Synthesis and electrochemical properties of Mg-doped LiNi<Subscript>0.6</Subscript>Co<Subscript>0.2</Subscript>Mn<Subscript>0.2</Subscript>O<Subscript>2</Subscript> cathode materials for Li-ion battery

The layered LiNi0.6Co0.2-xMn0.2MgxO2 (x=0.00,0.03,0.05,0.07) cathode materials were prepared by a co-precipitation method.The properties of the Mg-doped LiNi0.6Co0.2Mn0.2O2 were investigated by X-ray diffraction (XRD),scanning electron microscopy (SEM),and electrochemical measurements.XRD studies showed that the Mg-doped LiNi0.6Co0.2Mn0.2O2 had the same layered structure as the undoped LiNi0.6Co0.2Mn0.2O2.The SEM images exhibited that the particle size of Mg-doped LiNi0.6Co0.2Mn0.2O2 was finer than that of ...     

Synthesis and Characteristic of a New Niobate： BasNaCr0.5Nb9.5O30

A new niobate crystal was synthesized for the first time in BaO-NaO-Cr2O3-Nb2O3 system by the solid state reacition and the flux method. The new compound was studied by X-ray diffraction, electron probe, X-ray microanalysis, chemical analysis and SEM. The result of X-ray powder diffraction shows that Ba5NaCr0.5 Nb9.5O30 belongs to the tetragonal tungsten bronze structure, with space group P4 bin(100) and lattice parameters a=b=12. 4450 (2) A, c=3.9931 (2) A and Z=1. The X-ray powder diffraction lines of the compound were well indexed.     

Hydrothermally Synthesizing Nanospheres of Pd Loaded TiO<Subscript>2</Subscript> for Photocatalytically Reducing CO<Subscript>2</Subscript> in Isopropanol to Isopropyl Formate

Photocatalytic reduction of CO₂ was carried out on villiform spherical catalysts of Pd-TiO₂ in isopropanol solution. The catalysts were synthesized by hydrothermal method, their structures, morphologies and optical absorption properties were characterized by X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM) and UV-vis absorption spectroscopy (UV-vis). The photocatalytic activities with different loading amounts and morphologies were evaluated for determining the dominant effect and optimizing the catalyst preparation. Based on a villiform spherical TiO₂ with the largest specific surface area in our experiments, we prepared a set of catalysts with various loading amounts of palladium and tested them by bubbling CO₂ through the slurry of catalyst and isopropanol. The highest formation rate of isopropyl formate was 276.6 μmol/g·cat/h. Eventually we proposed the reaction mechanism.     

Solvothermal synthesis and photocatalytic performance of Bi<Subscript>2</Subscript>S<Subscript>3</Subscript> hierarchical nanostructure

The synthesis of Bi₂S₃ hierarchical nanostructure was reported by a solvothermal reaction using ethylene disulfhydrate as the sulfur source and chelating reagent. The as-synthesized samples were characterized by X-ray diffraction (XRD), Raman, X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and photoluminescence (PL). The XRD, Raman, and XPS data confirmed that the as-synthesized sample belongs to orthorhombic phase Bi₂S₃. The SEM observations displayed that Bi₂S₃ hierarchical nanostructure assembled from nanorods. A 410 nm ultraviolet photoluminescence (PL) emission of as-synthesized Bi₂S₃ was observed when the sample was excited with wavelength of 320-330 nm. The Bi₂S₃ hierarchical nanostructure also shows a significant enhancement of photocatalytic capability toward degrading methyl orange (MO) under UV light, the photodegradation of MO reaches 95% within 180 min.     

Preparation and characterization of nanocomposite MgFe<Subscript>2</Subscript>O<Subscript>4</Subscript>/SiO<Subscript>2</Subscript>

Nanocomposites MgFe₂O₄/SiO₂ were successfully synthesized by the sol-gel method in the presence of N, N-dimethylformamide (DMF). The formation of pure MgFe₂O₄ was confirmed by powder X-ray diffraction (XRD) and electron diffraction. The structural evolution of MgFe₂O₄ nanocrystals was followed by powder X-ray diffraction and IR absorption spectroscopy. The formation of spinel structure of MgFe₂O₄ started at 800 °C, and completed at 900 °C. The transmission electron microscopy (TEM) measurements suggest that the particle sizes increase with the increasing annealing temperature, and the mean particle sizes of the spherical samples annealed at 800 °C, 900 °C and 1 050 °C are ca. 3 nm, 8 nm and 11 nm, respectively. Magnetization measurements at room temperature and 78 K indicate superparamagnetic nature of these MgFe₂O₄ nanocrystals. Funded by the National Natural Science Foundation of China(No. 30771676), the Natural Science Foundation of Jiangsu Province (No. BK20081842), and the Foundation of Nanjing Bureau of Personal for the Returned Overseas Chinese Excellent Scholars     

Preparation and optical properties of Er<Superscript>3+</Superscript>: Na<Subscript>2</Subscript>O-Al<Subscript>2</Subscript>O<Subscript>3</Subscript>-SiO<Subscript>2</Subscript> transparent glass-ceramics

Na₂O-Al₂O₃-SiO₂ glass-ceramics doped with Er³⁺ ions were synthesized by the conventional melt quenching technique at a low melting temperature. The samples were characterized by differential scanning calorimetry (DSC), X-ray diffraction (XRD), scanning electron microscopy (SEM), UV-vis-NIR scanning spectrophotometry, and fluorescence spectrometry. The results show that the main crystalline phase of glass-ceramics is nepheline.The best heat-treatment process is at 520 °C for 2 h. Because the up-conversion luminescence and near infrared luminescence properties of glass doped with Eu³⁺ are studied in detail.     

Facile synthesis of nanocrystalline Cr<Subscript>2</Subscript>O<Subscript>3</Subscript> thin film

A novel and facile synthesis route for the manufacture of transparent and uniform self-assembled nanocrystalline Cr2O3 (nc-Cr2O3) thin films with different morphology was reported, utilizing chromium nitrate as the inorganic source and triblock copolymer F127 as the morphology-directing agent by the evaporation-induced assembly (EIA) method. X-ray powder diffraction (XRD), thermogravimetry-differential scanning calorimetry (TG-DSC), N2-sorption, scanning electron microscopy (SEM) and transmission electron microscopy (TEM) were used to characterize the as-prepared nc-Cr2O3 thin films. The Cr2O3 thin film with different morphology was obtained by changing the relative humidity. The possible formation mechanism of the nc-Cr2O3 thin films with different morphologies was discussed.     

Characterization and photocatalytic activity of KSr<Subscript>2</Subscript>Nb<Subscript>5</Subscript>O<Subscript>15</Subscript> with tungsten bronze structure

Tungsten bronze (TB) type potassium strontium niobate KSr₂Nb₅O₁₅ was prepared by solid-state reaction method, and was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and UV-vis diffuse spectrum. The photocatalyst shows high photocatalytic activity of photodegrading acid red G. The effects of photocatalyst dosage and initial concentration of acid red G on the photodegradation process were studied. The kinetics of photocatalytic degradation of acid red G by KSr₂Nb₅O₁₅ catalyst follows the first order reaction.     

Biomolecule-assisted solvothermal synthesis and enhanced visible light photocatalytic performance of Bi<Subscript>2</Subscript>S<Subscript>3</Subscript>/BiOCl composites

Novel Bi₂S₃/BiOCl photocatalysts were successfully synthesized via a facile biomolecule-assisted solvothermal method and biomolecule L-cysteine was used as the sulfur source. The structures, morphology, and optical properties of the synthesized samples were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, transmission electron microscopy (TEM), and UV-vis diffuse reflectance spectroscopy (DRS). The presence of Bi₂S₃ in the Bi₂S₃/BiOCl composites could not only improve the optical properties but also enhance the photocatalytic activities for the degradation of Rhodamine B (RhB) under visible-light irradiation (λ > 420 nm) as compared with single Bi₂S₃ and BiOCl. Especially, the sample displayed the best performance of the photodegradation when the feed molar ratio of BiCl3 and L-cysteine was 2.4:1, which was about 10 times greater than that of pure BiOCl. The enhanced photocatalytic activities could be ascribed to the effective separation of photoinduced electrons and holes and the photosensitization of dye. Moreover, the possible photodegradation mechanism was also proposed, and the results revealed that the active holes (h⁺) and superoxide radicals (?O₂ ^?) were the main reactive species during photocatalytic degradation.     

Influence of Aluminum Ions Implantation on Corrosion Behavior of Zircaloy-2 Alloy in 1M H2SO4

The specimens were implanted with aluminum ions with fluence ranging from 1× 10^16 to 1× 10^17 ions/cm^2 to study the effect of aluminum ion implantation on the aqueous corrosion behavior of zircaloy-2 by metal vapor vacuum arc source （MEVVA） at an extraction voltage of 40 kV. The valence states and depth distributions of elements in the surface layer of the samples were analyzed by X-ray photoelectron spectroscopy （XPS） and Auger electron spectroscopy （AES）, respectively. Transmission electron microscopy （TEM） was used to examine the microstructure of the aluminum-implanted samples. Glancing angle X-ray diffraction （GAXRD） was employed to examine the phase transformation due to the aluminum ion implantation. The potentiodynamic polarization technique was employed to evaluate the aqueous corrosion resistance of implanted zircaloy-2 in a 1 M H2SO4 solution. It is found that a significant improvement was achieved in the aqueous corrosion resistance of zircaloy-2 implanted with aluminum ions. Finally, the mechanism of the corrosion behavior of aluminum- implanted zircaloy-2 was discussed.     

Preparation of TiO2 Thin Film and Its Antibacterial Activity

TiO2 nanometer thin films with photocatalytic antibacterial activity were prepared by the sol-gel method on fused quartz and soda lime glass precoated with a SiO2 layer. The thin films were characterized by X-ray photoelectron spectroscopy ( XPS ), scanning electron microscopy (SEM), and X- ray diffraction ( XRD ). The results show that sodium and calcium diffusion into nascent TiO2 film is effectively retarded by the SiO2 layer precoated on the soda lime glass, The antibacterial activity of the films was determined. The crystalline of TiO2 nanometer thin film has important effects on the antibacterial activity of the film.     

Preparation and characterization of CeO<Subscript>2</Subscript>-TiO<Subscript>2</Subscript>/SnO<Subscript>2</Subscript>:Sb films deposited on glass substrates by R.F. sputtering

CeO2-TiO2 films and CeO2-TiO/SnO2：Sb （6 mol%） double films were deposited on glass substrates by radio-frequency magnetron sputtering （R.F. Sputtering）, using SnO2：Sb（6 mol%） target, and CeO2- TiO2 targets with different molar ratio of CeO2 to TiO2 （CeO2：TiO2-0：1.0; 0.1：0.9; 0.2：0.8; 0.3：0.7; 0.4：0.6; 0.5：0.5; 0.6：0.4; 0.7：0.3; 0.8：0.2; 0.9：0.1; 1.0：0）. The films are characterized by UV-visible transmission and infrared reflection spectra, scanning electron microscopy （SEM）, Raman spectroscopy, X-ray photoelectron spectroscopy （XPS） and X-ray diffraction （XRD）, respectively. The obtained results show that the amorphous phases composed of CeO2-TiO2 play an important role in absorbing UV, there are Ce^3-, Ce^4- and Ti^4- on the surface of the films; the glass substrates coated with CeO2-TiO2 （Ce/Ti=0.5：0.5; 0.6：0.4）/SnO2：Sb（6 mol%） double films show high absorbing UV（〉99）, high visible light transmission （75%） and good infrared reflection （〉70%）. The sheet resistance of the films is 30-50 Ω/□. The glass substrates coated with the double functional films can be used as window glass of buildings, automobile and so on.     

Fabrication and photocatalytic activity of Ag<Subscript>3</Subscript>PO<Subscript>4</Subscript>-TiO<Subscript>2</Subscript> heterostructural nanotube arrays

To extend the absorption capability of TiO₂ into visible light region and inhibit the recombination of photogenerated electrons and holes, we put forward an effective strategy of the coupling of TiO₂ with a suitable semiconductor that possesses a narrow band gap. Meanwhile, Ag₃PO₄-TiO₂ heterostructural nanotube arrays were prepared by the two-step anodic oxidation to obtain the TiO₂ nanotube arrays and then by a deposition-precipitation method to load Ag₃PO₄. The samples were characterized by field emission scanning electron microscopy (FESEM), energy dispersive spectrometry (EDS), X-ray diffraction (XRD), and UV-vis diffuse reflectance spectroscopy (UV-vis DRS). The experimental results showed that Ag₃PO₄ nanoparticles were uniformly dispersed on the highly ordered TiO₂ nanotube arrays, which increased the visible-light absorption of TiO₂ photocatalyst. The photocurrent density and photocatalytic degradation of methyl orange indicated that the performance of Ag₃PO₄-TiO₂ heterostructural nanotube arrays was better than that of the TiO₂ nanotube arrays, which could be attributed to the effective electron-hole separation and the improved utilization of visible light.     

Preparation and enhanced daylight-induced photo-catalytic activity of transparent C-Doped TiO<Subscript>2</Subscript> thin films

The transparent C-doped TiO₂ nanostructure films were fabricated on the silicate glass substrates by sol-gel spin-coated method. The as-prepared films were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), UV-visible absorption spectra (UV-vis) and X-ray photoelectron spectroscopy (XPS). The photocatalytic activity was evaluated via the photo-catalytic oxidation of methylene blue in aqueous under daylight irradiation at room temperature. The results show that the daylight-induced photocatalytic activities of the as-prepared films are improved by the C-doping. The calcination temperatures significantly affect the morphology, microstructure and photocatalytic activity of the as-prepared samples. At 723 K, the C-doped TiO₂ films exhibit the highest photocatalytic activity due to the synergetic effects of good crystallization, appropriate oxygen vacancies and strong absorption in the near UV and visible-light region.     

Synthesis of spin-ladder Sr<Subscript>14</Subscript>Cu<Subscript>24</Subscript>O<Subscript>41</Subscript> material by citrates sol-gel method

A new process to synthesize polycrystalline samples of Sr14Cu24O41 was presented. Firstly, dry gel powder of Sr14Cu24O41 was synthesized by the citrates sol-gel method, using Sr（NO3）2, Cu（NO3）2, ethylene glycol and citrate acid as raw materials. Then, polycrystalline samples of Sr14Cu24O41 were prepared by solid-state reaction. Thermal Gravimetric and Differential Thermal Analysis（TG-DTA） showed that the temperature for solid-state reaction is at 942 ℃. The samples are identified to be single phase by X-ray Diffraction（XRD） and Scanning Electron Microscopy（SEM）. The SEM pictures showed that the first-step particles were at even size of about 100 nm by this technique. The electronic transport measurements showed that the doping compound were semiconductor with a crossover temperature T in the Arrhenius plot of the resistivity versus temprature.     

Self-assembled SnO<Subscript>2</Subscript> colloidal particles and their gas sensing performance to H<Subscript>2</Subscript>, C<Subscript>2</Subscript>H<Subscript>5</Subscript>OH and LPG

Using organo-tin Sn(OC4H9)4 as precursor, sodium dodecyl sulfonate (SDS) and SDS-gelatin (SDS-G) complex as template, two tin dioxide colloidal particles were prepared by a self-assembly method. Both SnO2 products were respectively labelled SnO2-B particles with SDS and SnO2-C particles with SDS-G, which are applied in fabricating SnO2 gas sensors corresponding to SnO2-B’ and SnO2-C’ sensors. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and thermo-gravimetry and different thermal analysis (TG/DTA) were used for characterizations. The experimental results show that SnO2-B colloidal particles are composed of mesoporous piece-like particles, while SnO2-C particles mainly consist of spherical particles. Gas sensing measurements show that SnO2-B’ sensor performs the best sensing response to all target gases, including H2, C2H5OH and liquid petroleum gas (LPG). In particular, the sensing response of SnO2-B’ sensor is achieved at 32 in H2 atmosphere at the concentration of 1000×10-6 M. The gas sensing mechanism was purposely discussed from the electron transfer process and the microstructures of the as-prepared SnO2 products. It is found that serious agglomerations in SnO2-B’ particles facilitate the high gas sensing performance of SnO2-B’ sensor, while mesoporous structures in SnO2-C’ particles decrease the gas sensing response of SnO2-C’ sensor.     

二氧化碳气氛下改性SiO2负载V催化乙苯脱氢

以三嵌段共聚物P123为模板剂,正硅酸乙酯为硅源,采用水热法和浸渍法制备改性SiO2负载钒V/ZrO2-TiO2-SiO2催化剂.在CO2气氛下考察其催化乙苯脱氢的反应性能,并采用X射线衍射、BET比表面积、扫描电镜等技术对催化剂体相及表面性质进行表征.结果表明：催化剂在600℃、乙苯空速（LHSV）0.44 h-1、n（CO2）/n（EB）=5.4的条件下具有较好的催化活性,ZrO2和TiO2在SiO2负载型催化剂表面有相互修饰的作用.改性ZrO2-TiO2-SiO2载体有助于提高V2O5在载体表面的分散程度,抑制VOx的聚合,减小V2O5的微晶尺寸,提高其氧化还原能力.     

Sintering products molded by injecting ceramic and metal powders

The injection molding products with different volume ratios of ZrO2 ceramic powder to 316L stainless steel powder were prepared. Properties and structure of the products were characterized by X-ray diffraction(XRD), scanning electron microscope(SEM) and transmission electron microscope (TEM). The results show that the compressive stress exists in the products and the bend strength reaches 300 MPa. ZrO2 phase and stainless steel phase are uniform in samples. The toughness of ceramic increases with the increasing the content of stainless steel. Through TEM study of the interface, some crystalline orientation relationships are determined.     

Conformation of Organic Chain in Phase Transition of Hybrid （Cl2H25NH3）2MnCl4

The structural change in phase transition of hybrid （Cl2H25NH3）2MnCl4 was investigated. The temperature and the structures of the phase transition is investigated by thermal gravimetry （TG） and differential scanning calorimetry （DSC）, infrared spectrum （IR） and X-ray diffraction （XRD）. The results suggest that the phase transition is reversible and the structural change arises from the conformation change of the organic chain. The interlayer distance increases when the hybrid transforms from low temperature phase to high temperature phase. This is explained by the diffusion of gauche-bond along the organic chains and they move away from each other when the phase transition occurs. Combining the experimental data with theoretical calculation, we propose that organic chain of the hybrid in high temperature phase is the conformation of gauche-bond alternating with trans bond （noted as GTG＇TGTG＇TGTG＇T）.     

Effect of Al<Subscript>2</Subscript>O<Subscript>3</Subscript> content on residual stress and properties of CAS glass-ceramics

The structure and properties of the glass-ceramics were tested with X-ray diffraction testing instrument,correlative software,and other modern testing means.Then the effect of Al2O3 content on internal stresses in CaO-Al2O3-SiO2 glass-ceramics was studied deeply.In order to study the relationship of Al2O3 to the residual stress of CaO-Al2O3-SiO2 glass-ceramics,X-ray diffraction ＂sin2ψ＂ was used.The means utilized the x radial incidence produced from cathode radial tube,and took the space between crystals as measurement of strain.When the stresses produced,the space between crystals changed and the diffraction peak moved during Bragg diffraction.The magnitude of movement is related to the stresses.The experimental results show the residual stress is considerably high and Al2O3 can influence the mechanical properties of this material hugely.