Altering Glass Transition of TPD thin Films with UV Light
Аутори
Markesevic, NemanjaJovanović, Vladimir P.
Žikić, Radomir
Scarpellini, M.
Lucenti, E.
Milani, P.
Srdanov, V. I.
Конференцијски прилог (Објављена верзија)
Метаподаци
Приказ свих података о документуАпстракт
N,N´-Bis(3-methylphenyl)-N,N’dyphenilbenzidine (TPD) is a hole-transport material used in
electroluminescent devices whose glass transition temperature, Tg, depends on the film thickness.[1] For sufficiently thin films (d<30 nm), dewetting of amorphous TPD films deposited on a on fused silica or an ITO substrate occurs even at room temperature.[2] Following a brief report on increased thermal stability of UV irradiated TPD films,[3] we investigated the underlying mechanism responsible for it. From proton NMR and mass spectrometry measurements, coupled with morphology (AFM) and spectroscopy (UV-VIS) studies, we find that photo-excited TPD species react with oxygen in air. This leads to partially oxidized TPD films whose increased thermal stability we ascribe to stronger hydrogen bonding of photo-oxidized TPD species with hydrophilic substrates.
Кључне речи:
small organic molecule / TPD / thin film / glass transition temperature / UV lightИзвор:
XVIII Symposium on Condensed Matter Physics - SFKM 2011, Belgrade, 2011, 105-Издавач:
- Institute of physics, Pregrevica 118, Belgrade, Serbia
- CIMAINA, Università di Milano, Via Celoria 16, 20133 Milano, Italy
- 3 Institute for Terahertz Science and Technology, University of California Santa Barbara, Santa Barbara CA 93106
Институција/група
Institut za multidisciplinarna istraživanjaTY - CONF AU - Markesevic, Nemanja AU - Jovanović, Vladimir P. AU - Žikić, Radomir AU - Scarpellini, M. AU - Lucenti, E. AU - Milani, P. AU - Srdanov, V. I. PY - 2011 UR - http://rimsi.imsi.bg.ac.rs/handle/123456789/2163 AB - N,N´-Bis(3-methylphenyl)-N,N’dyphenilbenzidine (TPD) is a hole-transport material used in electroluminescent devices whose glass transition temperature, Tg, depends on the film thickness.[1] For sufficiently thin films (d<30 nm), dewetting of amorphous TPD films deposited on a on fused silica or an ITO substrate occurs even at room temperature.[2] Following a brief report on increased thermal stability of UV irradiated TPD films,[3] we investigated the underlying mechanism responsible for it. From proton NMR and mass spectrometry measurements, coupled with morphology (AFM) and spectroscopy (UV-VIS) studies, we find that photo-excited TPD species react with oxygen in air. This leads to partially oxidized TPD films whose increased thermal stability we ascribe to stronger hydrogen bonding of photo-oxidized TPD species with hydrophilic substrates. PB - Institute of physics, Pregrevica 118, Belgrade, Serbia PB - CIMAINA, Università di Milano, Via Celoria 16, 20133 Milano, Italy PB - 3 Institute for Terahertz Science and Technology, University of California Santa Barbara, Santa Barbara CA 93106 C3 - XVIII Symposium on Condensed Matter Physics - SFKM 2011, Belgrade T1 - Altering Glass Transition of TPD thin Films with UV Light SP - 105 UR - https://hdl.handle.net/21.15107/rcub_rimsi_2163 ER -
@conference{ author = "Markesevic, Nemanja and Jovanović, Vladimir P. and Žikić, Radomir and Scarpellini, M. and Lucenti, E. and Milani, P. and Srdanov, V. I.", year = "2011", abstract = "N,N´-Bis(3-methylphenyl)-N,N’dyphenilbenzidine (TPD) is a hole-transport material used in electroluminescent devices whose glass transition temperature, Tg, depends on the film thickness.[1] For sufficiently thin films (d<30 nm), dewetting of amorphous TPD films deposited on a on fused silica or an ITO substrate occurs even at room temperature.[2] Following a brief report on increased thermal stability of UV irradiated TPD films,[3] we investigated the underlying mechanism responsible for it. From proton NMR and mass spectrometry measurements, coupled with morphology (AFM) and spectroscopy (UV-VIS) studies, we find that photo-excited TPD species react with oxygen in air. This leads to partially oxidized TPD films whose increased thermal stability we ascribe to stronger hydrogen bonding of photo-oxidized TPD species with hydrophilic substrates.", publisher = "Institute of physics, Pregrevica 118, Belgrade, Serbia, CIMAINA, Università di Milano, Via Celoria 16, 20133 Milano, Italy, 3 Institute for Terahertz Science and Technology, University of California Santa Barbara, Santa Barbara CA 93106", journal = "XVIII Symposium on Condensed Matter Physics - SFKM 2011, Belgrade", title = "Altering Glass Transition of TPD thin Films with UV Light", pages = "105", url = "https://hdl.handle.net/21.15107/rcub_rimsi_2163" }
Markesevic, N., Jovanović, V. P., Žikić, R., Scarpellini, M., Lucenti, E., Milani, P.,& Srdanov, V. I.. (2011). Altering Glass Transition of TPD thin Films with UV Light. in XVIII Symposium on Condensed Matter Physics - SFKM 2011, Belgrade Institute of physics, Pregrevica 118, Belgrade, Serbia., 105. https://hdl.handle.net/21.15107/rcub_rimsi_2163
Markesevic N, Jovanović VP, Žikić R, Scarpellini M, Lucenti E, Milani P, Srdanov VI. Altering Glass Transition of TPD thin Films with UV Light. in XVIII Symposium on Condensed Matter Physics - SFKM 2011, Belgrade. 2011;:105. https://hdl.handle.net/21.15107/rcub_rimsi_2163 .
Markesevic, Nemanja, Jovanović, Vladimir P., Žikić, Radomir, Scarpellini, M., Lucenti, E., Milani, P., Srdanov, V. I., "Altering Glass Transition of TPD thin Films with UV Light" in XVIII Symposium on Condensed Matter Physics - SFKM 2011, Belgrade (2011):105, https://hdl.handle.net/21.15107/rcub_rimsi_2163 .