TY - JOUR
T1 - New blue emitters based on anthracene through charge transfer control
AU - Lee, Changmin
AU - Park, Sangwook
AU - Kwon, Hyukmin
AU - Lee, Kiho
AU - Lee, Hayoon
AU - Kang, Seokwoo
AU - Park, Dongmin
AU - Park, Jongwook
N1 - Publisher Copyright:
© 2024 Elsevier B.V.
PY - 2024/12
Y1 - 2024/12
N2 - We designed new moieties with varying electron-donating effects and sizes based on diphenylamine and introduced them into anthracene to synthesize three types of emitting materials. All three materials exhibited high thermal stability with glass transition temperatures above 175°C, confirming their potential as OLED emitters. Devices doped with N9,N9,N10,N10-tetraphenylanthracene-9,10-diamine (TAD), where diphenyl amine is substituted on both sides, and N9,N10-di([1,1′-biphenyl]-4-yl)-N9,N10-bis(dibenzo[b,d]furan-2-yl)anthracene-9,10 diamine (ABFA), with a fused side group of diphenyl amine and dibenzofuran, showed EQEs of 1.28 % and 3.57 % respectively. Due to the intramolecular charge transfer (ICT), they exhibited ELmax values at 517 nm and 538 nm. On the other hand, the device doped with N,N′-(anthracene-9,10-diylbis(4,1-phenylene))bis(N-([1,1′-biphenyl]-4-yl)dibenzo[b,d]furan-2-amine) (APBFA), which has optimized side groups that suppress ICT and intermolecular packing, achieved a relatively high EQE of 4.48 % and showed blue emission with CIE coordinates of (0.146, 0.142).
AB - We designed new moieties with varying electron-donating effects and sizes based on diphenylamine and introduced them into anthracene to synthesize three types of emitting materials. All three materials exhibited high thermal stability with glass transition temperatures above 175°C, confirming their potential as OLED emitters. Devices doped with N9,N9,N10,N10-tetraphenylanthracene-9,10-diamine (TAD), where diphenyl amine is substituted on both sides, and N9,N10-di([1,1′-biphenyl]-4-yl)-N9,N10-bis(dibenzo[b,d]furan-2-yl)anthracene-9,10 diamine (ABFA), with a fused side group of diphenyl amine and dibenzofuran, showed EQEs of 1.28 % and 3.57 % respectively. Due to the intramolecular charge transfer (ICT), they exhibited ELmax values at 517 nm and 538 nm. On the other hand, the device doped with N,N′-(anthracene-9,10-diylbis(4,1-phenylene))bis(N-([1,1′-biphenyl]-4-yl)dibenzo[b,d]furan-2-amine) (APBFA), which has optimized side groups that suppress ICT and intermolecular packing, achieved a relatively high EQE of 4.48 % and showed blue emission with CIE coordinates of (0.146, 0.142).
KW - Anthracene
KW - Blue
KW - Charge transfer
KW - Diphenyl amine
KW - OLED
UR - http://www.scopus.com/inward/record.url?scp=85205424211&partnerID=8YFLogxK
U2 - 10.1016/j.synthmet.2024.117762
DO - 10.1016/j.synthmet.2024.117762
M3 - Article
AN - SCOPUS:85205424211
SN - 0379-6779
VL - 309
JO - Synthetic Metals
JF - Synthetic Metals
M1 - 117762
ER -