We report the synthesis of nitrogen-doped
carbon nanotube sponges
(N-CNSs) by pyrolysis of solutions of benzylamine, ferrocene, thiophene,
and isopropanol-based mixture at 1020 °C for 4 h using an aerosol-assisted
chemical vapor deposition system. The precursors were transported
through a quartz tube using a dynamic flow of H2/Ar. We
characterized the N-CNSs by scanning electron microscopy, transmission
electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy,
Fourier transform infrared spectroscopy, Raman spectroscopy, and thermogravimetric
analysis. We found that isopropanol, isopropanol–ethanol, and
isopropanol–acetone as precursors promote the formation of
complex-entangled carbon fibers making knots and junctions. The N-CNSs
displayed an outstanding oxygen concentration reaching a value of
9.2% for those synthesized with only isopropanol. We identified oxygen
and nitrogen functional groups; in particular, the carbon fibers produced
using only isopropanol exhibited a high concentration of ether groups
(C–O bonds). This fact suggests the presence of phenols, carboxyl,
methoxy, ethoxy, epoxy, and more complex functional groups. Usually,
the functionalization of graphitic materials is carried out through
aggressive acid treatments; here, we offer an alternative route to
produce a superoxygenated surface. The understanding of the chemical
surface of these novel materials represents a huge challenge and offers
an opportunity to study complex oxygen functional groups different
from the conventional quinone, carboxyl, phenols, carbonyl, methoxy,
ethoxy, among others. The cyclic voltammetry measurements confirmed
the importance of oxygen in N-CNSs, showing that with high oxygen
concentration, the highest anodic and cathodic currents are displayed.
N-CNSs displayed ferromagnetic behavior with an outstanding saturation
magnetization. We envisage that our sponges are promising for anodes
in lithium-ion batteries and magnetic sensor devices.