Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/95968
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dc.contributor.authorDong, Xiaochenen
dc.contributor.authorLong, Qingen
dc.contributor.authorWei, Angen
dc.contributor.authorZhang, Wenjingen
dc.contributor.authorLi, Lain-Jongen
dc.contributor.authorChen, Pengen
dc.contributor.authorHuang, Weien
dc.date.accessioned2013-06-28T01:15:36Zen
dc.date.accessioned2019-12-06T19:23:50Z-
dc.date.available2013-06-28T01:15:36Zen
dc.date.available2019-12-06T19:23:50Z-
dc.date.copyright2011en
dc.date.issued2011en
dc.identifier.citationDong, X., Long, Q., Wei, A., Zhang, W., Li, L. J., Chen, P., et al. (2011). The electrical properties of graphene modified by bromophenyl groups derived from a diazonium compound. Carbon, 50(4), 1517-1522.en
dc.identifier.issn0008-6223en
dc.identifier.urihttps://hdl.handle.net/10356/95968-
dc.description.abstractGraphene field-effect transistors were fabricated with mechanically exfoliated single-layer graphene (SLG) and bilayer graphene (BLG) sheets and the functionalization effects of bromophenyl groups derived from a diazonium compound on its transfer properties were explored. Spectroscopic and electrical studies reveal that the bromophenyl grafting imposes p-doping to both SLG and BLG. The modification of SLG by bromophenyl groups significantly reduces the hole carrier mobility and the saturation current in SLG transistors, suggesting an increase in both long-range impurity and short-range defect scattering. Unexpectedly, the bromophenyl group functionalization on BLG does not obviously increase both types of scattering, indicating that the BLG is relatively more resistant to charge- or defect-induced scattering. The results indicate that chemical modification is a simple approach to tailor the electrical properties of graphene sheets with different numbers of layers.en
dc.language.isoenen
dc.relation.ispartofseriesCarbonen
dc.rights© 2011 Elsevier Ltd.en
dc.subjectDRNTU::Engineering::Bioengineeringen
dc.titleThe electrical properties of graphene modified by bromophenyl groups derived from a diazonium compounden
dc.typeJournal Articleen
dc.contributor.schoolSchool of Chemical and Biomedical Engineeringen
dc.identifier.doi10.1016/j.carbon.2011.11.029en
item.fulltextNo Fulltext-
item.grantfulltextnone-
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