钙钛矿(结构)
材料科学
磺酸盐
晶体生长
Crystal(编程语言)
接口(物质)
化学工程
光电子学
纳米技术
结晶学
复合材料
钠
计算机科学
化学
工程类
冶金
毛细管作用
程序设计语言
毛细管数
作者
Yuzhen Lv,Huifang Han,Huijing Liu,Xueqi Zhang,Yao Fu,Kun Lang,Zhen Sun,Xiaofei Zeng,Yihang Wei,Yahan Wu,Zhixue Li,Xu Pan,Xu Jia,Jianxi Yao
标识
DOI:10.1002/aenm.202502006
摘要
Abstract All inorganic CsPbI 3 perovskites have attracted significant attention due to their excellent thermal stability and ideal bandgap characteristics. However, interfacial defects at the perovskite/electron transport layer (ETL) interface and uncontrolled crystallization processes of the perovskite remain critical bottlenecks for advancing device performance. Herein, a multifunctional buried interface‐modifying additive, pentafluoroaniline trifluoromethane sulfonate (PFAT), is employed. Analytical results confirm that PFAT can effectively anchor at the TiO 2 /perovskite interface while passivating defects in both layers, thereby suppressing interfacial recombination losses. Furthermore, this modification can reduce the surface energy of the CsPbI 3 crystal plane, promoting perovskite crystallization and yielding films with enhanced crystallinity. To strengthen PFAT‐perovskite interactions, a PFAT‐PbI 2 hybrid solution (PFATLI) is synthesized for interfacial modification. Consequently, the optimized PFATLI‐modified device achieved a power conversion efficiency (PCE) of 21.36%, an open‐circuit voltage ( V OC ) of 1.23 V, and a fill factor (FF) of 83.44%. For the larger‐area devices with an active area of 1 cm 2 , the PCE reached 17.41%, while under the weak illumination conditions, the PCE further increased to 41.27%. After 800 h of storage in an ambient environment with 5% relative humidity (RH) at room temperature (RT), the unencapsulated device retained 87.27% of its initial efficiency.
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