Joule
Volume 1, Issue 3, 15 November 2017, Pages 548-562
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Article
Layer-by-Layer Degradation of Methylammonium Lead Tri-iodide Perovskite Microplates

https://doi.org/10.1016/j.joule.2017.08.005Get rights and content
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Highlights

  • An in situ TEM study reveals atomistic pathway of thermal degradation in MAPbI3

  • A surface reaction initiated layer-by-layer degradation model is discovered

  • Encapsulation by BN can restrain the surface reaction and retard the degradation

  • Theoretical calculations confirm the encapsulation slows down degradation rate

Context & Scale

The organolead halide perovskites have shown extraordinary potential for low-cost solution-processable photovoltaic devices, with the power conversion efficiency rapidly soaring beyond 20%. However, the perovskite devices today are generally plagued by their poor environmental and thermal instability, and the atomistic mechanism for the thermal degradation remains largely unexplored. Here we report a systematic in situ transmission electron microscopy investigation of perovskite structure transition at 85°C. Along with theoretical calculations, we discover a surface reaction initiated layer-by-layer degradation pathway during the MAPbI3 perovskite thermal degradation. Based on this finding, we developed a strategy using few-layer hBN encapsulation to restrain the surface reaction and thus considerably improve the thermal stability. This work reveals the atomistic pathway of perovskite structure evolution under heating and suggests a potential strategy for creating perovskite devices with improved stability.

Summary

The methylammonium lead iodide (MAPbI3) perovskite has attracted considerable interest for its high-efficiency, low-cost solar cells, but is currently plagued by its poor environmental and thermal stability. To aid the development of robust devices, we investigate here the microscopic degradation pathways of MAPbI3 microplates. Using in situ transmission electron microscopy to follow the thermal degradation process, we find that under moderate heating at 85°C the crystalline structure shows a gradual evolution from tetragonal MAPbI3 to trigonal lead iodide layered crystals with a fixed crystallographic direction. Our solid-state nudged elastic band calculations confirm that the surface-initiated layer-by-layer degradation path exhibits the lowest energy barrier for crystal transition. We further show experimentally and theoretically that encapsulation of the perovskites with boron nitride flakes suppresses the surface degradation, greatly improving its thermal stability. These studies provide mechanistic insight into the thermal stability of perovskites that suggests new designs for improved stability.

Keywords

hybrid perovskite
thermal stability
in situ TEM

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These authors contributed equally

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