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Articles

Design and synthesis of small molecules with difluoroquinoxaline units for OSCs

, , , , , , , & show all
Pages 79-86 | Published online: 18 Sep 2020
 

Abstract

We designed and synthesized three novel small molecule donors (SM1, SM2 and SM3) that consist of thiophene as the electron-donating end group and 6,​7-​difluoroquinoxaline moiety as a novel electron-withdrawing core group. The organic low band gap molecules with 6,​7-​difluoroquinoxaline and thiophene units were synthesized using Stille coupling to generate SM1, SM2 and SM3. The absorption of SM2 and SM3 in solution was red shifted due to increased conjugation length of added thiophene units. In case of SM2 and SM3, introduction of hexyl chain in terminal thiophene units improve solubility in organic solvent. The maximum absorption peaks of SM1, SM2 and SM3 in solid thin films were at 482, 505 and 518 nm, respectively. SM3 was red shifted as compare to SM2 due to increased π-π stacking of electron donor materials.

Additional information

Funding

This research was supported by the BB21+ Project in 2020, and the Korea Institute of Energy Technology Evaluation and Planning (KETEP) and the Ministry of Trade, Industry & Energy (MOTIE) of the Republic of Korea (No. 20194010201840).

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