The recent rapid development in perovskite solar cells (PSCs) has led to significant research interest due to their notable photovoltaic performance, currently exceeding 25% power conversion efficiency for small-area PSCs. The materials used to fabricate PSCs dominate the current photovoltaic market, especially with the rapid increase in efficiency and performance. The present work reviews recent developments in PSCs’ preparation and fabrication methods, the associated advantages and disadvantages, and methods for improving the efficiency of large-area perovskite films for commercial application. The work is structured in three parts. First is a brief overview of large-area PSCs, followed by a discussion of the preparation methods and methods to improve PSC efficiency, quality, and stability. Envisioned future perspectives on the synthesis and commercialization of large-area PSCs are discussed last. Most of the growth in commercial PSC applications is likely to be in building integrated photovoltaics and electric vehicle battery charging solutions. This review concludes that blade coating, slot-die coating, and ink-jet printing carry the highest potential for the scalable manufacture of large-area PSCs with moderate-to-high PCEs. More research and development are key to improving PSC stability and, in the long-term, closing the chasm in lifespan between PSCs and conventional photovoltaic cells.

Lead-free, bismuth-based perovskite solar cells (PSCs) are promising, non-toxic, and stable alternatives to lead-based PSCs, which are environmentally harmful and highly unstable under deprived air conditions. However, bismuth-based PSCs still suffer from low-power-conversion efficiency (PCE) due to their large bandgap and poor film morphology. Their poor film-forming ability is the greatest obstacle to Cs₃Bi₂I₉ progress in thin-film solar cell technology. This study synthesizes novel, lead-free perovskites with a small bandgap, excellent stability, and highly improved photovoltaic performance by integrating different amounts of potassium iodide (KI) into a perovskite precursor solution. KI incorporation improves the crystallinity of the perovskite, increases the grain size, and decreases the potential contact distribution, which is demonstrated by X-ray diffraction, electronic scanning microscopy, atomic force microscopy, and ultraviolet-visible spectroscopy. The Cs₃Bi₂I₉ PSC device with 2 vol. % incorporation of KI shows the highest PCE of 2.81% and Voc of 1.01 V as far as all the Bi-based cells fabricated for this study are concerned. The study demonstrates that incorporating KI in the Cs₃Bi₂I₉ perovskite layer highly stabilizes the resultant PSC device against humidity to the extent that it maintains 98% of the initial PCE after 90 days, which is suitable for solar cell applications. The devices also demonstrate greater resistance to airborne contaminants and high temperatures without encapsulation, opening up new possibilities for lead-free Cs₃Bi₂I₉ PSCs in future commercialization.

Thin and lightweight flexible lithium-ion batteries (LIBs) with high volumetric capacities are crucial for the development of flexible electronic devices. In the present work, we reported a paper-like ultrathin and flexible Si/carbon nanotube (CNT) composite anode for LIBs, which was realized by conformal electrodeposition of a thin layer of silicon on CNTs at ambient temperature. This method was quite simple and easy to scale up with low cost as compared to other deposition techniques, such as sputtering or CVD. The flexible Si/CNT composite exhibited high volumetric capacities in terms of the total volume of active material and current collector, surpassing the most previously reported Si-based flexible electrodes at various rates. In addition, the poor initial coulombic efficiency of the Si/CNT composites can be effectively improved by prelithiation treatment and a commercial red LED can be easily lighted by a full pouch cell using a Si/CNT composite as a flexible anode under flat or bent states. Therefore, the ultrathin and flexible Si/CNT composite is highly attractive as an anode material for flexible LIBs.

In this contribution, the efficiencies of perovskite solar cells have been further enhanced, based on optical optimization studies. The photovoltaic devices with textured perovskite film can be obtained and a power conversion efficiency (PCE) of the textured fluorine-doped tin oxide (FTO)/Ag nanoparticles (NPs) embedded in c-TiO₂/m-TiO₂/CH₃NH₃PbI₃/Spiro-OMeTAD/Au showed 33.7% enhancement, and a maximum of up to 14.01% was achieved. The efficiency enhancement can be attributed to the light trapping effect caused by the textured FTO and the incorporated Ag NPs, which can enhance scattering to extend the optical pathway in the photoactive layer of the solar cell. Interestingly, aside from enhanced light absorption, the charge transport characteristics of the devices can be improved by optimizing Ag NPs loading levels, which is due to the localized surface plasmon resonance (LSPR) from the incorporated Ag NPs. This light trapping strategy helps to provide an appropriated management for optical optimization of perovskite solar cells.

Two-dimensional nanomaterials hold great promise as electrode materials for the construction of excellent electrochemical energy storage and transformation apparatuses. In the study, metallic layered cobalt sulfide was, firstly, applied to the area of energy storage as a supercapacitor electrode. By a facile and scalable method for cathodic electrochemical exfoliation, metallic layered cobalt sulfide bulk can be exfoliated into high-quality and few-layered nanosheets with size distributions in the micrometer scale range and thickness in the order of several nanometers. With a two-dimensional thin sheet structure of metallic cobalt sulfide nanosheets, not only was a larger active surface area created, but also, the insertion/extraction of ions in the procedure of charge and discharge were enhanced. The exfoliated cobalt sulfide was applied as a supercapacitor electrode with obvious improvement compared with the original sample, and the specific capacitance increased from 307 F∙g⁻¹ to 450 F∙g⁻¹ at the current density of 1 A∙g⁻¹. The capacitance retention rate of exfoliated cobalt sulfide enlarged to 84.7% from the original 81.9% of unexfoliated samples while the current density multiplied by 5 times. Moreover, a button-type asymmetric supercapacitor assembled using exfoliated cobalt sulfide as the positive electrode exhibits a maximum specific energy of 9.4 Wh∙kg⁻¹ at the specific power of 1520 W∙kg⁻¹.