Source abstract
Abstract
High Resolution Image Download MS PowerPoint Slide Thermal annealing on hybrid perovskites is essential to prepare high-quality solar cells with extraordinary efficiency, whose benefits include transformation of inactive phases such as δ-FAPbI 3 to active α-FAPbI 3 . The detailed mechanism for such critical phase transition, however, has not yet been adequately studied. Here, we present multiscale microscopic observation to unravel the anisotropic δ-to-α transition in epitaxial FAPbI 3 thin films. We adopt polarized light microscopy that offers enhanced contrast to distinguish isotropic α-FAPbI 3 from the anisotropic δ-FAPbI 3 . Facilitated by in situ heating, it allows us to identify heterogeneous nucleation of α-FAPbI 3 and the subsequent diffusional phase transition preferentially occurring along ⟨0001⟩, which is underpinned by the smaller activation energy along the face-sharing direction of PbI 6 octahedra. We further reveal the morphology and orientation relationship at the δ-to-α transition front using four-dimensional scanning transmission electron microscopy (4D-STEM), evincing the surface energy dominated orientation rather than the interfacial energy. The presence of high-density planar defects is also discovered at the transition front, which can be considered as an intermediate state facilitating δ-to-α structure transformation. Besides filling the knowledge gap on the phase transition behavior in FAPbI 3, our work also demonstrates a multiscale microscopy approach to interrogate the phase transition mechanism in hybrid perovskites.
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Affiliations
Department of Applied Physics, Research Institute for Smart Energy, The Hong Kong Polytechnic University, Hung Hom, Kowloon 00000, Hong Kong, China
Department of Applied Physics, The Hong Kong Polytechnic University, Hung Hom, Kowloon 310028, Hong Kong, China
Department of Electrical and Electronic Engineering, Research Institute for Smart Energy, Photonic Research Institute, The Hong Kong Polytechnic University, Hung Hom, Kowloon 310028, Hong Kong, China
Funding
Research Grants Council of Hong Kong · CRF · Hong Kong Polytechnic University