Electronic-structural dynamics in graphene

We review our recent time- and angle-resolved photoemission spectroscopy experiments, which measure the transient electronic structure of optically driven graphene. For pump photon energies in the near infrared ( ℏ ω pump = 950   meV), we have discovered the formation of a population-inverted st...

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Main Authors: Isabella Gierz, Andrea Cavalleri
Format: Article
Language:English
Published: AIP Publishing LLC and ACA 2016-09-01
Series:Structural Dynamics
Online Access:http://dx.doi.org/10.1063/1.4964777
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spelling doaj-e2e9b001f0f04cb09f269faa3f7169a12020-11-24T21:40:37ZengAIP Publishing LLC and ACAStructural Dynamics2329-77782016-09-0135051301051301-810.1063/1.4964777010605SDYElectronic-structural dynamics in grapheneIsabella Gierz0Andrea Cavalleri1 Center for Free Electron Laser Science, Max Planck Institute for the Structure and Dynamics of Matter, Hamburg, Germany Center for Free Electron Laser Science, Max Planck Institute for the Structure and Dynamics of Matter, Hamburg, GermanyWe review our recent time- and angle-resolved photoemission spectroscopy experiments, which measure the transient electronic structure of optically driven graphene. For pump photon energies in the near infrared ( ℏ ω pump = 950   meV), we have discovered the formation of a population-inverted state near the Dirac point, which may be of interest for the design of THz lasing devices and optical amplifiers. At lower pump photon energies ( ℏ ω pump < 400   meV), for which interband absorption is not possible in doped samples, we find evidence for free carrier absorption. In addition, when mid-infrared pulses are made resonant with an infrared-active in-plane phonon of bilayer graphene ( ℏ ω pump = 200   meV), a transient enhancement of the electron-phonon coupling constant is observed, providing interesting perspective for experiments that report light-enhanced superconductivity in doped fullerites in which a similar lattice mode was excited. All the studies reviewed here have important implications for applications of graphene in optoelectronic devices and for the dynamical engineering of electronic properties with light.http://dx.doi.org/10.1063/1.4964777
collection DOAJ
language English
format Article
sources DOAJ
author Isabella Gierz
Andrea Cavalleri
spellingShingle Isabella Gierz
Andrea Cavalleri
Electronic-structural dynamics in graphene
Structural Dynamics
author_facet Isabella Gierz
Andrea Cavalleri
author_sort Isabella Gierz
title Electronic-structural dynamics in graphene
title_short Electronic-structural dynamics in graphene
title_full Electronic-structural dynamics in graphene
title_fullStr Electronic-structural dynamics in graphene
title_full_unstemmed Electronic-structural dynamics in graphene
title_sort electronic-structural dynamics in graphene
publisher AIP Publishing LLC and ACA
series Structural Dynamics
issn 2329-7778
publishDate 2016-09-01
description We review our recent time- and angle-resolved photoemission spectroscopy experiments, which measure the transient electronic structure of optically driven graphene. For pump photon energies in the near infrared ( ℏ ω pump = 950   meV), we have discovered the formation of a population-inverted state near the Dirac point, which may be of interest for the design of THz lasing devices and optical amplifiers. At lower pump photon energies ( ℏ ω pump < 400   meV), for which interband absorption is not possible in doped samples, we find evidence for free carrier absorption. In addition, when mid-infrared pulses are made resonant with an infrared-active in-plane phonon of bilayer graphene ( ℏ ω pump = 200   meV), a transient enhancement of the electron-phonon coupling constant is observed, providing interesting perspective for experiments that report light-enhanced superconductivity in doped fullerites in which a similar lattice mode was excited. All the studies reviewed here have important implications for applications of graphene in optoelectronic devices and for the dynamical engineering of electronic properties with light.
url http://dx.doi.org/10.1063/1.4964777
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