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Beilstein J. Nanotechnol. 2018, 9, 2750–2762, doi:10.3762/bjnano.9.257
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, ...
Beilstein J. Nanotechnol. 2012, 3, 345–350, doi:10.3762/bjnano.3.39
Figure 1: Schematic of the TXM for NEXAFS studies. Monochromated radiation from the undulator is focused by a...
Figure 2: (a) Average of aligned TXM images (283–311 eV). (b) Spectra extracted from the three regions indica...
Figure 3: Component map of (a) in-plane (σ) and (b) out-of-plane (π) bonds; (c) colour-coded composite of the...