2015
DOI: 10.1016/j.matchemphys.2015.05.063
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Low-temperature intermediates to oxygen reduction reaction catalysts based on amine-modified metal-loaded carbons. An XPS and ss-NMR investigation

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Cited by 24 publications
(14 citation statements)
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“…The N 1s and Si 2p peaks are presented in Figure b and the corresponding elemental relative concentrations are shown in the table embedded in Figure . Regarding nitrogen, Marzorati et al have reported binding energies for terminal amines between 398.4 and 398.8 eV, for secondary or tertiary amines between 400.0 and 400.5 eV, and in the case of intra- or intermolecular bonding, binding energies between 402.0 and 403.0 eV . These three peaks can be distinguished in the N 1s spectrum of Figure b.…”
Section: Resultsmentioning
confidence: 92%
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“…The N 1s and Si 2p peaks are presented in Figure b and the corresponding elemental relative concentrations are shown in the table embedded in Figure . Regarding nitrogen, Marzorati et al have reported binding energies for terminal amines between 398.4 and 398.8 eV, for secondary or tertiary amines between 400.0 and 400.5 eV, and in the case of intra- or intermolecular bonding, binding energies between 402.0 and 403.0 eV . These three peaks can be distinguished in the N 1s spectrum of Figure b.…”
Section: Resultsmentioning
confidence: 92%
“…An X-ray photoelectron spectroscopy (XPS) analysis was performed in order to obtain have reported binding energies for terminal amines between 398.4 and 398.8 eV, for secondary or tertiary amines between 400.0 and 400.5 eV and in the case of intra-or inter-molecular bonding a binding energy between 402.0 and 403.0 eV. 54 These three peaks can be distinguished in the N1s spectrum of Fig. 5b.…”
Section: Resultsmentioning
confidence: 99%
“…Quantitative XPS demonstrated that the O/C atomic ratio of P75-reduced biochar (0.27) was lower than that in P75 biochar (0.40), which indicated that P75-reduced biochar was more reduced than P75 biochar (Figure S4). The C 1s XPS spectra revealed the prominent peaks, i.e., C–C, C–O, and CO groups, with binding energies of ∼284.8, ∼286.0, and ∼288.3 eV, respectively, in P75 biochar. ,, In contrast, there were only C–C and C–O groups in P75-reduced biochar, with binding energies of 284.8 and 286.2 eV, respectively. Moreover, the O 1s XPS spectra also confirmed that the CO group was present only in P75 biochar (Figure D) .…”
Section: Results and Discussionmentioning
confidence: 98%
“…Nevertheless, as time increases, the amount of Fe 2+ gradually increasing while the Fe 3+ decreased. We attributed this iron reduction to the presence of the amide bond with the EDC-NHS, thus the nitrogen gradually displaces the Fe 3+ to Fe 2+ (Additional file 1 : Figure S2A and B) [ 60 ]. In the Additional file the evolution of compositions for Fe 3 O 4 NPs and Fe 3 O 4 –EDC-NHS-NPs for 30 days after synthesis is summarized (Additional file 1 : Figure S2A).…”
Section: Resultsmentioning
confidence: 99%