Phenanthro[110,9,8-cdefg]carbazole-Thiophene, Donor-Donor Copolymer for Narrow Band Green-Selective Organic Photodiode
- Authors
- Sung, Min Jae; Kim, Kyounghwan; Kwon, Soon-Ki; Kim, Yun-Hi; Chung, Dae Sung
- Issue Date
- Jul-2017
- Publisher
- American Chemical Society
- Citation
- The Journal of Physical Chemistry C, v.121, no.29, pp 15931 - 15936
- Pages
- 6
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- The Journal of Physical Chemistry C
- Volume
- 121
- Number
- 29
- Start Page
- 15931
- End Page
- 15936
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/13590
- DOI
- 10.1021/acs.jpcc.7b04793
- ISSN
- 1932-7447
1932-7455
- Abstract
- A new donor donor copolymer consisting of phenanthro[1,10,9,8-cdefg]carbazole and thiophene unit (PP-Th) was synthesized for narrow band green-selective organic photodiode application. Thanks to well-defined intramolecular conjugation and inhibited intermolecular interaction of PP-Th compared to its donor- acceptor type analogues, PP-Th revealed narrow band green-selective absorption peak at 510 nm with low full width at half-maximum value of 98 nm. In addition, deep ionization energy of PP-Th, as confirmed by photophysical analyses, made it less susceptible to oxidational degradation. Green-selective organic photodiodes (OPDs) were fabricated utilizing PP-Th as a green absorbing donor material and ZnO as a nonabsorbing acceptor material. The optimized OPD rendered a very low dark current of 2 nA cm(-2) and a high detectivity of 1.42 x 10(12) Jones with narrow band green-selectivity. Moreover, PP-Th enabled OPD with a high 3-dB bandwidth of 3.1 kHz and a high linear dynamic range of 84.9 dB. Furthermore, the responsivity of the OPD could be maintained for more than 30 days under atmospheric condition, revealing excellent stability of PP-Th.
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Collections - 공과대학 > School of Materials Science&Engineering > Journal Articles
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