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Inducing spontaneous electric polarizations in double perovskite iodide superlattices for ferroelectric photovoltaic materials
Journal article   Open access   Peer reviewed

Inducing spontaneous electric polarizations in double perovskite iodide superlattices for ferroelectric photovoltaic materials

Joshua Young and James M. Rondinelli
Physical review materials, v 2(6)
22 Jun 2018
url
https://doi.org/10.1103/physrevmaterials.2.065406View
Published, Version of Record (VoR) Open

Abstract

Materials Science Materials Science, Multidisciplinary Science & Technology Technology
In this work, we use density functional theory calculations to demonstrate how spontaneous electric polarizations can be induced via a hybrid improper ferroelectric mechanism in iodide perovskites, a family well known to display solar-optimal band gaps, to create materials for photoferroic applications. We first assemble three chemically distinct (AA')(BB')I-6 double perovskites using centrosymmetric ABI(3) perovskite iodides (where A = Cs, Rb, K and B = Sn, Ge) as building units. In each superlattice, we investigate the effects of three types of A- and B-site cation ordering schemes and three different BI6 octahedral rotation patterns. Out of these 27 combinations, we find that 15 produce polar space groups and display spontaneous electric polarizations ranging from 0.26 to 23.33 mu C/cm(2) . Furthermore, we find that a layered A-site/rock salt B-site ordering, in the presence of an a(0)a(0) c(+) rotation pattern, produces a chiral vortex-like A-site displacement pattern. We then investigate the effect of epitaxial strain on one of these compounds, (CsRb)(SnGe)I-6 , in layered and rock salt ordered configurations. In both phases, we find strong competition between the cation ordering schemes as well as an enhancement of the spontaneous polarization magnitude under tensile strain. Finally, using a hybrid density functional with fractional Fock exchange, we find the iodide superlattices display semiconducting band gaps ranging from 0.2 to 1.3 eV. These results demonstrate that cation ordering and epitaxial strain are powerful ways to induce and control functionalities in technologically useful families of materials.

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Collaboration types
Domestic collaboration
Web of Science research areas
Materials Science, Multidisciplinary
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