RESUMO
Wide-bandgap semitransparent perovskite photovoltaics are emerging as one of the ideal candidates for building-integrated photovoltaics (BIPV). However, surface defects in inorganic CsPbBr3 perovskite prepared by vapor deposition severely limit the optoelectronic performance of perovskite solar cells. To address this issue, a strategy of doping a trace amount of KBr into perovskite by vapor deposition is adopted, effectively improving the quality of the film, reducing surface defect concentration, and enhancing the transportation and extraction of charge carriers. Simultaneously, fully physical vapor deposition technology is employed to fabricate perovskite solar cells with an average visible light transmittance of 44%. These devices exhibited an ultrahigh open-circuit voltage of 1.55 V and a superior power conversion efficiency (PCE) of 7.28%, demonstrating excellent moisture and heat resistance. Moreover, the corresponding 5 cm × 5 cm modules achieve a PCE of 5.35% with great thermal insulation capability. This work provides an approach for fabricating highly efficient all-inorganic perovskite solar cells with high average visible light transmittance, demonstrating new insights into their application in building-integrated photovoltaics.
RESUMO
Vapor deposition is a promising technology for the mass production of perovskite solar cells. However, the efficiencies of solar cells and modules based on vapor-deposited perovskites are significantly lower than those fabricated using the solution method. Emerging evidence suggests that large defects are generated during vapor deposition owing to a specific top-down crystallization mechanism. Herein, a hybrid vapor deposition method combined with solvent-assisted recrystallization for fabricating high-quality large-area perovskite films with low defect densities is presented. It is demonstrated that an intermediate phase can be formed at the grain boundaries, which induces the secondary growth of small grains into large ones. Consequently, perovskite films with substantially reduced grain boundaries and defect densities are fabricated. Results of temperature-dependent charge-carrier dynamics show that the proposed method successfully suppresses all recombination reactions. Champion efficiencies of 21.9% for small-area (0.16 cm2 ) cells and 19.9% for large-area (10.0 cm2 ) solar modules under AM 1.5 G irradiation are achieved. Moreover, the modules exhibit high operational stability, i.e., they retain >92% of their initial efficiencies after 200 h of continuous operation.
RESUMO
To accelerate the commercial application of organic-inorganic hybrid perovskite solar cells (PSCs), it is necessary to develop simple and low-cost methods to prepare pinhole-free large-area perovskite films with high quality. A one-step blade coating method is regarded as a scalable technique. It is demonstrated that with the addition of N,N'-dimethylpropyleneurea (DMPU) in an FA-dominated perovskite precursor, a large-area high-quality perovskite film can be obtained by blade coating, achieving improved photovoltaic performance, thermal stability, and storage stability. It is found that the strong interaction between DMPU and Pb2+ ions is beneficial to delay the nucleation crystallization process, increase the size of crystal grains, and improve the crystallinity of the perovskite film. Planar n-i-p solar cells introducing DMPU exhibit power conversion efficiencies of 20.20% for 0.16 cm2 devices and 17.71% for 5 × 5 cm2 modules with an aperture area of 10 cm2. In addition, the devices without encapsulation placed at 50 °C for 500 h and with a relative humidity of 20 ± 5% for 1000 h still maintain efficiencies above 80 and 90%, respectively, showing outstanding stability.