Yu Wei, Cheng Xiafei, Chen Qiaoyun, Zhang Zelong, Zhou Junjie, Wang Rui, Nie Xiaoting, Zhang Jing, Ji Wenxi, Zhou Yi, Song Bo
College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, P. R. China.
Laboratory of Advanced Optoelectronic Materials, Suzhou Key Laboratory of Novel Semiconductor-optoelectronics Materials and Devices, Suzhou 215123, P. R. China.
ACS Appl Mater Interfaces. 2025 Jul 9;17(27):39270-39280. doi: 10.1021/acsami.5c09273. Epub 2025 Jun 24.
Hole-transport materials (HTMs) are essential for the efficient extraction and transport of holes from the perovskite layer to the electrodes, thus playing a crucial role in enhancing the performance of perovskite solar cells (PSCs). The introduction of halogens into the polymer-based HTMs contributes to the excellent charge transport and photovoltaic properties of the devices, which provides a promising avenue for improving PSC performance. In this study, three polymer-based HTMs, PM-2F (PM6), PM-4F, and PM-4Cl, were synthesized by strategically incorporating different numbers and types of halogen atoms. These polymers feature thiophene-substituted benzodithiophene (BDT-T) donor units and benzodithiophene-4,8-dione (BDD) acceptor units, along with longitudinal side-chain conjugation extensions. The effect of varying numbers and types of halogen atoms on the properties of HTMs and device performance was systematically investigated. The results indicated that PM-2F and PM-4F, which contain fluorine atoms in the branched chains, exhibit lower highest occupied molecular orbital energy levels, enhanced hole mobility, and superior electrical conductivity compared to PM-4Cl, which incorporates chlorine atoms in the branched chains. Therefore, due to the highest charge transport ability, energy levels highly compatible with perovskite materials, and effective defect passivation, the fluorine-substituted PM-2F and PM-4F achieved device efficiencies of 24.27 and 21.08%, respectively, with PM-2F outperforming PM-4F due to reduced fluorine-induced steric hindrance and optimized energy alignment. Furthermore, after 3500 h in a N environment, devices based on fluorine-substituted groups maintained 85% of their initial efficiency, while devices based on chlorine-substituted groups showed a decrease to approximately 30% of their initial efficiency after only 700 h. The findings suggest that fluorine-substituted organic HTLs have a significant effect on the photovoltaic performance of PSCs, highlighting their potential in developing high-performance organic HTMs for future applications.
空穴传输材料(HTMs)对于将空穴从钙钛矿层高效提取并传输到电极至关重要,因此在提高钙钛矿太阳能电池(PSC)的性能方面起着关键作用。将卤素引入基于聚合物的HTMs中有助于器件具有优异的电荷传输和光伏性能,这为提高PSC性能提供了一条有前景的途径。在本研究中,通过策略性地引入不同数量和类型的卤素原子,合成了三种基于聚合物的HTMs,即PM-2F(PM6)、PM-4F和PM-4Cl。这些聚合物具有噻吩取代的苯并二噻吩(BDT-T)供体单元和苯并二噻吩-4,8-二酮(BDD)受体单元,以及纵向侧链共轭延伸。系统研究了不同数量和类型的卤素原子对HTMs性能和器件性能的影响。结果表明,与在支链中引入氯原子的PM-4Cl相比,在支链中含有氟原子的PM-2F和PM-4F表现出更低的最高占据分子轨道能级、增强的空穴迁移率和优异的电导率。因此,由于电荷传输能力最高、与钙钛矿材料的能级高度兼容以及有效的缺陷钝化,含氟取代的PM-2F和PM-4F分别实现了24.27%和21.08%的器件效率,由于氟诱导的空间位阻减小和能量排列优化,PM-2F的性能优于PM-4F。此外,在氮气环境中放置3500小时后,基于氟取代基团的器件保持了其初始效率的85%,而基于氯取代基团的器件在仅700小时后就降至其初始效率的约30%。这些发现表明,氟取代的有机HTLs对PSC的光伏性能有显著影响,突出了它们在开发用于未来应用的高性能有机HTMs方面的潜力。