FA2PbBr4: synthesis, structure and unusual optical properties of two polymorphs of formamidinium-based layered (110) hybrid perovskite

TL;DR

This study reports the discovery and detailed analysis of two novel layered FA2PbBr4 polymorphs with unique optical properties, expanding understanding of formamidinium-based hybrid perovskites and their potential applications.

Contribution

The paper introduces two new polymorphs of FA2PbBr4, elucidates their structure, formation conditions, and optical properties, and demonstrates their potential for green photoluminescence.

Findings

FA2PbBr4 exists as two polymorphs with distinct layer arrangements.

FA2PbBr4 can form composites with FAPbBr3 3D perovskite.

UV irradiation induces green photoluminescence in FA2PbBr4.

Abstract

Small cations such as guanidinium and cesium can act as templating cations to form low dimensional phases (2D, 1D, 0D) in the case of excess of organic halides. However, such phases with the widely used formamidinium (FA+) cation have not been reported so far. In this study, we discovered two novel low dimensional phases with a composition of FA2PbBr4 and investigated the prerequisites of their formation upon crystallization of FABr-excessive solutions of FAPbBr3. We found that both phases have the structure of (110) layered perovskite but are represented by two different polymorphs with eclipsed and staggered arrangement of adjacent layers. It was shown that FA2PbBr4 phases usually exist in a labile equilibrium with FAPbBr3 3D perovskite and can form composites with it. The optical properties of both polymorphs were comprehensively studied by means of absorption spectroscopy, diffuse reflection spectroscopy and photoluminescence spectroscopy. DFT calculations were applied to investigate the band structure of the FA2PbBr4 and to corroborate the conclusions on their optoelectronic properties. As a result, we found that FA2PbBr4 phases irradiated by UV can exhibit effective green photoluminescence due to a transfer of excitation energy to defective states or 3D perovskite inclusions.