2020
Structure-Dependent Charge Transfer in Molecular Perylene-Based Donor/Acceptor Systems and Role of Side Chains
BELOVA, Valentina, Alexander HINDERHOFER, Clemens ZEISER, Timo STORZER, Jakub ROZBOŘIL et. al.Základní údaje
Originální název
Structure-Dependent Charge Transfer in Molecular Perylene-Based Donor/Acceptor Systems and Role of Side Chains
Autoři
BELOVA, Valentina, Alexander HINDERHOFER, Clemens ZEISER, Timo STORZER, Jakub ROZBOŘIL (203 Česká republika, domácí), Jan HAGENLOCHER, Jiří NOVÁK (203 Česká republika, domácí), Alexander GERLACH, Reinhard SCHOLZ a Frank SCHREIBER
Vydání
Journal of Physical Chemistry C, Washington D.C. American Chemical Society, 2020, 1932-7447
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10302 Condensed matter physics
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 4.126
Kód RIV
RIV/00216224:14310/20:00117387
Organizační jednotka
Přírodovědecká fakulta
UT WoS
000592366200001
Klíčová slova anglicky
Mixtures; Thin films; Energy; Molecular interactions; Molecules
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 18. 2. 2021 09:48, Mgr. Marie Šípková, DiS.
Anotace
V originále
In organic electronics and optoelectronics several crucial physical processes are related to charge transfer (CT) effects. In this work, we investigate mixing behavior and intermolecular coupling of donor and acceptor molecules in thin films prepared by organic molecular beam deposition (OMBD). Diindenoperylene (DIP) and pentacene (PEN) are used as the donor materials, and perylene diimide derivatives PDIR-CN2 and PDIF-CN2 as the acceptor materials.. The formation of charge transfer complexes coupled in the electronic excited state vs. noninteracting phase separating components is studied by structural and optical techniques. The CT mechanism and properties are considered in close connection with the thin film microstructure of the D/A blends which can be controlled via a change of the molecule geometry and/or growth temperature. We discuss two key findings for our systems: (1) The CT intensity correlates directly with the possibility of cocrystallization between acceptor and donor. (2) Side chain modification to tune the ground state energy levels has nearly no effect on the energy of the excited state CT, whereas replacement of molecular core modifies the CT energy correspondingly.
Návaznosti
LQ1601, projekt VaV |
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