Search Results (369)

The rapid advancement of photovoltaic (PV) technologies has transformed solar energy systems into intelligent, high-efficiency platforms. This review systematically examines next-generation PV materials, hybrid system architectures, and intelligent control strategies. Key technologies include perovskite-based tandem cells, N-type TOPCon, bifacial, heterojunction (HJT), and photovoltaic-thermal (PVT) systems. These innovations overcome the intrinsic limitations of conventional P-type silicon panels by reducing recombination losses, mitigating light- and temperature-induced degradation, and enhancing energy yield under real-world operating conditions. At the system level, AI-enabled inverters, adaptive maximum power point tracking (MPPT), predictive maintenance, and real-time grid interaction enable dynamic optimization under variable irradiance, thermal stress, and load fluctuations. A critical comparison across diverse deployment environments highlights current challenges, including manufacturing complexity, material stability, and AI data-quality limitations. Despite higher upfront costs and system complexity, these advanced PV systems offer superior long-term performance, improved reliability, and reduced levelized cost of electricity through lower degradation rates and enhanced operational resilience. Collectively, intelligent, material-optimized PV technologies represent a scalable, sustainable, and grid-compatible solution for solar energy deployment across diverse climates, supporting the global transition toward low-carbon energy infrastructures. 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

Additive engineering has become a critical strategy for optimizing the morphology and performance of bulk heterojunction (BHJ) organic solar cells (OSCs), while volatile solid additives have been widely employed to control nanoscale phase separation during film formation. Concerns regarding reproducibility, residual solvent effects, and long-term stability have stimulated increasing interest in non-volatile solid additives. In recent years, solid additive engineering has emerged as a promising approach for modulating molecular packing, regulating phase separation, enhancing charge transport, and improving device stability. However, a systematic analysis of its material design principles and performance impact remains limited. This review summarizes recent progress in solid additive engineering for OSCs, categorizing reported additives into non-volatile, volatile and nanomaterials. The effects of these additives on key photovoltaic parameters, including open-circuit voltage (Voc), short-circuit current density (Jsc), fill factor (FF), and power conversion efficiency (PCE), are comparatively analyzed based on the reported data. Particular emphasis is placed on morphology and structural performance relationships and stability enhancement mechanisms. Finally, current challenges, including the lack of universal molecular design rules and limited mechanistic understanding of additive host interactions, are discussed, and future research directions are proposed. This review aims to provide a comprehensive perspective on the material-level role of solid additives and to guide the rational design of next-generation high-performance and stable organic solar cells. Full article

Interdigitated back-contact solar cells were fabricated entirely with inkjet printing. poly(3,4-ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS), TiO₂, and metal lines were printed on a textured silicon substrate with only one inkjet printer. No vacuum deposition or diffusion of a back surface field is needed for the printed IBC solar cell. Adding co-solvent to the PEDOT:PSS and passivation of the Si surface significantly reduced the losses and enhanced the short-circuit current, Jsc, and, as a result, improved the fill factor and efficiency of the devices. The thickness of the PEDOT:PSS layer is approximately half a micrometer measured by profilometer, which is thicker than the optimal range typically reported; there is still a best short-circuit current, Jsc, of 19.2 mA/cm². To further improve the performance of the devices, an anti-reflective coating on the front side is required. Also, an improved metal contact ink is needed to improve the contact resistance between the PEDOT:PSS layer and the metal contact. The initial performance of all printed cells are compared to conventionally fabricated devices. Full article

In bulk heterojunction (BHJ) organic solar cells (OSCs) employing perylene diimide (PDI)-based non-fullerene acceptors, excessive intermolecular interactions among PDI units lead to severe aggregation and pronounced donor–acceptor phase separation, both of which critically limit device performance. To address these issues, numerous structurally engineered PDI derivatives have been developed. In particular, twisted multi-PDI architectures designed to suppress intermolecular aggregation have shown improved morphological control; however, such twisted structures are often highly amorphous, which reduces electron-transport efficiency and constrains OSC performance. In this work, we introduce a mixed-acceptor strategy combining a twisted PDI dimer (SF-PDI₂) with a planar monomeric PDI (m-PDI) to balance aggregation and morphological uniformity. Ternary blend OSCs consisting of PTB7-Th as the donor and these two PDI acceptors exhibit systematic performance variations depending on their relative ratios. At the optimized composition (SF-PDI₂:m-PDI = 90:10 by weight), the device outperforms single-acceptor systems, which is attributed to controlled aggregation arising from the complementary structural features of the two PDI acceptors. This study demonstrates that combining mixed PDI acceptors with similar molecular moieties enables precise control of aggregation, improving both morphology and photovoltaic performance. Full article

We report a comprehensive spectroscopic, microscopic, and device-level investigation of the ambient-driven degradation of PTQ10:IDIC bulk-heterojunction organic solar cells (BHJ-OSCs), up to 500 h. The power conversion efficiency dropped from 9.51% to 7.69% (≈19% relative loss), primarily due to a decrease in short-circuit current density (J_SC 15.93 to 13.82 mA cm⁻²), while the open-circuit voltage remained largely stable (0.92 to 0.90 V). Atomic force microscopy reveals surface smoothing upon ageing, with the root-mean-square roughness decreasing from 4.29 to 3.45 nm, and the UV–vis absorption spectra show negligible changes, indicating preserved bulk light-harvesting capability. In contrast, X-ray photoelectron spectroscopy indicates pronounced surface compositional evolution, with a decrease in oxygen (5.18 to 3.18%) and a substantial increase in fluorine content (3.23 to 7.23%), consistent with fluorine-rich surface segregation or reorientation. Ultraviolet photoelectron spectroscopy further reveals a 0.48 eV reduction in surface work function, indicative of surface dipole modification and near-surface electronic reorganization. Collectively, these results demonstrate that ambient ageing primarily impacts interfacial chemistry and morphology rather than bulk optoelectronic properties, highlighting interfacial engineering and encapsulation as effective strategies for improving long-term device stability. Full article

Owing to the excellent performance of zinc oxide materials under ultraviolet light, this paper proposes a process for fabricating ZnO/Au heterojunction nanostructures on the surface of silicon-based solar cells using anodic aluminum oxide as the template, ultimately resulting in a novel silicon-based solar cell with an embedded ZnO/Au nanostructure array. Through model optimization and analysis of the solar cells, it is found that compared with silicon-based solar cells with double grating nanostructures, silicon-based solar cells with surface silicon nanostructure arrays prepared by similar processes, and traditional planar silicon-based solar cells, the light absorption efficiency of the proposed solar cell structure is improved by 13.2%, 35.01%, and 63.78%, respectively; its short-circuit current density and power conversion efficiency reach 40 mA/cm² and 20.17%, respectively. Meanwhile, this paper conducts an in-depth study on the performance enhancement mechanism, providing new insights for the fabrication of ZnO/Au heterojunction nanostructures and their applications in the field of solar cells. Full article

The efficiency of organic solar cells is constantly improving thanks to more advanced materials. Electron donor polymers, such as PM6 and its derivatives, as well as non-fullerene acceptors (NFAs) Y6 and ITIC and their derivatives, have become the standard materials for organic solar cell studies. To broaden the absorption range of solar cells, so-called ternary organic solar cells have been developed, which add a third material to the active layer. In this work, two chromophores based on the derivatives of the Janus-dione (s-indacene-1,3,5,7(2H,6H)-tetraone) central acceptor fragment, namely TIIC-1 and TIIC-2, were synthesized. Materials were characterized using theoretical and experimental methods, including UV-Vis absorption measurements, cyclic voltammetry, photoemission yield spectroscopy, and photoconductivity. The materials were incorporated as ternary components in PM6:Y7 bulk heterojunction solar cells. The power conversion efficiency (PCE) of PM6:Y7:TIIC-1 ternary solar cells was improved compared to binary PM6:Y7 reference cells. The PCE increased from 11.9% in binary blends to 12.5% in ternary cells. This increase is attributed to the cascade-like energy level arrangement, which facilitates charge transfer in the photoactive layer. Full article

We report a notable enhancement in the performance of small-molecule-based organic photovoltaics (OPVs) through the use of a ternary blend comprising a small-molecule donor (DTS(FBTTh₂)₂), a polymer donor (PBDTTT-EFT), and a fullerene acceptor (PC₇₁BM). By optimizing the composition of this ternary active layer, we achieved a significant increase in power conversion efficiency from 7.99% to 9.08%. This improvement is attributed to the broader light absorption spectrum and enhanced charge transport pathways provided by the polymeric donor. PBDTTT-EFT optimizes the nanomorphology and ordering of the bulk heterojunction films and forms a cascade energy level that enhances charge carrier mobility. Our results demonstrate that semiconducting polymer donors can effectively control light absorption, charge transport, and exciton dissociation by optimizing morphology and crystallinity. This approach offers new possibilities for advancing the performance of various optoelectronic devices through strategic use of different semiconducting polymer donors. Full article

Cadmium-free buffer layers are pivotal for the sustainable development of thin-film photovoltaics. This work numerically investigates SnS₂ as a high-performance, environmentally benign alternative to CdS for antimony selenosulfide (Sb₂(S,Se)₃) solar cells using AFORS-HET software. The SnS₂/Sb₂(S,Se)₃ heterojunction exhibits a significantly lower conduction band offset (CBO ≈ 0.23 eV) than its CdS counterpart (CBO ≈ 0.49 eV), which is identified as the primary factor for suppressed interface recombination and enhanced electron injection efficiency. A comprehensive optimization strategy is presented: tuning the S content in Sb₂(S,Se)₃ to 40% optimizes the trade-off between band gap widening and hole transport barrier at the ETL/absorber interface; adjusting the absorber thickness to 340 nm balances light absorption and carrier collection efficiency; and elevating the SnS₂ carrier concentration to 10²¹ cm⁻³ strengthens the built-in potential and induces a beneficial hole-blocking “spike” at the front contact. The synergistically optimized device achieves a power conversion efficiency (PCE) of 10.39%, a substantial improvement over the 7.56% efficiency of the CdS-based reference cell in our simulation framework. Full article

Thin-film organic solar cells (TFOSCs) are gaining momentum as next-generation photovoltaic technologies due to their lightweight nature, mechanical flexibility, and low cost-effective fabrication. In this pioneering study, we report for the first time the incorporation of cobalt-doped zinc sulfide $(\mathrm{Z}\mathrm{n}\mathrm{S}/\mathrm{C}\mathrm{o})$ nanoparticles (NPs) into a poly(3-hexylthiophene) (P3HT) and [6,6]-phenyl-C61-butyric acid methyl ester (PC61BM) bulk-heterojunction photoactive layer. $\mathrm{Z}\mathrm{n}\mathrm{S}/\mathrm{C}\mathrm{o}$ NPs were successfully synthesized via a wet chemical method and integrated at varying concentrations (1%wt, 3%wt, and 5%wt) to systematically investigate their influence on device performance. The optimal doping concentration of 3%wt yielded a remarkable power conversion efficiency (PCE) of 4.76%, representing a 102% enhancement over the pristine reference device (2.35%) under ambient laboratory conditions. The observed positive trend is attributed to the localized surface plasmon resonance (LSPR) effect and near-field optical enhancement induced by the presence of ZnS/Co NPs in the active layer, thereby increasing light-harvesting capability and exciton dissociation. Comprehensive morphological and optical characterizations using high-resolution scanning electron microscopy (HRSEM), high-resolution transmission electron microscopy (HRTEM), and spectroscopic techniques confirmed uniform nanoparticle dispersion, nanoscale crystallinity, and effective light absorption. These findings highlight the functional role of $\mathrm{Z}\mathrm{n}\mathrm{S}/\mathrm{C}\mathrm{o}$ NPs as dopants in enhancing TFOSC performance, providing valuable insights into optimizing nanoparticle concentration. This work offers a scalable and impactful strategy for advancing high-efficiency, flexible, and wearable organic photovoltaic devices. Full article

We introduce a fully solution-processed interlayer strategy for n–p CdS/PbS thin film solar cells that combines a sol–gel ZnO compact coating with an electrospun ZnO nanofiber network. The synthesis and characterization of ZnO, CdS, and PbS thin films, complemented by electrospun ZnO nanofibers, are aimed at low-cost photovoltaic applications. Sol–gel ZnO films exhibited a hexagonal wurtzite structure with a bandgap (Eg) of approximately 3.28 eV, functioning effectively as electron transport and hole-blocking layers. CdS films prepared by chemical bath deposition (CBD) showed mixed cubic and hexagonal phases with an Eg of about 2.44 eV. PbS films deposited at low temperature displayed a cubic galena structure with a bandgap of approximately 0.40 eV. Scanning Electron Microscopy revealed uniform ZnO and CdS surface coatings and a conformal 1D ZnO network with nanofibers measuring about 50 nm in diameter (ranging from 49.9 to 53.4 nm), which enhances interfacial contact coverage. PbS films exhibited dense grains ranging from 50 to 150 nm, and EDS confirmed the expected stoichiometries. Electrical characterization indicated low carrier densities and high resistivities consistent with low-temperature processing, while mobilities remained within reported ranges. The incorporation of ZnO layers and nanofibers significantly improved device performance, particularly at the CdS/PbS heterojunction. The device achieved a V_oc of 0.26 V, an J_sc of 3.242 mA/cm², and an efficiency of 0.187%. These improvements are attributed to enhanced electron transport selectivity and reduced interfacial recombination provided by the percolated 1D ZnO network, along with effective hole blocking by the compact film and increased surface area. Fill-factor limitations are linked to series resistance losses, suggesting potential improvements through fiber densification, sintering, and control of the compact layer thickness. This work is a proof-of-concept of a fully solution-processed and low-temperature CdS/PbS architecture. Efficiencies remain modest due to low carrier concentrations typical of low-temperature CBD films and the deliberate omission of high-temperature annealing/ligand exchange. Overall, this non-vacuum, low-temperature coating method establishes electrospun ZnO as a tunable functional interlayer for CdS/PbS devices and offers a practical pathway to elevate power output in scalable productions. These findings highlight the potential of nanostructured intermediate layers to optimize charge separation and transport in low-cost PbS/CdS/ZnO solar cell architectures. Full article

Hybrid solar cells, which combine inorganic and organic materials, offer a promising pathway to achieve low cost, flexible, high-performance photovoltaic devices. This work explores the application of oxidative chemical vapor deposition (oCVD) to deposit poly(3,4-ethylenedioxythiophene) (PEDOT) as a transparent hole transfer layer in hybrid solar cells. Unlike solution-processed PEDOT with polystyrene sulfonate solubilizer (PEDOT:PSS), oCVD allows for growing high-purity PEDOT that provides conformal coverage on textured substrates, enabling enhanced antireflective effects and improved charge extraction. We discuss the advantages of oCVD PEDOT in hybrid architecture, its compatibility with textured substrates, and its potential to achieve higher efficiency. Full article

Cu₂O solar cells are regarded as a promising emerging inorganic photovoltaic technology due to their power conversion efficiency (PCE) potential and material sustainability. While previous studies primarily focused on the band offset between n-type buffer layers and Cu₂O optical absorption, this work systematically investigated an ETL/buffer/p-Cu₂O/HTL heterojunction structure using SCAPS-1D simulations. Key design parameters, including bandgap (Eg) and electron affinity (χ) matching across layers, were optimized to minimize carrier transport barriers. Furthermore, the doping concentration and thickness of each functional layer (ETL: transparent conductive oxide; HTL: hole transport layer) were tailored to balance electron conductivity, parasitic absorption, and Auger recombination. Through this approach, a maximum PCE of 14.12% was achieved (V_oc = 1.51V, J_sc = 10.52 mA/cm², FF = 88.9%). The study also identified candidate materials for ETL (e.g., GaN, ZnO:Mg) and HTL (e.g., ZnTe, NiO_x), along with optimal thicknesses and doping ranges for the Cu₂O absorber. These findings provide critical guidance for advancing high-performance Cu₂O solar cells. Full article

Due to its unique electrical and optical properties, as well as the tunable band structure based on thickness, 2D phosphorene recently emerged as a research hotspot and holds significant potential for applications across various fields. In this study, due to the special band structure and excellent electron transport performance of phosphorene, it formed a series structure with SnO₂ as the electron transport layer of perovskite solar cells. Consequently, the photocurrent density was enhanced by approximately 20%, and the energy conversion efficiency was effectively elevated from 16.38% for pure SnO₂ to 18.03% for the SnO₂/phosphorene composite. Electrochemical measurements and spectral analyses revealed that the incorporation of phosphorene augmented electron mobility within the absorption layer, reduced the electron–hole recombination rate, and decreased the cell’s series resistance, thereby leading to improved efficiency of the perovskite solar cell. This research not only introduces a novel approach to enhancing solar cell efficiency but also paves a new pathway for the application of phosphorene. Full article