Synthesis and Electronic Transport Studies of Single-Crystalline In2O3 Nanowires

2003 ◽  
Vol 775 ◽  
Author(s):  
Chao Li ◽  
Daihua Zhang ◽  
Song Han ◽  
Xiaolei Liu ◽  
Tao Tang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Thermal Emission ◽  
Field Effect Transistors ◽  
Growth Direction ◽  
X Ray Diffraction ◽  
Single Crystalline ◽  
Laser Ablation Method ◽  
Selected Area Electron Diffraction ◽  
Transport Studies ◽  
Transmission Electron

AbstractSingle crystalline In203 nanowires were successful synthesized using a laser ablation method. Extensive material characterization such as X-ray diffraction (XRD) and selected area electron diffraction (SAED) revealed a cubic crystal structure for these nanowires with [110] as the growth direction. Transmission electron microscopy (TEM) and scanning electron microscopy (SEM) are used to determine the diameter and length of our nanowires. By using monodispersed gold clusters as the catalyst, these nanowires can be grown with well-defined diameters around 10 nm. Individual In2O3 nanowires have been utilized to construct field effect transistors, which confirmed In2O3 nanowires as n-type semiconductors and exhibited on / off ratios as high as 104 at room temperature. The temperature-dependence of the conductance revealed thermal emission as the dominating transport mechanism. Our work can lead to important applications such as chemical sensing for In2O3 nanowires.

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.

scholarly journals Synthesis and Optical Properties of CdSxSe1-x Semiconductor Nanomaterials by Chemical Vapor Deposition Method

2019 ◽  
Vol 12 (3) ◽  
pp. 55-64
Author(s):  
Nadia M. Jassim
Keyword(s):  
Electron Microscopy ◽  
Chemical Vapor Deposition ◽  
Vapor Deposition ◽  
Chemical Vapor ◽  
Growth Direction ◽  
Chemical Vapor Deposition Method ◽  
X Ray Diffraction ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Vls Growth

Highly pure and crystalline CdSxSe1 -x nanostructures have been successfully synthesized via Chemical Vapor Deposition (CVD) method, changing the components of x, in order to adjust the band gap of materials, and the relationship with the lattice constant. Using X-ray Diffraction (XRD) to characterize the phase structures and elemental compositions of the samples, and using Field Emission Scanning Electron Microscopy (FESEM) to observe the surface morphology of CdSxSe1 -x nanomaterials and confirm the VLS growth mechanism. Using the High Resolution Transmission Electron Microscopy (HRTEM) and Selected Area Electron Diffraction (SAED) to analyze the crystal structure and the growth direction of the materials

scholarly journals Preparation of Biomorphic Porous SiC Ceramics from Bamboo by Combining Sol–Gel Impregnation and Carbothermal Reduction

Polymers ◽  
2019 ◽  
Vol 11 (9) ◽  
pp. 1442 ◽  
Author(s):  
Hung ◽  
Wu ◽  
Xu ◽  
Wu
Keyword(s):  
Electron Microscopy ◽  
Carbothermal Reduction ◽  
Sol Gel ◽  
Atomic Plane ◽  
Growth Direction ◽  
X Ray Diffraction ◽  
Selected Area Electron Diffraction ◽  
Sic Ceramics ◽  
Transmission Electron ◽  
Diffraction Patterns

This study investigated the feasibility of using bamboo to prepare biomorphic porous silicon carbide (bio-SiC) ceramics through a combination of sol–gel impregnation and carbothermal reduction. The effects of sintering temperature, sintering duration, and sol–gel impregnation cycles on the crystalline phases and microstructure of bio-SiC were investigated. X-ray diffraction patterns revealed that when bamboo charcoal–SiO2 composites (BcSiCs) were sintered at 1700 °C for more than 2 h, the resulting bio-SiC ceramics exhibited significant β-SiC diffraction peaks. In addition, when the composites were sintered at 1700 °C for 2 h, scanning electron microscopy micrographs of the resulting bio-SiC ceramic prepared using a single impregnation cycle showed the presence of SiC crystalline particles and nanowires in the cell wall and cell lumen of the carbon template, respectively. However, bio-SiC prepared using three and five repeated cycles of sol–gel impregnation exhibited a foam-like microstructure compared with that prepared using a single impregnation cycle. Moreover, high-resolution transmission electron microscopy and selected area electron diffraction revealed that the atomic plane of the nanowire of bio-SiC prepared from BcSiCs had a planar distance of 0.25 nm and was perpendicular to the (111) growth direction. Similar results were observed for the bio-SiC ceramics prepared from bamboo–SiO2 composites (BSiCs). Accordingly, bio-SiC ceramics can be directly and successfully prepared from BSiCs, simplifying the manufacturing process of SiC ceramics.

Synthesis and Photoluminescence Properties of Novel SnO2 Zigzag Nanoribbons

2010 ◽  
Vol 97-101 ◽  
pp. 4213-4216
Author(s):  
Jian Xiong Liu ◽  
Zheng Yu Wu ◽  
Guo Wen Meng ◽  
Zhao Lin Zhan
Keyword(s):  
Electron Microscopy ◽  
Room Temperature ◽  
Vapour Deposition ◽  
Chemical Vapour ◽  
Photoluminescence Properties ◽  
X Ray Diffraction ◽  
X Ray ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Ceramic Boat

Novel single-crystalline SnO2 zigzag nanoribbons have been successfully synthesized by chemical vapour deposition. Sn powder in a ceramic boat covered with Si plates was heated at 1100°C in a flowing argon atmosphere to get deposits on a Si wafers. The main part of deposits is SnO2 zigzag nanoribbons. They were characterized by means of X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectroscopy (EDX), transmission electron microscopy (TEM) and selected-area electron diffraction (SAED). SEM observations reveal that the SnO2 zigzag nanoribbons are almost uniform, with lengths near to several hundred micrometers and have a good periodically tuned microstructure as the same zigzag angle and growth directions. Possible growth mechanism of these zigzag nanoribbons was discussed. A room temperature PL spectrum of the zigzag nanoribbons shows three peaks at 373nm, 421nm and 477nm.The novel zigzag microstructures will provide a new candidate for potential application.

Control of Morphology and Growth Direction of Gallium Nitride Nanostructures

2003 ◽  
Vol 789 ◽  
Author(s):  
Seung Yong Bae ◽  
Hee Won Seo ◽  
Jeunghee Park
Keyword(s):  
Electron Microscopy ◽  
Gallium Nitride ◽  
Large Scale ◽  
Chemical Vapor ◽  
Growth Direction ◽  
Chemical Vapor Deposition Method ◽  
X Ray Diffraction ◽  
Oxide Mixture ◽  
Temperature Range ◽  
Transmission Electron

ABSTRACTVarious shaped single-crystalline gallium nitride (GaN) nanostructures were produced by chemical vapor deposition method in the temperature range of 900–1200 °C. Scanning electron microscopy, transmission electron microscopy, electron diffraction, x-ray diffraction, electron energy loss spectroscopy, Raman spectroscopy, and photoluminescence were used to investigate the structural and optical properties of the GaN nanostructures. We controlled the GaN nanostructures by the catalyst and temperature. The cylindrical and triangular shaped nanowires were synthesized using iron and gold nanoparticles as catalysts, respectively, in the temperature range of 900 – 1000 °C. We synthesized the nanobelts, nanosaws, and porous nanowires using gallium source/ boron oxide mixture. When the temperature of source was 1100 °C, the nanobelts having a triangle tip were grown. At the temperature higher up to 1200 °C the nanosaws and porous nanowires were formed with a large scale. The cylindrical nanowires have random growth direction, while the triangular nanowires have uniform growth direction [010]. The growth direction of the nanobelts is perpendicular to the [010]. Interestingly, the nanosaws and porous nanowires exhibit the same growth direction [011]. The shift of Raman, XRD, and PL bands from those of bulk was correlated with the strains of the GaN nanostructures.

Growth of epitaxial ZnO films on Si(111)

2002 ◽  
Vol 722 ◽  
Author(s):  
Chunming Jin ◽  
Ashutosh Tiwari ◽  
A. Kvit ◽  
J. Narayan
Keyword(s):  
Electron Microscopy ◽  
Transparent Conducting Oxide ◽  
Deposition Process ◽  
Growth Direction ◽  
Zno Films ◽  
X Ray Diffraction ◽  
Electrical Measurements ◽  
X Ray ◽  
Transmission Electron ◽  
Aln Buffer

AbstractEpitaxial ZnO films have been grown on Si(111) substrates by employing a AlN buffer layer during a pulsed laser-deposition process. The epitaxial structure of AlN on Si(111) substrate provides a template for ZnO growth. The resultant films are evaluated by transmission electron microscopy, x-ray diffraction, and electrical measurements. The results of x-ray diffraction and electron microscopy on these films clearly show the epitaxial growth of ZnO films with an orientational relationship of ZnO[0001]||Aln[0001]||Si[111] along the growth direction and ZnO[2 11 0]||AlN[2 11 0]||Si[0 11] along the in-plane direction. High electrical conductivity (103 S/m at 300 K) and a linear I-V characteristics make these epitaxial films ideal for microelectronic, optoelectronic, and transparent conducting oxide applications.

scholarly journals Synthesis and optical properties of self-assembled flower-like CdS architectures by mixed solvothermal process

2010 ◽  
Vol 8 (5) ◽  
pp. 1027-1033 ◽  
Author(s):  
Junhao Zhang ◽  
Yuhui Wu ◽  
Jia Zhu ◽  
Shaoxing Huang ◽  
Dongjing Zhang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Optical Properties ◽  
X Ray Diffraction ◽  
Wurtzite Phase ◽  
Strong Emission ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Self Assembled ◽  
Xrd Patterns ◽  
Hexagonal Wurtzite Phase

AbstractSelf-assembled CdS architectures with flower-like structures have been synthesized by a mixed solvothermal method using ethylene glycol and oleic acid as the mixed solvent at 160°C for 12 h. The results of X-ray diffraction (XRD) patterns, field-emission scanning electron microscopy (FESEM) and transmission electron microscopy (TEM) images indicate that the product exists as the hexagonal wurtzite phase and conatins of larger numbers of flower-like CdS architectures with diameters of 1.8–3 μm. The selected-area electron diffraction (SAED) pattern and the high resolution transmission electron microscope (HRTEM) image reveal that the grain has better crystallinity. The optical properties of flower-like CdS architectures were also investigated by ultraviolet-visable (UV-vis) and photoluminescence spectroscopy at room temperature. A strong peak at 490 nm is shown in the UV-vis absorption, while an emission at 486 nm and another strong emission at 712 nm are shown in the PL spectrum.

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.

On the destruction of kaolinite and gibbsite by phenylphosphonic, phenylphosphinic and phenylarsonic acids: evidence for the formation of new Al compounds

Clay Minerals ◽  
2004 ◽  
Vol 39 (4) ◽  
pp. 391-404 ◽  
Author(s):  
J. E. F. C. Gardolinski ◽  
G. Lagaly ◽  
M. Czank
Keyword(s):  
Electron Microscopy ◽  
Thermal Analysis ◽  
Transmission Electron Microscopy ◽  
Fourier Transform ◽  
Linear Chain ◽  
X Ray Diffraction ◽  
Phenylphosphonic Acid ◽  
X Ray ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron

AbstractKaolinite and synthetic γ-Al(OH)3 (gibbsite or hydrargillite) were reacted with phenylphosphonic, phenylphosphinic and 2-nitrophenol-4-arsonic acids. The products were studied by powder X-ray diffraction, transmission electron microscopy/selected area electron diffraction/ energy dispersive X-ray/Fourier transform infrared and simultaneous thermogravimetric/differential thermal analysis. The acids were not intercalated but, instead, easily destroyed the structure of the minerals. Lamellar Al phenylphosphonate and aluminium phenylphosphinate and phenylarsonate with polymeric linear-chain structures were formed from kaolinite. The reaction between gibbsite and the same acids yielded almost identical products. No evidence of formation of grafted kaolinite derivatives after the reaction with phenylphosphonic acid was found.

scholarly journals Fabrication of TiO2Nanotanks Embedded in a Nanoporous Alumina Template

2015 ◽  
Vol 2015 ◽  
pp. 1-7 ◽  
Author(s):  
C. Massard ◽  
S. Pairis ◽  
V. Raspal ◽  
Y. Sibaud ◽  
K. O. Awitor
Keyword(s):  
Electron Microscopy ◽  
Sol Gel ◽  
Thermal Treatments ◽  
X Ray Diffraction ◽  
Alumina Template ◽  
Nanoporous Alumina ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Sol Gel Process

The feasibility of surface nanopatterning with TiO2nanotanks embedded in a nanoporous alumina template was investigated. Self-assembled anodized aluminium oxide (AAO) template, in conjunction with sol gel process, was used to fabricate this nanocomposite object. Through hydrolysis and condensation of the titanium alkoxide, an inorganic TiO2gel was moulded within the nanopore cavities of the alumina template. The nanocomposite object underwent two thermal treatments to stabilize and crystallize the TiO2. The morphology of the nanocomposite object was characterized by Field Emission Scanning Electron Microscopy (FESEM). The TiO2nanotanks obtained have cylindrical shapes and are approximately 69 nm in diameter with a tank-to-tank distance of 26 nm. X-ray diffraction analyses performed by Transmission Electron Microscopy (TEM) with selected area electron diffraction (SAED) were used to investigate the TiO2structure. The optical properties were studied using UV-Vis spectroscopy.

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