Chemical modification of graphene via hyperthermal molecular reaction
dc.creator | Dubey, Girjesh | |
dc.creator | Urcuyo Solórzano, Roberto | |
dc.creator | Abb, Sabine | |
dc.creator | Rinke, Gordon | |
dc.creator | Burghard, Marko | |
dc.creator | Rauschenbach, Stephan | |
dc.creator | Kern, Klaus | |
dc.date.accessioned | 2022-03-15T16:15:03Z | |
dc.date.available | 2022-03-16T13:00:12Z | |
dc.date.issued | 2014 | |
dc.description.abstract | Chemical functionalization of graphene is achieved by hyperthermal reaction with azopyridine molecular ions. The one-step, room temperature process takes place in high vacuum (10–7 mbar) using an electrospray ion beam deposition (ES-IBD) setup. For ion surface collisions exceeding a threshold kinetic energy of 165 eV, molecular cation beams of 4,4′-azobis(pyridine) covalently attach to chemical vapor deposited (CVD) graphene. A covalent functionalization degree of 3% of the carbon atoms of graphene is reached after 3–5 h of ion exposure of 2 × 1014 azopyridinium/cm2 of which 50% bind covalently. This facile approach for the controlled modification of graphene extends the scope of candidate species that would not otherwise react via existing conventional methods. | en |
dc.description.procedence | UCR::Vicerrectoría de Investigación::Unidades de Investigación::Ciencias Básicas::Centro de Investigación en Electroquímica y Energía Química (CELEQ) | |
dc.format.extent | 13482-13485 | |
dc.identifier.citation | https://pubs.acs.org/doi/abs/10.1021/ja5046499 | |
dc.identifier.doi | 10.1021/ja5046499 | |
dc.identifier.issn | 0002-7863 | |
dc.identifier.uri | https://hdl.handle.net/10669/86056 | |
dc.language.iso | Inglés | |
dc.rights | acceso embargado | |
dc.source | Journal of American Chemical Society, 136(39), pp. 13482-13485 | |
dc.subject | Chemical | en |
dc.subject | Hyperthermal | en |
dc.subject | Molecular reaction | en |
dc.title | Chemical modification of graphene via hyperthermal molecular reaction | en |
dc.type | artículo original |
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