98-xFe0.02CuxO3 (x = 0.02, 0.04 or 0.06) compositions were prepared by adapted sol gel method. In all compositions, pure single phase with cubic structure of BaSnO3 was identified by the X-ray diffraction (XRD) technique. Pure BaSnO3 gives a band gap energy of 3.25 eV which red shifted to 3.1, 3.12 and 3.13 eV after incorporation of (2% Fe, 2% Cu), (2% Fe, 4% Cu) and (2% Fe, 6% Cu) ions, respectively. The scanning electron microscope (SEM) images reflects that the Fe/Cu blends obstruct the grains growth of BaSnO3 and also influenced on the particles shape and porosity. The energy dispersive X-ray (EDX) maps confirmed the homogenous spatial distribution of Fe and Cu in the codoped BaSnO3 structure. The X-ray photoelectron spectroscopy (XPS) results of BaSn0.92Fe0.02Cu0.06O3 prove that Ba, Sn, O, Fe and Cu elements possess the oxidation states of +2, +4, −2, +3 and +1/+2, respectively. The magnetic performance of BaSnO3 structure exhibits a minor ferromagnetic loop with measured coercivity (Hc) of 330 Oe, magnetization (Ms) of 0.0023 emu/g and retentivity of 0.00077 emu/g. Interestingly, the addition of 6 wt% Cu (nonmagnetic dopant) plus 2 wt% Fe (magnetic dopant) strongly boosts the saturation magnetization value of BaSnO3 to 1.85 emu/g. The results open the door to tune the ferromagnetic order of BaSnO3 using nonmagnetic dopant to avoid the formation of magnetic impurities. The F-center exchange interaction and the bound magnetic polarons model were used to explain the measured room temperature ferromagnetism.

Enhanced stability in InSnO transistors via ultrathin in-situ AlOx passivation

In this study, we present the impact of an ultrathin in-situ AlOx passivation layer on the electrical performance and stability of InSnO (ITO) transistors. Devices incorporating an ultrathin (∼2 nm) AlOx passivation layer demonstrate satisfactory electrical performance and stability, characterized by a decent field-effect mobility, enhancement mode operation, notably reduced subthreshold swing, negligible hysteresis, and, notably, a significantly reduced threshold voltage shift under negative bias stress (NBS) and positive bias stress (PBS), respectively. The total trap density (Ntot), extracted through the sub-threshold slope, and the trap density (Nt), measured using low-frequency noise (LFN) for the AlOx-passivated ITO transistors, are significantly decreased. Those improvements can be attributed to the suppression of oxygen vacancy formation during the reactively-sputtered AlOx and subsequent annealing processes, as demonstrated by comparing the in-depth X-ray photoelectron spectroscopy (XPS) results of the AlOx-passivated and un-passivated ITO films. These results underscore the potential of in-situ reactively-sputtered ultrathin AlOx passivation layers to enhance the stability of thin-film transistors with In-rich channels.

Rapidly reducing cadmium from contaminated farmland soil by novel magnetic recyclable Fe3O4/mercapto-functionalized attapulgite beads

Reducing cadmium (Cd) content from contaminated farmland soils remains a major challenge due to the difficulty in separating commonly used adsorbents from soils. This study synthesized novel millimeter-sized magnetic Fe3O4/mercapto-functionalized attapulgite beads (MFBs) through a facile one-step gelation process incorporating alginate. The MFBs inherit the environmental stability of alginate and enhance its mechanical strength by hybridizing Fe3O4 and clay mineral components. MFBs can be easily separated from flooded soils by magnets. When applied to 12 Cd-polluted paddy soils and 14 Cd-polluted upland soils, MFBs achieved Cd(II) removal rates ranging from 16.9% to 62.2% and 9.8%–54.6%, respectively, within a 12-h period. The MFBs predominantly targeted the exchangeable and acid soluble, and reducible fractions of Cd, with significantly enhanced removal efficiencies in paddy soils compared to upland soils. Notably, MFBs exhibited superior adsorption performance in soils with lower pH and organic matter (OM) content, where the bioavailability and mobility of Cd are heightened. The reduction of Cd content by MFBs is a sustainable and safe method, as it permanently removes the bioavailable Cd from soil, rather than temporarily reducing its bioavailability. The functional groups such as –SH, –OH, present in attapulgite and alginate of MFBs, played a crucial role in Cd(II) adsorption. Additionally, attapulgite and zeolite provided a porous matrix structure that further enhanced Cd(II) adsorption. The results of X-ray photoelectron spectroscopy suggested that both chemical precipitation and surface complexation contributed to Cd(II) removal. The MFBs maintained 87.6% Cd removal efficiency after 5 regeneration cycles. The surface of the MFBs exposed new adsorption sites and increased the specific surface area during multiple cycles with Cd-contaminated soil. This suggests that MFBs treatment with magnetic retrieval is a potentially effective pathway for the rapid removal of Cd from contaminated farmland soils.