Search Results (422)

Dye-sensitized solar cells (DSSCs) have emerged as a promising technology for converting sunlight into electricity at a low cost; however, it is still necessary to find a photostable, low-cost, and efficient photosensitizer. In this sense, the natural product bixin (Dye 1) has previously been reported as a potential photosensitizer. Thus, the present work reports the full synthesis of diester and diacid hybrids (Dyes 2 and 3, respectively, with corresponding yields of 93% and 52%) using the natural product bixin as a starting material and 1,3,4-oxadiazole ring as a connected point. The hydrolysis step of Dye 2 aims to obtain Dye 3 with a structural capacity to anchor the titanium dioxide (TiO₂) nanofilms via the carboxylic acid group. Both compounds (Dyes 1 and 3) can be adsorbed via pseudo-first order on the surface of TiO₂ nanofilms, reaching saturation after 10 and 6 min of exposure in an organic solution (1 × 10⁻⁵ M), respectively, with adsorption kinetics of the semisynthetic compound almost twofold higher than the natural product. Contrary to expectations, Dye 3 had spectral behavior similar to Dye 1, but with better frontier molecular orbital (FMO) parameters, indicating that Dye 3 will probably behave very similarly or have slightly better photovoltaic performance than Dye 1 in future DSSC measurements. Full article

Titanium dioxide (TiO₂) is a wide-bandgap semiconductor material with broad application potential, known for its excellent photocatalytic performance, high chemical stability, low cost, and non-toxicity. These properties make it highly attractive for applications in photovoltaic energy, environmental remediation, and optoelectronic devices. For instance, TiO₂ is widely used as a photocatalyst for hydrogen production via water splitting and for degrading organic pollutants, thanks to its efficient photo-generated electron–hole separation. Additionally, TiO₂ exhibits remarkable performance in dye-sensitized solar cells and photodetectors, providing critical support for advancements in green energy and photoelectric conversion technologies. Boron-doped diamond (BDD) is renowned for its exceptional electrical conductivity, high hardness, wide electrochemical window, and outstanding chemical inertness. These unique characteristics enable its extensive use in fields such as electrochemical analysis, electrocatalysis, sensors, and biomedicine. For example, BDD electrodes exhibit high sensitivity and stability in detecting trace chemicals and pollutants, while also demonstrating excellent performance in electrocatalytic water splitting and industrial wastewater treatment. Its chemical stability and biocompatibility make it an ideal material for biosensors and implantable devices. Research indicates that the combination of TiO₂ nanostructures and BDD into heterostructures can exhibit unexpected optical and electrical performance and transport behavior, opening up new possibilities for photoluminescence and rectifier diode devices. However, applications based on this heterostructure still face challenges, particularly in terms of photodetector, photoelectric emitter, optical modulator, and optical fiber devices under high-temperature conditions. This article explores the potential and prospects of their combined heterostructures in the field of optoelectronic devices such as photodetector, light emitting diode (LED), memory, field effect transistor (FET) and sensing. TiO₂/BDD heterojunction can enhance photoresponsivity and extend the spectral detection range which enables stability in high-temperature and harsh environments due to BDD’s thermal conductivity. This article proposes future research directions and prospects to facilitate the development of TiO₂ nanostructured materials and BDD-based heterostructures, providing a foundation for enhancing photoresponsivity and extending the spectral detection range enables stability in high-temperature and high-frequency optoelectronic devices field. Further research and exploration of optoelectronic devices based on TiO₂-BDD heterostructures hold significant importance, offering new breakthroughs and innovations for the future development of optoelectronic technology. Full article

Organic photovoltaic (OPV) technology, namely, organic solar cells (OSCs), have garnered attention as a sustainable and adaptable substitute for traditional silicon-based solar panels. Their lightweight construction, adaptability with various substrates, and capacity for low-energy production techniques make them formidable contenders for sustainable energy applications. Nonetheless, due to the swift advancement of OPV technology, there is increasing apprehension that existing life cycle assessment (LCA) studies may inadequately reflect their environmental consequences. This review aggregates and assesses LCA research to ascertain the extent to which existing studies accurately represent the genuine sustainability of OPVs. This paper conducts a comprehensive analysis of materials, manufacturing processes, device architecture, and end-of-life pathways, identifying methodological deficiencies, emphasizing critical environmental performance metrics, and examining how conceptual product design can improve environmental results. The results highlight the necessity for standardized, transparent LCA frameworks adapted to the changing OPV landscape. Full article

Conventional fabrication of high-efficiency organic solar cells (OSCs) predominantly relies on vacuum-evaporated metal top electrodes such as Ag and Al, which hinder large-scale industrial production. Gallium-based liquid metals (GaLMs), particularly the eutectic gallium–indium alloy (EGaIn), represent promising candidates to conventional vacuum-evaporated metal top electrodes due to their excellent printability and high electrical conductivity. In this study, we fabricated vacuum-free OSCs based on GaLM electrodes (Ga, EGaIn, and Galinstan) and analyzed the device performances. Rigid devices with EGaIn electrodes achieved a champion power conversion efficiency (PCE) of 15.6%. Remarkably, all-solution-processed ultrathin flexible devices employing silver nanowire (AgNW) bottom electrodes in combination with EGaIn top electrodes achieved a PCE of 13.8% while maintaining 83.4% of their initial performance after 100 compression–tension cycles (at 30% strain). This work highlights the potential of GaLMs as cost-effective, scalable, and high-performance top electrodes for next-generation flexible photovoltaic devices, paving the way for their industrial adoption. Full article

The aim of this study was the hydrothermal leaching of silver from waste monocrystalline silicon (m-Si) and polycrystalline silicon (p-Si) photovoltaic panel (PV) cells using organic acids, namely oxalic acid (OA) and citric acid (CA). Before leaching, two different pretreatment procedures were applied. First, the fluoropolymer backsheet was manually removed from the panel pieces and, then, the samples were subjected to high-temperature heating for the thermal degradation of the ethylene vinyl acetate (EVA) polymer. When removal by hand was not feasible, the second pretreatment procedure was followed by toluene immersion to remove the EVA and backsheet and separate the cells, glass, and films. After pretreatment, 4 M HCl leaching was applied to remove the aluminum layer from the cells. The remaining cells were subjected to hydrothermal leaching with organic acids to extract the silver. Several hydrothermal parameters were investigated, such as acid concentration (1-1.5-2 M), processing time (60-105-150 min), and temperature (150-180-210 °C), while the liquid-to-solid (L/S) ratio was fixed at 30 mL: 1 g, based on preliminary tests. Response surface methodology (RSM) was applied to optimize the hydrothermal leaching parameters. The optimized parameters were 210 °C, 95 min, 2 M CA or 210 °C, 60 min, 1 M OA. OA was more effective in Ag leaching than CA. The results were compared to HNO₃ leaching. The green leaching of silver from end-of-life PV panels with organic acids is an environmentally beneficial route. Full article

Recently, research and development in the field of dye-sensitized solar cells has been actively advanced, as the technology constitutes a potential alternative to silicon-based photovoltaic devices. Modification of the molecular structure of the dye can enhance the adsorption on the TiO₂ surface, improve the light absorption capacity, suppress the charge recombination, increase the electron injection rate, and thereby improve the overall performance of the solar cell. Carbazole and phenothiazine are rigid heterocyclic compounds containing nitrogen as a heteroatom with large π-conjugated skeletons. Phenothiazine differs from carbazole by the presence of sulfur as an additional electron-rich heteroatom. The inclusion of this heteroatom in the structure of the compounds can indeed improve the electron-donating properties, affect the conjugation, and thus affect the optical, electronic, and electrochemical properties of the chromophores as a whole. The difference in planarity when comparing carbazole with phenothiazine can be useful from several points of view. The planar structure of carbazole increases the degree of conjugation and the electron transfer capacity, which can increase the photocurrent of the cell. The nonplanar structure of phenothiazine helps to prevent π-stacking aggregation. This review comprehensively summarizes the progress in the field of synthesis of organic dyes for solar cells with an emphasis on the comparative analysis of two electron-donating moieties, carbazole and phenothiazine. In addition, the review describes in detail the relationship between the structure of the compounds (dyes), their properties, and the performance of solar cells. Full article

The field of photovoltaics (PV) continually seeks innovative materials solutions to enhance the efficiency and the stability of their standard devices. Core-shell nanoparticles have emerged as a promising new technology with unique structural attributes and widely tunable properties. This paper reviews the use of plasmonic core-shell nanoparticles in PV applications through various experimental validations. We describe advancements in the design and in the control over the properties of core-shell nanoparticles and highlight their integration into various solar cells, based on their ability to finely tune optical, electronic, and chemical properties. We also discuss experimental results for organic, perovskite, and dye-sensitized solar cells, where core-shell nanoparticles have been successfully deployed. Additionally, we identify gaps in the current research, such as the need for scalable synthesis methods and long-term stability assessments, and we will point out promising new developments at the frontier of that field. Full article

Organic–inorganic hybrid flexible perovskite solar cells (F-PSCs) have garnered considerable interest owing to their exceptional power conversion efficiency (PCE) and stable operational characteristics. However, F-PSCs continue to exhibit significantly lower PCE than their rigid counterparts. Herein, we employed 3-chloro-4-methoxybenzylamine hydrochloride (CMBACl) treatment to grow in situ two-dimensional (2D) perovskite layers on three-dimensional (3D) perovskite films. Through comprehensive physicochemical characterization, including X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and photoluminescence (PL) mapping, we demonstrated that CMBACl treatment enabled the in situ growth of two-dimensional (2D) perovskite layers on three-dimensional (3D) perovskite films via chemical interactions between CMBA⁺ cations and undercoordinated Pb²⁺ sites. The organic cation (CMBA⁺) bound to uncoordinated Pb²⁺ ions and residual PbI₂, while the chlorine anion (Cl⁻) filled iodine vacancies in the perovskite lattice, thereby forming a high-quality 2D/3D heterojunction structure. The CMBACl treatment effectively passivated surface defects in the perovskite films, prolonged charge carrier lifetimes, and enhanced the operational stability of the photovoltaic devices. Additionally, the hybrid 2D/3D architecture also improved energy band matching, thereby boosting charge transfer performance. The optimized flexible devices demonstrated a PCE of 23.15%, while retaining over 82% of their initial efficiency after enduring 5000 bending cycles under a 5 mm curvature radius (R = 5 mm). The unpackaged devices retained 94% of their initial efficiency after 1000 h under ambient conditions with a relative humidity (RH) of 45 ± 5%. This strategy offers practical guidelines for selecting interface passivation materials to enhance the efficiency and stability of F-PSCs. Full article

Conductive polymers play a crucial role in the advancement of modern technologies, particularly in the field of organic photovoltaics (OPVs). Due to advantages such as flexibility, low specific weight, ease of processing, and low production costs, polymeric materials present an attractive alternative to traditional photovoltaic materials. This study investigates the properties of a polymer blend composed of PCPDTBT (donor) and PNDI(2HD)2T (acceptor), used as the active layer in bulk heterojunction (BHJ) solar cells. The motivation behind this research was the search for a novel n-type polymer material with potentially better properties than the commonly used P(NDI2OD-T2). Comprehensive characterization of thin films made from the individual polymers and their blend was conducted using Fourier Transform Infrared Spectroscopy (FTIR), Atomic Force Microscopy (AFM), Scanning Electron Microscopy (SEM), Ultraviolet-Visible Spectroscopy (UV-Vis), four-point probe conductivity measurements, and photovoltaic testing. The prepared films were continuous, uniform, and exhibited low surface roughness (R_a < 2.5 nm). Spectroscopic analysis showed that the blend absorbs light in a broad range of the spectrum, with slight bathochromic shifts compared to individual polymers. Electrical measurements indicated that the blend’s conductivity (9.1 µS/cm) was lower than that of pure PCPDTBT but higher than that of PNDI(2HD)2T, with an optical band gap of 1.34 eV. Photovoltaic devices fabricated using the blend demonstrated an average power conversion efficiency (PCE) of 6.45%, with a short-circuit current of 14.37 mA/cm² and an open-circuit voltage of 0.89 V. These results confirm the feasibility of using PCPDTBT:PNDI(2HD)2T blends as active layers in BHJ solar cells and provide a promising direction for further optimization in terms of polymer ratio and processing conditions. Full article

The hole-transport layer (HTL) plays a pivotal role in engineering high-performance inverted perovskite solar cells (PSCs), as it governs both hole extraction/transport dynamics and critically impacts the crystallization quality of the perovskite absorber layer in device architectures. Recent advancements have highlighted self-assembled monolayers (SAMs) as promising candidates for next-generation HTL materials in inverted PSCs due to their intrinsic advantages over conventional counterparts. These molecularly engineered interfaces demonstrate superior characteristics including simplified purification processes, tunable molecular structures, and enhanced interfacial compatibility with device substrates. This review systematically examines the progress, existing challenges, and future prospects of SAM-based HTLs in inverted photovoltaic systems, aiming to establish a systematic framework for understanding their structure–property relationships. The review is organized into three sections: (1) fundamental architecture of inverted PSCs, (2) molecular design principles of SAMs with emphasis on head-group functionality, and (3) recent breakthroughs in SAM-engineered HTLs and their modification strategies for HTL optimization. Through critical analysis of performance benchmarks and interfacial engineering approaches, we elucidate both the technological merits and inherent limitations of SAM implementation in photovoltaic devices. Furthermore, we propose strategic directions for advancing SAM-based HTL development, focusing on molecular customization and interfacial engineering to achieve device efficiency and stability targets. This comprehensive work aims to establish a knowledge platform for accelerating the rational design of SAM-modified interfaces in next-generation optoelectronic devices. Full article

Perovskite/organic tandem solar cells, as a next-generation high-efficiency photovoltaic technology, integrate the tunable bandgap characteristics of perovskite materials with the broad spectral absorption advantages of organic semiconductors, demonstrating remarkable potential to surpass the theoretical efficiency limits of single-junction cells, enhance device stability, and expand application scenarios. This architecture supports low-temperature solution processing and offers tunable bandgaps, lightweight flexibility, and ecofriendly advantages. This review systematically summarizes research progress in this field, with a primary focus on analyzing the working principles, performance optimization strategies, and key challenges of the technology. Firstly, the article discusses strategies such as defect passivation, crystallization control, and suppression of phase separation in wide-bandgap perovskite sub-cells, offering insights into mitigating open-circuit voltage losses. Secondly, for the narrow-bandgap organic sub-cells, this paper highlights the optimization strategies for both the active layer and interfacial layers, aiming to improve spectral utilization and enhance power conversion efficiency. Additionally, this paper emphasizes the optimization of optical transparency, electrical conductivity, and energy level alignment in the recombination layer, providing theoretical guidance for efficient current matching and carrier transport. Full article

The growing demand for energy, coupled with the unsustainable nature of fossil fuels due to global warming and the greenhouse effect, have led to the advancement of renewable energy production concepts. Innovations such as photovoltaics, wind energy, and infrared energy harvesters are emerging as viable solutions. The challenge lies in the stochastic nature of renewable energy sources, which necessitates the implementation of electrical energy storage solutions, whether through batteries, supercapacitors, or hydrogen production. In this regard, innovative materials are essential to address the questions associated with these technologies. Metal-organic frameworks (MOFs) are crucial for achieving clean and efficient energy conversion in fuel cells and storage in batteries and supercapacitors. Metal-organic frameworks (MOFs) can be used as electrocatalytic materials, membranes for electrolytes, and energy storage materials. They exhibit exceptional design versatility, large surface, and can be functionalized with ligands with several charges and metallic centers. This article offers an in-depth examination of materials and devices utilizing metal-organic frameworks (MOFs) for electrochemical processes concerning the generation, transformation, and storage of electrical energy. This review specifically focuses on rechargeable batteries and fuel cells that incorporate MOFs. Finally, an outlook on the potential applications of MOFs in electrochemical industries is presented. Full article

In this study, the applicability of an integrated-hybrid process was performed in a divided electrochemical cell for removing organic matter from a polluted effluent with simultaneous production of green H₂. After that, the depolluted water was reused, for the first time, in the cathodic compartment once again, in the same cell to be a viable environmental alternative for converting water into energy (green H₂) with higher efficiency and reasonable cost requirements. The production of green H₂ in the cathodic compartment (Ni-Fe-based steel stainless (SS) mesh as cathode), in concomitance with the electrochemical oxidation (EO) of wastewater in the anodic compartment (boron-doped diamond (BDD) supported in Nb as anode), was studied (by applying different current densities (j = 30, 60 and 90 mA cm⁻²) at 25 °C) in a divided-membrane type electrochemical cell driven by a photovoltaic (PV) energy source. The results clearly showed that, in the first step, the water anodically treated by applying 90 mA cm⁻² for 180 min reached high-quality water parameters. Meanwhile, green H₂ production was greater than 1.3 L, with a Faradaic efficiency of 100%. Then, in a second step, the water anodically treated was reused in the cathodic compartment again for a new integrated-hybrid process with the same electrodes under the same experimental conditions. The results showed that the reuse of water in the cathodic compartment is a sustainable strategy to produce green H₂ when compared to the electrolysis using clean water. Finally, two implied benefits of the proposed process are the production of green H₂ and wastewater cleanup, both of which are equally significant and sustainable. The possible use of H₂ as an energetic carrier in developing nations is a final point about sustainability improvements. This is a win-win solution. Full article

This work explores the dispersed heterojunction of tris-(8-hydroxyquinoline) aluminum (AlQ₃) and 8-hydroxyquinoline zinc (ZnQ₂) with tetracyanoquinodimethane (TCNQ) and 2,6-diaminoanthraquinone (DAAq). Thin films of these organic semiconductors were deposited and analyzed, with their structures calculated with the B3PW91/6-31G** method. The optimized structure for AlQ₃-TCNQ, AlQ₃-DAAq, is achieved by means of three hydrogen bonds, whereas for ZnQ₂-DAAq, two hydrogen interactions are predicted. These structures were recalculated including the GD3 dispersion term. A stable ordering was also achieved for AlQ₃-TCNQ-GD3, AlQ₃-DAAq-GD3, and ZnQ₂-DAAq-GD3 with four and two hydrogen contacts for the former and the two latter, respectively. Infrared (IR) and UV-visible spectroscopy confirmed these theoretical predictions, in addition to obtaining the optical band gap for the films. The optical band gap values ranged between 1.62 and 2.97 eV (theoretical) and between 2.46 and 2.87 eV (experimental). Additional optical parameters and electrical behavior were obtained, which indicates the potential of the films to be used as organic semiconductors. All three films showed transmittance above 76%, which also broadens the range of applications in electrodes, transparent transistors, or photovoltaic cells. Devices fabricated using these materials displayed ohmic electrical behavior, with peak current values between 2 × 10⁻³ and 6 × 10⁻³ A. Full article

This study addresses the development and optothermal analysis of donor–acceptor thin layers, including materials universally used in organic photovoltaic cells. This article presents the impact of temperature on the optical properties and morphology of thin films made from materials commonly used in organic solar cells. This research focused on two donor materials (PTB7 and PTB7th) and two non-fullerene acceptors (Y5 and Y6), individually and in binary combinations with PTB7 and PTB7th. This study employed various techniques, including UV–Vis spectroscopy, ellipsometry, and atomic force microscopy (AFM), to analyze changes in the absorption, refractive index, extinction coefficient, and morphology at temperatures ranging from 30 °C to 120 °C. This research shows reversible changes in thickness and absorption with temperature, but the extent of these changes differs between PTB7 and PTB7th. Y5 shows some reversible changes, while Y6 demonstrates greater instability and more permanent changes at higher temperatures. The enhanced thermal stability of binary mixtures compared to single-component materials was observed. Full article