Interaction of UV irradiation with thin films of organic molecules
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There is an ongoing interest in organic materials due to their application in various organic electronic devices. However stability of organic materials limits their potential use. They are prone to degradation both during the working life and storage. One of the main causes is extrinsic degradation, under the influence of oxygen and moisture. This problem can be solved by encapsulation of devices. However no encapsulation is perfect. In the first part of this work a study of degradation of thin films of N,N′-bis(3-methylphenyl)-N,N′-bis(phenyl)benzidine (TPD) and 4,4′-bis(2,2-diphenylvinyl)-1,1′-biphenyl (DPVBi) under UV irradiation in air is given. Films of both materials are stable in vacuum, but readily degrade in the presence of oxygen. Thus, the necessary condition for degradation is the simultaneous presence of UV light and oxygen. Chemical analysis of irradiated films by NMR, mass and infrared spectroscopy revealed presence of oxidized species (impurities). These impurities are... responsible for increased morphological stability of irradiated films and quenching of photoluminescence. Only small amount of impurities, 0.4 % (0.2 %) for TPD (DPVBi), causes 50 % decrease of photoluminescence. This implies a non-trivial mechanism of quenching. For both molecules it was found that distance between impurities is smaller or equal to exciton diffusion length, which is the necessary condition for quenching. Following mechanism of quenching is proposed: exciton diffuses by hopping form one DPVBi (TPD) to another through FRET in a random walk manner. If, during its lifetime, it comes to proximity of an impurity, a Dexter-type energy transfer occurs and PL is quenched. Findings of DPVBi study are important because they show that even a small amount of oxygen that penetrates a DPVBi layer would impair luminescence efficiency of a device. Moreover, the absorption of own radiation (for DPVBi and TPD both) would additionally contribute to the rate of degradation of a device. It is reasonable to expect that transport properties would also be affected when materials are used as a hole-transporting layer in OLEDs.
Кључне речи:
thin organic films / morphology / photo-oxidation / degradation / photoluminescence quenching / exciton self-diffusionИзвор:
ADVANCED CERAMICS AND APPLICATION IV - PROGRAM AND THE BOOK OF ABSTRACTS, 2015, 43-Издавач:
- Serbian Ceramic Society
Финансирање / пројекти:
- Електронске, транспортне и оптичке особине нанофазних материјала (RS-171033)
- Интегрална студија идентификације регионалних генетских фактора ризика и фактора ризика животне средине за масовне незаразне болести хумане популације у Србији - INGEMA_S (RS-41028)
Напомена:
- Serbian Ceramic Society Conference ADVANCED CERAMICS AND APPLICATION IV New Frontiers in Multifunctional Material Science and Processing Serbian Academy of Sciences and Arts, Knez Mihailova 35 Serbia, Belgrade, 21-23. September 2015.
Институција/група
Institut za multidisciplinarna istraživanjaTY - GEN AU - Tomović, Aleksandar AU - Jovanović, Vladimir P. AU - Zikic, Radomir PY - 2015 UR - http://rimsi.imsi.bg.ac.rs/handle/123456789/1903 AB - There is an ongoing interest in organic materials due to their application in various organic electronic devices. However stability of organic materials limits their potential use. They are prone to degradation both during the working life and storage. One of the main causes is extrinsic degradation, under the influence of oxygen and moisture. This problem can be solved by encapsulation of devices. However no encapsulation is perfect. In the first part of this work a study of degradation of thin films of N,N′-bis(3-methylphenyl)-N,N′-bis(phenyl)benzidine (TPD) and 4,4′-bis(2,2-diphenylvinyl)-1,1′-biphenyl (DPVBi) under UV irradiation in air is given. Films of both materials are stable in vacuum, but readily degrade in the presence of oxygen. Thus, the necessary condition for degradation is the simultaneous presence of UV light and oxygen. Chemical analysis of irradiated films by NMR, mass and infrared spectroscopy revealed presence of oxidized species (impurities). These impurities are responsible for increased morphological stability of irradiated films and quenching of photoluminescence. Only small amount of impurities, 0.4 % (0.2 %) for TPD (DPVBi), causes 50 % decrease of photoluminescence. This implies a non-trivial mechanism of quenching. For both molecules it was found that distance between impurities is smaller or equal to exciton diffusion length, which is the necessary condition for quenching. Following mechanism of quenching is proposed: exciton diffuses by hopping form one DPVBi (TPD) to another through FRET in a random walk manner. If, during its lifetime, it comes to proximity of an impurity, a Dexter-type energy transfer occurs and PL is quenched. Findings of DPVBi study are important because they show that even a small amount of oxygen that penetrates a DPVBi layer would impair luminescence efficiency of a device. Moreover, the absorption of own radiation (for DPVBi and TPD both) would additionally contribute to the rate of degradation of a device. It is reasonable to expect that transport properties would also be affected when materials are used as a hole-transporting layer in OLEDs. PB - Serbian Ceramic Society T2 - ADVANCED CERAMICS AND APPLICATION IV - PROGRAM AND THE BOOK OF ABSTRACTS T1 - Interaction of UV irradiation with thin films of organic molecules SP - 43 UR - https://hdl.handle.net/21.15107/rcub_rimsi_1903 ER -
@misc{ author = "Tomović, Aleksandar and Jovanović, Vladimir P. and Zikic, Radomir", year = "2015", abstract = "There is an ongoing interest in organic materials due to their application in various organic electronic devices. However stability of organic materials limits their potential use. They are prone to degradation both during the working life and storage. One of the main causes is extrinsic degradation, under the influence of oxygen and moisture. This problem can be solved by encapsulation of devices. However no encapsulation is perfect. In the first part of this work a study of degradation of thin films of N,N′-bis(3-methylphenyl)-N,N′-bis(phenyl)benzidine (TPD) and 4,4′-bis(2,2-diphenylvinyl)-1,1′-biphenyl (DPVBi) under UV irradiation in air is given. Films of both materials are stable in vacuum, but readily degrade in the presence of oxygen. Thus, the necessary condition for degradation is the simultaneous presence of UV light and oxygen. Chemical analysis of irradiated films by NMR, mass and infrared spectroscopy revealed presence of oxidized species (impurities). These impurities are responsible for increased morphological stability of irradiated films and quenching of photoluminescence. Only small amount of impurities, 0.4 % (0.2 %) for TPD (DPVBi), causes 50 % decrease of photoluminescence. This implies a non-trivial mechanism of quenching. For both molecules it was found that distance between impurities is smaller or equal to exciton diffusion length, which is the necessary condition for quenching. Following mechanism of quenching is proposed: exciton diffuses by hopping form one DPVBi (TPD) to another through FRET in a random walk manner. If, during its lifetime, it comes to proximity of an impurity, a Dexter-type energy transfer occurs and PL is quenched. Findings of DPVBi study are important because they show that even a small amount of oxygen that penetrates a DPVBi layer would impair luminescence efficiency of a device. Moreover, the absorption of own radiation (for DPVBi and TPD both) would additionally contribute to the rate of degradation of a device. It is reasonable to expect that transport properties would also be affected when materials are used as a hole-transporting layer in OLEDs.", publisher = "Serbian Ceramic Society", journal = "ADVANCED CERAMICS AND APPLICATION IV - PROGRAM AND THE BOOK OF ABSTRACTS", title = "Interaction of UV irradiation with thin films of organic molecules", pages = "43", url = "https://hdl.handle.net/21.15107/rcub_rimsi_1903" }
Tomović, A., Jovanović, V. P.,& Zikic, R.. (2015). Interaction of UV irradiation with thin films of organic molecules. in ADVANCED CERAMICS AND APPLICATION IV - PROGRAM AND THE BOOK OF ABSTRACTS Serbian Ceramic Society., 43. https://hdl.handle.net/21.15107/rcub_rimsi_1903
Tomović A, Jovanović VP, Zikic R. Interaction of UV irradiation with thin films of organic molecules. in ADVANCED CERAMICS AND APPLICATION IV - PROGRAM AND THE BOOK OF ABSTRACTS. 2015;:43. https://hdl.handle.net/21.15107/rcub_rimsi_1903 .
Tomović, Aleksandar, Jovanović, Vladimir P., Zikic, Radomir, "Interaction of UV irradiation with thin films of organic molecules" in ADVANCED CERAMICS AND APPLICATION IV - PROGRAM AND THE BOOK OF ABSTRACTS (2015):43, https://hdl.handle.net/21.15107/rcub_rimsi_1903 .