Investigations of structure and morphology of the AlN nano-pillar crystal films prepared by halide chemical vapor deposition under atmospheric pressure

Aluminum nitride (AlN) prepared under atmospheric pressure using a halide chemical vapor deposition method has been examined by means of a variety of analytical techniques. Scanning electron microscopic observations showed that the crystals deposited onto a Si(100) substrate have hexagonal pillar structure. Based on the X-ray diffraction and X-ray pole-figure analyses, it was deduced that the each AlN pillar crystal grows with a different rotation angle around the 〈001〉 axis. Transmission electron diffraction showed that they are of single-like form. This was also confirmed by the selected area electron diffraction image as well. It was found that the diameter of pillar which constitutes an AlN film was significantly dependent upon the ratio of NH₃/AlCl₃ used as source materials and the growth temperature.     

High growth rate deposition of oriented InN pillar crystals

High growth rate deposition of highly oriented indium nitride (InN) pillar crystals were successfully grown on Si(100) substrate prepared under atmospheric pressure using a halide CVD method (AP-HCVD). The growth rate of InN pillar crystal can be enhanced threefold by AP-HCVD system with metal halide dual sources zone, and the maximum growth rate of 8.33 nm/s was achieved. X-ray diffraction and X-ray pole-figure analyses showed that the each InN pillar crystal grows with a different rotation angle around the 〈001〉 axis. Selected area transmission electron diffraction showed that that they are of high crystal quality.     

Fabrication of novel Cu microspheres assembled with nanoparticles by a solvothermal reduction route

Copper microspheres assembled with nanoparticles have been synthesized by a simple solvothermal route at 160 °C for 24 h. The samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectrometer (EDX), transmission electron microscopy (TEM) and electron diffraction (ED) techniques. The results show that the diameters of the microspheres range from 2 to 4 μm. The formation mechanism of the morphology control over the copper microspheres assembled by nanoparticles was investigated; the use of polyvinylpyrrolidone (PVP) as the surfactant and the choice of N,N-dimethylformamide (DMF) as the reducing agent were found to be important for the final generation of copper microspheres.     

Controlled synthesis and luminescence properties of LaPO4:Eu phosphors

Uniform single crystal LaPO₄ phosphors were selectively synthesized using a facile hydrothermal method without the aid of templates or catalysts. X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), high resolution transmission electron microscopy (HRTEM), and photoluminescence (PL) spectra were used to characterize the nanocrystal materials. The morphological evolution from nanorods to nanoparticles was brought about by altering the pH. In addition, the crystal structure was changed from hexagonal phase to monoclinic one by increasing the hydrothermal temperature. We propose a possible growth mechanism for LaPO₄ nanorods based on the results of our analyses. Furthermore, we compared the photoluminescence properties of LaPO₄:Eu with different morphologies. The results showed that the fluorescence intensity of monoclinic LaPO₄:Eu nanorods is stronger than that of nanoparticles.     

SERS activity of Au nanoparticles coated on an array of carbon nanotube nested into silicon nanoporous pillar

A novel composite structure, Au nanoparticles coated on a nest-shaped array of carbon nanotube nested into a silicon nanoporous pillar array (Au/NACNT/Si-NPA), was fabricated for surface-enhanced Raman scattering (SERS). The morphology of the Au/NACNT/Si-NPA composite structure was characterized with the aid of scanning electron microscopy, X-ray diffraction instrumentation and Transmission electron microscopy. Compared with SERS of rhodamine 6G (R6G) adsorbed on SERS-active Au substrate reported, the SERS signals of R6G adsorbed on these gold nanoparticles were obviously improved. This was attributed to the enlarged specific surface area for adsorption of target molecules brought by the nest-shaped CNTs structure.     

西峡红柱石化学物相分析

用氢氟酸-硝酸-盐酸作为选择性溶剂，采用X射线衍射分析结果指导选择性试验，试验了西峡红柱石矿的溶解特性。结果表明，使用X射线衍射分析结果指导选择性试验，可避免从混合矿中分离出单矿井逐个进行条件试验，提高了红柱石矿化学物相分析速度。     

Characterization of ultra-fast deposited polycrystalline graphite by a CO2 laser-assisted combustion-flame method

High deposition rate, 750 μm/min, crystalline graphite was deposited on WC substrates by a CO₂ laser-assisted combustion-flame method at laser powers between 300 and 800 W. The structures, which were identified as pillars, were characterized by various methods. The pillars were cylindrical in shape and grew to a size of approximately 3 mm in length and in a few minutes. The laser power did not affect the overall length of the pillar, but caused changes in the physical shape. X-ray and electron diffraction results revealed the pillars to be crystalline graphite regardless of the laser power. Investigation of the pillars by scanning electron microscopy showed two distinct microstructural areas: an inner core of dense material surrounded by an outer shell of lamellar-like material. The core/shell microstructure was unaffected by the level of CO₂ laser power.     

Facile synthesis of flower-like nickel nanocrystals and properties

A solvo-hydrothermal synthesis approach for the preparation of a new type of flowerlike nickel nanostructure is reported. The as-synthesized flower-like nickel nanocrystallites were characterized by X-ray diffraction and scanning electron microscopy. The nickel flowers modified glassy carbon electrode can be prepared and used to detect methanol and ethanol in the solution. The results show that the nickel flowers give a very high activity for detecting the methanol and ethanol, which provide a new application of nickel flowers. Compared with that of bulk nickel, thus-prepared nickel flowers showed a much enhanced coercivity.     

Microwave-assisted synthesis of flower-like and leaf-like CuO nanostructures via room-temperature ionic liquids

Flower-like and leaf-like cupric oxide (CuO) single-crystal nanostructures have been successfully synthesized using ionic liquid 1-octyl-3-methylimidazolium trifluoroacetate ([Omim]TA) under the microwave-assisted approach. By controlling the concentration of [Omim]TA and reaction temperature, shape transformation of CuO nanostructures could be achieved in a short period of time. The results indicate that ionic liquid [Omim]TA plays an important role in the formation of different morphologies of CuO crystals. The crystal structure and morphology of products were characterized by X-ray powder diffraction (XRD), infrared spectrum (IR), scanning electron microscope (SEM), transmission electron microscopy (TEM), and selected-area electron diffraction (SAED). A possible mechanism for CuO nanostructure was proposed. In addition, UV-vis spectroscopy was employed to estimate the band gap energies of CuO crystals.     

双掺杂LiNbO3:Ce:Cu晶体的光学性能

用提拉法生长出3种不同浓度的双掺杂LiNb03∶Ce∶Cu晶体,测试双掺杂晶体的红外吸收光谱、紫外可见光吸收光谱和X射线衍射谱,掺杂相对浓度较高时,紫外吸收边向长波方向红移,X射线谱峰半峰值宽度变小.测试掺杂晶体在生长态和氧化态时的衍射效率,氧化态的衍射效率比生长态衍射效率高,但响应时间较长.     

Controllable synthesis of Ag nanorods using a porous anodic aluminum oxide template

This paper describes a new approach to the synthesis of Ag nanorods. A solvothermal method was used to make Ag nanoparticles inside anodic aluminum oxide (AAO) templates. The nanoparticles were then annealed at 300 °C to produce Ag nanorods. The size of AAO templates, which is focused on in this study, would determine the diameter of Ag nanorods. The product was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). In this study, a nanorod growth mechanism is deduced, and understanding of the growth of nanorods inside AAO templates is furthered. This work demonstrates that it is possible to make crystalline nanorods that the size can be varied.     

Preparation,characterization and photocatalytic performance of noble metals (Ag,Pd, Pt,Rh) deposited on sponge-like ZnO microcuboids

Novel sponge-like ZnO microcuboids with a hierarchical structure were fabricated via an alcoholic thermal process. Then a series of noble metals (Ag, Pd, Pt, Rh) was loaded onto the microcuboids. The samples obtained were characterized by nitrogen physical adsorption, powder X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV-vis diffuse reflectance spectroscopy (DRS), and X-ray photoelectron spectroscopy (XPS). The results show that the ZnO microcuboids have a high surface area and a sponge-like hierarchical structure. Activity tests for the degradation of acid orange II dye showed that the noble metals enhanced the activity of ZnO to different extents. For loading of 0.5 wt.%, the activity enhancement decreased in the order Pd>Ag>Pt>Rh. Co-loading of Pd and Ag had a detrimental effect on activity compared to single loading. The enhanced photocatalytic performance can be attributed to an increase in the rate of separation of photogenerated e^–/h⁺ pairs induced by the noble metals.     

Ultrasound-assisted fabrication of a new nano-rods 3D copper(II)-organic coordination supramolecular compound

High-energy ultrasound irradiation has been used for the synthesis of a new copper(II) coordination supramolecular compound, [Cu₂(μ-O₂CCH₃)₂(μ-OOCCH₃)(phen)₂](BF₄) (1), (“phen” is 1,10-phenanthroline) with nano-rods morphology. The new nano-structure was characterized by scanning electron microscopy (SEM), X-ray powder diffraction (XRPD), FT-IR spectroscopy and elemental analyses. Compound 1 was structurally characterized by single crystal X-ray diffraction. The utilization of high intensity ultrasound has found as a facile, environmentally friendly, and versatile synthetic tool for the supramolecular coordination compounds.     

Effect of temperature on pulsed laser deposition of ZnO films

ZnO thin films have been deposited on Si(1 1 1) substrates at different substrate temperature by pulsed laser deposition (PLD) of ZnO target in oxygen atmosphere. An Nd:YAG pulsed laser with a wavelength of 1064 nm was used as laser source. The influences of the deposition temperature on the thickness, crystallinity, surface morphology and optical properties of ZnO films were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), selected area electron diffraction (SAED), photoluminescence (PL) spectrum and infrared spectrum. The results show that in our experimental conditions, the ZnO thin films deposited at 400 °C have the best surface morphology and crystalline quality. And the PL spectrum with the strongest ultraviolet (UV) peak and blue peak is observed in this condition.     

基于光栅衍射的晶体X射线衍射缺级的理论基础和实验研究

以光栅衍射缺级理论为切入点对晶体X射线衍射缺级的现象、产生的根源进行了理论分析,得出：(1) 晶体X射线衍射缺级存在的可能性在于某些晶体材料晶胞的几何结构因子为零;(2) 在复式格子晶体或具有某种特殊缺陷的晶体的X射线衍射图样中存在缺级是这方面实验研究的方向。这些结论在材料物相、材料结构类型和不完整性分析等方面具有一定的参考价值。     

Control synthesis of octahedral In2O3 crystals,belts, and nanowires

Octahedral In₂O₃ crystals were synthesized by evaporation of a mixture of In₂O₃ and graphite in a horizontal double-tube system. By adjusting the experimental conditions, In₂O₃ nanowires and nanobelts were also obtained. The microstructures of the resultant In₂O₃ materials were characterized by scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), selected-area electron diffraction (SAED), X-ray diffraction. In addition, the growth mechanism of the octahedral In₂O₃ crystals was discussed in detail.     

Microstructures and tribological properties of CrN/ZrN nanoscale multilayer coatings

Nanoscale multilayer CrN/ZrN coatings with bilayer thicknesses ranging from 11.7 to 66.7 nm were prepared by reactive magnetron sputtering techniques. The structure of the thin films was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). X-ray diffraction results showed that CrN individual layers presented a <1 1 1> preferred orientation in the multilayer coatings. The diffraction peaks of CrN shifted continuously to low diffraction angle with decreasing bilayer thickness. TEM observations showed that the multilayer did not form a superlattice structure instead of the coexistence of nanocrystalline CrN and ZrN layers. Columnar growth for all the coatings was observed by cross-sectional SEM. Nanoindentation tests showed that the multilayer coatings had almost a constant nanohardness of 29 GPa in spite of the variations of bilayer thickness. Pin-on-disk tests indicated that both the friction coefficients and wear rates increased when decreasing bilayer thickness. However, in comparison with the monolayer coating, the multilayer coatings exhibited excellent wear resistance.     

Preparation and characterization of silica-silver core-shell structural submicrometer spheres

Dense, uniform and thickness controllable silver layers were successfully coated on the mono-dispersed submicrometer silica spheres to obtain silica-silver core-shell structural spheres. The growth process of nanoscaled silver layer on silica spheres mainly includes two steps, i.e. nanoscaled nuclei formation and controllable layer growth process. The nuclear-growth mechanism is responsible for the deposition processes. The reagent concentrations and reaction time were found to be the key factors for the formation of controllable silver layer. High quality silver layer with dense and uniform structure was verified by transmission electron microscopy, X-ray diffraction and Energy Dispersive X-ray microanalysis.     

LiFePO4纳米管的制备与表征

采用溶胶凝胶法在氧化铝模板中成功的制备了LiFePO4一维纳米管阵列．扫描电子显微镜和透射电子显微镜表征结果表明所制备的LiFePO4纳米管具有单分散性,互相平行,高度有序。综合选区电子衍射、X射线衍射以及X光线能谱表征结果,所制备的LiFePO4纳米管为单一的橄榄石型结构．这种在室温和温和条件下合成的一维LiFePO4纳米管,可以做为新型的锂离子电池正极材料．     

Self-assembly of Sb2O3 nanowires into microspheres: Synthesis and characterization

Sb₂O₃ nanowires with diameters of ∼233 nm and microspheres assembled by these nanowires were successfully synthesized by a simple poly-(vinylpyrrolidone) (PVP) assisted hydrothermal method. The morphologies, nano/microstructures and optical properties of the as-grown nanowires and microspheres were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and UV-vis diffuse reflection spectrum. It has been found that the experimental parameters, such as mineralizers, played crucial roles in the morphological control of Sb₂O₃ nanowires. The possible growth mechanism of microspheres has been proposed.