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Negative Isotope Effect on Field‐Effect Hole Transport in Fully Substituted 13 C‐Rubrene
Author(s) -
Ren Xinglong,
Bruzek Matthew J.,
Hanifi David A.,
Schulzetenberg Aaron,
Wu Yanfei,
Kim ChangHyun,
Zhang Zhuoran,
Johns James E.,
Salleo Alberto,
Fratini Simone,
Troisi Alessandro,
Douglas Christopher J.,
Frisbie C. Daniel
Publication year - 2017
Publication title -
advanced electronic materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.25
H-Index - 56
ISSN - 2199-160X
DOI - 10.1002/aelm.201700018
Subject(s) - rubrene , organic semiconductor , materials science , electron mobility , semiconductor , chemical physics , optoelectronics , chemistry
Isotopic substitution is a useful method to study the influence of nuclear motion on the kinetics of charge transport in semiconductors. However, in organic semiconductors, no observable isotope effect on field‐effect mobility has been reported. To understand the charge transport mechanism in rubrene, the benchmark organic semiconductor, crystals of fully isotopically substituted rubrene, 13 C‐rubrene ( 13 C 42 H 28 ), are synthesized and characterized. Vapor‐grown 13 C‐rubrene single crystals have the same crystal structure and quality as native rubrene crystals (i.e., rubrene with a natural abundance of carbon isotopes). The characteristic transport signatures of rubrene, including room temperature hole mobility over 10 cm 2 V −1 s −1 , intrinsic band‐like transport, and clear Hall behavior in the accumulation layer of air‐gap transistors, are also observed for 13 C‐rubrene crystals. The field‐effect mobility distributions based on 74 rubrene and 13 C‐rubrene devices, respectively, reveal that 13 C isotopic substitution produces a 13% reduction in the hole mobility of rubrene. The origin of the negative isotope effect is linked to the redshift of vibrational frequencies after 13 C‐substitution, as demonstrated by computer simulations based on the transient localization (dynamic disorder) scenario. Overall, the data and analysis provide an important benchmark for ongoing efforts to understand transport in ordered organic semiconductors.