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The influence of the terminal acceptor and oligomer length on the photovoltaic properties of A-D-A small molecule donors

机译:终端受体和低聚物长度对A-D-A小分子供体的光伏性能的影响

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Four new A-D-A small molecules (denoted as FG1-4) have been designed and synthesized. The compounds have cyclopentadithiophene-vinylene (CPDTV) oligomers of different lengths as the central donor core linked with different terminal acceptor units (3-ethylrhodanine or dicyanomethylene-3-ethylrhodanine). The effects that conjugation length and terminal acceptor units have on the optical and electrochemical properties were investigated. These small molecules were used as donors in conjunction with PC71BM as an acceptor in the bulk heterojunction active layer for the fabrication of solution-processed organic solar cells. Solvent vapor annealing treatment improved the crystallinity and the interpenetrating networks of donor and acceptor phases for exciton dissociation and charge transfer, thus leading to significant improvements in the overall power conversion efficiency (PCE) of the organic solar cells. The PCE values for the organic solar cells based on the optimized FG1:PC71BM, FG2:PC71BM, FG3:PC71BM and FG4:PC71BM active layer were 5.58%, 6.99%, 7.51% and 8.43%, respectively. These results indicate that an enhancement in the PCE of small molecule organic solar cells can be achieved by an increase in conjugation-length and variation of terminal acceptor units in the molecular backbone of small molecules and optimization of the crystallinity and nanoscale interpenetrating morphology by appropriate solvent vapor annealing treatment.
机译:设计和合成了四种新的A-D-A小分子(表示为FG1-4)。该化合物具有不同长度的环戊二噻吩 - 乙烯烯 - 乙烯烯(CPDTV)低聚物,作为与不同末端受体单元(3-乙基硼胺或二氰基甲基-3-乙酸二乙酸二乙酸二乙酸二乙酸)连接的中央供体芯。研究了共轭长度和终端受体单元对光学和电化学性质的影响。将这些小分子与PC71BM一起用作供体,作为散装异质结的受体中的受体,用于制造溶液加工的有机太阳能电池。溶剂蒸汽退火处理改善了施主和受体阶段的结晶度和渗透网络,用于激子解离和电荷转移,从而导致有机太阳能电池的总功率转换效率(PCE)显着改善。基于优化的FG1:PC71BM,FG2:PC71BM,FG3:PC71BM和FG4:PC71BM活性层的PCE值分别为5.58%,6.99%,7.51%和8.43%。这些结果表明,小分子有机太阳能电池的PCE中的增强可以通过增加小分子的分子骨干中的末端受体单元的缀合长度和变化来实现,并通过适当的溶剂优化结晶度和纳米级渗透性形态蒸汽退火处理。

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