Mixed Formamidinium-Methylammonium Lead Iodide perovskite from first-principles: Hydrogen-bonding impact on the electronic properties

TL;DR

This study uses first-principles calculations to analyze how mixed methylammonium and formamidinium cations affect the structural and electronic properties of lead iodide perovskites, highlighting hydrogen bonding's stabilizing role.

Contribution

It provides new insights into the local structural variations and hydrogen-bonding effects in mixed A-site cation perovskites, advancing understanding of their stability and electronic behavior.

Findings

Octahedral tilting influences band gap more than unit-cell size.

Hydrogen bonds with iodine remain stronger for MA than FA across compositions.

Hydrogen bonding stabilizes specific orbitals, affecting electronic properties.

Abstract

Hybrid perovskites with mixed organic cations such as methylammonium and formamidinium have attracted interest due to their improved stability and capability to tune their properties varying the composition. In this work we report on the local variation of the structural and electronic properties in mixed A-site cation MA/FA lead iodide perovskites FAXMA1-XPBI3 evaluated from static first-principles calculations in certain structures where the orientations of organic cations result from examining the energy landscape of some compositions. The cation replacement at the A-site to form the solid solution causes an increase tilting of the inorganic PbI6 octahedra: in the FA-rich compounds the replacement of FA by a smaller cation like MA is to compensate the reduced space filling offered by the smaller cation, whereas in the MA-rich compounds is to expand the space needed for the larger cation. In fact, the effect of octahedron tiltings exceeds that of unit-cell size in determining the band gap for these organic cation mixtures. Our calculations indicate that the key role played by hydrogen bonds with iodine anions in pure compounds is preserved in the cation mixed perovskites. It is found that MA-I bonds remain stronger than FA-I bonds throughout the composition range regardless of the unit-cell expansion as the FA content increases. Our calculations reveal how the hydrogen bonds stabilize the no-bonding I-5p orbitals, spatially perpendicular to the Pb-I-Pb bond axis, lowering their energy when the H-I interaction occurs, which would explain the well-known role of hydrogen bonding in the structural stabilization of hybrid perovskites. These results contribute to the understanding on the role played by cation mixing at A sites in the physics of lead halide perovskites.