照亮过氧化物钝化层的演变过程

Marcin Giza, Aleksey Kozikov, Paula L. Lalaguna, Jake D. Hutchinson, Vaibhav Verma, Benjamin Vella, Rahul Kumar, Nathan Hill, Dumitru Sirbu, Elisabetta Arca, Noel Healy, Rebecca L. Milot, Malcolm Kadodwala, Pablo Docampo
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引用次数: 0

摘要

用层状对应材料对包晶石材料进行表面处理,已成为最大限度提高器件性能的普遍策略。虽然层状材料通过钝化缺陷和表面陷阱,对所产生的器件堆栈的寿命和长期效率大有裨益,但之前的大量报告显示,这些材料在暴露于光线和湿度下会发生变化,表明它们并不完全稳定。因此,研究这些材料在孤立和模拟器件堆栈条件下的行为至关重要。本文显示,在光照、溶剂和湿度等包晶制造过程中常见的条件下,由一系列阳离子模板在碘化甲铵铅之上的包晶封盖层会发生变化。光物理、结构和形态研究表明,这些层状包晶石的降解是通过针孔介导的自限制机制发生的。这导致整个包晶薄片的损失,从几个单层到几十纳米的材料,直到系统再次稳定,正如 PEA2PbI4 剥离薄片所证明的那样。这意味着最初的目标结构可能已经发生变化,这对设备制造的优化具有明显的影响。
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Illuminating the Devolution of Perovskite Passivation Layers
Surface treatment of perovskite materials with their layered counterparts has become an ubiquitous strategy for maximizing device performance. While layered materials confer great benefits to the longevity and long-term efficiency of the resulting device stack via passivation of defects and surface traps, numerous reports have previously demonstrated that these materials evolve under exposure to light and humidity, suggesting that they are not fully stable. Therefore, it is crucial to study the behavior of these materials in isolation and in conditions mimicking a device stack. Here, it is shown that perovskite capping layers templated by a range of cations on top of methylammonium lead iodide devolve in conditions commonly found during perovskite fabrication, such as exposure to light, solvent, and moisture. Photophysical, structural, and morphological studies are used to show that the degradation of these layered perovskites occurs via a self-limiting, pinhole-mediated mechanism. This results in the loss of whole perovskite sheets, from a few monolayers to tens of nanometers of material, until the system stabilizes again as demonstrated for exfoliated flakes of PEA2PbI4. This means that initially targeted structures may have devolved, with clear optimization implications for device fabrication.
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