Achieving structurally stable O3-type layered oxide cathodes through site-specific cation-anion co-substitution for sodium-ion batteries

O3-type layered oxides have garnered great attention as cathode materials for sodium-ion batteries because of their abundant reserves and high theoretical capacity.However,challenges persist in the form of uncontrollable phase transitions and intricate Na^(+)diffusion pathways during cycling,resulting in compromised structural stability and reduced capacity over cycles.This study introduces a special approach employing site-specific Ca/F co-substitution within the layered structure of O_(3)-NaNi_(0.5)Mn_(0.5)O_(2) to effectively address these issues.Herein,the strategically site-specific doping of Ca into Na sites and F into O sites not only expands the Na^(+)diffusion pathways but also orchestrates a mild phase transition by suppressing the Na^(+)/vacancy ordering and providing strong metal-oxygen bonding strength,respectively.The as-synthesized Na_(0.95)Ca_(0.05)Ni_(0.5)Mn_(0.5)O_(1.95)F_(0.05)(NNMO-CaF)exhibits a mild O3→O3+O'3→P3 phase transition with minimized interlayer distance variation,leading to enhanced structural integrity and stability over extended cycles.As a result,NNMO-CaF delivers a high specific capacity of 119.5 mA h g^(-1)at a current density of 120 mA g^(-1)with a capacity retention of 87.1%after 100 cycles.This study presents a promising strategy to mitigate the challenges posed by multiple phase transitions and augment Na^(+)diffusion kinetics,thus paving the way for high-performance layered cathode materials in sodium-ion batteries.

High‑Entropy Layered Oxide Cathode Enabling High‑Rate for Solid‑State Sodium‑Ion Batteries

Na-ion O3-type layered oxides are prospective cathodes for Na-ion batteries due to high energy density and low-cost.Nevertheless,such cathodes usually suffer from phase transitions,sluggish kinetics and air instability,making it difficult to achieve high performance solid-state sodium-ion batteries.Herein,the high-entropy design and Li doping strategy alleviate lattice stress and enhance ionic conductivity,achieving high-rate performance,air stability and electrochemically thermal stability for Na_(0.95)Li_(0.06)Ni_(0.25)Cu_(0.05)Fe_(0.15)Mn_(0.49)O_(2).This cathode delivers a high reversible capacity(141 mAh g^(−1)at 0.2C),excellent rate capability(111 mAh g^(−1)at 8C,85 mAh g^(−1)even at 20C),and long-term stability(over 85%capacity retention after 1000 cycles),which is attributed to a rapid and reversible O3–P3 phase transition in regions of low voltage and suppresses phase transition.Moreover,the compound remains unchanged over seven days and keeps thermal stability until 279℃.Remarkably,the polymer solid-state sodium battery assembled by this cathode provides a capacity of 92 mAh g^(−1)at 5C and keeps retention of 96%after 400 cycles.This strategy inspires more rational designs and could be applied to a series of O3 cathodes to improve the performance of solid-state Na-ion batteries.

Selective and mild oxidation of sulfides to sulfoxides by H_2O_2 using DBUH-Br_3 as catalyst

DBUH-Br_3 catalyzed selective conversion of sulfides to sulfoxides in the presence of H_2O_2 as oxidizing agent is described.The reaction was performed selectively at room temperature and relatively short reaction times.

Preparation of SiC_p/Al_2O_3-Al Composites by Directed Metal Oxidation

SiCp/Al2O3-Al composites were synthesized by means of direct metal oxidation method. The composition and microstructures of the composites were investigated using X-ray diffraction （XRD）, scanning electron microscopy （SEM） and metallurgical microscope. The effects of technical parameters on the properties of the product were analyzed. The results indicate that the composite possesses a dense microstructure, composed of three interpenetrated phases. Of them, SiO2 layer prohibits the powdering of the composites; Mg promotes the wetting and infiltration of the system and Si restricts the interfacial reaction while improving the wetting ability between reinforcement and matrix.

Al_2O_3包覆LiCoO_2对4.35V锂离子电池性能的影响

用固相法对钴酸锂(LiCoO2)正极材料进行纳米三氧化二铝(Al2O3)表面包覆,在充电终止电压为4.35 V时分析制备的495060AR型锂离子电池的性能。在放电截止电压为3.00 V时,以0.5 C放电,包覆、未包覆LiCoO2的比容量分别为167.6 mAh/g、170.9 mAh/g,平均电压分别为3.763 V、3.776 V;常温下1.0 C循环200次,包覆、未包覆LiCoO2的容量保持率分别为94.46%、96.40%。在55℃、48 h储存测试中,包覆LiCoO2制备的电池表现出更好的环境适应性;包覆LiCoO2制备的电池在高温45℃下以0.5 C循环200次,容量保持率为93.50%。对电池进行过充、热冲击测试,均未起火、爆炸。

Magnetic Fe_3O_4-Reduced Graphene Oxide Nanocomposites-Based Electrochemical Biosensing

An electrochemical biosensing platform was developed based on glucose oxidase(GOx)/Fe3O4-reduced graphene oxide(Fe3O4-RGO) nanosheets loaded on the magnetic glassy carbon electrode(MGCE).With the advantages of the magnetism, conductivity and biocompatibility of the Fe3O4-RGO nanosheets, the nanocomposites could be facilely adhered to the electrode surface by magnetically controllable assembling and beneficial to achieve the direct redox reactions and electrocatalytic behaviors of GOx immobilized into the nanocomposites. The biosensor exhibited good electrocatalytic activity, high sensitivity and stability. The current response is linear over glucose concentration ranging from 0.05 to 1.5 m M with a low detection limit of0.15 μM. Meanwhile, validation of the applicability of the biosensor was carried out by determining glucose in serum samples. The proposed protocol is simple, inexpensive and convenient, which shows great potential in biosensing application.

NITRIC OXIDE DECOMPOSITION ON ALKALI-PROMOTED Pd/AL_2o_3 CATALYSTS

Alkali-promoted Pd/Al2O3 catalysts exhibit much higher activities in NO decomposition than Pd/Al2O3. FTIR study shows that on the alkali promoted catalyst.nitric oxide exists on the surface mainly in negatively charged form(NO-)at high temperatures.which is consistent with the activity improvement.

Structure and Waveguide Properties of Sol-Gel Derived Gd_2O_3 Films

Pure and rare earth doped gadolinium oxide (Gd 2O 3) waveguide films were prepared by a simple sol-gel process and dip-coating method. Structure of Gd 2O 3 films annealed at different temperature was investigated by X-ray diffraction and transmission electron microscopy. Oriented growth of (400) face of Gd 2O 3 has been observed when the films were deposited on amorphous substrate. The refractive index and thickness of films were determined by m-lines spectroscopy. The laser beam (λ=632.8 nm) was coupled into the film by a prism coupler and the propagation length is about 3.5 cm. Luminescence properties of europium ions doped films were measured by waveguide fluorescence spectroscopy, which shows disordered environment for Eu 3+ at 400 ℃.

Perovskite Sr0.9Fe0.9Zr0.1O3-δ:Redox-stable Structure,Oxygen Vacancy,Electrical Properties and Steam Electrolysis Performance

Many researchers have studied on perovskite oxide for its unique structure.Perovskite oxides,ABO3-δ,with different A and B metals have shown wide applications in many fields,in particular solid oxide electrolysers.SrFeO3-δ,typical perovskite oxides,in which iron is the mixed-valence cation with the capacity to change the chemical valence,have a wide range of oxygen nonstoichiometry.In this study,Sr（0.9）Fe（0.9）Zr（0.1）O3-δ（SFZO） is synthesized and then treated in 5%H2/Ar and air at high temperature,exhibiting excellent redox stability.Redox-stable structure,oxygen vacancy and electrical properties of SFZO are investigated.Steam electrolysis is then performed with SFZO cathode under 5%H2O/5%H2/Ar and 5%H2O/Ar atmospheres,respectively.The present results indicate that the SFZO is a novel promising cathode material for solid oxide steam electrolyser.

Review of gallium oxide based field-effect transistors and Schottky barrier diodes

Gallium oxide(Ga_2O_3), a typical ultra wide bandgap semiconductor, with a bandgap of ~4.9 e V, critical breakdown field of 8 MV/cm, and Baliga's figure of merit of 3444, is promising to be used in high-power and high-voltage devices.Recently, a keen interest in employing Ga_2O_3 in power devices has been aroused. Many researches have verified that Ga_2O_3 is an ideal candidate for fabricating power devices. In this review, we summarized the recent progress of field-effect transistors(FETs) and Schottky barrier diodes(SBDs) based on Ga_2O_3, which may provide a guideline for Ga_2O_3 to be preferably used in power devices fabrication.

Structure and properties of brazed joints on dispersion-strengthened copper

Development of the technological process for brazing of heat-resistant copper alloy strengthened with Al2O3 oxide particles is an important task of fabrication of high-temperature application structures. As mechanical properties of the brazed joints directly depend on the structural factor and morphological peculiarities of the brazed seams, the latter are of technological interest in terms of making of permanent joints. This study gives results of X-ray spectral microanalysis of the brazed joints on dispersion-strengthened copper alloy （ Gridcop Al-25 ） produced by using the Ti-Cu system adhesion-active brazing filler alloy, different heat sources and temperature-time parameters of the brazing process. Shown are differences in formation of structure of the seams made by vacuum brazing using radiation and high-frequency heating. Vacuum brazing with radiation heating provides the homogeneous seams with crystallisation of the phases based on the CuTi and CuTi2 compounds in the form of discrete faceted particles 2 - 9μm in size against the background of the copper matrix. Based on investigation of structural peculiarities of the brazed seams, the temperature-time conditions of vacuum brazing with radiation heating were selected for manufacture of specimens for mechanical tests. Analysis of the results of strength tests of the butt brazed specimens proved the expediency of preliminary heat treatment of the base material, providing strength of the joints at a level of about 92% of that of the base material.

Modeling,simulations,and optimizations of gallium oxide on gallium-nitride Schottky barrier diodes

With technology computer-aided design(TCAD)simulation software,we design a new structure of gallium oxide on gallium-nitride Schottky barrier diode(SBD).The parameters of gallium oxide are defined as new material parameters in the material library,and the SBD turn-on and breakdown behavior are simulated.The simulation results reveal that this new structure has a larger turn-on current than Ga2O3 SBD and a larger breakdown voltage than Ga N SBD.Also,to solve the lattice mismatch problem in the real epitaxy,we add a Zn O layer as a transition layer.The simulations show that the device still has good properties after adding this layer.

Effect of SO_2 on Performance of Solid Oxide Fuel Cell Cathodes

Effects of SO2 in ambient air on the performance and durability of solid oxide fuel cell（SOFC） cathode were evaluated by galvanostatic measurement. Comparison between two cathode materials was made to consider the cathode degradation mechanisms. The degradation performance is associated with a slow decomposition of the La0.6Sr0.4Co0.2Fe0.8O3（LSCF） due to the segregation of strontium oxide. Negligible deterioration for （La0.7Sr0.3）MnO3 （LSM） cathode was caused by SO2 poisoning under a current density of 200 mA/cm2. Metal sulphate formation may explain a slight deterioration under increasing high the concentration of SO2. It was verified that the poisoning mechanism for the two cathode materials resulted from the gradual decomposition of the cathode materials.

Sulfur poisoning and regeneration of MnO_x-CeO_2-Al_2O_3 catalyst for soot oxidation

MnOx-CeO2-Al2O3 mixed oxides were prepared by impregnating manganese and cerium precursors on alumina powders via a sol- gel deposition method. The oxide catalyst exhibited a poor resistance to sulfur dioxide after the treatment in 100 ppm SO2/air at 350 °C for 50 h. The formation of manganese sulfate and especially cerium sulfate reduced the availability of surface active metal oxides, blocked the pore structure and decreased the surface area of the catalyst. These changes in chemical and structural and textural properties resulted in a severe loss in the activities of the sulfated catalyst for NO and soot oxidation. The decomposition of sulfates was almost complete during the calcina-tion in air at 800 °C for 30 min, which partially recovered the surface active sites and the catalyst surface area despite the significant sintering of metal oxides. Consequently, the NOx-assisted soot oxidation activity of the catalyst was regenerated to some extent by the oxidation treatment.

Selective oxidation of methane and carbon deposition over Fe_2O_3/Ce_(1-x)Zr_xO_2 oxides

A series of Fe2O3/Al2O3, Fe2O3/CeO2, Ce0.7Zr0.3O2, and Fe2O3/Ce1-xZrxO2（x = 0.1–0.4） oxides was prepared and their physicochemical features were investigated by X-ray diffraction（XRD）, transmission electron microscope（TEM）, and H2-temperature-programmed reduction（H2-TPR） techniques. The gas–solid reactions between these oxides and methane for syngas generation as well as the catalytic performance for selective oxidation of carbon deposition in O2-enriched atmosphere were investigated in detail. The results show that the samples with the presence of Fe2O3show much higher activity for methane oxidation compared with the Ce0.7Zr0.3O2solid solution,while the CeO2-contained samples represent higher CO selectively in methane oxidation than the Fe2O3/Al2O3sample. This suggests that the iron species should be the active sites for methane activation, and the cerium oxides provide the oxygen source for the selective oxidation of the activated methane to syngas during the reaction between methane and Fe2O3/Ce0.7Zr0.3O2. For the oxidation process of the carbon deposition, the CeO2-containing samples show much higher CO selectivity than the Fe2O3/Al2O3sample, which indicates that the cerium species should play a very important role in catalyzing the carbon selective oxidation to CO. The presence of the Ce–Zr–O solid solution could induce the growth direction of the carbonfilament, resulting in a loose contact between the carbon filament and the catalyst. This results in abundant exposed active sites for catalyzing carbon oxidation, strongly improving the oxidation rate of the carbon deposition over this sample. In addition, the Fe2O3/Ce0.7Zr0.3O2also represents much higher selectivity（ca. 97 %） for the conversion of carbon to CO than the Fe2O3/CeO2sample, which can be attributed to the higher concentration of reduced cerium sites on this sample. The increase of the Zr content in the Fe2O3/Ce1-xZrxO2samples could improve the reactivity of the materials for methane oxidation, but it also reduces the selectivity for CO formation.

Fe(NO_3)_3-9H_2O-catalyzed aerobic oxidation of sulfides to sulfoxides under mild conditions with the aid of trifluoroethanol

Selective oxidation of sulfides to sulfoxides was successfully performed by employing readily available Fe（NO3）3-9H2O as the active catalyst with oxygen as the oxidant in 2,2,2-trifluoroethanol （TFE） without the formation of sulfones. Nitrate anion could play a crucial role in promoting the reaction due to the oxidation capacity under acidic media. High yields of sulfoxides were exclusively obtained from the corresponding sulfides. Furthermore, both aromatic and aliphatic sulfides gave moderate to high yields of sulfoxides with this protocol.

Preparation and thermoelectric transport properties of Ba-, La- and Ag- doped Ca3Co4O9 oxide materials

The Ba-, La- and Ag-doped polycrystalline Ca2.9M0.1Co4O9 （M=Ca, Ba, La, Ag） thermoelectric bulk samples were pre- pared via citrate acid sol-gel synthesis method followed by spark plasma sintering technique. The bulk samples were characterized and analyzed with regard to their phase compositions, grain orientations as well as microstructures. The high temperature thermoelec- tric transport properties of the bulk samples were studied in detail. All bulk samples were found to be single-phased with modified body texture. The electrical resistivity was modulated as a result of carrier concentration modification, however the carrier transport process was not influenced; the Seebeck coefficient was deteriorated simultaneously. The total thermal conductivity was remarkably reduced, on account of the decreasing of phonon thermal conductivity. The thermoelectric properties of the Ba-, La-, and Ag-doped bulk samples were optimized, and the Ba-doped Ca2.9Ba0.1Co4O9 system was found to have the highest dimensionless figure of merit ZT0.20 at 973 K, which was remarkably higher than that of the un-doped sample.

Multi-dimensionally ordered, multi-functionally integrated r-GO@TiO2（B）@Mn304 yolk-membranc shell superstructures for ultrafast lithium storage

TiO2（B） is an attractive new anode candidate for lithium-ion batteries （LIBs） due to its unique and highly desirable properties, including high structural integrity, long cycle life, and low cost. However, despite these merits, its inherent slow lithium and electron transport kinetics hinder its practical application to LIBs. Here, we propose a novel, simple route towards multi-dimensionally ordered, multi-functionally integrated reduced graphene oxide （r-GO）@TiO2（B）@Mn304 yolk-membrane-shell superstructures in which r-GO nanosheets, TiO2（B） nanosheets, and Mn304 nanoparticles are hierarchically organized to achieve remarkable synergistic interactions. This hybridization design is fundamentally bilateral in nature, aiming to overcome the conductivity and capacity deficiencies of TiO2（B） simultaneously. The resulting r-GO@TiO2（B）@Mn304 yolk-membrane- shell superstructures have great potential as advanced anode materials for ultrafast lithium storage, delivering a strikingly high reversible capacity of 662 mA.h-g-1 at 500 mA-g^-1 after 500 charge-discharge cycles.

Magnetic CuO nanoparticles supported on graphene oxide as an efficient catalyst for A^3-coupling synthesis of propargylamines

Magnetically separable CuO nanoparticles supported on graphene oxide（Fe3O4 NPs/GO-CuO NPs） is synthesized and characterized for the preparation of propargylamines in EtOH,at 90 C.Fe3O4 NPs/GOCuO NPs is found to be an efficient catalyst for the A^3-coupling of aldehydes,amines,and alkynes through C-H activation.Both aromatic and aliphatic aldehydes and alkynes are combined with secondary amines to provide a wide range of propargylamines in moderate to excellent yields.

Electromagnetic wave absorption in reduced graphene oxide functionalized with Fe3O4/Fe nanorings

We report the preparation of nanocomposites of reduced graphene oxide with embedded Fe3O4/Fe nanorings （FeNR@rGO） by chemical hydrothermal growth. We illustrate the use of these nanocomposites as novel electromagnetic wave absorbing materials. The electromagnetic wave absorption properties of the nanocomposites with different compositions were investigated. The preparation procedure and nanocomposite composition were optimized to achieve the best electromagnetic wave absorption properties. Nanocomposites with a GO：cx-Fe203 mass ratio of 1：1 prepared by annealing in HdAr for 3 h exhibited the best properties. This nanocomposite sample （thickness = 4.0 mm） showed a minimum reflectivity of -23.09 dB at 9.16 GHz. The band range was 7.4-11.3 GHz when the reflectivity was less than -10 dB and the spectrum width was up to 3.9 GHz. These figures of merit are typically of the same order of magnitude when compared to the values shown by traditional ferric oxide materials. However, FeNR@rGO can be readily applied as a microwave absorbing material because the production method we propose is highly compatible with mass production standards.