2012
DOI: 10.1134/s0022476612060054
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X-ray spectral and photoelectron study of the electronic structure of copper phthalocyanine and its fluoro-substituted analog

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Cited by 5 publications
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“…The possible mechanism of DTA decomposition will be discussed below. Similar findings were reported by Cosultchi et al, who investigated the surface structure of copper sliding using petroleum, and also by Mazalov and Semushkina, who analyzed adhesion of organic thin films on metal substrates.…”
Section: Resultssupporting
confidence: 87%
“…The possible mechanism of DTA decomposition will be discussed below. Similar findings were reported by Cosultchi et al, who investigated the surface structure of copper sliding using petroleum, and also by Mazalov and Semushkina, who analyzed adhesion of organic thin films on metal substrates.…”
Section: Resultssupporting
confidence: 87%
“…The elements with high electronegativity are more likely to bond with Cu, and the sequence of the electronegativity of the elements is O < N < S (Cosultchi et al, 2003). Therefore, the order of the binding energies of S2p, N1s, O1s and Cu 2p follows Cu-S < Cu-N < Cu-O (Mazalov et al, 2012), which is consistent with the results above. The observed peaks of O1s located at 530.0 and 531.1 eV are assigned with CuO and Figure 7 Three-dimensional SPM images (left) and the roughness (right) of the samples in emulsion for 300 h at 298 K Figure 8 XRD images of (a) the raw specimen, the corrode specimen (b) and the specimens protected by 0.5 mM (c) pyrrole, (d) thiophene, (e) furan, (f) 2 H-1,2,3-triazole and (g) 1,2,5-thiadiazole and (h) 1,2,5oxadiazole Cu 2 O in emulsion without inhibitor (Biesinger et al, 2010); the others are C-O, R-OH and CuCO 3 /Cu(OH) 2 (Hussein et al, 1985).…”
Section: X-ray Photoelectron Spectroscopy Analysissupporting
confidence: 89%