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dc.contributor.authorLin, Cheng-Teen_US
dc.contributor.authorChen, Wen-Chaoen_US
dc.contributor.authorYen, Ming-Yuen_US
dc.contributor.authorWang, Lung-Shenen_US
dc.contributor.authorLee, Chi-Youngen_US
dc.contributor.authorChin, Tsung-Shuneen_US
dc.contributor.authorChlu, Hsin-Tienen_US
dc.date.accessioned2014-12-08T15:14:46Z-
dc.date.available2014-12-08T15:14:46Z-
dc.date.issued2007-02-01en_US
dc.identifier.issn0008-6223en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.carbon.2006.09.002en_US
dc.identifier.urihttp://hdl.handle.net/11536/11162-
dc.description.abstractUsing porous anodic aluminum oxide as template and petroleum pitch as precursor, a massive amount of uniform carbon nanofibers was obtained after thermal treatment. The diameter and length were 300 nm and 60 pm, respectively. The difference between these and the classic herringbone structure is that the angle between the graphenes and the fiber axis increases regularly along the axis instead of being fixed. TEM observations show that the nanofiber consists of stacked conical graphenes with cone angles that steadily increase from 60 degrees to 180 degrees along the fiber axis. This structure is the first to be produced without using catalytic CVD, and has not been reported using template procedures. The large deformation of the graphene planes at the tip of the nanofiber may produce interesting electronic applications. (c) 2006 Elsevier Ltd. All rights reserved.en_US
dc.language.isoen_USen_US
dc.titleCone-stacked carbon nanofibers with cone angle increasing along the longitudinal axisen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.carbon.2006.09.002en_US
dc.identifier.journalCARBONen_US
dc.citation.volume45en_US
dc.citation.issue2en_US
dc.citation.spage411en_US
dc.citation.epage415en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000244270600025-
dc.citation.woscount8-
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