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dc.contributor.authorShearer, C.
dc.contributor.authorYu, J.
dc.contributor.authorO’Donnell, Kane
dc.contributor.authorThomsen, L.
dc.contributor.authorDastoor, P.
dc.contributor.authorQuinton, J.
dc.contributor.authorShapter, J.
dc.date.accessioned2017-01-30T12:04:05Z
dc.date.available2017-01-30T12:04:05Z
dc.date.created2014-08-31T20:00:27Z
dc.date.issued2008
dc.identifier.citationShearer, C. and Yu, J. and O’Donnell, K. and Thomsen, L. and Dastoor, P. and Quinton, J. and Shapter, J. 2008. Highly resilient field emission from aligned single-walled carbon nanotube arrays chemically attached to n-type silicon. Journal of Materials Chemistry. 18 (47): pp. 5753-5760.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/17798
dc.identifier.doi10.1039/b811546j
dc.description.abstract

Single-walled carbon nanotubes (SWNTs) were chemically attached to an n-type silicon (100) substrate (n-Si) by exposing the surface to a nanotube-containing suspension for attachment times varying from 2 to 72 h. The SWNTs were imaged by atomic force microscopy (AFM) revealing a high density of vertically aligned SWNT bundles. Cyclic voltammetry experiments demonstrated that the n-type character of the substrate was maintained after the chemical attachment process. The SWNT/n-Si surfaces were found to field emit with a turn-on field ranging from 1.37–1.64 V µm-1. From the Fowler–Nordheim (F–N) plots the field enhancement factor, ß, was found to vary between ~5000–7000 depending upon attachment time, which is consistent with changes in the sharpness of the SWNT tips as shown by AFM. The robustness of the field emitters was tested by maintaining a constant current and measuring the change in voltage required. The structures were found to have excellent stability over several days. The prospect for chemically attached SWNT arrays in field emission displays is discussed.

dc.publisherThe Royal Society of Chemistry
dc.titleHighly resilient field emission from aligned single-walled carbon nanotube arrays chemically attached to n-type silicon
dc.typeJournal Article
dcterms.source.volume18
dcterms.source.number47
dcterms.source.startPage5753
dcterms.source.endPage5760
dcterms.source.issn0959-9428
dcterms.source.titleJournal of Materials Chemistry
curtin.departmentDepartment of Imaging and Applied Physics
curtin.accessStatusFulltext not available


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