Abstract
The mixed cation lead iodide perovskite photovoltaics show improved stability following site substitution of cesium ions (Cs+) onto the formamidinium cation sites (FA(+)) of (CH(NH2)(2)PbI3 (FAPbI(3)) and increased resistance to formation of the undesirable.-phase. The structural phase behavior of Cs(0.1)FA(0.9)PbI(3) has been investigated by neutron powder diffraction (NPD), complemented by single crystal and power X-ray diffraction and photoluminescence spectroscopy. The Cs-substitution limit has been determined to be less than 15%, and the cubic alpha-phase, Cs(0.1)FA(0.9)PbI(3), is shown to be synthesizable in bulk and stable at 300 K. On cooling the cubic Cs(0.1)FA(0.9)PbI(3), a slow, second-order cubic to tetragonal transition is observed close to 290 K, with variable temperature NPD indicating the presence of the tetragonal beta-phase, adopting the space group P4/mbm between 290 and 180 K. An orthorhombic phase or twinned tetragonal phase is formed below 180 K, and the temperature for further transition to a disordered state is lowered to 125 K compared to that seen in phase pure alpha-FAPbI(3) (140 K). These results demonstrate the importance of understanding the effect of cation site substitution on structure-property relationships in perovskite materials.
Dokumententyp: | Zeitschriftenartikel |
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Fakultät: | Physik |
Themengebiete: | 500 Naturwissenschaften und Mathematik > 530 Physik |
ISSN: | 0897-4756 |
Sprache: | Englisch |
Dokumenten ID: | 89211 |
Datum der Veröffentlichung auf Open Access LMU: | 25. Jan. 2022, 09:29 |
Letzte Änderungen: | 25. Jan. 2022, 09:29 |