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


ABSTRACT: 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 ?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.

SUBMITTER: Aeschlimann S 

PROVIDER: S-EPMC7220367 | biostudies-literature | 2020 May

REPOSITORIES: biostudies-literature

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Direct evidence for efficient ultrafast charge separation in epitaxial WS<sub>2</sub>/graphene heterostructures.

Aeschlimann Sven S   Rossi Antonio A   Chávez-Cervantes Mariana M   Krause Razvan R   Arnoldi Benito B   Stadtmüller Benjamin B   Aeschlimann Martin M   Forti Stiven S   Fabbri Filippo F   Coletti Camilla C   Gierz Isabella I  

Science advances 20200513 20


We use time- and angle-resolved photoemission spectroscopy (tr-ARPES) to investigate ultrafast charge transfer in an epitaxial heterostructure made of monolayer WS<sub>2</sub> 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-excit  ...[more]

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