Growth and Density Control of Carbon Tubule Nanocoils Using Catalyst of Iron Compounds

2002 ◽  
Vol 17 (1) ◽  
pp. 145-148 ◽  
Author(s):  
Lujun Pan ◽  
Taichi Hayashida ◽  
Yoshikazu Nakayama

We synthesized carbon tubule nanocoils by catalytic thermal chemical vapor deposition. The iron catalyst necessary in the growth of carbon nanocoils was prepared only by coating the iron compound solution on indium tin oxide–coated glass substrate. It was found that the iron compounds have the same catalytic function as iron thin film prepared by evaporation or electroplating. Furthermore, the density of the prepared carbon nanocoils could be easily controlled by changing the density of the solution of iron compounds. In addition, the poly(methylphenylsilane) proved to be an excellent dispersive medium for the iron compound in preparation of the carbon nanocoils in desired densities.

2011 ◽  
Vol 1309 ◽  
Author(s):  
Lamartine Meda ◽  
Geoffrey D. Stevens

ABSTRACTBy carefully manipulating and controlling the growth conditions, Ruthenium (Ru) and ruthenium oxide (RuO2) two-dimensional (2-D) nanostructure were self-assembled into a stack of plates on indium tin oxide coated glass substrate. The nanoplates were grown in a horizontal hot-wall metalorganic chemical vapor deposition (MOCVD) from ruthenocene. Each nanoplate has a thickness in the range of 25 - 60 nm and the average area is 1000 x 300 nm2. Each stack of nanoplates is approximately 1.2 m in height. A continuous layer of Ru and RuO2 thin film, which may serve as the growth template, is observed on the bottom of the nanoplate stacks. Field-emission scanning electron microscopy reveals that each stack of nanoplates was grown vertically aligned on the substrate and exhibited elongated shape. Structural properties which were examined by X-ray diffraction show that the nanoplates are polycrystalline.


2014 ◽  
Vol 2014 ◽  
pp. 1-11 ◽  
Author(s):  
Mohamed Shuaib Mohamed Saheed ◽  
Norani Muti Mohamed ◽  
Zainal Arif Burhanudin

The paper reported the investigation of the substrate preparation technique involving deposition of iron catalyst by electron beam evaporation and ferrocene vaporization in order to produce vertically aligned multiwalled carbon nanotubes array needed for fabrication of tailored devices. Prior to the growth at 700°C in ethylene, silicon dioxide coated silicon substrate was prepared by depositing alumina followed by iron using two different methods as described earlier. Characterization analysis revealed that aligned multiwalled carbon nanotubes array of 107.9 µm thickness grown by thermal chemical vapor deposition technique can only be achieved for the sample with iron deposited using ferrocene vaporization. The thick layer of partially oxidized iron film can prevent the deactivation of catalyst and thus is able to sustain the growth. It also increases the rate of permeation of the hydrocarbon gas into the catalyst particles and prevents agglomeration at the growth temperature. Combination of alumina-iron layer provides an efficient growth of high density multiwalled carbon nanotubes array with the steady growth rate of 3.6 µm per minute for the first 12 minutes and dropped by half after 40 minutes. Thicker and uniform iron catalyst film obtained from ferrocene vaporization is attributed to the multidirectional deposition of particles in the gaseous form.


2015 ◽  
Vol 804 ◽  
pp. 47-50 ◽  
Author(s):  
Udomdej Pakdee ◽  
Santipab Srabua ◽  
Aphichard Phongphala ◽  
Chutchai Pawong

The effects of cobalt, nickel and iron catalyst on carbon nanotubes (CNTs) were examined with scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray diffractrometer (XRD) and Fourier transform Raman spectrometer (FT-Raman). The samples were prepared by the thermal chemical vapor deposition (CVD) method at 780 °C under pressure of acetylene gas (C2H2) at 0.5 bar. The average diameter of CNTs grown on Co, Fe and Ni catalyst obtained from SEM image is 100, 90, 70 nm, respectively. The crystallinity and the yield of CNTs synthesized from Ni catalyst were higher than that from Fe or Co catalyst. The Raman peak of radial breathing mode (RBM) region and the TEM images highlighted the hollow tubes of the CNTs. The results indicated that the diameter, the yield and the crystallinity for synthesis of carbon nanotubes were manipulated by the selection of the catalyst.


2012 ◽  
Vol 490-495 ◽  
pp. 3211-3214 ◽  
Author(s):  
Lei Shan Chen ◽  
Cun Jing Wang

Synthesis reactions were carried out by chemical vapor deposition using iron catalyst supported on aluminum hydroxide at 400 °C and 420 °C, in the presence of argon as carrier gas and acetylene as carbon source. The aluminum hydroxide support was separated by refluxing the samples in 40% NaOH solution for 2 h and 36% HCl solution for 24 h, respectively. The samples were characterized by field-emission scanning electron microscopy, energy dispersive spectroscopy, high-resolution transmission electron microscopy and X-ray diffraction. The results show that carbon nanotubes were the main products at 420 °C, while large scale high purity nano onion-like fullerenes encapsulating Fe3C, with almost uniform sizes ranging from 10-50 nm, were obtained at the low temperature of 400 °C.


2007 ◽  
Vol 1057 ◽  
Author(s):  
Abhishek Prasad ◽  
Samuel Mensah ◽  
Jiesheng Wang ◽  
Archana Pandey ◽  
Yoke Khin Yap

ABSTRACTThe growth of ZnO nanotubes and nanosquids is obtained by conventional thermal chemical vapor deposition (CVD) without the use of catalysts or templates. Characterization of these ZnO nanostructures was conducted by X-ray powder diffraction (XRD), Field-emission scanning electron microscopy (FESEM), Raman spectroscopy, and photoluminescence (PL). Results indicate that these ZnO nanostructures maintain the crystalline structures of the bulk wurtzite ZnO crystals. Our results show that rapid cooling can be used to induce the formation of ZnO nanotubes and ZnO nanosquids. The self-assembly of these novel ZnO nanostructures are guided by the theory of nucleation and the vapor-solid crystal growth mechanism.


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