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Unraveling low-temperature structural and dielectric characteristics in lead-free bismuth halide perovskites

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Peer-reviewed

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Abstract

Bismuth halide perovskite crystals have garnered a lot of interest lately because of their superior optoelectronic qualities, affordability, and ease of processing. Bismuth halide perovskite crystals have garnered a lot of interest lately because of their superior optoelectronic qualities, affordability, and ease of processing. Nonetheless, most of the research has concentrated on their room-temperature characteristics, leaving their low-temperature behavior largely unknown. Here, we have investigated the low-temperature behavior of bismuth halide perovskite crystals to understand their structural and dielectric characteristics. The low-temperature X-ray diffraction pattern revealed a sharp phase transition in MA 3 Bi 2 I 9 , a gradual phase transition in FA 3 Bi 2 I 9 and a ferroelastic phase transition in Cs 3 Bi 2 I 9 . These structural characteristics are directly mirrored and linked to the material's dielectric function. The dielectric properties of these crystals revealed that the features of the A-site cations, rather than the inorganic bioctahedral cage, have the greatest influence on the behavior of these materials. The presence of microscopic dipoles has a significant influence on the macroscopic dielectric constant, resulting in a dielectric constant hierarchy. It was found that MA 3 Bi 2 I 9 exhibits a higher value of dielectric constant than FA 3 Bi 2 I 9 and Cs 3 Bi 2 I 9 , due to the rotational dynamics of MA + ions with large dipole moments. The findings of this study would contribute to the advancement of perovskite-based optoelectronics by providing a detailed understanding of the low-temperature properties of bismuth halide perovskites with A-site cation variation.

Description

Journal Title

Journal of Materials Chemistry C

Conference Name

Journal ISSN

2050-7526
2050-7534

Volume Title

Publisher

Royal Society of Chemistry (RSC)

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Except where otherwised noted, this item's license is described as Attribution 4.0 International
Sponsorship
Royal Society (UF150033)
European Research Council (756962)