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A new non-fullerene acceptor based on the combination of a heptacyclic benzothiadiazole unit and a thiophene-fused end group achieving over 13% efficiency.
Zhang, Yunqiang; Cai, Fangfang; Yuan, Jun; Wei, Qingya; Zhou, Liuyang; Qiu, Beibei; Hu, Yunbin; Li, Yongfang; Peng, Hongjian; Zou, Yingping.
Affiliation
  • Zhang Y; College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, China. hongjianpeng@126.com yingpingzou@csu.edu.cn.
Phys Chem Chem Phys ; 21(48): 26557-26563, 2019 Dec 11.
Article in En | MEDLINE | ID: mdl-31782431
A new non-fullerene acceptor, namely Y10, based on dithienothiophen[3,2-b]-pyrrolobenzothiadiazole (TPBT) as the central core and 2-(6-oxo-5,6-dihydro-4H-cyclopenta[c]thiophen-4-ylidene)malononitrile (TC) as the electron-deficient end group, has been designed and synthesized. Y10 reveals a narrow optical energy gap (Eoptg) of 1.35 eV with a broad absorption band from 600 to 900 nm. A wide bandgap polymer, J11, as the donor material (Eoptg = 1.96 eV) is used to blend with Y10 for the construction of organic solar cell devices, which achieve an impressive power conversion efficiency (PCE) of 13.46% with an open circuit voltage (Voc) of 0.89 V, a short circuit current (Jsc) of 21.21 mA cm-2, and a fill factor (FF) of 71.55%, with thermal annealing treatment at 100 °C for 5 min and 0.8 wt% 1-chloronaphthalene (CN) as an additive. These results indicate that the incorporation of the TPBT unit as the central core and the TC unit as the electron-deficient end group provides an efficient strategy for the construction of high performance solar cells.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Phys Chem Chem Phys Journal subject: BIOFISICA / QUIMICA Year: 2019 Document type: Article Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Phys Chem Chem Phys Journal subject: BIOFISICA / QUIMICA Year: 2019 Document type: Article Country of publication: United kingdom