Search Results (5,516)

The ambient stability of ambient-processed lead-free perovskite absorbers remains a critical challenge toward scalable, eco-friendly photovoltaics. Herein, we systematically investigate the time-dependent structural and morphological evolution of drop-cast ambient-processed Cs₃Sb₂I₉ thin films, being a potential non-toxic and stable solar absorber candidate (energy bandgap ~2 eV) for solar cells, stored under uncontrolled ambient condition (~60% Relative humidity) for 28 days. Sequential X-ray diffraction (XRD) and surface morphology analyses using scanning electron microscope (SEM) reveal that the films preserve their trigonal P3̅m1 phase throughout aging, confirming phase stability. Moderate moisture exposure may induce partial recrystallization and subtle structural reorganization, possibly including minor c-axis realignment, leading to reduced lattice strain and improved crystallite coherence. Even after prolonged aging, no secondary phases or micro-cracks are detected, underscoring the slow degradation kinetics and robust Sb–I bonding that stabilize the layered [Sb₂I₉]³⁻ dimers. The late-stage increase in diffraction intensity and partial recovery of crystallographic parameters could indicate transient structural reorganization, potentially associated with moisture-mediated reordering within an overall degradation pathway. These observations suggest some degree of morphological persistence and structural tolerance of Cs₃Sb₂I₉ under ambient conditions, rather than complete stability. This behavior offers useful insights into ambient processing and the long-term reliability of lead-free perovskite photovoltaics. Full article

Organic-type solar cells containing an active layer of block copolymer donor PTB7-Fx (x = 0, 20, and 100), based on benzo [1,2-b:4,5-b’]dithiophene and variably fluorinated thieno [3,4-b]thiophene units, and fullerene acceptor [6,6]phenyl-C₇₁-methylbutyrate, were constructed. The active layer thin film of the solar cells was obtained from a dichlorobenzene solution at an established concentration via spin-coating of the donor–acceptor mixture in the presence of solvent additives such as 3% diiodooctane and 1% triethyl phosphate. Organic photovoltaic elements with normal device architecture were prepared on glass substrates using an indium tin oxide anode, a spin-coated hole transporting layer of poly(ethylene dioxythiophene):polystyrenesulfonate, the aforementioned active layer, followed by an electron transporting layer of zinc oxide nanoparticles, and finally a magnetron sputtered silver (Ag) top-electrode. The optical properties, thin film morphology, and the thickness of the active layers were investigated. Additionally, current density–voltage characteristics and impedance spectra of photovoltaic devices were measured. It was found that PTB7-Fx:PC₇₁BM-based solar cells processed in the presence of two types of solvent additives, diiodooctane and triethyl phosphate, with a sputtered Ag top-electrode display similar absorption and quantum efficiency spectra, as well as comparable current density–voltage characteristics and efficiencies to the same devices fabricated without additives. The diiodooctane solvent additive preferably dissolves the fullerene component and has a positive effect on fill factor enhancement, impedance spectra improvement, and amelioration in charge carrier transport and collection, whereas the triethyl phosphate solvent additive preferentially dissolves the copolymer donor and has a more pronounced impact on the refined morphology of the thin film active layers. Full article

Maritime transport is under increasing pressure to cut greenhouse gas and pollutant emissions to meet global decarbonization goals and tighter environmental standards. Ship electric propulsion systems offer a promising solution for short-range maritime operations, particularly for small vessels and coastal activities. Full-electric vessels can significantly reduce operational emissions; however, a key challenge is the extensive charging time for onboard energy storage, which can affect operational continuity and logistical efficiency. This study examines mission planning and energy management for a hybrid multi-source electric mail boat operating in the Aeolian archipelago. It evaluates the viability and performance of a daily inter-island route powered by a high-temperature methanol fuel cell, batteries, and photovoltaic panels. A routing and simulation framework was developed to model the boat’s itinerary among seven islands, accounting for realistic navigation speeds, scheduled stops, solar energy availability, and battery state-of-charge constraints. The study analyzes distance, travel time, energy consumption, solar power generation, and fuel–electric usage with high temporal resolution, enabling detailed analysis of power flows during sailing and docking. Several operational strategies were assessed, including periods of increased speed supported by battery assistance and fuel–electric cell output, combined with coordinated energy management to keep battery levels above a lower acceptable threshold while completing the route in a single day. The methodology provides a practical tool for planning low-emission island networks and supports the integration of innovative energy systems into small electric workboats operating in specific maritime regions. Full article

To enhance the energy efficiency and environmental sustainability of solar greenhouses, precise microclimate control is essential. Composite thermal blankets critically influence heating demand and carbon footprint, yet conventional heat transfer models often neglect their internal structural characteristics, limiting simulation accuracy and optimization. Accordingly, a heat transfer model for composite thermal blankets was developed based on the law of energy conservation. The model discretizes the internal structure and integrates radiation, convection, conduction, and latent heat from condensation. It uniquely incorporates dynamic environmental factors and blanket properties including layered composition, porosity, and moisture content. Accuracy was validated through numerical simulations and field experiments in both traditional brick-wall and prefabricated flexible-wall solar greenhouses under various weather conditions. Validation showed strong agreement: for the brick-wall greenhouse, mean absolute error (MAE) was 1.21 °C, root mean square error (RMSE) 1.27 °C, and R² 0.97; for the flexible-wall greenhouse, MAE was 0.56 °C, RMSE 1.08 °C, and R² 0.85. These indicators confirm that the model reliably quantifies the impact of thermal insulation blanket material and structure on thermal performance, providing a basis for design optimization and a reduction in supplemental heating demand and carbon emissions. Further analysis examined the porosity and moisture effects on spray-bonded cotton, PE foam, and needle-punched felt. Under low moisture, higher porosity reduced thermal conductivity by up to 27.4%, 57.6%, and 52.4%, respectively. However, under high moisture, conductivity increased with porosity in materials with interconnected pores (spray-bonded cotton and Needle-punched felt) due to continuous water channels, while closed-cell PE foam conductivity continued decreasing. All materials showed linearly increasing conductivity with moisture content, with higher-porosity materials exhibiting greater sensitivity. For example, at porosities of 0.95, 0.95, and 0.85, moisture content rising from 0 to 0.225 increased conductivity by 264%, 209.6%, and 196.7%. This model provides a robust theoretical foundation for the scientific selection, structural optimization, and performance evaluation of composite thermal blankets in greenhouse applications. Full article

Crystalline silicon solar cells have long dominated the global photovoltaic market due to their mature manufacturing processes, excellent stability, and abundant raw material reserves, accounting for over 90% of the total PV market share. However, single−junction c−Si solar cells are approaching the Shockley–Queisser (SQ) efficiency limit of ~29.4%, creating an urgent need for next−generation PV technologies to achieve higher power conversion efficiency (PCE). Monolithic perovskite/silicon tandem solar cells (PSTSCs) stand as the most commercially promising technology to surpass the single−junction efficiency limit. Since their first demonstration in 2015, PSTSCs have experienced rapid technological advancement, with the certified PCE reaching 35.0% in 2026. This review posits that their rapid efficiency ascent is not serendipitous but driven by synergistic innovations across critical subsystems. We systematically deconstruct these efficiency drivers, encompassing top−cell materials, bottom−cell architecture, and optical management. We conclude by outlining future research frontiers essential for transforming this lab−champion technology into a mainstream energy solution. Full article

This research study conducts a computational analysis of a two-terminal (2T) Perovskite-on-silicon (PVK-Si) solar cell with a tandem configuration. The motivation for this analysis arises from the outstanding potential of PVK-Si solar cells to surpass the efficiency limitations of conventional photovoltaic technology. The tandem configuration utilizes a combination of CsSnBr₃ in the top sub-cell and crystalline silicon (c-Si) in the bottom sub-cell. After optimizing parameters of the top sub-cell (FTO/TiO₂/CsSnBr₃/rGO/Au), which included the thicknesses of CsSnBr₃ (500 nm), TiO₂ (40 nm), rGO (50 nm), the interface defects (10¹³ cm⁻²), and the bandgap of CsSnBr₃ (1.78 eV), the PVK-Si tandem device was simulated. As a result, the top CsSnBr₃ sub-cell achieved an efficiency of 21.62%, while the bottom silicon sub-cell achieved an efficiency of 23.48%. Subsequently, the sub-cells were interconnected in series using filtered spectra and current-density matching. After interpolating the J-V curves, the tandem exhibited a global efficiency of 29.76%, a fill factor (FF) of 85.30%, a matched current density (J_SC) of 19.02 mA/cm², and an open-circuit voltage (V_OC) of 1.83 V. The EQE results confirmed efficient photon management via complementary sub-cell absorption. The performance is competitive with experimental lead-based tandems and exceeds that of current lead-free simulations. Therefore, this research proposes a viable pathway for the development of non-toxic, cost-effective tandem solar systems with manufacturing capabilities. Full article

CuIn₅Se₈ is reported as a remarkable copper-deficient layer that contains ordered vacancy compounds (OVCs) for high-efficiency chalcopyrite-based solar cells; however, the understanding of its carrier characteristics has remained limited. OVCs could naturally form on the surface of chalcopyrite absorber. In this study, the carrier dynamics characteristics of OVCs were investigated by constructing a junction consisting of chalcopyrite absorber and CdS buffer layer. At first, the band structure of CuIn₅Se₈ was studied to determine the bandgap properties. Then, thermodynamic stability, defect formation energy, defects and carrier concentration, defect transition energy level of CuIn₅Se₈ and its Cd doping state (caused by CdS) were comparatively studied. The results suggest that Cd doping has different effects on the defect and carrier characteristics of OVCs with various chemical potentials. However, the OVC always remains n-type under the whole thermodynamically stable region, with contribution from the hallow-level In_Cu donor defect. Finally, the OVC’s carrier dynamics characteristics were assessed using the collected defect and carrier data. It is indicated that the OVC layer may contribute to the formation of a p-n homojunction in solar cells. Under selenium-rich conditions, the OVC layer increases the carrier density on the n-type side of p-n junction nearly 30-fold, which helps reduce the difference in carrier density and minority current density between two sides of the p-n junction. The conversion efficiency of the solar cell with OVC shows a 7.25% improvement when compared to the control. The distinct behavior of OVCs may serve as a valuable reference for the creation or improvement of a related functional film layer or device. Full article

Photovoltaic technologies represent an increasingly relevant alternative for developing renewable energy sources, particularly those based on light-harvesting materials such as perovskite solar cells (PSCs) and dye-sensitized solar cells (DSSCs), which have achieved efficiencies of 27.3% and 13.0%, respectively. In this context, phenothiazine (PTZ) has attracted considerable interest as a structural block due to its outstanding structural and photophysical properties, which also represent low production costs and reduced environmental impact. This review presents recent advances in the design and development of phenothiazine-based organic materials for photovoltaic applications, analyzing the main synthetic routes for obtaining this nucleus, as well as the fundamental aspects related to the operation of solar cells, including relevant device parameters. Furthermore, several studies focused on the synthesis, characterization, and performance of new phenothiazine-derived molecules used in photovoltaic devices are also examined. Finally, the most relevant conclusions are discussed, and future perspectives for the use of these materials in solar technologies are proposed. Full article

Dye-sensitized solar cells (DSSCs) remain attractive as low-cost photovoltaic devices; however, their practical efficiency is still constrained by electron-transport losses, interfacial recombination, and incomplete light harvesting in conventional titanium dioxide (TiO₂) photoanodes. The effects of TiO₂ film thickness, multi-walled carbon nanotube (MWCNT) incorporation, and multilayer oxide interface engineering on DSSC performance were examined. Degussa P25-TiO₂ photoanodes were first optimized with respect to thickness, after which controlled MWCNT loadings and sequential compact sol–gel TiO₂ and tin dioxide (SnO₂) sublayers were introduced. The optimum pristine P25-TiO₂ photoanode thickness was 9.11 μm, yielding an open-circuit voltage of 0.74 ± 0.01 V, a short-circuit current density of 14.10 ± 0.40 mA/cm², a fill factor of 56.24 ± 1.00%, and a power-conversion efficiency of 5.93 ± 0.20%. The incorporation of 0.025 wt% MWCNTs increased the efficiency to 6.04 ± 0.20%, corresponding to an absolute gain of 0.11 percentage points. The best performance was obtained with the sol–gel SnO₂/sol–gel TiO₂/P25-CNT multilayer photoanode, which delivered 0.74 ± 0.02 V, 16.22 ± 0.40 mA/cm², 57.59 ± 1.00%, and 6.89 ± 0.30%, respectively. FE-SEM, EIS, XRD, Heated Ultrasonic Cleaner and UV–visible analyses indicate that the multilayer architecture preserves porosity, enhances light harvesting, and suppresses interfacial recombination, while the CNT network facilitates charge transport. Full article

The development of sustainable encapsulation materials with tunable thermomechanical properties remains a critical challenge for photovoltaic reliability. Currently, the mainstream encapsulant for polycrystalline silicon solar cells is crosslinked EVA (Ethylene-Vinyl Acetate), which complicates the end-of-life recycling and reuse of modules. There is an urgent need to develop a novel encapsulant that combines excellent barrier properties with thermoplastic recyclability. Herein, we report a novel series of thermally decomposable CO₂-based thermoplastic polyurethane (PPC-TE) films engineered through the rational design of soft and hard segments. Utilizing polycarbonate diol (PPCDL) and polyether glycol (PEG) as soft segments, we systematically tailor material properties by modulating PEG-to-PPCDL ratios (5–20 wt%) and PEG molecular weights (1000–4000 g/mol). The optimized PPC-TE films exhibit excellent transmittance (>90%), adjustable glass transition temperature (T_g: 35.1 °C~11.6 °C), and remarkable mechanical adaptability (51~92 HA). The PPC-TE films exhibit water vapor permeability (WVP) as low as 14.8 g·mm·m⁻²·day⁻¹ and oxygen permeability (OP) of 4.13 cc·mm·m⁻² day⁻¹ at 15 wt% PEG content, surpassing commercial ethylene–vinyl acetate (EVA) encapsulants. Notably, these films demonstrate fully thermal decomposition above 350 °C, facilitating eco-friendly photovoltaic device recycling. Superior adhesion to glass substrates is evidenced by peel strengths up to 37 N/cm (PPC-TE2000-20) and the shrinkage rate is as low as 3%. This work contributes to improving the long-term stability of solar cells and has the potential for large-scale production. Full article

This work proposes the doping of bi-electron transport layers consisting of TiO₂/SnO₂ with iron to facilitate electron movement and recombination reduction, which results in increases in power conversion efficiency and stability enhancement. Two different PSC structures are used: device 1—FTO/TiO₂/SnO₂/MAPbI₃/Spiro-OMETAD/Ag; device 2, a modified device—FTO/TiO₂/SnO₂ + Fe/MAPbI₃/Spiro-OMETAD/Ag. Characterization analysis revealed an improvement in perovskite crystallinity in the modified device; this leads to reductions in trap state density and the recombination of charges that enhance charge extraction. UV-vis absorbance enhancement in the modified device revealed an enhancement in the perovskite layer morphology and good coverage. As a result, PSCs with a short circuit current of 23.35 mA/cm², open circuit voltage of 1.07 V, fill factor of 0.73, and high PCE of 18.17% are obtained from device 2, compared to PSCs with only 22.13 mA/cm², 1.03 V, 0.7, and 16.053% for device 1 without Fe doping, respectively. The results reveal that the device based on Fe doping is more stable than the pristine one under stability tests with regard to aging, thermal, stress and prolonged light. Full article

Nanophotonics, an interdisciplinary field merging nanotechnology and photonics, has enabled transformative advancements across diverse sectors, including green energy, biomedicine, and optical computing. This review comprehensively examines recent progress in nanophotonic principles and applications, highlighting key innovations in material design, device engineering, and system integration. In renewable energy, nanophotonics allows the use of light-trapping nanostructures and spectral control in perovskite solar cells, concentrating solar power systems, and thermophotovoltaics. This has significantly enhanced solar conversion efficiencies, approaching theoretical limits. In biosensing, nanophotonic platforms achieve unprecedented sensitivity in detecting biomolecules, pathogens, and pollutants, enabling real-time diagnostics and environmental monitoring. Medical applications leverage tailored light–matter interactions for precision photothermal therapy, image-guided surgery, and early disease detection. Furthermore, nanophotonics underpins next-generation optical neural networks and neuromorphic computing, offering ultrafast, energy-efficient alternatives to von Neumann architectures. Despite rapid growth, challenges in scalability, fabrication costs, and material stability persist. Future advancements will rely on novel materials, AI-driven design optimization, and multidisciplinary approaches to enable scalable, low-cost deployment. This review summarizes recent progress and highlights future trends, including novel material systems, multidisciplinary approaches, and enhanced computational capabilities, paving the way for transformative applications in this rapidly evolving field. Full article

Nano–bio hybrid catalysts have emerged as a promising platform for sustainable energy conversion by integrating the high selectivity of enzymes with the structural robustness and conductivity of nanomaterials. In recent years, the growing demand for clean energy technologies has driven the development of biohybrid systems capable of efficient electron transfer, enhanced catalytic activity, and improved operational stability. This review comprehensively discusses the design principles, mechanistic foundations, and performance metrics of enzyme–nanomaterial interfaces for energy-related applications. We first outline the fundamentals of enzymatic redox catalysis and the limitations of free enzymes in practical systems. Subsequently, we examine the functional roles of nanomaterials including carbon-based materials, metal and metal oxide nanoparticles, and two-dimensional platforms such as MXenes in facilitating enzyme immobilization and promoting direct or mediated electron transfer. Special emphasis is placed on engineering strategies at the bio–nano interface, including immobilization techniques, surface functionalization, and structural tuning to optimize catalytic efficiency. The review further highlights representative hybrid systems based on laccase, glucose oxidase, peroxidase, and hydrogenase enzymes, and evaluates their applications in biofuel cells, solar–bio hybrid systems, green oxidation reactions, and self-powered biosystems. Stability challenges, deactivation mechanisms, and enhancement strategies such as polymer coatings, cross-linking, and nanoconfinement are critically analyzed. Finally, emerging directions including artificial enzymes, AI-guided catalyst design, and self-healing bioelectrodes are discussed to provide a forward-looking perspective on next-generation sustainable bioelectrocatalytic systems. Full article

Activating PIK3CA mutations occur in approximately 40% of hormone receptor-positive (HR+)/HER2-negative breast cancers and represent a major driver of endocrine resistance. The PI3Kα-selective inhibitor alpelisib, in combination with fulvestrant, significantly improves progression-free survival in patients with PIK3CA-mutant disease, as demonstrated in the SOLAR-1 trial. However, this therapeutic strategy is frequently complicated by treatment-induced hyperglycemia, a metabolic disturbance that promotes oxidative stress, mitochondrial dysfunction, and inflammatory signaling, thereby increasing cardiovascular vulnerability. Sodium–glucose cotransporter-2 (SGLT2) inhibitors have emerged as cardiometabolic modulators with benefits extending beyond glucose lowering. In this study, we used a human cardiomyocyte in vitro model designed to recapitulate the hyperglycemic metabolic milieu observed in breast cancer patients receiving PI3Kα-targeted therapy, to investigate whether the SGLT2 inhibitor dapagliflozin directly protects cardiomyocytes from alpelisib- and fulvestrant-induced injury. Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) were cultured under hyperglycemic conditions (25 mM glucose) to mimic the metabolic environment associated with PI3Kα inhibitor-induced dysglycemia. Cells were exposed to alpelisib (100 nM) and fulvestrant (100 nM), alone or in combination, in the absence or presence of dapagliflozin (1 μM). Cardiomyocyte viability was assessed using the MTS assay, mitochondrial function by TMRM-based mitochondrial membrane potential (ΔΨm) measurements, and apoptosis by caspase-3 quantification. Cardiomyocyte injury was evaluated by release of cardiac troponin I and heart-type fatty acid binding protein (H-FABP). Lipid peroxidation markers (MDA and 4-HNE) were measured to assess oxidative membrane damage. Intracellular inflammasome-related signaling (NLRP3 and MyD88) and secreted inflammatory mediators (IL-1β, IL-18, IL-6, TNF-α, and CCL2) were quantified by ELISA. Exposure to alpelisib, particularly in combination with fulvestrant, significantly reduced cardiomyocyte viability, induced mitochondrial depolarization, and increased caspase-3-mediated apoptotic signaling. These alterations were accompanied by elevated lipid peroxidation (MDA and 4-HNE) and increased release of cardiac injury biomarkers (troponin I and H-FABP). Alpelisib-based treatments also activated inflammasome-related signaling, as indicated by increased intracellular NLRP3 and MyD88 levels and enhanced secretion of pro-inflammatory mediators (IL-1β, IL-18, IL-6, TNF-α, and CCL2). Co-treatment with dapagliflozin significantly attenuated these alterations, preserving mitochondrial membrane potential, reducing apoptotic signaling, limiting oxidative membrane damage, and suppressing inflammatory cytokine release. This study provides evidence that alpelisib-based therapy under hyperglycemic conditions is associated with oxidative, mitochondrial, and inflammatory stress responses in human cardiomyocytes, recapitulating key features of cardiometabolic stress relevant to PI3Kα-targeted therapy. Importantly, dapagliflozin markedly attenuated these alterations, supporting a potential cardioprotective role that may extend beyond glycemic control. These findings provide a mechanistic rationale for further investigation of SGLT2 inhibition as a cardiometabolic protective strategy in patients receiving PI3Kα inhibitor-based cancer therapy. Full article