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Unraveling the Elastic Properties of (Quasi)Two-Dimensional Hybrid Perovskites: A Joint Experimental and Theoretical Study
Author(s) -
Marcos Reyes-Martinez,
Peng Tan,
Arvin Kakekhani,
Sayan Banerjee,
Ayan A. Zhumekenov,
Wei Peng,
Osman M. Bakr,
Andrew M. Rappe,
YuehLin Loo
Publication year - 2020
Publication title -
acs applied materials and interfaces
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.535
H-Index - 228
eISSN - 1944-8252
pISSN - 1944-8244
DOI - 10.1021/acsami.0c02327
Subject(s) - materials science , van der waals force , density functional theory , nanoindentation , ionic bonding , mesoscopic physics , elastic modulus , condensed matter physics , stiffness , chemical physics , nanotechnology , computational chemistry , composite material , physics , molecule , chemistry , quantum mechanics , ion
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 ab initio 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) 2 PbI 4 (MAPbI 3 ) n -1 , and their 3D counterpart, MAPbI 3 . 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 ( n ) 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 ab initio 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.

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