Deep insight into the electronic structure of organic single crystal: rubrene
DIPC Seminars
- Speaker
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Satoshi Kera, Institute for Molecular Science, Okazaki, Japan
- When
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2022/11/16
13:00 - Place
- Hybrid Seminar: Donostia International Physics Center
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Understanding the impacts of weak electronic interaction on the electron
delocalization is required to discuss the rich functionalities of organic
molecular materials. Moreover, effects of the strong coupling of phonon
(collective lattice vibration) and/or local molecular vibration to the
electron must be unveiled. Angle-resolved UPS (ARUPS) is known to be a
powerful technique to study the electronic structure. The HOMO-band features
can offer a wide variety of key information, that is essential to comprehend
charge- hopping transport (small-polaron related transport) [1] as well as to
coherent band transport in the molecular single crystal [2,3]. However, the
experimental study of fine features in the HOMO state has not been progressed
till recently due to difficulty in the sample preparation, damages upon
irradiation, and so on [4,5]. We present recent findings regarding on the
precise measurements of the electronic structure of rubrene (C42H28) single
crystals by using synchrotron-light based, high-resolution ARUPS. We describe
the characteristic electronic structure of rubrene that 1) the UPS HOMO bands
show a clear linear dichroism for bonding and anti-bonding HOMO, 2) a band-
unfolding behavior as for intrinsic spectral function of HOMO, and 3) polaron-
like quasiparticle effects on the electronic structure. The precise
experiments of the 2D momentum scan in the ARUPS would provide a perspective
of designing the organic semiconductor devices in non-trivial way.
References
[1] S. Kera, H. Yamane. N. Ueno, Prog. Surf. Sci. 84 (2009) 135-154.
[2] N. Ueno and S. Kera, Prog. Surf. Sci. 83 (2009) 490- 557.
[3] Y. Nakayama, S. Kera, and N. Ueno, J. Mater. Chem. C 8 (2020) 9090-9132.
[4] S. Machida, et al. Phys Rev. Lett. 104 (2010) 156401. [5] F. Bussolotti,
et al., Nat. Comm. 8 (2017) 173.
Host: Frederik Schiller
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