Nisa Qurrotun Ayuni Khoirun, Son Dong Hwan, Nasrun Rahmatia Fitri Binti, Kim Joo Hyun
Department of Polymer Engineering, Pukyong National University, Busan 48513, Korea.
CECS Research Institute, Core Research Institute, Busan 48513, Korea.
ACS Appl Mater Interfaces. 2025 Aug 6;17(31):45234-45248. doi: 10.1021/acsami.5c11948. Epub 2025 Jul 26.
As an interface engineering method for high-performance inverted perovskite solar cells (PSCs), self-assembled monolayers (SAMs) with hole-transport properties have been used to reduce energy losses at the hole-transport layer/perovskite interface. However, the application of -butyl carbazole-based SAMs has been limited by poor wettability of the perovskite precursor on the carbazole surface. To address this, a self-assembled bilayer (SAB) comprising a novel -butyl functionalized CBZC2 SAM and a conjugated polyelectrolyte wetting layer (PFN-Br) is proposed as the hole-transport layer (HTL) in CsI.FA.MA.Pb(I.Br.) PSCs. The steric hindrance of the bulky -butyl group prevents aggregation and enhances hole extraction efficiency while reducing interfacial recombination losses. Notably, the -butyl carbazole SAB mitigates the stability issues of MeO-2PACz, leading to outstanding stability. CBZC2/PFN-Br-based PSCs achieved 24.1% efficiency, outperforming CBZC4/PFN-Br and MeO-2PACz. These devices showed a higher fill factor of 81.5%, compared to 73.8% for MeO-2PACz control based devices, and retained 96% of their initial efficiency after 500 h of maximum power point tracking. They also retained 90% and 85% efficiency after long-term stability test for 30 days at room temperature and under 85 °C heat exposure in nitrogen, respectively. These results highlight the potential of the -butyl carbazole SAM for the realization of high-performance PSCs.
作为高性能倒置钙钛矿太阳能电池(PSC)的一种界面工程方法,具有空穴传输特性的自组装单分子层(SAM)已被用于减少空穴传输层/钙钛矿界面处的能量损失。然而,基于丁基咔唑的SAM的应用受到钙钛矿前驱体在咔唑表面润湿性差的限制。为了解决这个问题,提出了一种由新型丁基功能化的CBZC2 SAM和共轭聚电解质润湿层(PFN-Br)组成的自组装双层(SAB),作为CsI.FA.MA.Pb(I.Br.)PSC中的空穴传输层(HTL)。庞大的丁基的空间位阻防止了聚集,提高了空穴提取效率,同时减少了界面复合损失。值得注意的是,丁基咔唑SAB减轻了MeO-2PACz的稳定性问题,从而具有出色的稳定性。基于CBZC2/PFN-Br的PSC实现了24.1%的效率,优于CBZC4/PFN-Br和MeO-2PACz。与基于MeO-2PACz对照的器件的73.8%相比,这些器件显示出更高的填充因子81.5%,并且在最大功率点跟踪500小时后保留了其初始效率的96%。在室温下进行30天的长期稳定性测试以及在氮气中85°C热暴露后,它们分别还保留了90%和85%的效率。这些结果突出了丁基咔唑SAM在实现高性能PSC方面的潜力。