Abstract
The pressure-induced structural evolution of formamidinium-based perovskite FAPbI3 was investigated using in situ synchrotron X-ray diffraction and laser-excited photoluminescence methods. Cubic α-FAPbI3 (Pm3m) partially and irreversibly transformed to hexagonal δ-FAPbI3 (P63mc) at a pressure less than 0.1 GPa. Structural transitions of α-FAPbI3 followed the sequence of Pm3m → P4/mbm → Im3 → partial amorphous during compression to 6.59 GPa, whereas the δ-phase converted to an orthorhombic Cmc21 structure between 1.26 and 1.73 GPa. During decompression, FAPbI3 recovered the P63mc structure of the δ-phase as a minor component (∼18 wt %) from 2.41-1.40 GPa and the Pm3m structure of the α-phase becomes dominant (∼82 wt %) at 0.10 GPa but with an increased fraction of δ-FAPbI3. The photoluminescence behaviors from both the α- and δ-forms were likely controlled by radiative recombination at the defect levels rather than band-edge emission during pressure cycling. FAPbI3 polymorphism is exquisitely sensitive to pressure. While modest pressures can engineer FAPbI3-based photovoltaic devices, irreversible δ-phase crystallization may be a limiting factor and should be taken into account.
Original language | English |
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Pages (from-to) | 13952-13957 |
Number of pages | 6 |
Journal | Journal of the American Chemical Society |
Volume | 140 |
Issue number | 42 |
DOIs | |
Publication status | Published - Oct 24 2018 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:Copyright © 2018 American Chemical Society.
ASJC Scopus Subject Areas
- Catalysis
- General Chemistry
- Biochemistry
- Colloid and Surface Chemistry