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Development of low bandgap polymers for red and near-infrared fullerene-free organic photodetectors

Authors
Jeong, WonJoKang, JinhyeonJeong, Moon-KiWon, Jong HoJung, In Hwan
Issue Date
Jun-2021
Publisher
ROYAL SOC CHEMISTRY
Citation
NEW JOURNAL OF CHEMISTRY, v.45, no.24, pp.10872 - 10879
Indexed
SCIE
SCOPUS
Journal Title
NEW JOURNAL OF CHEMISTRY
Volume
45
Number
24
Start Page
10872
End Page
10879
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/1082
DOI
10.1039/d1nj01694f
ISSN
1144-0546
Abstract
Two photoconductive conjugated polymers (PDTPTT and PCPDTTT) were synthesized to be utilized in red and near-infrared (NIR) organic photodetectors (OPDs). The low bandgap was achieved by stabilizing the quinoidal structure of the conjugated backbone, and both donor polymers showed strong red and NIR absorption in the range of 500-900 nm. To enhance the exciton separation and intensify the red and NIR absorption, p-n bulk heterojunction OPDs were fabricated by blending a PDTPTT (or PCPDTTT) and a low bandgap nonfullerene acceptor (IDIC). The PCPDTTT:IDIC devices showed excellent OPD performances with a detectivity (D*) of 1.14 x 10(12) Jones and a -3 dB bandwidth (f(-3dB)) of 211.7 Hz at -1 V, whereas the PDTPTT:IDIC devices were not successful due to the high dark current density (J(D)) at negative bias. The interfacial energies of the PDTPTT:IDIC and PCPDTTT:IDIC blends were calculated by measuring the solvent contact angles and we found that the lower interfacial energy of the PCPDTTT:IDIC blends could make a well-mixed nanomorphology in the blend films, resulting in superior OPD properties. On the other hand, the shallow HOMO energy level (-4.66 eV) of PDTPTT could make substantial J(D), which showed suboptimal OPD performances.
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