卤化物
钙钛矿(结构)
纳米
化学
开尔文探针力显微镜
纳米尺度
结晶
纳米技术
碘化物
分析化学(期刊)
化学物理
矿物学
化学工程
结晶学
原子力显微镜
材料科学
无机化学
工程类
色谱法
作者
Paul Gratia,Giulia Grancini,Johannes M. C. Mol,Xavier A. Jeanbourquin,Edoardo Mosconi,Iwan Zimmermann,David Dowsett,Yonghui Lee,Michael Grätzel,Filippo De Angelis,Kevin Sivula,Tom Wirtz,Mohammad Khaja Nazeeruddin
摘要
Compositional engineering of a mixed cation/mixed halide perovskite in the form of (FAPbI3)0.85(MAPbBr3)0.15 is one of the most effective strategies to obtain record-efficiency perovskite solar cells. However, the perovskite self-organization upon crystallization and the final elemental distribution, which are paramount for device optimization, are still poorly understood. Here we map the nanoscale charge carrier and elemental distribution of mixed perovskite films yielding 20% efficient devices. Combining a novel in-house-developed high-resolution helium ion microscope coupled with a secondary ion mass spectrometer (HIM-SIMS) with Kelvin probe force microscopy (KPFM), we demonstrate that part of the mixed perovskite film intrinsically segregates into iodide-rich perovskite nanodomains on a length scale of up to a few hundred nanometers. Thus, the homogeneity of the film is disrupted, leading to a variation in the optical properties at the micrometer scale. Our results provide unprecedented understanding of the nanoscale perovskite composition.
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