التفاصيل البيبلوغرافية
| العنوان: |
Effect of order and disorder on degradation processes of copper phthalocyanine nanolayers |
| المؤلفون: |
Lucyna Grządziel, Georgi Genchev, Andreas Erbe, Maciej Krzywiecki |
| المصدر: |
Synthetic metals |
| بيانات النشر: |
Elsevier BV, 2017. |
| سنة النشر: |
2017 |
| مصطلحات موضوعية: |
010302 applied physics, Materials science, Mechanical Engineering, Metals and Alloys, Nanotechnology, 02 engineering and technology, 021001 nanoscience & nanotechnology, Condensed Matter Physics, 01 natural sciences, Electronic, Optical and Magnetic Materials, symbols.namesake, chemistry.chemical_compound, Nanoelectronics, chemistry, Mechanics of Materials, Copper phthalocyanine, 0103 physical sciences, Materials Chemistry, symbols, Phthalocyanine, Degradation (geology), 0210 nano-technology, Raman spectroscopy |
| الوصف: |
The impact was examined of surface ordering of 50 nm-thick copper phthalocyanine (CuPc) layers on the layer's susceptibility to ambience-induced degradation processes. The surface morphology of CuPc layers obtained by physical vapor deposition with different deposition rates, 0.01 nm/s (r1) and 0.02 nm/s (r2), was diagnosed applying atomic force and scanning electron microscopes. The images exhibited compact, ordered surface topography with crystallites of homogeneous geometry for a layer with r1 while randomly distributed bigger crystallites on a rougher and more expanded surface for a layer with r2. X-ray diffraction revealed the α-form of phthalocyanine, mostly with an orientation of the a axis perpendicular to the substrate plane. Mean grain size in bulk was slightly larger for CuPc with r2. Energy dispersive X-ray spectroscopy demonstrated an increase of C/Cu and N/Cu elemental ratios compared to the expected composition for both layers but significantly more pronounced for layer with r2. Morphological features and traces of CuPc-air interaction were mirrored also in the Raman spectra. Samples with r2 exhibited an increased peak width, and their peaks were shifted compared to samples with r1, which was attributed to surface disorder. The Raman spectra exhibited the appearance of additional peaks of oxidation products indicating Csingle bondOsingle bondC, Cdouble bond; length as m-dashO and Nsingle bondO bonds, with intensities coinciding to an increased carbon and nitrogen content. More intensive peaks were recorded for layers obtained with higher deposition rate, proving their stronger susceptibility to environment-induced degradation processes. © 2017 Elsevier Ltd. All rights reserved. This is the authors' accepted and refereed manuscript to the article. Locked until January 31st 2019 due to copyright restrictions |
| تدمد: |
0379-6779 |
| URL الوصول: |
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ad0839caf1d2ed2865894a1fdae8dbe
https://doi.org/10.1016/j.synthmet.2016.11.024 |
| حقوق: |
OPEN |
| رقم الأكسشن: |
edsair.doi.dedup.....4ad0839caf1d2ed2865894a1fdae8dbe |
| قاعدة البيانات: |
OpenAIRE |
