TY - JOUR
T1 - F8BT Oligomers for Organic Solid-State Lasers
AU - Mamada, Masashi
AU - Komatsu, Ryutaro
AU - Adachi, Chihaya
N1 - Funding Information:
We thank Sumitomo Chemical Co. Ltd. for providing F8BT and Ms. K. Kusuhara and Ms. N. Nakamura for the characterization of materials. This work was financially supported by JST ERATO grant number JPMJER1305, JSPS KAKENHI grant number 19H02790, and the JSPS Core-to-Core Program.
Publisher Copyright:
Copyright © 2020 American Chemical Society.
PY - 2020/6/24
Y1 - 2020/6/24
N2 - The yellow-green emissive poly(9,9-dioctylfluorene-alt-benzothiadiazole) (F8BT) polymer is widely used because of its suitability for a variety of applications. However, we have found that F8BT shows huge performance variations that depend on the chemical supplier, with photoluminescence quantum yields (PLQYs) ranging from 7 to 60% in neat films. Polymers generally face problems including purity, polydispersity, and reproducibility, which also affect F8BT polymers. Therefore, to overcome these problems, we investigated oligomers of F8BT, which can easily be purified and can thus be obtained in a high-purity form. In the three oligomers (M1-M3) that we synthesized, the PLQYs were much higher than those of conventional F8BT (>80% in their neat films) although their PL spectra were nearly the same as that of F8BT, and their amplified spontaneous emission (ASE) thresholds were lower than that of the polymer (e.g., 1.9 μJ cm-2 for M3 and 2.7 μJ cm-2 for F8BT) because of a higher net gain and better film morphology. Furthermore, the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) energies of the oligomers were found to be similar to those of F8BT, making them candidate materials for use as hosts in light-emitting devices. The ASE using a near-infrared laser emitter doped in F8BT and oligomer hosts showed a clear difference despite nearly the same properties for steady-state emission.
AB - The yellow-green emissive poly(9,9-dioctylfluorene-alt-benzothiadiazole) (F8BT) polymer is widely used because of its suitability for a variety of applications. However, we have found that F8BT shows huge performance variations that depend on the chemical supplier, with photoluminescence quantum yields (PLQYs) ranging from 7 to 60% in neat films. Polymers generally face problems including purity, polydispersity, and reproducibility, which also affect F8BT polymers. Therefore, to overcome these problems, we investigated oligomers of F8BT, which can easily be purified and can thus be obtained in a high-purity form. In the three oligomers (M1-M3) that we synthesized, the PLQYs were much higher than those of conventional F8BT (>80% in their neat films) although their PL spectra were nearly the same as that of F8BT, and their amplified spontaneous emission (ASE) thresholds were lower than that of the polymer (e.g., 1.9 μJ cm-2 for M3 and 2.7 μJ cm-2 for F8BT) because of a higher net gain and better film morphology. Furthermore, the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) energies of the oligomers were found to be similar to those of F8BT, making them candidate materials for use as hosts in light-emitting devices. The ASE using a near-infrared laser emitter doped in F8BT and oligomer hosts showed a clear difference despite nearly the same properties for steady-state emission.
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U2 - 10.1021/acsami.0c05449
DO - 10.1021/acsami.0c05449
M3 - Article
C2 - 32453542
AN - SCOPUS:85087111058
SN - 1944-8244
VL - 12
SP - 28383
EP - 28391
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 25
ER -