Vapor deposition of perovskite solar cells (PSCs) has attracted considerable interest for its dry processing characteristics. However, a two-step sequential vapor deposition method suffers from ineffective conversion of PbI2 to perovskite with reasons still unclear. In this report, we carefully investigated the crystallization orientation of PbI2 films deposited by physical vapor deposition via synchrotron grazing-incidence wide-angle X-ray scattering (GIWAXS) and observed an asymmetric scattering pattern with respect to the qz -axis. The observed oriented morphology and texture hinder the diffusion of MAI molecules in the PbI2 films synthesized by vapor deposition, resulting in over 15% PbI2 remaining at the buried interface after reaction with MAI vapor. As a result, the MAPbI3 synthesized in this way was also highly oriented, especially in the surface layers. Surface fumigation (SF) step was introduced to decrease the orientational anisotropy of PbI2, which successfully breaks the diffusion barriers of MAI molecules by forming a complex layer on the PbI2 surface with polar solvent vapors, like dimethyl sulfoxide or 1,3-dimethyl-2-imidazolidinone. We infer that the SF treatment changes the vapor–solid reaction mechanism from reaction–crystallization to dissolution–recrystallization, which largely promotes the conversion of PbI2 to perovskite. Defects were reduced in perovskite synthesized in this way, and a p-i-n device with 19.56% efficiency was fabricated, which is among the highest efficiencies reported for sequential-vapor-deposited PSCs. Notably, this method enables the fabrication of conformal perovskite layers on uneven substrates. An exemplary PSC showing efficiency of 8.93% was fabricated on a precurved substrate. We believe that the method is applicable to the fabrication of tandem or curved PSCs that are compatible with wearable or building/autocar-integrated photovoltaics in the future.
The efficiency and stability of perovskite solar cells (PSCs) can be either deteriorated or enhanced by strain at interfaces, which is sensitive to various external conditions, particularly light illumination. Here we investigated the vertical strain distribution in perovskite films synthesized under light illumination with various wavelengths. The films were formed by reacting formamidinium iodide (FAI)/methylammonium chloride (MACl) vapor with vapor-deposited PbI2 (CsBr) films. Strain in the films was evaluated with incident-angle-dependent grazing-incidence wide-angle X-ray scattering, which showed out-of-plane compressive and in-plane tensile strains, particularly on the surface. Short-wavelength light relaxed the strain on the perovskite surface via promotion of ionic diffusion, including FA, MA, Cs, and I, to reach vertical ionic homogeneity. With the charge trap concentration being reduced, both the efficiency and stability were greatly improved. This finding provides deep insight into the effect of light on strain in PSCs.
Silver nanowires (AgNWs) are important materials for flexible transparent electrodes (FTEs). However, the loose stacking of nanowire junctions greatly affects the electric conductivity across adjacent nanowires. Soldering can effectively reduce the wire−wire contact resistance of AgNWs by epitaxially depositing nanosolders at the junctions, but the process normally needs to be performed with high energy consumption. In this work, we proposed a simple room-temperature method to achieve precise welding of junctions by adjusting the wettability of the soldered precursor solution on the surfaces of AgNWs. The nanoscale welding at nanowire cross junctions forms efficient conductive networks. Furthermore, reduced graphene oxide (rGO) was used to improve the stability of FTEs by wrapping the rGO around the AgNW surface. The obtained FTE shows a figure-of-merit (FoM) of up to 439.3 (6.5 Ω/sq at a transmittance of 88%) and has significant bending stability and environmental and acidic stability. A flexible transparent heater was successfully constructed, which could reach up to 160 °C within a short response time (43 s) and exhibit excellent switching stability. When laminating this FTE onto half perovskite solar cells as the top electrodes, the obtained double-side devices achieved power conversion efficiencies as high as 16.15% and 13.91% from each side, pointing out a convenient method for fabricating double-sided photovoltaic devices.
2D perovskites are widely employed to improve efficiency and stability of perovskite solar cells (PSCs), but the processes are rarely accomplished in air due to the difficulty of controlling the formation processes. An ultra-thin 2D capping layer with an alternating cation interlayer (ACI) structure is in situ formed by fumigating 3D perovskites with benzylamine vapor. The whole process is finished in air within 10 s regardless of the humidity, after which both defects and tensile strain are reduced and the interfacial energy band gets benignly aligned to a type-I heterojunction, avoiding direct charge recombination at the interface. Theoretical analysis reveals that the ACI phase is thermodynamically more stable than an analogous Ruddlesden-Popper phase. The strategy can passivate various perovskites, including methylammonium (or multi-cation) lead (or lead/tin mixed) halide perovskites, prepared via either vapor or solution approaches, increasing the absolute power conversion efficiency by up to 2.5%. It can uniformly passivate PSCs without area limitation, and provide a repeatable methodology for passivating perovskites.
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