钙钛矿(结构)
材料科学
磁滞
背景(考古学)
电荷(物理)
化学物理
光电子学
纳米技术
凝聚态物理
结晶学
化学
物理
古生物学
量子力学
生物
作者
Laura Canil,Jagadish K. Salunke,Qiong Wang,Maning Liu,Hans Köbler,Marion A. Flatken,Luca Gregori,Daniele Meggiolaro,Damiano Ricciarelli,Filippo De Angelis,Martin Stolterfoht,Dieter Neher,Arri Priimägi,Paola Vivo,Antonio Abate
标识
DOI:10.1002/aenm.202101553
摘要
Abstract Interfaces play a crucial role in determining perovskite solar cells, (PSCs) performance and stability. It is therefore of great importance to constantly work toward improving their design. This study shows the advantages of using a hole‐transport material (HTM) that can anchor to the perovskite surface through halogen bonding (XB). A halo‐functional HTM (PFI) is compared to a reference HTM (PF), identical in optoelectronic properties and chemical structure but lacking the ability to form XB. The interaction between PFI and perovskite is supported by simulations and experiments. XB allows the HTM to create an ordered and homogenous layer on the perovskite surface, thus improving the perovskite/HTM interface and its energy level alignment. Thanks to the compact and ordered interface, PFI displays increased resistance to solvent exposure compared to its not‐interacting counterpart. Moreover, PFI devices show suppressed nonradiative recombination and reduced hysteresis, with a V oc enhancement of ≥20 mV and a remarkable stability, retaining more than 90% efficiency after 550 h of continuous maximum‐power‐point tracking. This work highlights the potential that XB can bring to the context of PSCs, paving the way for a new halo‐functional design strategy for charge‐transport layers, which tackles the challenges of charge transport and interface improvement simultaneously.
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