Oxygen etching mechanism in carbon-nitrogen ( C N x ) domelike nanostructures

We report a comprehensive study involving the ion beam oxygen etching purification mechanism of domelike carbon nanostructures containing nitrogen. The C N x nanodomes were prepared on Si substrate containing nanometric nickel islands catalyzed by ion beam sputtering of a carbon target and assisting...

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Veröffentlicht in:Journal of applied physics 2008-06, Vol.103 (12), p.124907-124907-6
Hauptverfasser: Acuña, J. J. S., Figueroa, C. A., Biggemann, D., Kleinke, M. U., Alvarez, F.
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container_end_page 124907-6
container_issue 12
container_start_page 124907
container_title Journal of applied physics
container_volume 103
creator Acuña, J. J. S.
Figueroa, C. A.
Biggemann, D.
Kleinke, M. U.
Alvarez, F.
description We report a comprehensive study involving the ion beam oxygen etching purification mechanism of domelike carbon nanostructures containing nitrogen. The C N x nanodomes were prepared on Si substrate containing nanometric nickel islands catalyzed by ion beam sputtering of a carbon target and assisting the deposition by a second nitrogen ion gun. After preparation, the samples were irradiated in situ by a low energy ion beam oxygen source and its effects on the nanostructures were studied by x-ray photoelectron spectroscopy in an attached ultrahigh vacuum chamber, i.e., without atmospheric contamination. The influence of the etching process on the morphology of the samples and structures was studied by atomic force microscopy and field emission gun-secondary electron microscopy, respectively. Also, the nanodomes were observed by high resolution transmission electron microscopy. The oxygen atoms preferentially bond to carbon atoms by forming terminal carbonyl groups in the most reactive parts of the nanostructures. After the irradiation, the remaining nanostructures are grouped around two well-defined size distributions. Subsequent annealing eliminates volatile oxygen compounds retained at the surface. The oxygen ions mainly react with nitrogen atoms located in pyridinelike structures.
doi_str_mv 10.1063/1.2948941
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S.</creatorcontrib><creatorcontrib>Figueroa, C. A.</creatorcontrib><creatorcontrib>Biggemann, D.</creatorcontrib><creatorcontrib>Kleinke, M. U.</creatorcontrib><creatorcontrib>Alvarez, F.</creatorcontrib><collection>CrossRef</collection><collection>OSTI.GOV</collection><jtitle>Journal of applied physics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Acuña, J. J. S.</au><au>Figueroa, C. A.</au><au>Biggemann, D.</au><au>Kleinke, M. U.</au><au>Alvarez, F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Oxygen etching mechanism in carbon-nitrogen ( C N x ) domelike nanostructures</atitle><jtitle>Journal of applied physics</jtitle><date>2008-06-15</date><risdate>2008</risdate><volume>103</volume><issue>12</issue><spage>124907</spage><epage>124907-6</epage><pages>124907-124907-6</pages><issn>0021-8979</issn><eissn>1089-7550</eissn><coden>JAPIAU</coden><abstract>We report a comprehensive study involving the ion beam oxygen etching purification mechanism of domelike carbon nanostructures containing nitrogen. The C N x nanodomes were prepared on Si substrate containing nanometric nickel islands catalyzed by ion beam sputtering of a carbon target and assisting the deposition by a second nitrogen ion gun. After preparation, the samples were irradiated in situ by a low energy ion beam oxygen source and its effects on the nanostructures were studied by x-ray photoelectron spectroscopy in an attached ultrahigh vacuum chamber, i.e., without atmospheric contamination. The influence of the etching process on the morphology of the samples and structures was studied by atomic force microscopy and field emission gun-secondary electron microscopy, respectively. Also, the nanodomes were observed by high resolution transmission electron microscopy. The oxygen atoms preferentially bond to carbon atoms by forming terminal carbonyl groups in the most reactive parts of the nanostructures. After the irradiation, the remaining nanostructures are grouped around two well-defined size distributions. Subsequent annealing eliminates volatile oxygen compounds retained at the surface. The oxygen ions mainly react with nitrogen atoms located in pyridinelike structures.</abstract><cop>United States</cop><pub>American Institute of Physics</pub><doi>10.1063/1.2948941</doi></addata></record>
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source AIP Journals Complete; AIP Digital Archive; Alma/SFX Local Collection
subjects ANNEALING
ATOMIC FORCE MICROSCOPY
CARBON
CARBONYLS
DEPOSITION
ETCHING
FIELD EMISSION
ION BEAMS
MATERIALS SCIENCE
MORPHOLOGY
NANOSTRUCTURES
NICKEL
NITROGEN
NITROGEN IONS
OXYGEN
OXYGEN IONS
PURIFICATION
SCANNING ELECTRON MICROSCOPY
SPUTTERING
TRANSMISSION ELECTRON MICROSCOPY
X-RAY PHOTOELECTRON SPECTROSCOPY
title Oxygen etching mechanism in carbon-nitrogen ( C N x ) domelike nanostructures
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