Realization of the welding of individual TiO2 semiconductor nano-objects using a novel 1D Au80Sn20 nanosolder

Individual semiconductor nanowires (NWs) TiO2 were successfully welded together using novel one-dimensional (1D) Au80Sn20 (mass ratio) nanosolders at the nano-scale for the first time. The nanosolders were electrodeposited into nanoporous templates to form a 1D structure, and their morphology, crystal structure, chemistry and elemental electronic states were systematically characterized. Individual Au80Sn20 nanowires were proved to consist of mixed crystal phases, including a Au5Sn phase with a trigonal structure, a AuSn phase with a hexagonal structure and a small SnO2 phase produced the by oxidation of the surface portion. Chemical analysis indicated that the composition was Au80Sn20. The testing of the welding capability by either in situ TEM or in situ SEM by nanomanipulators and infiltration experiment revealed a good wet ability and diffusion ability between the Au80Sn20 nanosolder and the TiO2 nanowire. It is believed that our study contributes to the field a special nanosolder for future nano-scale welding techniques, which also make the bonding of titanium-based semiconductor oxide nanomaterials at the nano-scale a reality

Carbon Nanotubes by a CVD Method. Part II: Formation of Nanotubes from (Mg, Fe)O Catalysts

The aim of this paper is to study the formation of carbon nanotubes (CNTs) from different Fe/MgO oxide powders that were prepared by combustion synthesis and characterized in detail in a companion paper. Depending on the synthesis conditions, several iron species are present in the starting oxides including Fe2+ ions, octahedral Fe3+ ions, Fe3+ clusters, and MgFe2O4-like nanoparticles. Upon reduction during heating at 5 °C/min up to 1000 °C in H2/CH4 of the oxide powders, the octahedral Fe3+ ions tend to form Fe2+ ions, which are not likely to be reduced to metallic iron whereas the MgFe2O4-like particles are directly reduced to metallic iron. The reduced phases are R-Fe, Fe3C, and ç-Fe-C. Fe3C appears as the postreaction phase involved in the formation of carbon filaments (CNTs and thick carbon nanofibers). Thick carbon nanofibers are formed from catalyst particles originating from poorly dispersed species (Fe3+ clusters and MgFe2O4-like particles). The nanofiber outer diameter is determined by the particle size. The reduction of the iron ions and clusters that are well dispersed in the MgO lattice leads to small catalytic particles (<5 nm), which tend to form SWNTS and DWNTs with an inner diameter close to 2 nm. Well-dispersed MgFe2O4-like particles can also be reduced to small metal particles with a narrow size distribution, producing SWNTs and DWNTs. The present results will help in tailoring oxide precursors for the controlled formation of CNTs

Fe/Co Alloys for the Catalytic Chemical Vapor Deposition Synthesis of Single- and Double-Walled Carbon Nanotubes (CNTs). 1. The CNT−Fe/Co−MgO System

Mg0.90FexCoyO (x + y ) 0.1) solid solutions were synthesized by the ureic combustion route. Upon reduction at 1000 °C in H2-CH4 of these powders, Fe/Co alloy nanoparticles are formed, which are involved in the formation of carbon nanotubes, which are mostly single and double walled, with an average diameter close to 2.5 nm. Characterizations of the materials are performed using 57Fe Mo¨ssbauer spectroscopy and electron microscopy, and a well-established macroscopic method, based on specific-surface-area measurements, was applied to quantify the carbon quality and the nanotubes quantity. A detailed investigation of the Fe/Co alloys’ formation and composition is reported. An increasing fraction of Co2+ ions hinders the dissolution of iron in the MgO lattice and favors the formation of MgFe2O4-like particles in the oxide powders. Upon reduction, these particles form R-Fe/Co particles with a size and composition (close to Fe0.50Co0.50) adequate for the increased production of carbon nanotubes. However, larger particles are also produced resulting in the formation of undesirable carbon species. The highest CNT quantity and carbon quality are eventually obtained upon reduction of the iron-free Mg0.90Co0.10O solid solution, in the absence of clusters of metal ions in the starting material. Introduction Catalyti

Growth of few-wall carbon nanotubes with narrow diameter distribution over Fe-Mo-MgO catalyst by methane/acetylene catalytic decomposition

Few-wall carbon nanotubes were synthesized by methane/acetylene decomposition over bimetallic Fe-Mo catalyst with MgO (1:8:40) support at the temperature of 900°C. No calcinations and reduction pretreatments were applied to the catalytic powder. The transmission electron microscopy investigation showed that the synthesized carbon nanotubes [CNTs] have high purity and narrow diameter distribution. Raman spectrum showed that the ratio of G to D band line intensities of IG/ID is approximately 10, and the peaks in the low frequency range were attributed to the radial breathing mode corresponding to the nanotubes of small diameters. Thermogravimetric analysis data indicated no amorphous carbon phases. Experiments conducted at higher gas pressures showed the increase of CNT yield up to 83%. Mössbauer spectroscopy, magnetization measurements, X-ray diffraction, high-resolution transmission electron microscopy, and electron diffraction were employed to evaluate the nature of catalyst particles

Titanium Dioxide Nanoparticles: Synthesis, X-Ray Line Analysis and Chemical Composition Study

TiO2 nanoparticleshave been synthesized by the sol-gel method using titanium alkoxide and isopropanolas a precursor. The structural properties and chemical composition of the TiO2 nanoparticles were studied usingX-ray diffraction, scanning electron microscopy, and X-ray photoelectron spectroscopy.The X-ray powder diffraction pattern confirms that the particles are mainly composed of the anatase phase with the preferential orientation along [101] direction.The physical parameters such as strain, stress and energy density were investigated from the Williamson- Hall (W-H) plot assuming a uniform deformation model (UDM), and uniform deformation energy density model (UDEDM). The W-H analysis shows an anisotropic nature of the strain in nanopowders. The scanning electron microscopy image shows clear TiO2 nanoparticles with particle sizes varying from 60 to 80nm. The results of mean particle size of TiO2 nanoparticles show an inter correlation with the W-H analysis and SEM results. Our X-ray photoelectron spectroscopy spectra show that nearly a complete amount of titanium has reacted to TiO2

Single-wall carbon nanotubes production by heterogeneous catalytic reaction.

A synergistic effect between Co and Mo has been observed. When both metallic species are simultaneously present, particularly when Mo is in excess, the catalyst is very effective. However, when they are separated they are either inactive (Mo alone) or unselective (Co alone). To understand this synergistic effect, X-ray absorption spectroscopy (EXAFS and XANES) has been used to characterize the state of Co and Mo on the catalysts before and after the production of SWNT. Co species has found to alter from cobalt oxide in fresh catalyst to metallic cobalt after the reaction, with its particle size growing with reaction time. In the case of Mo species, the molybdenum carbide is identified in the catalyst after the reaction while molybdenum oxide is observed in the fresh catalyst.Carbon nanotubes has shown their outstanding properties and potential applications. However the production of carbon nanotubes is still in the gram-scale that results in the very high cost, particularly single-wall type. The production of single-wall carbon nanotubes (SWNTs) by heterogeneous catalytic reaction is the most promising technique to manufacture this material. Among several catalysts tested in this study, a family of Co-Mo catalysts on silica support has been found to be able to produce SWNTs from carbon monoxide (CO) disproportionation with high selectivity, depending on the Co:Mo ratio, and the reaction condition. The catalyst composition and operating conditions for the synthesis of SWNTs from CO disproportionation have been systematically varied in order to maximize the selectivity towards SWNTs. A simple quantification method based on the standard Temperature Programmed Oxidation (TPO) technique has developed in order to determine the distribution of the different forms of carbonaceous deposits presenting on the catalysts after the CO decomposition reaction

チタニアケイ フクゴウ キンゾク サンカブツ ナノ ザイリョウ オ モチイタ シキソ ゾウカン タイヨウ デンチ ノ ケンキュウ

京都大学0048新制・課程博士博士(エネルギー科学)甲第12422号エネ博第129号新制||エネ||32(附属図書館)24258UT51-2006-J413京都大学大学院エネルギー科学研究科エネルギー基礎科学専攻(主査)教授 吉川 暹, 教授 八尾 健, 教授 萩原 理加学位規則第4条第1項該当Doctor of Energy ScienceKyoto UniversityDA