2 article(s) from Mamane, Victor
Figure 1: A working electrode (WE) incorporating the f-SWCNTs deposited on the GCE surface.
Figure 2: a) HRTEM micrographs of the raw HIPCO material. The arrows point out residual iron nanoparticles. b...
Figure 3: Three-step covalent functionalization of HIPCO SWCNTs using different acidic conditions for step 1.
Figure 4: Ferrocene derivatives (FcAlkyl and FcETGn) with different linkers.
Figure 5: Detailed C 1s spectra of A) raw HIPCO and B) HIPCO-HNO3-FcETG8. The binding energies of the Fe 2p c...
Figure 6: A) TGA curves obtained under He for three samples. B) Derivative curve of the weight loss for the s...
Figure 7: Mass spectrometry channels used to show the departure peaks of the cyclopentadienyl group and its m...
Figure 8: Raman data of raw and f-SWCNTs taken with a laser at 514 nm.
Figure 9: An example of a STEM HAADF image of the HIPCO-HNO3-FcETG2 sample. Inset: EELS spectra of the cataly...
Figure 10: HIPCO-HNO3-FcETG2 sample analyzed by STEM: a) HAADF image. The inset focuses on the FcETG molecule,...
Figure 11: Cyclic voltammograms obtained of GCEs modified with A) HIPCO-H2SO4 immobilized with diaphorase; B) ...
Figure 12: Molecular-dynamics simulated structures after 6 ns: A) HIPCO-FcETG8 without the presence of water, ...
Scheme 1: SWNT functionalization by diazonium addition under microwave heating.
Figure 1: Photographs of f-SWNT-5min, f-SWNT-10min and f-SWNT-15min dispersed in THF 1 week after their prepa...
Figure 2: Raman spectra of the starting and functionalized SWNTs and typical HRTEM images. a) Raman spectrum ...
Figure 3: TGA weight loss under helium of raw SWNTs (blue curve), phys-SWNT (violet curve), f-SWNT-5min (red ...
Figure 4: Mass spectrometry intensities for the main m/z corresponding to chlorobenzene. a) f-SWNT-5min, b) f...
Figure 5: Mass spectrometry intensities for xylene. a) main m/z of xylene for f-SWNT-15min, b) m/z 91 for f-S...
Scheme 2: Over-reactions after 15 min under microwaves.