Crystal structure features of CH3NH3PbI3−xBrx hybrid perovskites prepared by ball milling: a route to more stable materials. Issue 4 (24th December 2019)

• Record Type: Journal Article
• Authors: López, Carlos Alberto; Alvarez-Galván, María Consuelo; Martínez-Huerta, María Victoria; Fauth, Francois; Alonso, José Antonio
• Is Part Of: CrystEngComm. Volume 22:Issue 4(2020)
• Page Start: 767
• Page End: 775
• Publication Date: 2019-12-24
• Subjects: Crystals -- Periodicals; Crystal growth -- Periodicals; Crystallography -- Periodicals; Cristaux -- Périodiques; Cristaux -- Croissance -- Périodiques; Cristallographie -- Périodiques; 548
• DOI: 10.1039/c9ce01461f
• Languages: English
• ISSNs: 1466-8033

Abstract

Abstract : Hybrid organic–inorganic perovskites, MAPbX3 (MA: CH3 –NH3 + ; X = halogen), prepared by ball milling are, by far, much more stable towards ambient conditions (air, humidity) than the conventional materials prepared from solution chemistry. Abstract : Hybrid organic–inorganic perovskites, MAPbX3 (MA: methylammonium, CH3 –NH3 + ; X = halogen), are active absorption materials in the new generation of solar cells. The triiodide specimen (MAPbI3 ) remains the most widely studied perovskite due to its ability to absorb broadband light below its band gap of 1.6 eV, but its degradation in a humid atmosphere has remained a major obstacle for commercialization. Here we found that CH3 NH3 PbI3− x Br x ( x = 0.0, 1.0) perovskites, prepared by ball milling, exhibit superior stability, showing no signs of degradation after several months of exposure to humid air. A synchrotron X-ray diffraction (SXRD) investigation was useful to determine some peculiar structural features that may account for the improved stability. The crystal structure was analysed to be in the I 4/ mcm and acentric I 4 cm space groups, yielding similar agreement factors. In both, the inorganic framework presents a conspicuously lower tilting effect than that observed in samples prepared by wet methods; an additional difference arises since the tetragonal structure is stable down to 140 K. The orientation of the organic MA units may play an important role in the properties, given the degrees of freedom for internal motion of MA groups within the PbX6 network. From the refined C/N positions, the MA + units lie along the c axis with 25% probability. The structure at 140 K shows that the MA + contribution along the c axis vanishes at this temperature. By contrast, MAPbI2 Br crystallizes in the cubic phase with the space group Pm 3̄ m, also with a larger unit-cell volume than that previously described. The absence of phase transitions down to 120 K suggests that the anion disorder prevents the localization of MA units upon cooling.