Unprecedented Richness of Temperature- and Pressure-Induced Polymorphism in 1D Lead Iodide Perovskite.

Inherent features of metal halide perovskites are their softness, complex lattice dynamics, and phase transitions spectacularly tuning their structures and properties. While the structural transformations are well described and classified in 3D perovskites, their 1D analogs are much less understood. Herein, both temperature- and pressure-dependent structural evolutions of a 1D AcaPbI3 perovskitoid incorporating acetamidinium (Aca) cation are examined. The study reveals the existence of nine phases of δ-AcaPbI3, which present the most diverse polymorphic collection among known perovskite materials. Interestingly, temperature- and pressure-triggered phase transitions in the 1D perovskotoid exhibit fundamentally different natures: the thermal transformations are mainly associated with the collective translations of rigid polyanionic units and ordering/disordering dynamics of Aca cations, while the compression primarily affects inorganic polymer chains. Moreover, in the 1-D chains featuring the face-sharing connection mode of the PbI6 octahedra the Pb···Pb distances are significantly shortened compared to the corner-sharing 3D perovskite frameworks, hence operating in the van der Waals territory. Strikingly, a good correlation is found between the Pb···Pb distances and the pressure evolution of the bandgap values in the δ-AcaPbI3, indicating that in 1D perovskitoid structures, the contacts between Pb2+ ions are one of the critical parameters determining their properties.

Mechanoperovskites for Photovoltaic Applications: Preparation, Characterization, and Device Fabrication.

Hybrid organic-inorganic metal halide perovskites (MHPs) have emerged as excellent absorber materials for next generation solar cells owing to their simple solution-processed synthesis and high efficiency. This breakthrough in photovoltaics along with an accompanying impact in light-emitting applications prompted a renaissance of interest in the broad family of MHPs. Notably, the optoelectronic properties and the photovoltaic parameters of MHPs are highly sensitive to the adopted synthetic strategy. The preparation of MHPs has commonly relied on solution-based methods requiring elevated temperatures for homogeneity of reaction mixtures. While the solution-based approach is relatively versatile, it faces challenges such as limitations in compositional engineering of MHPs or their long-term storage among others. Therefore, there is a continuous great challenge to develop efficient synthetic strategies affording various high-quality MHP materials for numerous technological optoelectronic applications. In the past decade, mechanochemistry has appeared as a green alternative to traditional synthesis. This solid-state, re-emerging efficient synthetic methodology mediated by direct absorption of mechanical energy is growing explosively across organic and inorganic chemistry and materials science. In this Account, we describe our shared interest in the productive use of mechanical force in chemistry of MHPs, as well as assembly of the respective solar cell devices. We highlight the milestones achieved by our groups along with the seminal contributions by other groups. In particular, we demonstrate that mechanochemistry efficiently allows the formation of various phase pure hybrid lead and lead-free halide perovskite compositions (called hereafter "mechanoperovskites"). The progress in solvent-free solid-state synthesis is greatly enhanced by the integration of advanced methods of solid-state analysis like powder X-ray diffraction (pXRD), solid-state nuclear magnetic resonance (ss-NMR) and UV-vis spectroscopies, and we aim to illustrate this ongoing integration through appropriate examples. Furthermore, we show that thin films based on mechanoperovskites have the advantage of providing a higher degree of control of the stoichiometry and higher reproducibility, stability, and material phase purity. The impact of using powdered mechanoperovskite as a precursor for thin film formation on the electrochemical and photovoltaic properties of the solar cells is also discussed. Finally, our view of current challenges and future directions in this emerging interdisciplinary area of research is provided.

Formation of Stable Mixed Guanidinium-Methylammonium Phases with Exceptionally Long Carrier Lifetimes for High-Efficiency Lead Iodide-Based Perovskite Photovoltaics.

Methylammonium (MA)- and formamidinium (FA)-based organic-inorganic lead halide perovskites provide outstanding performance as photovoltaic materials, due to their versatility of fabrication and their power conversion efficiencies reaching over 22%. The proposition of guanidinium (GUA)-doped perovskite materials generated considerable interest due to their potential to increase carrier lifetimes and open-circuit voltages as compared to pure MAPbI3. However, simple size considerations based on the Goldschmidt tolerance factor suggest that guanidinium is too big to completely replace methylammonium as an A cation in the APbI3 perovskite lattice, and its effect was thus ascribed to passivation of surface trap states at grain boundaries. As guanidinium was not thought to incorporate into the MAPbI3 lattice, interest waned since it appeared unlikely that it could be used to modify the intrinsic perovskite properties. Here, using solid-state NMR, we provide for the first time atomic-level evidence that GUA is directly incorporated into the MAPbI3 and FAPbI3 lattices, forming pure GUA xMA1- xPbI3 or GUA xFA1- xPbI3 phases, and that it reorients on the picosecond time scale within the perovskite lattice, which explains its superior charge carrier stabilization capacity. Our findings establish a fundamental link between charge carrier lifetimes observed in photovoltaic perovskites and the A cation structure in ABX3-type metal halide perovskites.

Halide Mixing and Phase Segregation in Cs2AgBiX6 (X = Cl, Br, and I) Double Perovskites from Cesium-133 Solid-State NMR and Optical Spectroscopy.

All-inorganic double perovskites (elpasolites) are a promising potential alternatives to lead halide perovskites in optoelectronic applications. Although halide mixing is a well-established strategy for band gap tuning, little is known about halide mixing and phase segregation phenomena in double perovskites. Here, we synthesize a wide range of single- and mixed-halide Cs2AgBiX6 (X = Cl, Br, and I) double perovskites using mechanosynthesis and probe their atomic-level microstructure using 133Cs solid-state MAS NMR. We show that mixed Cl/Br materials form pure phases for any Cl/Br ratio while Cl/I and Br/I mixing is only possible within a narrow range of halide ratios (<3 mol % I) and leads to a complex mixture of products for higher ratios. We characterize the optical properties of the resulting materials and show that halide mixing does not lead to an appreciable tunability of the PL emission. We find that iodide incorporation is particularly pernicious in that it quenches the PL emission intensity and radiative charge carrier lifetimes for iodide ratios as low as 0.3 mol %. Our study shows that solid-state NMR, in conjunction with optical spectroscopies, provides a comprehensive understanding of the structure-activity relationships, halide mixing, and phase segregation phenomena in Cs2AgBiX6 (X = Cl, Br, and I) double perovskites.

Reduction in the Interfacial Trap Density of Mechanochemically Synthesized MAPbI3.

Organo-lead halide perovskites have emerged as promising light harvesting materials for solar cells. The ability to prepare high quality films with a low concentration of defects is essential for obtaining high device performance. Here, we advance the procedure for the fabrication of efficient perovskite solar cells (PSCs) based on mechanochemically synthesized MAPbI3. The use of mechano-perovskite for the thin film formation provides a high degree of control of the stoichiometry and allows for the growth of relatively large crystalline grains. The best device achieved a maximum PCE of 17.5% from a current-voltage scan (J-V), which stabilized at 16.8% after 60 s of maximum power point tracking. Strikingly, PSCs based on MAPbI3 mechanoperovskite exhibit lower "hysteretic" behavior in comparison to that comprising MAPbI3 obtained from the conventional solvothermal reaction between PbI2 and MAI. To gain a better understanding of the difference in J-V hysteresis, we analyze the charge/ion accumulation mechanism and identify the defect energy distribution in the resulting MAPbI3 based devices. These results indicate that the use of mechanochemically synthesized perovskites provides a promising strategy for the formation of crystalline films demonstrating slow charge recombination and low trap density.