Search

Highlights from the article: Photovoltaic Devices: In Situ Observation of Crystallization Dynamics and Grain Orientation in Sequential Deposition of Metal Halide Perovskites (Adv. Funct. In article number 1902319, featuring a synchrotron-based in situ X-ray diffraction technique, Gang Chen and co-workers investigate the sequential deposition process of FAPbI SB 3 sb from a smooth PbI SB 2 sb film to a trilayer PbI SB 2 sb -FAI composite film and finally to the oriented perovskite film. The effects of the additive ions of Br SP - sp , Cl SP - sp , and MA SP + sp on the crystallization dynamics and grain orientation of the resultant perovskite films are also surveyed.

Metal halide perovskites have revolutionized the development of highly efficient, solution‐processable solar cells. Further advancements rely on improving perovskite film qualities through a better understanding of the underlying growth mechanism. Here, a systematic in situ grazing‐incidence X‐ray diffraction investigation is performed, facilitated by other techniques, on the sequential deposition of formamidinium lead iodide (FAPbI3)‐based perovskite films. The active chemical reaction, composition distribution, phase transition, and crystal grain orientation are all visualized following the entire perovskite formation process. Furthermore, the influences of additive ions on the crystallization speed, grain orientation, and morphology of FAPbI3‐based films, along with their photovoltaic performances, are fully evaluated and optimized, which leads to highly reproducible and efficient perovskite solar cells. The findings provide key insights into the perovskite growth mechanism and suggest the fabrication of high‐quality perovskite films for widespread optoelectronic applications. [ABSTRACT FROM AUTHOR]

The methylammonium (MA)‐free perovskite solar cells (PSCs) have drawn broad attention due to their excellent thermostability. However, the efficiency of these devices is inferior to most state‐of‐the‐art PSCs. Herein, the photovoltaic performance of the MA‐free PSCs is enhanced by constructing interfacial capping layers with a pair of alkylammonium halides, n‐propylammonium (PA) iodide and propane‐1,3‐diammonium (PDA) iodide. The structure and composition of the interfacial layers are comprehensively investigated and their correlation with the device performance is presented in terms of defect passivation efficacy, energy level alignment, and hydrophobicity for moisture resistance. The PSC devices based on the PAI and PDAI2 treated MA‐free perovskite films demonstrate better power conversion efficiencies (PCEs) and stabilities than the reference devices without the interfacial layers. Although the PAI‐treated devices exhibit the highest PCE of 21.1%, the PDAI2‐treated PSCs demonstrate the exceptional thermal and humidity stabilities. [ABSTRACT FROM AUTHOR]