Chemical tuning of dynamic cation off-centering in the cubic phases of hybrid tin and lead halide perovskites

Geneva Laurita, Douglas H. Fabini, Constantinos C. Stoumpos, Mercouri G. Kanatzidis, Ram Seshadri

Research output: Contribution to journalArticle

31 Citations (Scopus)

Abstract

Hybrid halide perovskites combine ease of preparation and relatively abundant constituent elements with fascinating photophysical properties. Descriptions of the chemical and structural drivers of the remarkable properties have often focused on the potential role of the dynamic order/disorder of the molecular A-site cations. We reveal here a key aspect of the inorganic framework that potentially impacts the electronic, thermal, and dielectric properties. The temperature evolution of the X-ray pair distribution functions of hybrid perovskites ABX3 [A+ = CH3NH3 (MA) or CH(NH2)2 (FA); B2+ = Sn or Pb; X- = Br, or I] in their cubic phases above 300 K reveals temperature-activated displacement (off-centering) of the divalent group 14 cations from their nominal, centered sites. This symmetry-lowering distortion phenomenon, previously dubbed emphanisis in the context of compounds such as PbTe, is attributed to Sn2+ and Pb2+ lone pair stereochemistry. Of the materials studied here, the largest displacements from the center of the octahedral sites are found in tin iodides, a more moderate effect is found in lead bromides, and the weakest effect is seen in lead iodides. The A-site cation appears to play a role as well, with the larger FA resulting in greater off-centering for both Sn2+ and Pb2+. Dynamic off-centering, which is concealed within the framework of traditional Bragg crystallography, is proposed to play a key role in the remarkable defect-tolerant nature of transport in these semiconductors via its effect on the polarizability of the lattice. The results suggest a novel chemical design principle for future materials discovery.

Original languageEnglish
Pages (from-to)5628-5635
Number of pages8
JournalChemical Science
Volume8
Issue number8
DOIs
Publication statusPublished - 2017

ASJC Scopus subject areas

  • Chemistry(all)

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