Reyes-Martinez Marcos A, Tan Peng, Kakekhani Arvin, Banerjee Sayan, Zhumekenov Ayan A, Peng Wei, Bakr Osman M, Rappe Andrew M, Loo Yueh-Lin
Chemical and Biological Engineering, Princeton University, Princeton, New Jersey 08544-5263, United States.
Department of Chemistry, University of Pennsylvania, Philadelphia, Pennsylvania 19104-6323, United States.
ACS Appl Mater Interfaces. 2020 Apr 15;12(15):17881-17892. doi: 10.1021/acsami.0c02327. Epub 2020 Mar 31.
The unique properties of hybrid organic-inorganic perovskites (HOIPs) promise to open doors to next-generation flexible optoelectronic devices. Before such advances are realized, a fundamental understanding of the mechanical properties of HOIPs is required. Here, we combine density functional theory (DFT) modeling with a diverse set of experiments to study the elastic properties of (quasi)2D HOIPs. Specifically, we focus on (quasi)2D single crystals of phenethylammonium methylammonium lead iodide, (PEA)PbI(MAPbI), and their 3D counterpart, MAPbI. We used nanoindentation (both Hertzian and Oliver-Pharr analyses) in combination with elastic buckling instability experiments to establish the out-of-plane and in-plane elastic moduli. The effect of Van der Waals (vdW) forces, different interlayer interactions, and finite temperature are combined with DFT calculations to accurately model the system. Our results reveal a nonmonotonic dependence of both the in-plane and out-of plane elastic moduli on the number of inorganic layers () rationalized by first-principles calculations. We discuss how the presence of defects in as-grown crystals and macroscopic interlayer deformations affect the mechanical response of (quasi)2D HOIPs. Comparing the in- and out-of-plane experimental results with the theory reveals that perturbations to the covalent and ionic bonds (which hold a 2D layer together) is responsible for the relative out-of-plane stiffness of these materials. In contrast, we conjecture that the in-plane softness originates from macroscopic or mesoscopic motions between 2D layers during buckling experiments. Additionally, we learn how dispersion and π interactions in organic bilayers can have a determining role in the elastic response of the materials, especially in the out-of-plane direction. The understanding gained by comparing and experimental techniques paves the way for rational design of layered HOIPs with mechanical properties favorable for strain-intensive applications. Combined with filters for other favorable criteria, e.g., thermal or moisture stability, one can systematically screen viable (quasi)2D HOIPs for a variety of flexible optoelectronic applications.
有机-无机杂化钙钛矿(HOIPs)的独特性质有望为下一代柔性光电器件打开大门。在实现这些进展之前,需要对HOIPs的机械性能有基本的了解。在此,我们将密度泛函理论(DFT)建模与多种实验相结合,以研究(准)二维HOIPs的弹性性质。具体而言,我们专注于苯乙铵甲基铵碘化铅(PEA)PbI(MAPbI)的(准)二维单晶及其三维对应物MAPbI。我们使用纳米压痕(赫兹分析和奥利弗-法尔分析)结合弹性屈曲不稳定性实验来确定面外和面内弹性模量。将范德华(vdW)力、不同的层间相互作用和有限温度的影响与DFT计算相结合,以准确模拟该系统。我们的结果揭示了面内和面外弹性模量对无机层数()的非单调依赖性,这通过第一性原理计算得到了合理的解释。我们讨论了生长晶体中的缺陷和宏观层间变形的存在如何影响(准)二维HOIPs的机械响应。将面内和面外实验结果与理论进行比较表明,对将二维层结合在一起的共价键和离子键的扰动是这些材料相对面外刚度的原因。相比之下,我们推测面内柔软性源于屈曲实验中二维层之间的宏观或介观运动。此外,我们了解到有机双层中的色散和π相互作用如何在材料的弹性响应中起决定性作用,特别是在面外方向。通过比较理论和实验技术所获得的理解为合理设计具有有利于应变密集型应用的机械性能的层状HOIPs铺平了道路。结合用于其他有利标准(例如热稳定性或湿度稳定性)的过滤器,可以系统地筛选适用于各种柔性光电器件应用的可行(准)二维HOIPs。