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dc.contributor.authorHuang, J
dc.contributor.authorHuang, Z
dc.contributor.authorYi, S
dc.contributor.authorLiu, Y
dc.contributor.authorFang, M
dc.contributor.authorZhang, S
dc.date.accessioned2016-05-11T10:47:44Z
dc.date.issued2013-12-16
dc.description.abstractPreparation of nanomaterials with various morphologies and exploiting their novel physical properties are of vital importance in nanoscientific field. Similarly to the III-N compound semiconductors, Si3N4 nanostructures also could be potentially used for making optoelectronic devices. In this paper, we report on an improved Fe-catalyzed chemical vapour deposition method for synthesizing ultra-long α-Si3N4 nanobelts along with a few nanowires and nanobranches on a carbon felt substrate. The ultra-long α-Si3N4 nanobelts grew via a combined VLS-base and nanobranches via a combined double-stage VLS-base and VS-tip mechanism, as well as nanowires via VLS-tip mechanism. The three individual nanostructures showed variant optical properties as revealed by a cathodoluminescence spectroscopy. A single α-Si3N4 nanobelt or nanobranch gave a strong UV-blue emission band as well as a broad red emission, whereas a single α-Si3N4 nanowire exhibited only a broad UV-blue emission. The results reported would be useful in developing new photoelectric nanodevices with tailorable or tunable properties.en_GB
dc.identifier.citationVol. 3: 3504en_GB
dc.identifier.doi10.1038/srep03504
dc.identifier.urihttp://hdl.handle.net/10871/21473
dc.language.isoenen_GB
dc.publisherNature Publishing Groupen_GB
dc.relation.urlhttp://www.ncbi.nlm.nih.gov/pubmed/24336316en_GB
dc.rightsThis work is licensed under a Creative Commons AttributionNonCommercial-NoDerivs 3.0 Unported license. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0en_GB
dc.titleFe-catalyzed growth of one-dimensional α-Si3N4 nanostructures and their cathodoluminescence propertiesen_GB
dc.typeArticleen_GB
dc.date.available2016-05-11T10:47:44Z
exeter.place-of-publicationEngland
dc.descriptionThis is the final version of the article. Available from the publisher via the DOI in this record.en_GB
dc.identifier.journalScientific Reportsen_GB


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