Photovoltaic Field Research Articles

Camphorsulfonic‐Salified Chitosan Allowing MACl‐Free Stabilization of Pure FAPbI3 α‐Phase via Gravure Printing in Ambient Air

Metal–halide perovskites have gained extreme interest in the photovoltaic field with formamidinium lead iodide (FAPbI3) currently being one of the best‐performing materials for single‐junction solar cells. Despite the outstanding record efficiencies, there are still several major issues hindering the large‐scale fabrication of perovskite solar cells. The vulnerability to environmental agents along with the need of controlled atmosphere and crystallization aids for the perovskite film deposition represents the major roadblocks. This is particularly true for FAPbI3 for which the thermodynamically stable phase at room temperature is photovoltaically inactive δ‐phase. To address those challenges, herein, a camphorsulfonic‐salified chitosan is specifically designed with the aid of DTF calculations to strongly interact with the perovskite and, as a result, improve the morphology and optoelectronic quality of the FAPbI3. Thanks to the numerous interactions and then the modulation of the solution viscosity, FAPbI3 devices are fabricated by gravure printing deposition without either antisolvent bath or inclusion of methylammonium chloride (MACl) as additive. The gravure‐printed devices with the chitosan feature an enhanced efficiency and stability in air, retaining 80% of the original efficiency after 1200 h in ambient air without any encapsulation.

The Feasibility of Egypt's Photovoltaic Industry Drawing on China's Successful Experience

This study aims to evaluate the feasibility of Egypt's photovoltaic industry drawing on China's successful experience. Firstly, based on Egypt's national conditions and actual situation, the current situation, development potential, and challenges faced by the Egyptian photovoltaic market were analyzed.Egypts economic foundation remains less competitive, with outdated electricity infrastructure and long-term dependence on natural gas, posing challenges to its transformation. Egypt is one of the regions with the most concentrated solar energy resources in the world, which gives it the possibility and new opportunities to overtake in the photovoltaic field. Secondly, by analyzing the development process of China's photovoltaic industry, this paper explores China's successful experiences in policy support, market demand, technological level, financial support, and talent cultivation.Compared with China, Egypt's photovoltaic industry is still in an underdeveloped and developing stage, and requires sustained efforts in multiple aspects. This article compares the significant differences in the development of photovoltaic industries between China and Egypt, and analyzes the opportunities and challenges faced by Egypt's photovoltaic industry, as well as the corresponding strategies from three aspects: policy stability, demand activation, and desert photovoltaics. Finally, based on the research results, policy recommendations and development paths are proposed to promote the development of Egypt's photovoltaic industry, to provide reference and inspiration for the sustainable development of Egypt's photovoltaic industry.

High efficiency homojunction tandem organic solar cells with all solution processable interconnect layer

In the field of organic photovoltaics, the power conversion efficiency of single junction solar cells continues to improve. However, tandem organic solar cells are poised to push the efficiency limits even further and offer a promising avenue for improving the performance of organic photovoltaic devices. This study reports the development of an all-solution processed interconnecting layer (ICL) based on ZnO NPs:PEI/PEI/PEDOT:PSS/2PACz for tandem solar cells. The PM6:BTP-eC9 active layer material was adjusted for its donor-to-acceptor (D/A) ratio and film thickness as the front and back sub-cells. The ICL exhibits favorable mechanical, electrical and optical properties. Through multidimensional modulation, the front and rear sub-cells have been optimized to obtain highly efficient homojunction tandem solar cells. The tandem solar cell has a structure of indium tin oxide (ITO)/PEDOT:PSS/2PACz/active layer/ICL/active layer/PNDIT-F3N/Ag. This optimization resulted in a power conversion efficiency (PCE) of 19.9 %, which is the highest reported efficiency for homojunction tandem organic solar cells to date. Our research demonstrates that the PCE of homojunction tandem cells can be significantly improved by careful design of the interconnecting layers and optimization of the donor-to-acceptor (D/A) ratio. This strategy may provide guidance for further improvements in homojunction tandem cells.

In-situ and ex-situ preparation of Bi2S3 on the BiVO4/TiO2 to construct Bi2S3/BiVO4/TiO2 heterojunction for efficient Cr(VI) reduction

The environmentally friendly and rapid removal of hexavalent chromium (Cr(VI)) from wastewater has garnered significant attention, driven by the severe acute toxicity and carcinogenic properties associated with Cr(VI). The design and synthesis of heterojunctions are recognized as effective solutions for enhancing the photocatalytic performance of TiO2 based materials. BiVO4/TiO2 and Bi2S3/BiVO4/TiO2 composite films (BVT) were prepared via a simple hydrothermal method. The influence of Bi2S3 preparation methods (In-situ and Ex-situ) on the morphology, structure and properties of BVT was studied. The relative crystallinity of TiO2, BiVO4/TiO2, BVT(In-situ) and BVT(Ex-situ) were 50 %, 62 %, 72 % and 92 %, respectively. SEM shows that the morphology of Bi2S3 in BVT(In-situ) was nanoribbon and that of Bi2S3 in BVT(Ex-situ) was radioactive sphere. Compared with pure TiO2 and BiVO4/TiO2, the light absorption range of BVT composite material has been expanded from the ultraviolet light region to the visible region, the bandgap has been significantly narrowed, and the photocurrent density has been increased. The BVT(In-situ) shows stronger photoelectrical performance and reduction efficiency of Cr (VI) compared to BVT(Ex-situ), reaching 93.9 %. The photocatalytic reaction rate of BVT(In-situ) and BVT(Ex-situ) are 0.0291 min−1 and 0.0266 min−1, respectively. Density functional theory (DFT) calculations indicate that the work function of BiVO4 is higher than that of Bi2S3, and electrons will transfer from Bi2S3 to BiVO4 at the heterojunction interface. The BVT(In-situ) heterojunction constructed in this experiment greatly improves the separation and transport efficiency of photo-generated carriers, laying the foundation for the wide application of BVT heterojunction in the field of optoelectronics and providing a strategy for photocatalytic reduction of Cr(VI). The BVT(In-situ) with FTO conductive glass, it also can be applied to photovoltaic fields such as solar cells, photocatalysis and photodetectors.

Fused Hexabenzocoronene‐Porphyrin Conjugates with Tailorable Excited‐State Lifetimes

AbstractA new clear‐cut strategy for fusing N‐heterocyclic and carbon‐pure systems is introduced en route to a versatile platform of multi‐purpose tetrapyrrolic chromophores. In particular, three novel C−C bond‐fused porphyrin‐hexabenzocoronene (HBC) conjugates were synthesized under oxidative cyclodehydrogenation conditions, starting from tailor‐made nickel porphyrin precursors. The fusion of the individual aromatic systems via 5‐membered rings led to highly soluble π‐extended porphyrins in excellent yields. The resulting porphyrin‐HBC conjugates exhibit absorption cross‐sections that are of interdisciplinary interest in the ever‐growing field of organic photovoltaics and near‐infrared (NIR) dyes. Quantum chemical calculations show that the newly formed 5‐membered rings induce biradicaloid character in the porphyrin core, which has a strong impact on excited state lifetimes. This is confirmed by a thorough optoelectronic and time‐resolved characterization in order to understand these unique features better. Broadened absorption characteristics go hand‐in‐hand with short‐lived excited states with up to six orders of magnitude faster decay rates.

Fused Hexabenzocoronene-Porphyrin Conjugates with Tailorable Excited-State Lifetimes.

A new clear-cut strategy for fusing N-heterocyclic and carbon-pure systems is introduced en route to a versatile platform of multi-purpose tetrapyrrolic chromophores. In particular, three novel C-C bond-fused porphyrin-hexabenzocoronene (HBC) conjugates were synthesized under oxidative cyclodehydrogenation conditions, starting from tailor-made nickel porphyrin precursors. The fusion of the individual aromatic systems via 5-membered rings led to highly soluble π-extended porphyrins in excellent yields. The resulting porphyrin-HBC conjugates exhibit absorption cross-sections that are of interdisciplinary interest in the ever-growing field of organic photovoltaics and near-infrared (NIR) dyes. Quantum chemical calculations show that the newly formed 5-membered rings induce biradicaloid character in the porphyrin core, which has a strong impact on excited state lifetimes. This is confirmed by a thorough optoelectronic and time-resolved characterization in order to understand these unique features better. Broadened absorption characteristics go hand-in-hand with short-lived excited states with up to six orders of magnitude faster decay rates.

Novel Green Solvent for Sustainable Fabrication of Quasi‐2D Perovskite Solar Cells

AbstractDespite the remarkable advances in the field of perovskite photovoltaics, the use of toxic solvents for their fabrication poses a significant challenge to their scale‐up and commercialization. The vast majority of studies rely on using the highly hazardous N, N‐Dimethylformamide (DMF), with green alternatives remaining scarce. In this work, the use of glycerol formal (Gly‐F) is reported as a green solvent for fabricating quasi‐2D (n = 5) perovskite solar cells. Quasi‐2D perovskite films processed from Gly‐F exhibit a high degree of uniformity and a compact microstructure. When integrated into solar cells, the green solvent‐processed films reach a promising power conversion efficiency of 14.53%. This performance is lower than that of DMF‐based perovskites, most likely due to the presence of laterally oriented low n perovskite phases. Interestingly, while the performance of DMF‐based devices is rather irreproducible, the performance of Gly‐F‐based devices is robust and consistent. These results demonstrate the potential of Gly‐F‐ as a promising green alternative to DMF.

Temperature dependence of gold nanostar particles morphology and its SERS application

ABSTRACT Gold nano-star particles (GNS) have broad application prospects in Raman enhancement, photovoltaic, and catalysis fields because of the hot spot effect of their tip structure. However, metal nanoparticles will accumulate heat during applications of high-power laser-focused irradiation, which may lead to the morphological degradation of the nanoparticles. In this paper, we have studied the effect of annealing temperature on the surface tip structure of GNS. Firstly, GNS with the multi-tip structure were synthesised by the two-step method, and GNS thin films were prepared by self-assembly technique without auxiliaries. By means of SEM characterisation, the film is found to be compact and uniform. Secondly, we systematically studied the morphology degradation of GNS at 100°C, 150°C, 200°C and 250°C. The results show that the tip of GNS does not change obviously until the temperature reaches 200°C. Then the four kinds of GNS films were used as surface-enhanced Raman scattering (SERS) substrates, and their Raman enhancement properties have been studied with adenine as the analyte, and stronger Raman enhancement effect can be found for the tip of nanoparticles. For a SERS substrate corresponding to an annealing temperature of 100°C, we have obtained the limit sensitivity of adenine molecule of 10−9 M. Finally, the surface electric field distribution and local resonance spectrum curves of four kinds of gold nanoparticles with different tip sizes were simulated theoretically by using the finite element method, and the results are consistent with the experimental data.

Optoelectronic properties of GaP:Ti photovoltaic devices

Supersaturated GaP is of interest for the photovoltaic field since optical transitions at energies below the bandgap (2.26 eV) could enhance the overall device efficiency up to theoretically 60%. We have previously demonstrated that Ti supersaturated GaP can be obtained by means of ion implantation and pulsed-laser melting with high structural quality and measured its below-bandgap photoconductivity. In this work we report the first results of a GaP:Ti based photovoltaic device. We have fabricated and measured photovoltaic devices with a GaP:Ti absorber layer showing enhanced external quantum efficiency at wavelengths above 550 nm. Also, we have measured the absorption coefficient (around 104 cm-1) and refractive index of this absorber layer. Finally, current-voltage curves in darkness were measured and analysed using a two-diodes model, showing improvable characteristics. Ideas to enhance the properties of the devices are suggested.

Exergy and thermoeconomic analysis of a novel polygeneration system based on gasification and power-to-x strategy

This study introduces a novel polygeneration system that integrates biomass gasification, anaerobic digestion, photovoltaic (PV) energy, and electrolysis to enhance system flexibility and efficiency. The system includes an allothermal gasification unit that processes lignocellulosic biomass sourced from a botanical garden. The gasifying agent, either steam or oxygen, is supplied by an alkaline electrolyzer, which operates under a Power-to-X strategy, utilizing surplus energy from a PV field. The resulting syngas and hydrogen are blended with biogas from an anaerobic digester, which treats municipal waste, to power a cogenerator. This cogenerator meets the electricity, heating, and cooling demands of a hospital, while the PV field powers the botanical garden. The systems components are modeled using various tools and integrated into the TRNSYS environment for dynamic simulation. An exergy analysis identifies the main sources of exergy destruction, while a thermo-economic analysis evaluates the energy, environmental, and economic impacts of a demonstration plant located in Bogotá’s Botanical Garden. Simulation results show that the system achieves an overall exergy efficiency of around 35 %, with a 96 % reduction in primary energy consumption compared to a reference system, avoiding nearly 6000 tons of CO2 emissions annually. From an economic perspective, the system is profitable, with a payback period of 3.02 years and a Net Present Value of $15.23 million, almost double the capital cost. The gasification unit's exergy efficiency is significantly higher when using oxygen (0.50) compared to steam (0.25), underscoring the importance of integrating electrolysis for improved biomass conversion. The alkaline electrolyzer operates efficiently within its optimal range, with an energy efficiency close to 0.70 and an exergy efficiency around 0.60, effectively utilizing 25 % of the total PV production.

On-Grid Hybrid PV/WT Renewable Energy System for Green Hydrogen Production

The term "Power-to-X" (PtX) refers to a set of techniques for converting electrical energy into another form of energy, primarily focusing on hydrogen production. Produced hydrogen can be stored, distributed, and then used directly (to regenerate electricity, generate heat, or in transportation, steel, and chemical industries) or indirectly to produce ammonia, fertilizers, methane, methanol, e-fuels, and more. Thus, PtX is a mean of storing intermittent energy and a key contributor to the energy transition and decarbonization. In this article, we examine a grid-connected green hydrogen production system. This 1 MW renewable capacity system consists of a 300 kW wind turbine, a 700 kW photovoltaic field, and a 209 kW electrolyzer. In this system, any excess energy is integrated into the grid, enhancing overall energy sustainability. Conversely, when energy output is insufficient for the electrolyzer, the deficit is sourced from the grid, ensuring continuous and reliable operation. This dynamic interaction with the grid optimizes energy usage and reinforces the stability of the system. The results show an annual hydrogen production of about 16 tons, renewable energy production of approximately 1.9 GWh/year, a 20.85% capacity factor, a shortage of about 144.5 MWh, and an energy excess of about 824 MWh.

Theoretical investigation of benzodithiophene-based donor molecules in organic solar cells: from structural optimization to performance metrics.

Achieving high power conversion efficiency (PCE) remains a significant challenge in the advancement of organic solar cells (OSCs). In the field of organic photovoltaics (OPVs), considerable progress has been made in optimizing molecular structures to improve the PCE. However, innovative material design strategies specifically aimed at enhancing PCE are still needed. Here, we have designed BDTS-2DPP-based molecules and propose a molecular design approach to develop donor materials that can significantly improve the PCE of OSCs. Density functional theory (DFT) and time-dependent DFT (TD-DFT) methods have been adopted in both gas and solvent phases. Our newly designed molecule M1 shows the highest absorption value (λ max = 846 nm), highest electron reorganization energy (λ e = 0.18 eV), and the lowest energy gap (E g = 1.81 eV) among all the designed molecules. M1 molecule also exhibits the highest dipole moment in both gas (10.62 D) and solvent phase (13.62 D), and their ground and excited state dipole moment difference is also higher (μ e - μ g = 2.99 D), which enhances its separation to make it a suitable candidate for charge transfer between HOMO-LUMO (97%). Newly designed molecule M3 is observed to have the highest voltage when the current is zero (V oc = 1.15 V) highest PCE value (21.90%) and highest fill factor (FF) value (89.42%). The lowest excitation binding energy is estimated by newly designed molecule M2 (E b = 0.30 eV), which indicates a higher rate of dissociation during the excitation as observed in transition density matrix (TDM) plots. Utilizing electron density difference maps, the newly designed molecules in dichloromethane solvent exhibited consistent intramolecular charge transfer (ICT). The designed molecules were evaluated against reference molecule R to determine if they exhibit superior optoelectronic capabilities. It is found that all designed molecules (M1-M5) exhibit reduced band gaps, are red-shifted in wavelength in comparison to a reference molecule R, and have remarkable charge motilities in terms of reorganisation energies.

Geometric optimisation and structural properties of organic−inorganic halide perovskites from van der Waals density functional theory calculations

Organic–inorganic hybrid perovskites have attracted extensive attention in the photovoltaic field due to their unique photoelectric properties and low production costs. Using the density functional theory-based first-principles calculations, we reported the geometric optimisation and structural properties of halide perovskites using van der Waals density functional theory calculations. The strongly constrained and appropriately normed (SCAN) meta-GGA with the revised Vydrov-van Voorhis no-local correlation functional (SCAN + rVV10) are promising van der Waals density functional for solving van der Waals (vdW) interaction problems that many non-empirical semilocal functionals fail to include. We found the optimised structure parameters of halide perovskites based on the SCAN + rVV10 functionals are much closer to the experimental results than other functional including PBE and PBE + vdW-TS functionals, which provides the fundamental aspect for the theoretical calculations of surfaces, interfaces, optical properties, and structure-properties relationship.

Short‐term power prediction of distributed PV based on multi‐scale feature fusion with TPE‐CBiGRU‐SCA

AbstractTo address the challenge of insufficient comprehensive extraction and fusion of meteorological conditions, temporal features, and power periodic features in short‐term power prediction for distributed photovoltaic (PV) farms, a TPE‐CBiGRU‐SCA model based on multiscale feature fusion is proposed. First, multiscale feature fusion of meteorological features, temporal features, and hidden periodic features is performed in PV power to construct the model input features. Second, the relationships between PV power and its influencing factors are modelled from spatial and temporal scales using CNN and Bi‐GRU, respectively. The spatiotemporal features are then weighted and fused using the SCA attention mechanism. Finally, TPE‐based hyperparameter optimization is used to refine network parameters, achieving PV power prediction for a single field station. Validation with data from a PV field station shows that this method significantly enhances feature extraction comprehensiveness through multiscale fusion at both data and model layers. This improvement leads to a reduction in MAE and RMSE by 26.03% and 38.15%, respectively, and an increase in R2 to 96.22%, representing a 3.26% improvement over other models.

Energy Level Tuning in CsPbBr3 Perovskite Solar Cells through In Situ-Polymerized PEDOT Hole Transport Layer.

The all-inorganic CsPbBr3 perovskite solar cells exhibit excellent stability against humidity and thermal conditions as well as relatively low production cost, rendering them a gradually emerging research hot spot in the field of photovoltaics. However, the absence of a hole transport layer (HTL) in its common structure and the substantial energy level difference of up to 0.6 eV between the highest occupied molecular orbital (HOMO) level of CsPbBr3 and the work function of the carbon electrode have emerged as the primary factor limiting the improvement of its power conversion efficiency (PCE). In this work, the monomer 2,5-dibromo-3,4-ethylenedioxythiophene (DBEDOT) is spin-coated onto the surface of the CsPbBr3 film directly and then subjected to annealing; DBEDOT undergoes in situ polymerization to form poly(3,4-ethylenedioxythiophene) (PEDOT), which aims to ameliorate the issue of excessive energy level difference between CsPbBr3 and the carbon electrode, and to facilitate the extraction and transport efficiency of holes between the CsPbBr3 perovskite and the carbon electrode. Compared to the pristine device, the PCE of the device based on in situ polymerization is enhanced and achieves a maximum efficiency of 9.81%. Furthermore, the unencapsulated devices based on in situ polymerization maintain 95.9% of their original efficiency after 40 days of stability testing.

An Updated Review for Performance Enhancement of Solar Cells by Spectral Modification

Photovoltaic technology has become one of the major renewable ways to generate electric power. However, the mismatch between the incident solar spectrum and photo-electric response efficiency of solar cells severely constrains their performance. Hence, spectral modification technologies, e.g., up-conversion (UC), down-conversion (DC), and luminescent down-shifting (LDS) technologies have been applied widely in the photovoltaic field to reform the incident spectrum to match the best response band possible. In this paper, we review the latest developments of the three technologies above in terms of material selection, optical characteristics, and photovoltaic performance. It is found that the three most popular materials for conversion are NaYF4: Er3+, Yb3+, and Yb3+. The excitation bands for the three technologies are 800–1550 nm, 250–488 nm, and 250–488 nm, respectively, while the emission bands are 523–669 nm, 520–1031 nm, and 490–1010 nm, respectively. Furthermore, issues hindering the development of spectral modification technologies are pointed out, e.g., low absorption efficiency, poor quantum conversion efficiency, and hurdles in commercialization. Finally, suggestions and solutions to address the above-mentioned issues are provided.

The impact of halogens on the structural, electronic, and optical properties of vacancy-ordered double perovskites Rb2SeX6 (X=I, Br, Cl)

Lead-based perovskite materials have become one of the most widely used materials in the field of photovoltaics due to their excellent properties. However, concerns over lead toxicity and the stability of materials have prompted the search for alternative, eco-friendly, and stable perovskite materials. To address this need, our study conducts an in-depth analysis of the electronic and optical properties of the lead-free double perovskite materials Rb2SeX6 (X = Cl, Br, I) using first-principles calculations. The results indicate that Rb2SeX6 perovskites possess an indirect bandgap, with values of 3.26 eV, 2.52 eV and 1.39 eV for Rb2SeCl6/Br6/I6, respectively. Rb2SeI6 has larger dielectric function and superior absorption spectrum across the visible range than the other two materials. Thus, Rb2SeI6 has a promising future as a photoelectric material for solar cells. Rb2SeCl6 and Rb2SeBr6 also have the potential for use in photodetectors, light-emitting diodes and other optoelectronic devices.

Heavy-duty vehicles with solar panels as a regenerative power source

Abstract Road transportation represents more than a third of all CO2-producing sources on Earth, being the main producer of greenhouse gas (GHG) emissions. Nowadays, continuous development of technology has reduced fossil-fuel consumption by integrating clean energy sources as a range extender. Solar energy has the largest potential of all renewable energy sources worldwide. The photovoltaic and energy storage research fields have grown exponentially during the last decade and, forced by the current energy crisis, had a great contribution to the hybrid solar vehicles (HSV) industry. Vehicle Integrated Photovoltaics (VIPV) comply with requirements on vehicles aesthetics, and they convert solar energy into electric energy to supply the low-voltage and high-voltage battery packs onboard HSV. Heavy-load road transportation by commercial vehicles equipped with PV-integrated modules or retrofit installation will contribute to global decarbonization. A study is done on a configuration of a heavy-duty vehicle with its cuboid cargo body covered with solar panels and a regulated driving route during different weather conditions [3]. The energy management system is designed to maximize solar energy conversion in order to reduce fuel consumption and extend the vehicle’s total driving distance.

Study of the Management of the Electrical Energy Production and Distribution System Within the National School of Teachers of Mamou, Guinea

With the energy transition, marked essentially by the mass integration of energy production based on renewable resources, the missions and challenges of electrical energy distribution networks are evolving. This study is part of this dynamic, its objective is the study of the management of the production and distribution system of electrical energy within the National School of Teachers of Mamou. It emerges from this study that the supply of electrical energy to the National School of Teachers of Mamou is ensured by a hybrid system of three power sources: photovoltaic solar fields, Generator Group and Electricity of Guinea. The current electrical energy requirements of the Mamou NST are 40 kW. The total power of the installed photovoltaic solar fields is 70 kWp; the Generator used has a power of 10 kVA; the site’s Electricity of Guinea network is made up of transformers, cabin substations and protective equipment. The electricity distribution network is characterized by: Four (4) 250 A circuit breakers; a 32 A circuit breaker for the departure of lamps, sockets and fans; a 10 A circuit breaker for the lamps; a 10 A circuit breaker for the fans; a 16 A circuit breaker for the sockets and an 800 A mechanical inverter. The study shows that the power of photovoltaic solar fields is largely sufficient to cover the current electrical energy needs of the National School of Teachers of Mamou.

Synthesis of hydrophobic silica without traditional aging process to construct the anti-reflective film with ultralow refractive index for improving power conversion efficiency

The fabrication of anti-reflective films to optimize sunlight utilization encounters various challenges. Herein, we have synthesized modified silica with hydrophobic properties, eliminating the conventional aging process to create an anti-reflective film with an ultralow refractive index of 1.05, marking the lowest value reported to date. This innovative methodology reduces tasks that typically require days or weeks to just a few hours, thereby significantly accelerating production. The power conversion efficiency of the photovoltaic device can increase by 6.2 % when coated with this film. This research not only advances the synthesis of silica but also develops anti-reflective films with record-low refractive indices. This breakthrough represents a substantial contribution, highlighting its significant impact on the photovoltaic field.