Perovskite solar cells (PSCs) are gaining popularity due to their high efficiency and low-cost fabrication. In recent decades, noticeable research efforts have been devoted to improving the stability of these cells under ambient conditions. Moreover, researchers are exploring new materials and fabrication techniques to enhance the performance of PSCs under various environmental conditions. The mechanical stability of flexible PSCs is another area of research that has gained significant attention. The latest research also focuses on developing tin-based PSCs that can overcome the challenges associated with lead-based perovskites. This review article provides a comprehensive overview of the latest advances in materials, fabrication techniques, and stability enhancement strategies for PSCs. It discusses the recent progress in perovskite crystal structure engineering, device construction, and fabrication procedures that has led to significant improvements in the photo conversion efficiency of these solar devices. The article also highlights the challenges associated with PSCs such as their poor stability under ambient conditions and discusses various strategies employed to enhance their stability. These strategies include the use of novel materials for charge transport layers and encapsulation techniques to protect PSCs from moisture and oxygen. Finally, this article provides a critical assessment of the current state of the art in PSC research and discusses future prospects for this technology. This review concludes that PSCs have great potential as a low-cost alternative to conventional silicon-based solar cells but require further research to improve their stability under ambient conditions in view of their definitive commercialization.

In this study, the influence of zinc oxide (ZnO) nanostructures with various morphologies on the performance of dye-sensitized solar cells (DSSCs) was investigated. Photo-electrodes were fabricated incorporating ZnO transport layers of distinct nanoscale morphologies—namely nanoparticles, microballs, spiky microballs, belts, and triangles—and their respective current–voltage characteristics were evaluated. It was observed that the DSSCs employing the triangular ZnO nanostructures, with a side length of approximately 30 nm, achieved the highest power conversion efficiency of 2.62%. This was closely followed by the DSSCs using spherical nanoparticles with an average diameter of approximately 20 nm, yielding an efficiency of 2.54%. In contrast, the efficiencies of DSSCs with microball and spiky microball ZnO nanostructures were significantly lower, measuring 0.31 and 1.79%, respectively. The reduction in efficiency for the microball-based DSSCs is attributed to the formation of micro-cracks within the thin film during the fabrication process. All DSSC configurations maintained a uniform active area of 4 mm². Remarkably, the highest fill factor of 59.88% was recorded for DSSCs utilizing the triangular ZnO morphology, with the spherical nanoparticles attaining a marginally lower fill factor of 59.38%. This investigation corroborates the hypothesis that reduced particle size in the transport layer correlates with enhanced DSSC performance, which is further amplified when the nanoparticles possess pointed geometries that induce strong electric fields due to elevated charge concentrations.

The present work systematically investigates the impact of multilayer architecture—specifically 5, 10, and 15 layers—on the structural, morphological, optical, and dielectric properties of zinc oxide (ZnO) thin films, aiming to tailor their characteristics for optoelectronic applications. The films were characterized using a comprehensive suite of techniques. X-ray diffraction (XRD) analysis of the 15-layer sample confirmed the formation of polycrystalline ZnO with a hexagonal wurtzite crystal structure, showing prominent (100), (002), and (101) diffraction peaks. Measurements indicated that the film thickness progressively increased from 43.81 nm for 5 layers to 80.68 nm for 15 layers. Concurrently, the surface roughness significantly decreased from 5.54 nm (5 layers) to 2.00 nm (15 layers) with increasing layer count, suggesting enhanced film quality and densification. Optical studies using ultraviolet–visible (UV-Vis) spectroscopy revealed an increase in absorbance and a corresponding decrease in transmittance in the UV-Vis spectrum as the film thickness increased. The calculated optical band gap showed a slight redshift, decreasing from 3.26 eV for the 5-layer film to 3.23 eV for the 15-layer film. Photoluminescence (PL) spectra exhibited characteristic near-band-edge UV emission, with the 5-layer film demonstrating the highest PL intensity. Furthermore, analysis of optical constants revealed that the refractive index, extinction coefficient, optical conductivity, and both the real and imaginary parts of the dielectric constant generally increased with an increasing number of layers, particularly in the visible region, while more nuanced and non-monotonic trends were observed in the UV range. These results underscore the significant influence of layer number on the physical properties of ZnO thin films, providing valuable insights for optimizing their performance in various optoelectronic devices.

The present study investigates the influence of photosensitizer selection and the polymer electrolyte composition on the performance of quasi-solid-state dye-sensitized solar cells (QsDSSCs). Two benchmark ruthenium dyes, N719 and Z907, alongside a novel photoactive phenothiazine dye were used. Each dye was incorporated into a QsDSSC architecture employing poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) as the gel electrolyte matrix, with varying molecular weights, to investigate their impacts on the overall device performance and long-term stability. Our results demonstrated that the N719 dye exhibited the highest power conversion efficiency (PCE), attributed to its strong absorption in the visible spectrum and efficient electron injection into the TiO₂ photoanode. Z907, on the other hand, showed moderate PCE due to its broader absorption profile but slower electron injection kinetics. The phenothiazine dye revealed promising PCE, with tunable absorption properties and efficient charge transfer. Furthermore, the impact of PVDF-HFP polymer gel electrolytes with varying molecular weights on cell stability was explored. The QsDSSC incorporating the PVH80 polymer with the phenothiazine dye exhibited reduced dye desorption, due to the effective dye molecules’ immobilization by the gel matrix, and consequently enhanced long-term stability over 600 h. This comparative study sheds light on the interplay between dye selection, the polymer gel’s properties, and QsDSSCs’ performance. These insights are crucial in designing robust and efficient QsDSSCs for practical applications.

This study introduces novel phenothiazine-based organic dyes, 2-LBH-100, 2-LBH-44, and 2-Ryu-4, specifically designed for quasi-solid-state dye-sensitized solar cells (QsDSSCs). Employing a donor-π-acceptor architecture, these dyes incorporate varying electron-donating moieties, including bis(3-(hexyloxy)phenyl)amine and diphenylamino, coupled with a cyanoacrylic acid acceptor. Alkoxy substitutions in 2-LBH-100 and 2-LBH-44 enhanced solubility and dye loading on TiO₂, leading to improved performance in QsDSSCs. 2-LBH-100 exhibited a power conversion efficiency (PCE) exceeding 5% with excellent stability, while 2-LBH-44 demonstrated a PCE of over 3%, increasing to 4% over time. 2-Ryu-4, with its diphenylamino donor, achieved an initial PCE of over 6%. This research highlights the crucial role of donor–acceptor interactions in optimizing organic dye design for high-performance QsDSSCs, paving the way for efficient and stable next-generation solar energy technologies.