TY - JOUR
T1 - Synthesis and Opto-Electrical Properties of Novel Conjugated Small Molecule Bearing a B←N Moiety
AU - Ryu, Ka Yeon
AU - Sung, Dan Bi
AU - Kwon, Yong Ju
AU - Kim, Hyun Yeong
AU - Lee, Chongmok
AU - Kim, Won Suk
AU - Kim, Kyungkon
N1 - Publisher Copyright:
© 2020, The Polymer Society of Korea and Springer.
PY - 2020/9/1
Y1 - 2020/9/1
N2 - Effects of the B←N unit on the energy level of conjugated small molecule were investigated by synthesizing a new small molecule BPDPP (3,8-bis(5-(2,5-dioctyl-3,6-dioxo-4-(thiophen-2-yl)-2,3,5,6-tetrahydropyrrolo[3,4-c]pyrrol-1-yl)-thiophen-2-yl)-6,6-dioctyl-6H-benzo[3,4] [1,2]azaborolo[1,5-a]pyridin-5-ium-6-uide) via Suzuki coupling. For comparison, CPDPP (6,6′-(5,5′-(9,9-dioctyl-9H-fluorene-2,7-diyl)bis(thiophene-5,2-diyl))bis(2,5-dioctyl-3-(thiophen-2-yl)pyrrolo[3,4-c] pyrrole-1,4(2H,5H)-dione)) having the same chemical structure with BPDPP except the B←N unit is synthesized through the same coupling reaction. Absorption spectra and cyclovoltammetry analysis for these small molecules revealed that the B←N unit reduces the band gap of BPDPP by maintaining large oxidation potential. As a result, the blend film of BPDPP and PC71BM maintained 87.4% of the initial absorption intensity after 1sun light soaking test for 315 h. The photo stability of the BPDPP is significantly higher than the blend film of P3HT: PC71BM, which maintained only 19.8% of the initial absorption intensity only after light soaking for 23 h.[Figure not available: see fulltext.].
AB - Effects of the B←N unit on the energy level of conjugated small molecule were investigated by synthesizing a new small molecule BPDPP (3,8-bis(5-(2,5-dioctyl-3,6-dioxo-4-(thiophen-2-yl)-2,3,5,6-tetrahydropyrrolo[3,4-c]pyrrol-1-yl)-thiophen-2-yl)-6,6-dioctyl-6H-benzo[3,4] [1,2]azaborolo[1,5-a]pyridin-5-ium-6-uide) via Suzuki coupling. For comparison, CPDPP (6,6′-(5,5′-(9,9-dioctyl-9H-fluorene-2,7-diyl)bis(thiophene-5,2-diyl))bis(2,5-dioctyl-3-(thiophen-2-yl)pyrrolo[3,4-c] pyrrole-1,4(2H,5H)-dione)) having the same chemical structure with BPDPP except the B←N unit is synthesized through the same coupling reaction. Absorption spectra and cyclovoltammetry analysis for these small molecules revealed that the B←N unit reduces the band gap of BPDPP by maintaining large oxidation potential. As a result, the blend film of BPDPP and PC71BM maintained 87.4% of the initial absorption intensity after 1sun light soaking test for 315 h. The photo stability of the BPDPP is significantly higher than the blend film of P3HT: PC71BM, which maintained only 19.8% of the initial absorption intensity only after light soaking for 23 h.[Figure not available: see fulltext.].
KW - B-N containing dye
KW - organic solar cell
KW - small molecule organic solar cell
KW - stability
UR - http://www.scopus.com/inward/record.url?scp=85087444990&partnerID=8YFLogxK
U2 - 10.1007/s13233-020-8113-1
DO - 10.1007/s13233-020-8113-1
M3 - Article
AN - SCOPUS:85087444990
SN - 1598-5032
VL - 28
SP - 919
EP - 924
JO - Macromolecular Research
JF - Macromolecular Research
IS - 10
ER -