TY - JOUR
T1 - Evolution of crystallinity at a well-defined molecular interface of epitaxial C 60 on the single crystal rubrene
AU - Tsuruta, Ryohei
AU - Hosokai, Takuya
AU - Yamanaka, Soichiro
AU - Yoshida, Koki
AU - Mizuno, Yuta
AU - Koganezawa, Tomoyuki
AU - Nakayama, Yasuo
N1 - Funding Information:
A part of this work was done under the approval of JASRI (Proposal 2016A1676, 2016B1612, 2017A1570, and 2017A1815 as collaborating proposals with Keysight Technologies). Financial supports from KAKENHI Grant Numbers JP15H05498, JP16K14102, and JP16K17975 of the Japan Society for the Promotion of Science (JSPS), The Futaba Foundation, and Iketani Science and Technology Foundation are gratefully acknowledged. This work was also partially supported by Murata Science Foundation.
Publisher Copyright:
© 2019 IOP Publishing Ltd.
PY - 2019
Y1 - 2019
N2 - Uniform and well-defined interfaces are required for clarification of fundamental processes at internal interfaces between donor and acceptor molecules constituting organic optoelectronic devices. In this study, evolution of a well-ordered molecular interface, epitaxially grown C 60 on the single crystal rubrene (C 42 H 28 ) surface, was accurately investigated by grazing incidence x-ray diffraction (GIXD) techniques. Contrasting to the case of C 60 on the single crystal pentacene forming uniquely aligned epitaxial interfaces, coexistence of two inequivalent crystalline domains of C 60 was identified on the single crystal rubrene. Nevertheless, crystallinity of C 60 /rubrene exhibited even more remarkable improvement to extend its in-plane average crystallite size up to 250 nm as the growth temperature was raised. Probable leading factors determining the structures and crystallinity of the well-defined molecular interfaces are discussed based on close comparison of the present results with the C 60 /pentacene interfaces. The techniques presented herein for enhancement of the crystallinity in epitaxial molecular interfaces are potentially applicable to development in the photoelectric power conversion efficiency of organic photovoltaics (OPVs) via improved charge carrier mobility in donor-acceptor interfaces.
AB - Uniform and well-defined interfaces are required for clarification of fundamental processes at internal interfaces between donor and acceptor molecules constituting organic optoelectronic devices. In this study, evolution of a well-ordered molecular interface, epitaxially grown C 60 on the single crystal rubrene (C 42 H 28 ) surface, was accurately investigated by grazing incidence x-ray diffraction (GIXD) techniques. Contrasting to the case of C 60 on the single crystal pentacene forming uniquely aligned epitaxial interfaces, coexistence of two inequivalent crystalline domains of C 60 was identified on the single crystal rubrene. Nevertheless, crystallinity of C 60 /rubrene exhibited even more remarkable improvement to extend its in-plane average crystallite size up to 250 nm as the growth temperature was raised. Probable leading factors determining the structures and crystallinity of the well-defined molecular interfaces are discussed based on close comparison of the present results with the C 60 /pentacene interfaces. The techniques presented herein for enhancement of the crystallinity in epitaxial molecular interfaces are potentially applicable to development in the photoelectric power conversion efficiency of organic photovoltaics (OPVs) via improved charge carrier mobility in donor-acceptor interfaces.
KW - Organic semiconductor
KW - donor-acceptor interface
KW - grazing incidence x-ray diffraction
KW - heteroepitaxy
KW - synchrotron radiation
UR - http://www.scopus.com/inward/record.url?scp=85062409668&partnerID=8YFLogxK
U2 - 10.1088/1361-648X/aafde0
DO - 10.1088/1361-648X/aafde0
M3 - Article
C2 - 30634171
AN - SCOPUS:85062409668
SN - 0953-8984
VL - 31
JO - Journal of Physics Condensed Matter
JF - Journal of Physics Condensed Matter
IS - 15
M1 - 154001
ER -