Hydrogen-Assisted Synthesis and Optical Properties of Single-Crystalline Cd0.9Mn0.1S Nanobelts

2008 ◽  
Vol 8 (8) ◽  
pp. 3883-3888 ◽  
Author(s):  
Guohua Li ◽  
Yang Jiang ◽  
Chun Wang ◽  
Jianfeng Shi ◽  
Zhongping Zhang
Keyword(s):  
Electron Microscopy ◽  
Large Scale ◽  
Hexagonal Wurtzite Structure ◽  
High Quality ◽  
Thermal Evaporation Method ◽  
Single Crystalline ◽  
X Ray ◽  
Transmission Electron ◽  
Room Temperature Photoluminescence Spectrum ◽  
One Step

High quality Cd0.9Mn0.1S nanobelts have been synthesized using a one-step thermal evaporation method in large scale. Their morphology and microstructures were determined by X-ray powder diffraction, scanning electron microscopy, high-resolution transmission electron microscopy, energy-dispersive X-ray spectroscopy, Raman spectroscopy and photoluminescence spectroscopy. The observations revealed that the as-synthesized Cd0.9Mn0.1S nanobelts were high quality single crystalline with hexagonal wurtzite structure. The nanobelts grew along [0 −1 1 0] direction with side surfaces of ± (0 0 0 1) and top surfaces of ± (2 1 1 0). The nanobelts can range in length from several tens to a hundred microns, in thickness about 50 nm and in tapered width 50 to 300 nm. A hydrogen-assisted vapor-liquid-solid (VLS) combined with vapor-solid (VS) formation mechanism is also proposed to interpret the growth of Cd0.9Mn0.1S nanobelts in our work. The room-temperature photoluminescence spectrum of Cd0.9Mn0.1S nanobelts featured two luminescence peaks around 515 and 596 nm, which could be attributed to surface state emission and Mn2+ ion intra-3d (4T1–6A1) transition, respectively.

SYNTHESIS OF In2O3 NANOWIRES ENHANCED BY ANODIC ALUMINA MEMBRANE

2006 ◽  
Vol 05 (04n05) ◽  
pp. 479-485
Author(s):  
C. W. LAI ◽  
X. Y. ZHANG ◽  
H. C. ONG ◽  
J. Y. DAI ◽  
H. L. W. CHAN
Keyword(s):  
Electron Microscopy ◽  
Large Scale ◽  
Anodic Alumina ◽  
X Ray Diffraction ◽  
Alumina Membrane ◽  
Thermal Evaporation Method ◽  
Single Crystalline ◽  
X Ray ◽  
Alumina Membranes ◽  
Transmission Electron

Large-scale single crystalline In 2 O 3 nanowires were successfully synthesized on anodic alumina membranes by a simple thermal evaporation method at 570°C. X-ray diffraction, transmission electron microscopy, and scanning electron microscopy studies revealed the formation of single crystalline In 2 O 3 nanowires with diameters of 50–100 nm and lengths of up to a few hundreds of micrometers. Cathodeluminescence study revealed existence of oxygen vacancies evidenced by a strong and broad emission at 470 nm with a shoulder at 400 nm. The growth mechanism of the nanostructures is also discussed.

Synthesis and Properties of GaN Nanostructures

2005 ◽  
Vol 475-479 ◽  
pp. 3367-3370
Author(s):  
Hong-Lei Ma ◽  
Cheng Shan Xue ◽  
Ying Ge Yang ◽  
Hui Zhao Zhang ◽  
Jin Ma ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Hexagonal Wurtzite Structure ◽  
X Ray Diffraction ◽  
High Quality ◽  
One Dimensional ◽  
X Ray ◽  
Gan Nanowires ◽  
Transmission Electron ◽  
Morphology And Structure ◽  
Scanning Electron

One-dimensional GaN nanostructure films were successfully synthesized by the recently developed sputtering post-nitridation technique. The morphology and structure of GaN nanowires are investigated by X-ray diffraction (XRD), transmission electron microscopy (TEM), and scanning electron microscopy (SEM). The results indicate that the crystalline GaN nanostructures have a hexagonal wurtzite structure, and there is not any other phase such as Ga2O3 or Ga in the specimen. It also confirms that high quality crystal was obtained in the resulting sample due to the lattice defects decreased and the crystallinity improved in the process of nitridation at high temperature. The growth mechanism of the GaN nanostructures is briefly discussed.

scholarly journals A facile synthesis of a carbon-encapsulated Fe3O4 nanocomposite and its performance as anode in lithium-ion batteries

2013 ◽  
Vol 4 ◽  
pp. 699-704 ◽  
Author(s):  
Raju Prakash ◽  
Katharina Fanselau ◽  
Shuhua Ren ◽  
Tapan Kumar Mandal ◽  
Christian Kübel ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Lithium Ion ◽  
Iron Pentacarbonyl ◽  
X Ray Diffraction ◽  
Facile Synthesis ◽  
X Ray ◽  
Transmission Electron ◽  
Lithium Ion Cell ◽  
Carbon Framework ◽  
One Step

A carbon-encapsulated Fe3O4 nanocomposite was prepared by a simple one-step pyrolysis of iron pentacarbonyl without using any templates, solvents or surfactants. The structure and morphology of the nanocomposite was investigated by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, Brunauer–Emmett–Teller analysis and Raman spectroscopy. Fe3O4 nanoparticles are dispersed intimately in a carbon framework. The nanocomposite exhibits well constructed core–shell and nanotube structures, with Fe3O4 cores and graphitic shells/tubes. The as-synthesized material could be used directly as anode in a lithium-ion cell and demonstrated a stable capacity, and good cyclic and rate performances.

Activation of persulfate by heterogeneous catalyst ZnCo2O4–RGO for efficient degradation of bisphenol A

2020 ◽  
Vol 98 (12) ◽  
pp. 771-778
Author(s):  
Xin Chang ◽  
Xiangyang Xu ◽  
Zhifeng Gao ◽  
Yingrui Tao ◽  
Yixuan Yin ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Bisphenol A ◽  
Photoelectron Spectroscopy ◽  
X Ray Diffraction ◽  
Reaction Conditions ◽  
X Ray ◽  
Transmission Electron ◽  
Nucleation Sites ◽  
One Step ◽  
Application Potential

A nanocomposite, reduced graphene oxide (RGO) modified ZnCo2O4 (ZnCo2O4–RGO) was synthesized via one-step solvothermal method for activating persulfate (PS) to degrade bisphenol A (BPA). The morphology and structure of the nanocomposite were identified by X-ray diffraction, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy, and transmission electron microscopy. RGO provides nucleation sites for ZnCo2O4 to grow and inhibits the agglomeration of the nanoparticles. The influence of different reaction conditions on the oxidation of BPA catalyzed by ZnCo2O4–RGO was investigated, including the content of RGO, the dosage of catalyst, the concentration of humic acid (HA), anions in the environment, the reaction temperature, and pH. BPA can be totally degraded within 20 min under optimized reaction conditions. The presence of HA, Cl−, and NO3− only has a slight effect on the oxidation of BPA, whereas the presence of either H2PO4− or HCO3− can greatly inhibit the reaction. ZnCo2O4–RGO shows good cycling stability and practical application potential. A reaction mechanism of the degradation of BPA was also explored.

Uniform Cerium-Based Coordination Polymer Microspheres: Preparation and Upconversion Emission

2016 ◽  
Vol 16 (4) ◽  
pp. 3705-3709 ◽  
Author(s):  
Zhi-Wen Nie ◽  
Cheng-Hui Zeng ◽  
Gang Xie ◽  
Sheng-Liang Zhong
Keyword(s):  
Electron Microscopy ◽  
Coordination Polymer ◽  
Large Scale ◽  
Upconversion Emission ◽  
X Ray Diffraction ◽  
X Ray ◽  
Band Emission ◽  
Transmission Electron ◽  
Light Excitation ◽  
Luminescent Spectra

Homogeneously doped Yb3+ and Er3+ cerium-based coordination polymer (CP) microspheres have been successfully synthesized on a large scale through a simple solvothermal route with 2, 5-pyridinedicarboxylic acid (2, 5-H2PDC) as the organic linker. CeO2:Yb3+, Er3+ porous microspheres were obtained by annealing the corresponding CP microspheres at 600 °C for 4 h under atmospheric pressure. These as-prepared products were characterized by Powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR), energy-dispersion X-ray (EDX) spectroscopy, Thermogravimetric (TG) and derivative thermogravimetric (DTG) analysis. The room temperature upconversion luminescent spectra of the as-prepared microspheres were carried out by 980 nm NIR light excitation. Interestingly, Yb3+ and Er3+ codoped CP microspheres give a single-band emission centered at 673 nm, while the CeO2:Yb3+, Er3+ microspheres give emission in green and red region, with red being the dominant emission. The emission intensity of the CeO2:Yb3+, Er3+ microspheres were much stronger than that of the Yb3+ and Er3+ codoped CP microspheres.

Characterization and Growth Mechanism of B12As2 Epitaxial Layers Grown on (1-100) 15R-SiC

2008 ◽  
Vol 1069 ◽  
Author(s):  
Hui Chen ◽  
Guan Wang ◽  
Michael Dudley ◽  
Zhou Xu ◽  
James. H. Edgar ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
High Resolution ◽  
Growth Mechanism ◽  
Heteroepitaxial Growth ◽  
High Quality ◽  
X Ray ◽  
Transmission Electron ◽  
Substrate Choice

ABSTRACTA systematic study is presented of the heteroepitaxial growth of B12As2 on m-plane 15R-SiC. In contrast to previous studies of B12As2 on other substrates, including (100) Si, (110) Si, (111) Si and (0001) 6H-SiC, single crystalline and untwinned B12As2 was achieved on m-plane 15R-SiC. Observations of IBA on m-plane (1100)15R-SiC by synchrotron white beam x-ray topography (SWBXT) and high resolution transmission electron microscopy (HRTEM) confirm the good quality of the films on the 15R-SiC substrates. The growth mechanism of IBA on m-plane 15R-SiC is discussed. This work demonstrates that m-plane 15R-SiC is potentially a good substrate choice to grow high quality B12As2 epilayers.

scholarly journals One-Step Synthesis of Copper and Cupric Oxide Particles from the Liquid Phase by X-Ray Radiolysis Using Synchrotron Radiation

2016 ◽  
Vol 2016 ◽  
pp. 1-16 ◽  
Author(s):  
Akinobu Yamaguchi ◽  
Ikuo Okada ◽  
Takao Fukuoka ◽  
Mari Ishihara ◽  
Ikuya Sakurai ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Synchrotron Radiation ◽  
Cupric Oxide ◽  
Oxide Particle ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Transmission ◽  
One Step ◽  
Oxide Particles

The deposition of copper (Cu) and cupric oxide (Cu4O3, Cu2O, and CuO) particles in an aqueous copper sulfate (CuSO4) solution with additive alcohol such as methanol, ethanol, 2-propanol, and ethylene glycol has been studied by X-ray exposure from synchrotron radiation. An attenuated X-ray radiation time of 5 min allows for the synthesis of Cu, Cu4O3, Cu2O, and CuO nano/microscale particles and their aggregation into clusters. The morphology and composition of the synthesized Cu/cupric oxide particle clusters were characterized by scanning electron microscopy, scanning transmission electron microscopy, and high-resolution transmission electron microscopy with energy dispersive X-ray spectroscopy. Micro-Raman spectroscopy revealed that the clusters comprised cupric oxide core particles covered with Cu particles. Neither Cu/cupric oxide particles nor their clusters were formed without any alcohol additives. The effect of alcohol additives is attributed to the following sequential steps: photochemical reaction due to X-ray irradiation induces nucleation of the particles accompanying redox reaction and forms a cluster or aggregates by LaMer process and DLVO interactions. The procedure offers a novel route to synthesize the Cu/cupric oxide particles and aggregates. It also provides a novel additive manufacturing process or lithography of composite materials such as metal, oxide, and resin.

Mixed-Solvothermal Preparation of Mace-Like CdS Nanocrystals

2012 ◽  
Vol 502 ◽  
pp. 164-168
Author(s):  
Ling Xu ◽  
Han Mei Hu ◽  
Hai Yan Xu
Keyword(s):  
Electron Microscopy ◽  
Large Scale ◽  
Volume Ratio ◽  
X Ray Diffraction ◽  
Visible Absorption ◽  
X Ray ◽  
Transmission Electron ◽  
Cds Nanostructures ◽  
Uv Visible ◽  
Solvothermal Preparation

Novel mace-like (wolf-teeth clubs) CdS nanostructures were successfully prepared on a large scale using CdCl2•2.5H2O and NH2CSNH2 as starting materials through a convenient mixed-solvothermal route. The as-synthesized products were characterized by X-ray diffraction (XRD), energy dispersive X-ray spectrometry (EDX), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM) and UV-visible absorption spectroscopy. The experimental results reveal that the morphology of CdS products was greatly affected by the volume ratio of anhydrous ethanol and distilled water. The possible mechanism for the formation of mace-like CdS nanostructures is simply discussed.

One-step synthesis of Sb2O3 broom-like belts with controllable morphology

2005 ◽  
Vol 83 (8) ◽  
pp. 1093-1097 ◽  
Author(s):  
Qingrui Zhao ◽  
Xuanjun Zhang ◽  
Qing Yang ◽  
Yi Xie
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Solvothermal Reaction ◽  
Antimony Trioxide ◽  
Reactant Ratio ◽  
Reaction Conditions ◽  
X Ray ◽  
Transmission Electron ◽  
One Step ◽  
Template Free

A direct and simple surfactant- and template-free route has been developed for the controlled synthesis of Sb2O3 belt-like microstructures. By adjusting the reactant ratio between SbCl3 and urea under solvothermal reaction conditions, broom-like belts and rods of Sb2O3 have been successfully prepared. X-ray powder diffraction (XRD), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HR-TEM), and X-ray photoelectron spectroscopy (XPS) has been used to characterize the phases and morphologies of the as-prepared products. A possible formation mechanism is also discussed.Key words: antimony trioxide, solvothermal synthesis, broom-like belts.

scholarly journals Hydrothermal Synthesis and Characterization of Single-Crystalline -Fe2O3Nanocubes

2011 ◽  
Vol 2011 ◽  
pp. 1-5 ◽  
Author(s):  
Wenqing Qin ◽  
Congren Yang ◽  
Ran Yi ◽  
Guanhua Gao
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Infrared Spectrometry ◽  
X Ray Diffraction ◽  
Single Crystalline ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Alkaline Agent ◽  
One Step

Single-crystalline - nanocubes were successfully obtained in large quantities through a facile one-step hydrothermal synthetic route under mild conditions. In this synthetic system, aqueous iron (III) nitrate () served as iron source and triethylamine served as precipitant and alkaline agent. By prolonging reaction time from 1 h to 24 h, the evolution process of -, from nanorhombohedra to nanohexahedron, and finally nanocube, was observed. The products were characterized by Powder X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), High-resolution Transmission Electron Microscopy (HRTEM), Selected-Area Electron Diffraction (SAED), and Fourier Transform Infrared Spectrometry (FTIR). The possible formation mechanism was discussed on basis of the experimental results.

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