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Transient and Steady-State Photoconductivity of a Solid C60 Film

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dc.contributor.authorLee, C. H.-
dc.contributor.authorYu, G.-
dc.contributor.authorMoses, D.-
dc.contributor.authorSrdanov, V. I.-
dc.contributor.authorWei, X.-
dc.contributor.authorVardeny, Z. V.-
dc.date.accessioned2009-11-19-
dc.date.available2009-11-19-
dc.date.issued1993-09-15-
dc.identifier.citationPhys. Rev. B 48, 8506en
dc.identifier.issn1098-0121-
dc.identifier.urihttps://hdl.handle.net/10371/13605-
dc.description.abstractWe report the experimental results of the subnanosecond time-resolved transient photoconductivity (PC) of solid C60 film at various photon energies, and the spectral response of the steady-state PC in the energy range between 1.5 and 4.5 eV. The initial fast transient PC response decays exponentially in the subnanosecond time regime, followed by a weak slower component. Decay time at ħω=2.0 eV is longer than that at ħω=2.6 and 2.9 eV. At ħω=2.0 eV, transient PC peak shows a superlinear intensity dependence, suggesting carrier generation via exciton-exciton collision ionization, consistent with the recent results of fast photoinduced absorption. However, the linear intensity dependence of the transient PC at ħω=2.6 and 2.9 eV and a sharp increase of the transient and steady-state PC response at ħω≊2.3 eV indicate direct photogeneration of free electrons and holes at ħω>2.3 eV.en
dc.language.isoenen
dc.publisherThe American Physical Societyen
dc.titleTransient and Steady-State Photoconductivity of a Solid C60 Filmen
dc.typeArticleen
dc.identifier.doi10.1103/PhysRevB.48.8506-
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