结晶
材料科学
钙钛矿(结构)
离子液体
化学工程
离子键合
工程物理
工艺工程
离子
化学
工程类
有机化学
催化作用
作者
Shiying Tang,Yunsheng Gou,Deng Chen,Chunlong Yuan,Pan Zhao,Can Li,Jingyu Chen,Haimin Li,Hua Yu
出处
期刊:Solar RRL
[Wiley]
日期:2025-03-18
卷期号:9 (10)
被引量:3
标识
DOI:10.1002/solr.202500104
摘要
The premature reaction of PbI 2 with organic cations in perovskite (PVK) precursor solutions often leads to compromised film quality. To mitigate this, the ionic liquid (IL) pyridinium trifluoromethanesulfonate is introduced into the precursor solution. The strong interaction between pyridinium trifluoromethanesulfonate and PbI 2 promotes the formation of nucleation clusters, effectively lowering the nucleation barrier and regulating the crystallization of perovskite, resulting in high‐quality, homogeneous PVK films. In situ characterization shows that the prenucleation strategy yields PVK films with an average grain size exceeding 1 μm. The hydrophobicity of the trifluoromethyl group modulates humidity, facilitating perovskite crystallization in moist environments. This is in contrast to the typical negative effects of moisture, which can induce defects in perovskite structures. As a result, IL‐modified perovskite solar cells (PSCs) achieved a remarkable power conversion efficiency (PCE) of 25.11% under ambient conditions. These PSCs retained 80.43% of their initial PCE after 820 h of continuous maximum power point (MPP) tracking. Furthermore, after 1000 h of exposure to air with 30%–50% relative humidity (RH) at room temperature, the devices maintained 87% of their initial efficiency, demonstrating excellent air stability for long‐term PSC applications.
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