ABSTRACT
Formamidinium lead triiodide (FAPbI3) perovskite thin films are commonly deposited through a solution process, often incorporating a specific amount of methylammonium halide to stabilize the α-phase or enhance their crystallinity. The precursor solution for such coatings significantly influences the fabrication of perovskite solar cells (PSCs), involving time-dependent aging and byproduct formation. The chemical principle underlying this behavior is believed to be related to the deprotonation of methylamine cations (MA+) and subsequent chemical reactions with FA+ to generate N-methylformamidinium. Nevertheless, the role of the solvent in the side reactions between these organic cations remains unclear. This work systematically investigates the reaction reactivity in three protic solvents and three aprotic solvents. We uncover the hidden role of dimethylamine from the hydrolysis products of N,N-dimethylformamide, promoting the reaction between FA+ and MA+. Additionally, we elucidate the impact of environmental factors, such as water and oxygen, in stabilizing precursor solutions. This work establishes a basic concept and scientific direction for rationalizing high-efficiency, reproducible, and long-term-stable PSCs.
ABSTRACT
Defects at the top and bottom interfaces of three-dimensional (3D) perovskite photoabsorbers diminish the performance and operational stability of perovskite solar cells owing to charge recombination, ion migration and electric-field inhomogeneities1-5. Here we demonstrate that long alkyl amine ligands can generate near-phase-pure 2D perovskites at the top and bottom 3D perovskite interfaces and effectively resolve these issues. At the rear-contact side, we find that the alkyl amine ligand strengthens the interactions with the substrate through acid-base reactions with the phosphonic acid group from the organic hole-transporting self-assembled monolayer molecule, thus regulating the 2D perovskite formation. With this, inverted perovskite solar cells with double-side 2D/3D heterojunctions achieved a power conversion efficiency of 25.6% (certified 25.0%), retaining 95% of their initial power conversion efficiency after 1,000 h of 1-sun illumination at 85 °C in air.
ABSTRACT
Although antimony selenoiodide (SbSeI) exhibits a suitable bandgap as well as interesting physicochemical properties, it has not been applied to solar cells. Here the fabrication of SbSeI solar cells is reported for the first time using multiple spin-coating cycles of SbI3 solutions on Sb2Se3 thin layer, which is formed by thermal decomposition after depositing a single-source precursor solution. The performance exhibits a short-circuit current density of 14.8 mA cm-2, an open-circuit voltage of 473.0 mV, and a fill factor of 58.7%, yielding a power conversion efficiency (PCE) of 4.1% under standard air mass 1.5 global (AM 1.5 G, 100 mW cm-2). The cells retain ≈90.0% of the initial PCE even after illuminating under AM 1.5G (100 mW cm-2) for 2321 min. Here, a new approach is provided for combining selenide and iodide as anions, to fabricate highly efficient, highly stable, green, and low-cost solar cells.
