Published November 1, 2012 | Version v1
Journal article

Thermally stable aromatic amine derivative with symmetrically substituted double spirobifluorene core as a hole transport material for green phosphorescent organic light-emitting diodes

Description

A thermally stable aromatic amine derivative with a symmetrically substituted double spirobifluorene core was synthesized as a hole transport material for green phosphorescent organic light-emitting diodes. A high glass transition temperature of 142 °C was obtained and a film morphology of the hole transport material was kept stable up to 120 °C. The hole transport material showed a high triplet energy of 2.53 eV and a quantum efficiency of 17.4% in green phosphorescent organic light-emitting diodes. - Highlights: ► Synthesis of symmetrically substituted double spirobifluorene core ► Stable film morphology up to 120 °C ► High quantum efficiency in green phosphorescent organic light emitting diode

Availability note (English)

Available from http://dx.doi.org/10.1016/j.tsf.2012.08.034

Additional details

Identifiers

DOI
10.1016/j.tsf.2012.08.034;
PII
S0040-6090(12)01071-1;

Publishing Information

Journal Title
Thin Solid Films
Journal Volume
522
Journal Page Range
p. 415-419
ISSN
0040-6090
CODEN
THSFAP

Conference

Title
Engineering of wide bandgap semiconductor materials for energy saving
Acronym
E-MRS 2011 Symposium Q
Dates
9-10 May 2011
Place
Nice (France)

INIS

Country of Publication
Netherlands
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
44103728
Subject category
S36: MATERIALS SCIENCE;
Resource subtype / Literary indicator
Conference
Descriptors DEI
AMINES; EV RANGE 01-10; FILMS; GLASS; HOLES; LIGHT EMITTING DIODES; MORPHOLOGY; QUANTUM EFFICIENCY; STABILITY; SYNTHESIS; TRANSITION TEMPERATURE; TRIPLETS
Descriptors DEC
EFFICIENCY; ENERGY RANGE; EV RANGE; MULTIPLETS; ORGANIC COMPOUNDS; PHYSICAL PROPERTIES; SEMICONDUCTOR DEVICES; SEMICONDUCTOR DIODES; THERMODYNAMIC PROPERTIES

Optional Information

Copyright
Copyright (c) 2012 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.