RESUMEN
A highly transparent NiO layer was prepared by a solution processing method with nickel(II) 2-ethylhexanoate in non-polar solvent and utilized as HTM in perovskite solar cells. Excellent optical transmittance and the matched energy level lead to the enhanced power conversion efficiency (PCE, 18.15 %) than that of conventional sol-gel-processed NiO-based device (12.98 %).
RESUMEN
As one of the most promising light-harvesting materials, perovskites have drawn tremendous attention for their unique advantages, such as high efficiency, low cost and facile fabrication compared with other photovoltaic materials. Nevertheless, poor moisture tolerance of the perovskites greatly hampers the operation of such devices and hinders their commercialization. Herein, we demonstrate a facile dipping treatment using sulfur-oleylamine solution for surface atomic modulation of perovskite films. Oleylammonium polysulfides (OPs) would be self-assembled on the etched perovskite film as an ultrathin outer layer. This layer could passivate the surface chemical activity of the outer perovskite layers. Moreover, the hydrophobic OPs significantly enhance moisture stability of such devices. As a result, the obtained device without encapsulation retains more than 70% of its initial power conversion efficiency (PCE) after 14 days of exposure to a relative humidity of 40 ± 10%.
RESUMEN
A gradient heterosturcture is one of the basic methods to control the charge flow in perovskite solar cells (PSCs). However, a classical route for gradient heterosturctures is based on the diffusion technique, in which the guest ions gradually diffuse into the films from a concentrated source of dopants. The gradient heterosturcture is only accessible to the top side, and may be time consuming and costly. Here, the "intolerant" n-type heteroatoms (Sb3+ , In3+ ) with mismatched cation sizes and charge states can spontaneously enrich two sides of perovskite thin films. The dopants at specific sides can be extracted by a typical hole-transport layer. Theoretical calculations and experimental observations both indicate that the optimized charge management can be attributed to the tailored band structure and interfacial electronic hybridization, which promote charge separation and collection. The strategy enables the fabrication of PSCs with a spontaneous graded heterojunction showing high efficiency. A champion device based on Sb3+ doped film shows a stabilized power-conversion efficiency of 21.04% with a high fill factor of 0.84 and small hysteresis.