RESUMO
The CsPbI3 perovskite has a suitable bandgap (≈1.7 eV) for application in tandem solar cells. One challenge for this compound is that the semiconducting perovskite phase is not stable at room temperature, when it tends to form a yellow nonperovskite phase with a bandgap of approximately 2.8 eV. Therefore, many reports have been focused on the stabilization of the CsPbI3 black perovskite phase through the use of additives during solution processing. Vacuum deposited CsPbI3 has been seldom reported, as in this case, the insertion of stabilizing agents is more challenging. In this work, we demonstrate the vacuum processing of CsPbI3 perovskite films at room temperature, obtained by incorporating dimethylammonium iodide by cosublimation with CsI and PbI2. As-prepared films were applied in planar solar cells, leading to an average power conversion efficiency (PCE) exceeding 12%. In order to improve the device performance, we introduced a third A-site cation (methylammonium) in a four-source deposition process. This pure iodide formulation can be used in wide bandgap solar cells with a PCE up to 14.8%.
RESUMO
Vacuum processing of multicomponent perovskites is not straightforward, because the number of precursors is in principle limited by the number of available thermal sources. Herein, we present a process which allows increasing the complexity of the formulation of vacuum-deposited lead halide perovskite films by multisource deposition and premixing both inorganic and organic components. We apply it to the preparation of wide-bandgap CsMAFA triple-cation perovskite solar cells, which are found to be efficient but not thermally stable. With the aim of stabilizing the perovskite phase, we add guanidinium (GA+) to the material formulation and obtained CsMAFAGA quadruple-cation perovskite films with enhanced thermal stability, as observed by X-ray diffraction and rationalized by microstructural analysis. The corresponding solar cells showed similar performance with improved thermal stability. This work paves the way toward the vacuum processing of complex perovskite formulations, with important implications not only for photovoltaics but also for other fields of application.
RESUMO
We have developed a general protocol for the preparation of hybrid nanostructures formed by nanoparticles (NPs) of molecule-based magnets based on Prussian Blue Analogues (PBAs) decorated with plasmonic Au NPs of different shapes. By adjusting the pH, Au NPs can be attached preferentially along the edges of the PBA or randomly on the surface. The protocol allows tuning the plasmonic properties of the hybrids in the whole visible spectrum.