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Emissive Material Optimization for Solution-Processed Excip..:

Jaber Saghaei (8211396) ; Tanja Leitner (11661918) ; Van Thi Ngoc Mai (11661921)...
https://figshare.com/articles/journal_contribution/Emissive_Material_Optimization_for_Solution-Processed_Exciplex_OLEDs/16953660. , 2021

Link: https://doi.org/10.1021/acsaelm.1c00630.s001

RT Journal
T1 <Title>Emissive Material Optimization for Solution-Processed Exciplex OLEDs</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_16953660&Exemplar=1&LAN=DE
				
A1 Jaber Saghaei (8211396)
A1 Tanja Leitner (11661918)
A1 Van Thi Ngoc Mai (11661921)
A1 Chandana Sampath Kumara Ranasinghe (4232491)
A1 Paul L. Burn (1460572)
A1 Ian R. Gentle (1444540)
A1 Almantas Pivrikas (1471633)
A1 Paul E. Shaw (1744702)
YR 2021
K1 Biophysics
K1 Biochemistry
K1 Molecular Biology
K1 Pharmacology
K1 Biotechnology
K1 Biological Sciences not elsewhere classified
K1 Chemical Sciences not elsewhere classified
K1 Physical Sciences not elsewhere classified
K1 simple bilayer oleds
K1 photoluminescence quantum yield
K1 ethylhexyloxy ) phenyl
K1 charge transfer emission
K1 best overall performance
K1 oxadiazole derivative exhibited
K1 charge transfer blends
K1 hole transporting 4
K1 >- butylphenyl moieties
K1 synthesized oxadiazole derivatives
K1 yl ] benzene
K1 emissive material optimization
K1 3 ± 0
K1 4 -( 2
K1 oxadiazole derivatives
K1 exciplex blends
K1 >- propyl
K1 >- hexyl
K1 >- alkylfluoren
K1 4 -<
K1 similar manner
K1 part due
K1 organic light
K1 neat films
K1 mainly used
K1 magnitude higher
K1 good solubility
K1 evaporable materials
K1 end groups
K1 electron mobilities
K1 di -<
K1 covalent linkages
K1 commercial 1
K1 alkyl groups
K1 acceptor materials
K1 3 %
JF https://figshare.com/articles/journal_contribution/Emissive_Material_Optimization_for_Solution-Processed_Exciplex_OLEDs/16953660
LK http://dx.doi.org/https://doi.org/10.1021/acsaelm.1c00630.s001
DO https://doi.org/10.1021/acsaelm.1c00630.s001
SF ELIB - SuUB Bremen

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