Carbon Nanotubes Grown with Non-Ferromagnetic Catalysts in Alcohol CVD

2010 ◽  
Vol 636-637 ◽  
pp. 703-708 ◽  
Author(s):  
E. Borowiak-Palen ◽  
A. Steplewska ◽  
A. Bachmatiuk ◽  
M.H. Rümmeli ◽  
R.K. Kalenczuk

In this contribution we present high resolution transmission electron microscopy (HR-TEM) and Raman studies on the synthesis of carbon nanotubes using platinum supported on MgO in alcohol - chemical vapour deposition (A-CVD). For comparison copper and iron catalysts mixed with the same metal loading in MgO and the same process parameters in A-CVD have been tested. Our findings show that the choice of catalyst utilized under the same experimental conditions strongly influences the final morphology of the carbon nanostructures. Application of Pt/MgO in CVD results in doublewalled carbon nanotubes (DWCNT) and multiwalled carbon nanotubes (MWCNT). Cu/MgO mixtures lead to the synthesis of copper filled multiwalled carbon nanotubes (Cu-MWCNT) and iron capsules surrounded by multiwalled carbon shells (Fe-MWCS), respectively. Our findings indicate that the three discussed metals interact differently with the substrate leading to the formation of different sized catalyst particles. The analysis of the particles size in the catalyst precursors and in the final products is also described in this contribution.

2004 ◽  
Vol 99-100 ◽  
pp. 269-272
Author(s):  
R.J. Kalenczuk ◽  
E. Borowiak-Palen ◽  
T. Pichler ◽  
M. Rümmeli ◽  
J. Fink

We present a study on the preparation of multiwalled carbon nanotubes (MWCNT) using chemical vapour deposition (CVD). The CVD produced MWCNT and single wall carbon nanotubes (SWCNT) produced with a laser ablation technique were then chemically modified by substituting carbon atoms with boron and nitrogen atoms. The morphology and the crystal structure of the new class of nanostructures were analyzed by means of scanning electron microscopy (SEM) and transmission electron microscopy (TEM).


2012 ◽  
Vol 3 ◽  
pp. 360-367 ◽  
Author(s):  
Luca Camilli ◽  
Manuela Scarselli ◽  
Silvano Del Gobbo ◽  
Paola Castrucci ◽  
Eric Gautron ◽  
...  

We have taken advantage of the native surface roughness and the iron content of AISI-316 stainless steel to grow multiwalled carbon nanotubes (MWCNTs) by chemical vapour deposition without the addition of an external catalyst. The structural and electronic properties of the synthesized carbon nanostructures have been investigated by a range of electron microscopy and spectroscopy techniques. The results show the good quality and the high graphitization degree of the synthesized MWCNTs. Through energy-loss spectroscopy we found that the electronic properties of these nanostructures are markedly different from those of highly oriented pyrolytic graphite (HOPG). Notably, a broadening of the π-plasmon peak in the case of MWCNTs is evident. In addition, a photocurrent was measured when MWCNTs were airbrushed onto a silicon substrate. External quantum efficiency (EQE) and photocurrent values were reported both in planar and in top-down geometry of the device. Marked differences in the line shapes and intensities were found for the two configurations, suggesting that two different mechanisms of photocurrent generation and charge collection are in operation. From this comparison, we are able to conclude that the silicon substrate plays an important role in the production of electron–hole pairs.


2011 ◽  
Vol 306-307 ◽  
pp. 1325-1329
Author(s):  
Shu Shan Yao

Carbon nanotubes, carbon spheres and slices of vertically aligned multiwalled carbon nanotubes (MWNTs) were synthesized simultaneously by chemical vapour deposition (CVD). Electron microscopy image showed carbon nanotubes were multiwalled carbon nanotubes, several micrometers in length. Carbon spheres were of uniform diameter (about 1 μm). Slices of vertically aligned multiwalled carbon nanotubes were about 5 mm in length, 3 mm in width and 8 μm in thickness. The interior of the slice was composed of densely packed, vertical aligned MWNTs, and faceted carbon beads. They were stable and easily separated from each other. The formation mechanism of slice was also discussed.


2019 ◽  
Vol 6 (1) ◽  
pp. 72-80 ◽  
Author(s):  
Longze Zhao ◽  
Yong Cheng ◽  
Qiaobao Zhang ◽  
Ming-Sheng Wang

Two multiwalled carbon nanotubes are seamlessly joined via the crystallization of an amorphous carbon joint using a transmission electron microscope.


2015 ◽  
Vol 60 (3) ◽  
pp. 2053-2060 ◽  
Author(s):  
A.D. Dobrzańska-Danikiewicz ◽  
D. Łukowiec ◽  
D. Cichocki ◽  
W. Wolany

Abstract Carbon-metal nanocomposites consisting of multiwalled carbon nanotubes coated with rhodium or rhenium nanoparticles by the high-temperature method were fabricated during the research undertaken. Multiwalled carbon nanotubes fabricated by Catalytic-Chemical Vapour Deposition (CCVD) were used in the investigations. Multiwalled carbon nanotubes functionalisation in acid or in a mixture of acids was applied to deposit rhodium or rhenium nanoparticles onto the surface of carbon nanotubes, and then the material was placed in a solution being a precursor of metallic nanoparticles. The material prepared was next subjected to high-temperature reduction in the atmosphere of argon and/or hydrogen to deposit rhodium or rhenium nanoparticles onto the surface of multiwalled carbon nanotubes. The investigations performed include, respectively: fabrication of a CNT-NPs (Carbon NanoTube-NanoParticles) nanocomposite material; the characterisation of the material produced including examination of the structure and morphology, and the assessment of rhodium and/or rhenium nanoparticles distribution on the surface of carbon nanotubes. Micro- and spectroscopy techniques were employed to characterise the structure of the nanocomposites obtained.


2010 ◽  
Vol 442 ◽  
pp. 7-14 ◽  
Author(s):  
M. Mansoor ◽  
Ian Kinloch ◽  
Brian Derby

The production of substrates coated with carbon nanotubes (CNTs) in well-defined patterns is desirable for sensor applications. In the present work, nickel based catalytic inks were prepared and printed on silicon substrates using inkjet delivery. Subsequently, the substrates were subjected to calcination and chemical vapour deposition for the growth of aligned CNTs. Scanning electron microscopy, transmission electron microscopy and Raman spectroscopy were used to characterize the CNTs. Various concentrations and formulations of ink preparations were studied to investigate the effect of these parameters on the growth and structure of the CNTs.


2020 ◽  
Vol 16 (7) ◽  
pp. 905-913
Author(s):  
Youyuan Peng ◽  
Qingshan Miao

Background: L-Ascorbic acid (AA) is a kind of water soluble vitamin, which is mainly present in fruits, vegetables and biological fluids. As a low cost antioxidant and effective scavenger of free radicals, AA may help to prevent diseases such as cancer and Parkinson’s disease. Owing to its role in the biological metabolism, AA has also been utilized for the therapy of mental illness, common cold and for improving the immunity. Therefore, it is very necessary and urgent to develop a simple, rapid and selective strategy for the detection of AA in various samples. Methods: The molecularly imprinted poly(o-phenylenediamine) (PoPD) film was prepared for the analysis of L-ascorbic acid (AA) on gold nanoparticles (AuNPs) - multiwalled carbon nanotubes (MWCNTs) modified glass carbon electrode (GCE) by electropolymerization of o-phenylenediamine (oPD) and AA. Experimental parameters including pH value of running buffer and scan rates were optimized. Scanning electron microscope (SEM), fourier-transform infrared (FTIR) spectra, cyclic voltammetry (CV) and differential pulse voltammetry (DPV) were utilized for the characterization of the imprinted polymer film. Results: Under the selected experimental conditions, the DPV peak currents of AA exhibit two distinct linear responses ranging from 0.01 to 2 μmol L-1 and 2 to 100 μmol L-1 towards the concentrations of AA, and the detection limit was 2 nmol L-1 (S/N=3). Conclusion: The proposed electrochemical sensor possesses excellent selectivity for AA, along with good reproducibility and stability. The results obtained from the analysis of AA in real samples demonstrated the applicability of the proposed sensor to practical analysis.


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