Phase segregation control in mixed halide and mixed cation perovskite films: Synergistic effects of Cs and Rb (Conference Presentation)

Hoang X. Dang, Kai Wang, Masoud Ghasemi, M. De Bastiani, Detlef-Matthias Smilgies, S. De Wolf, A. Amassian
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Abstract

Mixed halide, mixed cation lead perovskite films have been demonstrated to benefit tremendously from the addition of Cs and Rb into the perovskite formulation, resulting in high performance, enhanced reproducibility and stability. However, the root cause of these effects in these complicated systems is not well understood. We address the above challenge by tracking in situ the solidification of perovskite precursors during solution-casting using time-resolved grazing incidence wide-angle X-ray scattering (GIWAXS). In doing so, we can directly link the formation or suppression of different crystalline phases to the presence of Cs and/or Rb. In the absence of these elements, the multi-component perovskite film is inherently unstable, phase segregating into a solvated MAI-rich phase and a FABr-rich phase. Adding even one of the two (Cs or Rb) is shown to alter the solidification quite dramatically, promoting different solidification pathways. Importantly, the addition of both components in the optimal ratio can drastically suppress phase segregation and promotes the spontaneous formation of the desired perovskite phase. This result is also confirmed by elemental mapping of organic cations (FA+, MA+) and halide anions (I-, Br-) via time-of-flight secondary ion mass spectroscopy (ToF-SIMS). Perovskite precursors with an optimal combination of additives (7% Cs, 3% Rb) result in solar cells with 20.1% power conversion efficiency (PCE), outperforming formulation excluding Cs and Rb (PCE=14.6%). We propose that the synergistic effect is due to the collective benefits of Cs and Rb on the formation kinetics of the perovskite phase, and on the halides redistribution throughout the film. Importantly, our study points to new design rules for tuning the crystallization pathway of multi-component hybrid perovskites.
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混合卤化物和混合阳离子钙钛矿薄膜中的相偏析控制:Cs和Rb的协同效应(会议报告)
混合卤化物、混合阳离子、混合铅钙钛矿薄膜已被证明在钙钛矿配方中添加Cs和Rb会极大地受益,从而获得高性能、增强的再现性和稳定性。然而,在这些复杂的系统中产生这些影响的根本原因尚不清楚。我们通过使用时间分辨掠入射广角x射线散射(GIWAXS)原位跟踪钙钛矿前驱体在溶液铸造过程中的凝固来解决上述挑战。这样,我们可以直接将不同晶相的形成或抑制与Cs和/或Rb的存在联系起来。在缺乏这些元素的情况下,多组分钙钛矿膜本质上是不稳定的,相分离为溶剂化的富mai相和富f - f相。结果表明,即使添加两者中的一种(Cs或Rb)也会显著改变凝固,促进不同的凝固途径。重要的是,以最佳比例添加这两种成分可以显著抑制相偏析,促进所需钙钛矿相的自发形成。通过飞行时间二次离子质谱(ToF-SIMS)对有机阳离子(FA+, MA+)和卤化物阴离子(I-, Br-)的元素映射也证实了这一结果。钙钛矿前驱体的最佳添加剂组合(7% Cs, 3% Rb)使太阳能电池的功率转换效率(PCE)达到20.1%,优于不含Cs和Rb的配方(PCE=14.6%)。我们认为这种协同效应是由于Cs和Rb对钙钛矿相的形成动力学和卤化物在整个薄膜中的再分配的共同利益。重要的是,我们的研究指出了调整多组分杂化钙钛矿结晶路径的新设计规则。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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Front Matter: Volume 11094 The crucial role of end group planarity for fused-ring electron acceptors in organic solar cells (Conference Presentation) Phase segregation control in mixed halide and mixed cation perovskite films: Synergistic effects of Cs and Rb (Conference Presentation) Aqueous processing of Ag-nanowire electrodes on top of semi-transparent perovskite solar cells (Conference Presentation) Investigations on band structure engineering in organic semiconductors (Conference Presentation)
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