Tiny spots to light the future: advances in synthesis, properties, and application of perovskite nanocrystals in solar cells.

Perovskites are in the hotspot of material science and technology. Outstanding properties have been discovered, fundamental mechanisms of defect formation and degradation elucidated, and applications in a wide variety of optoelectronic devices demonstrated. Advances through adjusting the bulk-perovskite composition, as well as the integration of layered and nanostructured perovskites in the devices, allowed improvement in performance and stability. Recently, efforts have been devoted to investigating the effects of quantum confinement in perovskite nanocrystals (PNCs) aiming to fabricate optoelectronic devices based solely on these nanoparticles. In general, the applications are focused on light-emitting diodes, especially because of the high color purity and high fluorescence quantum yield obtained in PNCs. Likewise, they present important characteristics featured for photovoltaic applications, highlighting the possibility of stabilizing photoactive phases that are unstable in their bulk analog, the fine control of the bandgap through size change, low defect density, and compatibility with large-scale deposition techniques. Despite the progress made in the last years towards the improvement in the performance and stability of PNCs-based solar cells, their efficiency is still much lower than that obtained with bulk perovskite, and discussions about upscaling of this technology are scarce. In light of this, we address in this review recent routes towards efficiency improvement and the up-scaling of PNC solar cells, emphasizing synthesis management and strategies for solar cell fabrication.

Improving the Stability and Efficiency of Perovskite Solar Cells by a Bidentate Anilinium Salt.

We report improvement in the perovskite solar cell efficiency and stability after passivation with an organic molecule decorated with two anilinium cations. We compare this salt with its neutral analog and found that the change in the electron density distribution upon protonation and the presence of the halide anion are key to explaining the better passivation ability of the salt. In addition, we show that the counteranion has a significant impact on the performance of the device.