Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Polarity Switching in Organic Electronic Devices via Terminal Substitution of Active-Layer Molecules. / Dominskii, D. I.; Kharlanov, O.G.; Trukhanov, V.A.; Sosorev, A.Yu.; Sorokina, N.I.; Kazantsev, M.S.; Лазнева, Элеонора Федоровна; Герасимова, Наталия Борисовна; Соболев, Виталий Сергеевич; Комолов, Алексей Сергеевич; Борщев, О.В.; Пономаренко, С. А.
в: ACS Applied Electronic Materials, Том 4, № 12, 07.12.2022, стр. 6345–6356.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Polarity Switching in Organic Electronic Devices via Terminal Substitution of Active-Layer Molecules
AU - Dominskii, D. I.
AU - Kharlanov, O.G.
AU - Trukhanov, V.A.
AU - Sosorev, A.Yu.
AU - Sorokina, N.I.
AU - Kazantsev, M.S.
AU - Лазнева, Элеонора Федоровна
AU - Герасимова, Наталия Борисовна
AU - Соболев, Виталий Сергеевич
AU - Комолов, Алексей Сергеевич
AU - Борщев, О.В.
AU - Пономаренко, С. А.
PY - 2022/12/7
Y1 - 2022/12/7
N2 - Organic electronic devices often suffer from poor charge injection limiting their performance. Specifically, high-performance electronic devices usually need Ohmic contacts, but it is not easy to realize them in junctions of the organic semiconductor with the electrodes because of the contact problems. In this work, polarity switching in organic field-effect transistors (OFETs) that is independent of the electrode work function is demonstrated-the switching of charge injection from the p-type to ambipolar and to the n-type-via modification of the donor/acceptor character of the molecular terminal substituents. By using three thiophene-phenylene co-oligomers with the same conjugated core, similar crystal packings, but different terminal substituents (methyl, trimethylsilyl, and trifluoromethyl), the polarity switching in both thin-film and single-crystal OFETs is demonstrated. The ultraviolet photoelectron spectroscopy studies and electronic structure calculations justify a definitive role of the interface dipole stemming from the terminal groups in controlling the heights of charge injection barriers and hence in charge injection into the OFET active layer. The results obtained are expected to facilitate rational design of organic semiconductors for high-performance electronic devices.
AB - Organic electronic devices often suffer from poor charge injection limiting their performance. Specifically, high-performance electronic devices usually need Ohmic contacts, but it is not easy to realize them in junctions of the organic semiconductor with the electrodes because of the contact problems. In this work, polarity switching in organic field-effect transistors (OFETs) that is independent of the electrode work function is demonstrated-the switching of charge injection from the p-type to ambipolar and to the n-type-via modification of the donor/acceptor character of the molecular terminal substituents. By using three thiophene-phenylene co-oligomers with the same conjugated core, similar crystal packings, but different terminal substituents (methyl, trimethylsilyl, and trifluoromethyl), the polarity switching in both thin-film and single-crystal OFETs is demonstrated. The ultraviolet photoelectron spectroscopy studies and electronic structure calculations justify a definitive role of the interface dipole stemming from the terminal groups in controlling the heights of charge injection barriers and hence in charge injection into the OFET active layer. The results obtained are expected to facilitate rational design of organic semiconductors for high-performance electronic devices.
KW - contacts
KW - electronic structure calculations
KW - interface dipole
KW - organic field-effect transistor
KW - organic semiconductor
UR - https://www.mendeley.com/catalogue/bec7c867-2e62-3da1-90d2-4e75e98d85d4/
U2 - 10.1021/acsaelm.2c01481
DO - 10.1021/acsaelm.2c01481
M3 - Article
VL - 4
SP - 6345
EP - 6356
JO - ACS Applied Electronic Materials
JF - ACS Applied Electronic Materials
SN - 2637-6113
IS - 12
ER -
ID: 101344095