Raji Ibrahim Oladayo, Wen Shuguang, Li Yonghai, Huang Da, Shi Xiaoyan, Saparbaev Aziz, Gu Chuantao, Yang Chunming, Bao Xichang
CAS Key Laboratory of Bio-based Materials, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Qingdao 266101, China.
University of Chinese Academy of Sciences, Beijing 100049, China.
ACS Appl Mater Interfaces. 2021 Aug 4;13(30):36071-36079. doi: 10.1021/acsami.1c07822. Epub 2021 Jul 20.
Alkylthio groups can be used to modulate energy levels and molecular packing of organic semiconductors, which makes it important in the design of materials for organic solar cell. However, its effect has not been sufficiently exploited as most of the studies report introducing an alkylthio group to the donor unit and seldom to the acceptor unit of donor-acceptor conjugated polymers. In this report, two alkylthio-substituted polymers, namely, PBB-TSA and PBB-TSD, with benzo1,2-:4,5-' (BBT) as the acceptor unit and benzo[1,2-:4,5-']dithiophene (BDT) as the donor unit, were rationally designed, synthesized, and applied in organic photovoltaics. An alkylthio side chain was substituted on the BBT-accepting unit for PBB-TSA, while for PBB-TSD, the alkylthio side chain was substituted on the BDT donor unit. PBB-TSA and PBB-TSD show upshifted and downshifted energy levels, respectively, compared to the nonsulfur-substituted material. Both polymers exhibit dominate face-on orientation, while PBB-TSD exhibits higher crystallinity compared to PBB-TSA. With the contribution of lower energy level and beneficial film morphology, the device based on PBB-TSD/IT-4F has much higher power conversion efficiency (PCE) of 14.6%, whereas the PBB-TSA blend had a lower PCE of 10.7%. 1,8-Diiodooctane can effectively optimize the blend film morphology, and the effect on device performance has also been demonstrated in detail. This result indicates that introducing an alkylthio side chain into the donor or acceptor moieties would result in materials with different energy levels and thus would be utilized to match with various acceptors, achieving optimized performance in organic solar cells.
烷硫基可用于调节有机半导体的能级和分子堆积,这使其在有机太阳能电池材料设计中具有重要意义。然而,其作用尚未得到充分利用,因为大多数研究报告的是将烷硫基引入给体单元,而很少引入给体-受体共轭聚合物的受体单元。在本报告中,合理设计、合成了两种以苯并[1,2-:4,5-']噻唑(BBT)为受体单元、苯并[1,2-:4,5-']二噻吩(BDT)为给体单元的烷硫基取代聚合物,即PBB-TSA和PBB-TSD,并将其应用于有机光伏领域。对于PBB-TSA,烷硫基侧链取代在BBT受体单元上;而对于PBB-TSD,烷硫基侧链取代在BDT给体单元上。与无硫取代材料相比,PBB-TSA和PBB-TSD分别表现出能级上移和下移。两种聚合物均呈现主导的面取向,而PBB-TSD与PBB-TSA相比具有更高的结晶度。由于较低的能级和良好的薄膜形态,基于PBB-TSD/IT-4F的器件具有高达14.6%的功率转换效率(PCE),而PBB-TSA共混物的PCE较低,为10.7%。1,8-二碘辛烷可有效优化共混薄膜形态,并且对器件性能的影响也已得到详细证明。该结果表明,将烷硫基侧链引入给体或受体部分会导致具有不同能级的材料,从而可用于与各种受体匹配,在有机太阳能电池中实现优化性能。