4.8 Article

Direct evidence for efficient ultrafast charge separation in epitaxial WS2/graphene heterostructures

Journal

SCIENCE ADVANCES
Volume 6, Issue 20, Pages -

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/sciadv.aay0761

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Funding

  1. German Science Foundation via the Collaborative Research Center 925 Light induced dynamics and control of correlated quantum systems
  2. German Science Foundation via the Collaborative Research Center 173 Spin + X: spin in its collective environment
  3. European Union [696656 - GrapheneCore1, 785219 - GrapheneCore2]

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We use time- and angle-resolved photoemission spectroscopy (tr-ARPES) to investigate ultrafast charge transfer in an epitaxial heterostructure made of monolayer WS2 and graphene. This heterostructure combines the benefits of a direct-gap semiconductor with strong spin-orbit coupling and strong light-matter interaction with those of a semimetal hosting massless carriers with extremely high mobility and long spin lifetimes. We find that, after photoexcitation at resonance to the A-exciton in WS2, the photoexcited holes rapidly transfer into the graphene layer while the photoexcited electrons remain in the WS2 layer. The resulting charge-separated transient state is found to have a lifetime of similar to 1 ps. We attribute our findings to differences in scattering phase space caused by the relative alignment of WS2 and graphene bands as revealed by high-resolution ARPES. In combination with spin-selective optical excitation, the investigated WS2/graphene heterostructure might provide a platform for efficient optical spin injection into graphene.

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