Chelate Coordination Strengthens Surface Termination to Attain High-Efficiency Perovskite Solar Cells.

Solar cell efficiency and stability are two key metrics to determine whether a photovoltaic device is viable for commercial applications. The surface termination of the perovskite layer plays a pivotal role in not only the photoelectric conversion efficiency (PCE) but also the stability of assembled perovskite solar cells (PSCs). Herein, a strong chelate coordination bond is designed to terminate the surface of the perovskite absorber layer. On the one hand, the ligand anions bind with Pb cations via a bidentate chelating bond to restrict the ion migration, and the chelate surface termination changes the surface from hydrophilic to hydrophobic. Both are beneficial to improving the long-term stability. On the other hand, the formation of the chelating bonding effectively eliminates the deep-level defects including PbI and Pb clusters on the Pb-I and FA-I terminations, respectively, as confirmed by theoretical simulation and experimental results. Consequently, the PCE is increased to 24.52%, open circuit voltage to 1.19 V, and fill factor to 81.53%; all three are among the highest for hybrid perovskite cells. The present strategy provides a straightforward means to enhance both the PCE and long-term stability of PSCs.

Polar Species for Effective Dielectric Regulation to Achieve High-Performance CsPbI3 Solar Cells.

Nonradiative losses caused by defects are the main obstacles to further advancing the efficiency and stability of perovskite solar cells (PSCs). There is focused research to boost the device performance by reducing the number of defects and deactivating defects; however, little attention is paid to the defect-capture capacity. Here, upon systematically examining the defect-capture capacity, highly polarized fluorinated species are designed to modulate the dielectric properties of the perovskite material to minimize its defect-capture radius. On the one hand, fluorinated polar species strengthen the defect dielectric-screening effect via enhancing the dielectric constant of the perovskite film, thus reducing the defect-capture radius. On the other, the fluorinated iodized salt replenishes the I-vacancy defects at the surface, hence lowering the defect density. Consequently, the power-conversion efficiency of an all-inorganic CsPbI3 PSC is increased to as high as 20.5% with an open-circuit voltage of 1.2 V and a fill factor of 82.87%, all of which are among the highest in their respective categories. Furthermore, the fluorinated species modification also produces a hydrophobic umbrella yielding significantly improved humidity tolerance, and hence long-term stability. The present strategy provides a general approach to effectually regulate the defect-capture radius, thus enhancing the optoelectronic performance.

Molten-Salt-Assisted CsPbI3 Perovskite Crystallization for Nearly 20%-Efficiency Solar Cells.

Dynamic manipulation of crystallization is pivotal to the quality of polycrystalline films. A molten-salt-assisted crystallization (MSAC) strategy is presented to improve grain growth of the all-inorganic perovskite films. Compared with the traditional solvent annealing, MSAC enables more intensive mass transfer by means of convection and diffusion, which is beneficial to the interaction among the precursor colloids and to inducing in-plane growth of perovskite grains, resulting in the formation of high-quality perovskite films with suppressed pinhole and crack formation. Additionally, the introduction of molten salt alters the intermediate phases, and thus changes the crystallization pathways by reducing the energy barrier to produce films with desired optical and electrical properties. As a result, the MSAC strategy endows the devices with champion steady-state output efficiency of 19.83% and open-circuit voltage (Voc ) as high as 1.2 V, among the highest for this type of solar cell, thanks to its effectively reduced Voc deficit.