Probing exciton dissociation in C60/Au(111) using TR-ARPES
ORAL
Abstract
While optical techniques have been used to study the ultrafast response of organic semiconductors for several years, a lack of momentum resolution has limited their interpretation. Time- and angle-resolved photoemission spectroscopy (TR-ARPES) is a technique that allows a user to visualize the energy-momentum landscape of a material and enables real-time observation of the material’s response to photoexcitation.
Using TR-ARPES to track the dynamics and resolve the momentum dependent dispersion of the excitations, we are able to probe excitons in C60 and charge separation at the C60/Au(111) interface. We do this for a variety of film thicknesses grown using our two-stage growth method to produce highly-ordered films [1]. This will allow us to better understand the processes that occur post-photoexcitation both at and away from the organic-metal interface.
[1] Tully, Greenwood, Burke, et al., J. Phys. Chem. C, 128, 42 (2024)
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Publication: A. Tully, R. Greenwood, S.A. Burke et al., Two-stage growth for highly ordered epitaxial C60 films on Au(111), J. Phys. Chem. C 2024, 128, 42, 18128–18134
Presenters
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Rysa Greenwood
University of British Columbia, The University of British Columbia
Authors
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Rysa Greenwood
University of British Columbia, The University of British Columbia
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Alexandra Tully
The University of British Columbia
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MengXing Na
University of British Columbia
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Bradley G Guislain
University of British Columbia
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Sergey Zhdanovich
University of British Columbia
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Jerry I Dadap
University of British Columbia, The University of British Columbia
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Giorgio Levy
The University of British Columbia, University of British Columbia
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Arthur K Mills
University of British Columbia, The University of British Columbia
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Matteo Michiardi
University of British Columbia
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Andrea Damascelli
University of British Columbia
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Sarah Burke
University of British Columbia, The University of British Columbia
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David Jones
University of British Columbia, The University of British Columbia