کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
10610906 | 986027 | 2005 | 11 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Structural and chemical evolution of single-wall carbon nanotubes under atomic and molecular deuterium interaction
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موضوعات مرتبط
مهندسی و علوم پایه
مهندسی انرژی
انرژی (عمومی)
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چکیده انگلیسی
The interaction of atomic (D) and molecular (D2) deuterium, as present in a (DÂ +Â D2) gas mixture, with single-wall carbon nanotubes (SWNTs) has been studied by means of a combination of scanning electron microscopy, transmission electron microscopy and X-ray photoelectron spectroscopy. The SWNT samples were exposed to the gas mixture, produced by thermal dissociation of D2 on a hot W filament, its temperature, TW, being kept at 1020 and 1550Â K for a deuterium pressure of 0.6 and 60Â Pa, respectively. Prolonged interaction of the low-pressure (DÂ +Â D2) gas mixture produced at TWÂ =Â 1020Â K leads to a conglomeration of the SWNT bundles into larger diameter ropes of square and triangular cross-section, covered by nano-aggregates of graphite material. Both the coalescence of single SWNTs and a massive reconstruction of bundles of SWNTs into a “coral reef”-like structure were found to occur after prolonged exposure of SWNTs to the high-pressure (DÂ +Â D2) gas mixture produced at TWÂ =Â 1550Â K. This structure is formed by the encapsulated Fe nanoparticles and deuterocarbon-like species appearing as a result of the deuterium interaction with the SWNT bundles accompanied by partial erosion of the SWNT material. The XPS valence-band spectra disclose electronic features characteristic for a hydrogen-plasma modified multi-wall carbon nanotube (MWNT)-like structure as a result of an intensive (DÂ +Â D2) induced transformation of the SWNTs into the “coral reef”-like structure.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Carbon - Volume 43, Issue 5, 2005, Pages 1073-1083
Journal: Carbon - Volume 43, Issue 5, 2005, Pages 1073-1083
نویسندگان
W. Lisowski, E.G. Keim, A.H.J. van den Berg, M.A. Smithers,