Over the past few decades, silicon-based solar cells have been used in the photovoltaic (PV) industry because of the abundance of silicon material and the mature fabrication process. However, as more electrical devices with wearable and portable functions are required, silicon-based PV solar cells have been developed to create solar cells that are flexible, lightweight, and thin. Unlike flexible PV systems (inorganic and organic), the drawbacks of silicon-based solar cells are that they are difficult to fabricate as flexible solar cells. However, new technologies have emerged for flexible solar cells with silicon. In this paper, we describe the basic energy-conversion mechanism from light and introduce various silicon-based manufacturing technologies for flexible solar cells. In addition, for high energy-conversion efficiency, we deal with various technologies (process, structure, and materials).

Over the past few decades, solar water splitting has evolved into one of the most promising techniques for harvesting hydrogen using solar energy. Despite the high potential of this process for hydrogen production, many research groups have encountered significant challenges in the quest to achieve a high solar-to-hydrogen conversion efficiency. Recently, ferroelectric materials have attracted much attention as promising candidate materials for water splitting. These materials are among the best candidates for achieving water oxidation using solar energy. Moreover, their characteristics are changeable by atom substitute doping or the fabrication of a new complex structure. In this review, we describe solar water splitting technology via the solar-to-hydrogen conversion process. We will examine the challenges associated with this technology whereby ferroelectric materials are exploited to achieve a high solar-to-hydrogen conversion efficiency.

Conventional sputtering method uses a single cathode with a permanent magnet. Facing targets sputtering (FTS) methods consists of two cathodes. Because of a unique structure, FTS can prepare high quality films with low temperature and low plasma damage. During the film sputtering process, density and confinement of discharged plasma depend on the arrangement of a permanent magnet in the cathode. In this study, we designed two types of permanent magnet arrangements in the FTS system and the designed permanent magnet was inserted into two cathodes in the FTS system. The system was operated in different permanent magnet conditions, and their discharge voltage and properties of as-grown films were recorded. In the designed FTS, compared to a conventional magnetron sputtering method, the substrate temperature increased to a value under 80 °C, which is relatively low, even though the films’ sputtering process was completed.

The electron transport layer (ETL) of organic–inorganic perovskite solar cells plays an important role in their power conversion efficiency (PCE). In this study, TiO₂ hollow nanospheres with a diameter of 150 nm were prepared by a facile synthesis method. The synthesized TiO₂ hollow nanospheres had a highly porous structure with a surface area of 85.23 m² g⁻¹, which is significantly higher than commercial TiO₂ (P25) (54.32 m² g⁻¹), indicating that they can form an ideal mesoporous layer for Formamidinium iodide-based perovskite solar cells (PSCs). In addition, the nanospheres achieved a remarkable perovskite performance, and the average PCE increased from 12.87% to 14.27% with a short circuit current density of 22.36 mAcm⁻², an open voltage of 0.95 V, and a fill factor of 0.65. The scanning electron microscopy images revealed that the enhanced PCE could be due to the improved carrier collection and transport properties of the nanosphere, which enabled efficient filtration of perovskite into the TiO₂ mesoporous ETL. The TiO₂ hollow nanospheres fabricated in this study show high potential as a high-quality ETL material for efficient (FAPbI₃)_0.97(MAPbBr₃)_0.03-based PSCs.

Perovskite solar cells (PSCs) are usually fabricated by using the spin coating method. During the fabrication process, the surface status is very important for energy conversion between layers coated in the substrate. PSCs have multilayer-stacked structures, such as the transparent electrode layer, the perovskite layer, and a metal electrode. The efficiency and uniformity of all layers depend on the surface status of the transparent electrode coated on the glass substrate. Until now, etching methods by chemical processes have been introduced to make the substrate surface smooth and uniform by decreasing surface roughness. However, highly reactive chemical treatments can be harmful to the environment. In this study, we employed an eco-friendly chemical-mechanical polishing (CMP) process to ensure the fluorine-doped tin oxide (FTO) substrate is treated with a smooth surface. Before the perovskite layer and electron transport layer (ETL) are applied, the TiO₂ layer is coated with the FTO substrate, and the surface of the FTO substrate is polished using CMP. As a result, the CMP-treated surface of the FTO substrate showed a smooth surface, and the PSCs with CMP treatment did not require conventional TiCl₄ treatment.

We employed ultra-violet (UV) light treatment on the TiO₂ layer prior to coating the perovskite layer to improve the solar conversion efficiency of perovskite solar cells (PSCs). A laboratory-made UV treatment system was equipped with various UV light sources (8 W power; maximum wavelengths of 254, 302, and 365 nm). The UV light treatment improved the power conversion efficiency (PCE) while coating the uniformity layer and removing impurities from the surface of cells. After the PSCs were exposed to UV light, their PCE developed approximately 10% efficiency; PBI₂ decreased without changing the structure.