A single step process for the simultaneous purification and opening of multiwalled carbon nanotubes

2005 ◽  
Vol 412 (1-3) ◽  
pp. 184-189 ◽  
Author(s):  
E. Raymundo-Piñero ◽  
T. Cacciaguerra ◽  
P. Simon ◽  
F. Béguin
Nanoscale ◽  
2011 ◽  
Vol 3 (9) ◽  
pp. 3876 ◽  
Author(s):  
Upendra Kumar Parashar ◽  
Suraj Bhandari ◽  
Rajesh Kumar Srivastava ◽  
Deep Jariwala ◽  
Anchal Srivastava

2012 ◽  
Vol 2012 ◽  
pp. 1-8 ◽  
Author(s):  
Matthew Cole ◽  
Pritesh Hiralal ◽  
Kai Ying ◽  
Chi Li ◽  
Yan Zhang ◽  
...  

Herein we present an inexpensive facile wet-chemistry-free approach to the transfer of chemical vapour-deposited multiwalled carbon nanotubes to flexible transparent polymer substrates in a single-step process. By controlling the nanotube length, we demonstrate accurate control over the electrical conductivity and optical transparency of the transferred thin films. Uniaxial strains of up to 140% induced only minor reductions in sample conductivity, opening up a number of applications in stretchable electronics. Nanotube alignment offers enhanced functionality for applications such as polarisation selective electrodes and flexible supercapacitor substrates. A capacitance of 17 F/g was determined for supercapacitors fabricated from the reported dry-transferred MWCNTs with the corresponding cyclic voltagrams showing a clear dependence on nanotube length.


Author(s):  
Stefania Sandoval ◽  
Gerard Tobias

We have employed fullerenes as versatile agents to “cork” the open tips of multiwalled carbon nanotubes (MWCNTs), and as promoting species for the release of the inorganic material filled within the nanotubes’ cavities. High Z element compounds, namely, PbI2, ZnI2, and CeI3, were chosen to easily determine the presence of the filler inside the hosting nanotubes by transmission electron microscopy (TEM). Fullerenes can isolate inorganic nanostructures confined within the hollow cavities of MWCNTs, which allows the removal of the external material remnant after the filling. Otherwise, taking advantage of the affinity of fullerenes with selected solvents, we have confirmed the ability of the C60 molecules to promote the displacement of the inorganic guest from the host. We propose two different strategies to trigger the release, employing vapor and liquid phase treatments. The first protocol involves annealing filled MWCNTs in presence of fullerenes (to obtain C60PbI2@MWCNTs) and the subsequent washing of the sample in ethanol under mild conditions. On the other hand, the simultaneous introduction of the C60 molecules and the liberation of the guest are produced by a single step wet procedure; the latter being potentially useful when materials that are not stable at high temperatures are employed for filling.


Energies ◽  
2020 ◽  
Vol 13 (9) ◽  
pp. 2322 ◽  
Author(s):  
Thi Ngoc Tuyen Pham ◽  
Young Soo Yoon

Double-oxide Mn3O4-Co3O4 nanoparticles were synthesized and anchored on multiwalled carbon nanotubes (MWCNTs) via a single-step solvothermal method. The largest specific area (99.82 m2g−1) of the catalyst was confirmed via a nitrogen adsorption isotherm. Furthermore, the uniform coating of the Mn3O4-Co3O4 nanoparticles on the surface of the MWCNTs was observed via scanning electron microscopy and transmission electron microscopy; the uniform coating provided an effective transport pathway during the electrocatalytic activities. The rotating disk electrode and rotating ring disk electrode measurements indicated that the electron transfer number was 3.96 and the evolution of H2O2 was 2%. In addition, the Mn3O4-Co3O4/MWCNT catalyst did not undergo urea poisoning and remained stable in an alkaline solution. Conversely, commercial Pt/C could not withstand urea poisoning for long. The performance cell achieved a power density of 0.4226 mW cm−2 at 50 °C. Therefore, Mn3O4-Co3O4/MWCNT is an efficient and inexpensive noble-metal-free cathodic catalyst for direct urea fuel cells.


2012 ◽  
Vol 2 (6) ◽  
pp. 166-168 ◽  
Author(s):  
Dr.T.Ch.Madhavi Dr.T.Ch.Madhavi ◽  
◽  
Pavithra.P Pavithra.P ◽  
Sushmita Baban Singh Sushmita Baban Singh ◽  
S.B.Vamsi Raj S.B.Vamsi Raj ◽  
...  

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