TY - JOUR
T1 - Improved EL efficiency of fluorene-thieno[3,2-b] thiophene-based conjugated copolymers with hole-transporting or electron-transporting units in the main chain
AU - Lim, Eunhee
AU - Jung, Byung Jun
AU - Shim, Hong Ku
PY - 2006/1/1
Y1 - 2006/1/1
N2 - New electroluminescent polymers (poly(9,9′-dioctylfluorene-co-thieno[3,2-6]thiophene-co-benzo[2,3,5] thiadiazole) (P1) and poly(9,9′-dioctylfluorene-co-thieno[3, 2-b]thiophene-co-benzo[2,3,5]thiadiazole-co-[4-(2-ethylhexyloxyl)phenyl] diphenylamine (P2)) possess hole-transporting or electron-transporting units or both in the main chains. Electron-deficient benzothiadiazole and electron-rich triphenylamine moieties were incorporated into the polymer backbone to improve the electron-transporting and hole-transporting characteristics, respectively. P1 and P2 show greater solubility than poly(9,9′-dioctylfluorene-co-thieno[3,2-b]thiophene (PFTT), without sacrificing their good thermal stability. Moreover, owing to the incorporation of the electron-deficient benzothiadiazole unit, P1 and P2 exhibit remarkably lower LUMO levels than PFTT, and thus, it should facilitate the electron injection into the polymer layer from the cathode electrode. Consequently, because of the balance of charge mobility, LED devices based on P1 and P2 exhibit greater brightness and efficiency (up to 3000 cd/m2 and 1.35 cd/A) than devices that use the pristine PFTT.
AB - New electroluminescent polymers (poly(9,9′-dioctylfluorene-co-thieno[3,2-6]thiophene-co-benzo[2,3,5] thiadiazole) (P1) and poly(9,9′-dioctylfluorene-co-thieno[3, 2-b]thiophene-co-benzo[2,3,5]thiadiazole-co-[4-(2-ethylhexyloxyl)phenyl] diphenylamine (P2)) possess hole-transporting or electron-transporting units or both in the main chains. Electron-deficient benzothiadiazole and electron-rich triphenylamine moieties were incorporated into the polymer backbone to improve the electron-transporting and hole-transporting characteristics, respectively. P1 and P2 show greater solubility than poly(9,9′-dioctylfluorene-co-thieno[3,2-b]thiophene (PFTT), without sacrificing their good thermal stability. Moreover, owing to the incorporation of the electron-deficient benzothiadiazole unit, P1 and P2 exhibit remarkably lower LUMO levels than PFTT, and thus, it should facilitate the electron injection into the polymer layer from the cathode electrode. Consequently, because of the balance of charge mobility, LED devices based on P1 and P2 exhibit greater brightness and efficiency (up to 3000 cd/m2 and 1.35 cd/A) than devices that use the pristine PFTT.
KW - Conducting polymers
KW - Conjugated polymer
KW - Light-emitting diodes (LED)
KW - Photophysics
KW - Polyfluorene
UR - http://www.scopus.com/inward/record.url?scp=30344464396&partnerID=8YFLogxK
U2 - 10.1002/pola.21144
DO - 10.1002/pola.21144
M3 - Article
AN - SCOPUS:30344464396
SN - 0887-624X
VL - 44
SP - 243
EP - 253
JO - Journal of Polymer Science, Part A: Polymer Chemistry
JF - Journal of Polymer Science, Part A: Polymer Chemistry
IS - 1
ER -