1. Donor End-Capped Hexafluorinated Oligomers for Organic Solar Cells with 9.3% Efficiency by Engineering the Position of π-Bridge and Sequence of Two-Step Annealing
- Author
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Ru-Bo Zhang, Yu-Qing Zheng, Jin-Hu Dou, Hongbin Wu, Jian Pei, Jin-Liang Wang, Yong Cao, Fei Xiao, Zheng-Feng Chang, Sha Liu, and Kai-Kai Liu
- Subjects
Fabrication ,Materials science ,Organic solar cell ,Annealing (metallurgy) ,Atomic force microscopy ,General Chemical Engineering ,Two step ,02 engineering and technology ,General Chemistry ,010402 general chemistry ,021001 nanoscience & nanotechnology ,01 natural sciences ,0104 chemical sciences ,Crystallography ,chemistry.chemical_compound ,chemistry ,Materials Chemistry ,Thiophene ,Organic chemistry ,0210 nano-technology - Abstract
A pair of isomeric hexafluorinated oligomers (Th6FSe and Se6FTh), which are with the same aromatic compositions (difluorobenzothiadiazoles central core, IDT units, and donor end-capped groups), but differ in the π-bridge position (selenophene and thiophene), were designed and successfully synthesized. The potential of the resulted oligomers as donor materials for BHJ-OSCs was systematically investigated through optical absorption, AFM, TEM, GIXD, charge mobility measurement, and photovoltaic device fabrication. It was found that the π-bridge sequences in the resulted oligomers play a subtle but key role in device performances. Moreover, as a result of increase of crystalline content and desired phase separation after rapid SVA or combined TA and SVA treatment, the device performance of the resultant devices undergo significant enhancement. Notably, the Se6FTh devices showed a best PCE of ca. 9.3% with SVA+TA treatment, which is the highest PCE of BHJ-OSCs based on donor end-capped oligomers. These primary...
- Published
- 2017