TY - JOUR
T1 - Organic electroluminescence devices fabricated with chemical vapour deposited polyazomethine films
AU - Weaver, M. S.
AU - Bradley, D. D.C.
N1 - Generated from Scopus record by KAUST IRTS on 2019-11-27
PY - 1996/1/1
Y1 - 1996/1/1
N2 - We demonstrate the use of chemical vapour deposition polymerization as an effective method to fabricate conjugated polymer films as constituents in organic electroluminescence (EL) devices. This technique provides excellent compatibility with vacuum sublimation deposition of low molecular weight materials for construction of hybrid devices. The specific polyazomethine polymer studied here, namely, poly(1,4-phenylenemethylidynenitrilo-1,4-phenylenenitrilomethylidyne), is shown to be an addition to the range of polymer structures that provide electron transport functionality and, in combination with suitable emissive materials, provides the basis for new device structures. From measurements on a series of devices we propose an energy level structure for this material. Despite remaining isoelectronic with poly (1,4-phenylenevinylene) the energy levels of the polyazomethine are strongly shifted through the replacement of a vinylene CH with a N atom.
AB - We demonstrate the use of chemical vapour deposition polymerization as an effective method to fabricate conjugated polymer films as constituents in organic electroluminescence (EL) devices. This technique provides excellent compatibility with vacuum sublimation deposition of low molecular weight materials for construction of hybrid devices. The specific polyazomethine polymer studied here, namely, poly(1,4-phenylenemethylidynenitrilo-1,4-phenylenenitrilomethylidyne), is shown to be an addition to the range of polymer structures that provide electron transport functionality and, in combination with suitable emissive materials, provides the basis for new device structures. From measurements on a series of devices we propose an energy level structure for this material. Despite remaining isoelectronic with poly (1,4-phenylenevinylene) the energy levels of the polyazomethine are strongly shifted through the replacement of a vinylene CH with a N atom.
UR - https://linkinghub.elsevier.com/retrieve/pii/S0379677997800537
UR - http://www.scopus.com/inward/record.url?scp=0030262791&partnerID=8YFLogxK
U2 - 10.1016/S0379-6779(97)80053-7
DO - 10.1016/S0379-6779(97)80053-7
M3 - Article
SN - 0379-6779
VL - 83
JO - Synthetic Metals
JF - Synthetic Metals
IS - 1
ER -