Search Results (69)

Melanin-like polymers, particularly polydopamine, have gained significant attention as photothermal materials due to their broad light absorption (ultraviolet to near-infrared), high photothermal conversion efficiency, negligible fluorescence, good biocompatibility regarding unmodified melanin-like polymers, and universal adhesion. Upon light irradiation, these bioinspired polymers convert absorbed optical energy into heat through molecular vibration and electron–phonon coupling, making them ideal for diverse photothermal applications. This review comprehensively summarizes recent advances in using melanin-like polymers for photothermal purposes. In biomedical engineering, they serve as efficient agents for photothermal therapy and synergistic antibacterial treatment. In catalysis, their photothermal effect enhances pollutant degradation, hydrogen production, and chemical warfare agent detoxification. For water remediation, melanin-like polymers are fabricated into evaporators, membranes, and aerogels for solar-driven steam generation, desalination, and oil spill cleanup. They also enable sensitive photothermal sensing, near-infrared imaging, and laser desorption ionization mass spectrometry imaging. Furthermore, these materials are incorporated into soft actuators and self-healing elastomers for light-controlled shape memory, programmable folding, and remote manipulation. Finally, we discuss remaining challenges such as long-term stability, biocompatibility, scalability, and color limitations and provide future perspectives for advancing melanin-like photothermal materials toward practical applications. Full article

Polymer–ceramic hybrid composites are emerging as attractive candidates for lightweight, corrosion-resistant absorber components in solar thermal collectors; however, their adoption is constrained by the intrinsically low thermal conductivity of polymers, processing-induced anisotropic heat transport, interfacial thermal resistance at tube/laminate joints, and durability challenges under outdoor exposure. This review provides a collector-centered synthesis of polymer–ceramic hybrid materials, emphasizing the translation of composite properties into collector-level outcomes rather than conductivity enhancement alone. A structure–property–performance mapping approach is presented to connect directional thermal conductivity ((k_in-plane), (k_perp)), thermal diffusivity, heat capacity, coefficient of thermal expansion, and service temperature with collector performance parameters such as heat removal effectiveness, overall heat losses, and stagnation behavior. Ceramic fillers (e.g., boron nitride, aluminum nitride, silicon carbide, alumina) are examined for stable conduction-network formation, coating compatibility, and long-term reliability, while carbon fillers (graphite, graphene nanoplatelets, carbon nanotubes) are evaluated for combined heat spreading and solar absorption benefits, with attention to emissivity penalties. Hybrid ceramic–carbon architectures and multilayer absorber designs are identified as the most promising routes to balance thermal transport, optical selectivity (high solar absorptance and low thermal emittance), manufacturability, and durability under UV, humidity, and thermal cycling. Full article

Utility-scale energy storage can help improve grid reliability, reduce costs, and promote faster adoption of intermittent sources such as solar and wind. This paper analyzes the technical aspects and economics of standalone microgrids operating on intermittent power combined with hydrogen energy storage. It explores the feasibility of using dibenzyltoluene (DBT) as a liquid organic hydrogen carrier to absorb excess energy during periods of high supply and polymer electrolyte fuel cells to generate electrical energy during periods of low supply. A comparative analysis is conducted on three power demand scenarios (industrial, residential, and office), in conjunction with three alternative energy sources: solar, wind and wind–solar mix. A mixed system of solar and wind energy can maintain an annual average efficiency above 70%, except for residential power demand, which lowered the efficiency to 67%. A balanced combination of wind and solar power was the most cost-effective option. The current levelized cost of electricity (LCOE) for industrial power demand was estimated to 15 ¢/kWh, and it is projected to decrease to 9 ¢/kWh in the future. For residential power demand, the LCOE was 45% higher due to the demand profile. In comparison, battery storage is significantly more expensive than hydrogen storage, even with future cost projections, increasing the LCOE between 60 and 120 ¢/kWh. 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

Controlling traps and structural defects in perovskite absorber layers is crucial for enhancing both the device efficiency and long-term stability of perovskite solar cells (PSCs). Here we demonstrate the modification of perovskite films by introducing low-cost green polymers, polysuccinimide (PSI) and polyasparagine (PASP), into the perovskite layer. Structural, morphological and optoelectronic properties of polymer-modified perovskite films were probed by scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared (FTIR) and UV-Vis spectroscopy. The incorporation of PSI triggers interactions between the polymer and perovskite, leading to the passivation of surface defects at the grain boundaries and improved morphology of perovskite films. This defect passivation boosted PSC performance, providing power conversion efficiency (PCE) values up to 20.1%. An optimal polymer concentration of 0.1 mg/mL in the perovskite precursor solution was identified for an improvement in the photovoltaic performance. It was shown that the primary factor leading to the observed enhancement in the power conversion efficiency for PSI-modified PSCs is the increase in the lifetime of charge carriers due to the efficient passivation of surface defects and suppression of recombination losses. Additionally, PSI-modified PSCs demonstrated enhanced stability, retaining over 80% of their initial efficiency after 40 days of storage under ambient conditions without encapsulation. The obtained results highlight the effectiveness of green polymer additives in passivating surface defects in perovskite films and provide a viable approach for improving the stability and performance of perovskite solar cells. Full article

Global warming and environmental pollution due to the overuse and exploitation of fossil fuels are the main issues affecting humans’ well-being. Solar energy is considered to be one of the most promising candidates for providing human society with a clean and sustainable energy supply. Thin-film organic solar cells (TFOSCs) use organic semiconductors as light-absorbing layer materials. TFOSCs have attracted wide research interest due to several advantages, such as easy fabrication, affordability, light weight, and environmental friendliness. Over the years, TFOSCs have been dominated by donor–acceptor blends based on polymer donors and fullerene acceptors. However, a new class of non-fullerene acceptors (NFAs) has gained prominence in TFOSCs owing to their significant improvement in the power conversion efficiency (PCE) of non-fullerene-based devices. In this study, the One-Dimensional Solar Cell Capacitance Simulator (SCAPS-1D) numerical simulator was used to study the performance of a device with a configuration of FTO/PDINO/PBDB-T/ITIC/CFTS/Al. Here, the PBDB-T/ITIC polymer blend represents poly[(2,6-(4,8-bis(5-(2 ethylhexyl)thiophen-2-yl)benzo [1,2-b:4,5-b]dithiophene)-co-(1,3-di(5-thiophene-2-yl)-5,7-bis(2-ethylhexyl)benzo [1,2-c:4,5-c]dithiophene-4,8-dione)] (PBDB)/3,9-bis(2-methylene-(3-(1,1-dicyanomethylene)-indanone)-5,5,11,11-tetraki(4-hexylphenyl)-dithieno[2,3-d:2,3-d]-s-indaceno [1,2-b:5,6-b]dithiophene) (ITIC) and the non-fullerene acceptor (NFA) and serves as the absorber layer. The electron transport layer (ETL) was 2,9-Bis[3-(dimethyloxidoamino)propyl]anthra[2,1,9-def:6,5,10-d’e’f’]diisoquinoline-1,3,8,10(2H,9H)-tetrone (PDINO), and Cu₂FeSnS₄ (CFTS) was used as a hole transport layer (HTL). This research article aims to address the global challenges of environmental pollution and global warming caused by the overuse of fossil fuels by exploring alternative energy solutions. Upon optimization, the device achieved a power conversion efficiency (PCE) of 16.86%, a fill factor (FF) of 79.12%, a short-circuit current density (J_SC) of 33.19 mA cm⁻², and an open-circuit voltage (V_OC) of 0.64 V. The results obtained can guide the fabrication of NFA-based TFOSCs in the near future. Full article

Flexibility, light weight, and mechanical robustness are the key advantages of flexible photovoltaic (PV) modules, making them highly versatile for sustainable energy solutions. Unlike traditional rigid PV modules, their flexible nature makes them incredibly versatile for harnessing energy in places where doing so was once impossible. They have a wide range of applications due to their flexibility and moldability, making it possible to conform these modules to surfaces like curved rooftops and other irregular structures. In this paper, we provide a comprehensive review of all the materials used in flexible PV modules with a focus on their role in sustainability. We thoroughly discuss the active-layer materials for crystalline silicon (c-Si)-based solar cells (SC) and thin-film solar cells such as cadmium telluride (CdTe), as well as copper indium gallium diselenide (CIGS), amorphous thin-film silicon (a-Si), perovskite and organic solar cells. Various properties, such as the optical, barrier, thermal, and mechanical properties of different substrate materials, are reviewed. Transport layers and conductive electrode materials are discussed with a focus on emerging trends and contributions to sustainable PV technology. Various fabrication techniques involved in making flexible PV modules, along with advantages, disadvantages, and future trends, are highlighted in the paper. The commercialization of flexible PV is also discussed, which is a crucial milestone in advancing and adapting new technologies in the PV industry with a focus on contributing toward sustainability. Full article

A flat-plate unglazed solar water heater (SWH) with a polymer thermal absorber was developed and experimented with. Polymer thermal absorbers could be a viable alternative to metal thermal absorbers for SWH systems. The performance of this polymer SWH system was measured based on inlet and outlet water temperature, water flow rate, ambient air temperature and solar irradiance. The polymer thermal absorbers were hollow Polyvinyl Chloride (PVC) tubes with a 20 mm external diameter and 3 mm thickness and were painted black to enhance radiation absorption. The pipes are arranged in a rectangular spiral inward–outward alternating-flow (RSioaf) pattern. The collector pipes were placed in a 1 m × 1 m enclosure with bottom insulation and a reflective surface for maximized radiation absorption. Water circulated through a closed loop with an uninsulated 16 L storage tank, driven by a pump and controlled by two valves to maintain a mass flow rate of 0.0031 to 0.0034 kg·s⁻¹. The test was conducted under a partially clouded sky from 9 a.m. to 5 p.m., with solar irradiance between 105 and 1003 W·m⁻² and an ambient air temperature of 27–36 °C. This SWH system produced outlet hot water at 65 °C by midday and maintained the storage temperature at 63 °C until the end of the test period. Photothermal energy conversion was recorded, showing a maximum value of 23%. Results indicate that a flat-plate solar water heater with a polymer thermal absorber in an RSioaf design can be an effective alternative to an SWH with a metal thermal absorber. Its performance can be improved with glazing and optimized tube sizing. Full article

Information on the detection of the presence and potential for degradation of synthetic polymers (SPs) under various environmental conditions is of increasing interest and concern to a wide range of specialists. At this stage, there is a need to understand the relationship between the main participants in the processes of (bio)degradation of SPs in various ecosystems (reservoirs with fresh and sea water, soils, etc.), namely the polymers themselves, the cells of microorganisms (MOs) participating in their degradation, and humic substances (HSs). HSs constitute a macrocomponent of natural non-living organic matter of aquatic and soil ecosystems, formed and transformed in the processes of mineralization of bio-organic substances in environmental conditions. Analysis of the main mechanisms of their influence on each other and the effects produced that accelerate or inhibit polymer degradation can create the basis for scientifically based approaches to the most effective solution to the problem of degradation of SPs, including in the form of microplastics. This review is aimed at comparing various aspects of interactions of SPs, MOs, and HSs in laboratory experiments (in vitro) and environmental investigations (in situ) aimed at the biodegradation of polymers, as well as pollutants (antibiotics and pesticides) that they absorb. Comparative calculations of the degradation velocity of different SPs in different environments are presented. A special place in the analysis is given to the elemental chemical composition of HSs, which are most successfully involved in the biodegradation of SPs. In addition, the role of photo-oxidation and photoaging of polymers under the influence of the ultraviolet spectrum of solar radiation under environmental conditions on the (bio)degradation of SPs in the presence of HSs is discussed. Full article

The development of absorber materials with strong light absorption properties and low-cost fabrication processes is highly significant for the application of photothermal conversion technology. In this work, a mixed powder consisting of NaCl, polypropylene (PP), and scale-like carbon flakes was ultrasonically pressed into sheets, and the NaCl was then removed by salt dissolution to obtain porous carbon polypropylene composite sheets (P-CPCS). This process is simple, green, and suitable for the low-cost, large-area fabrication of P-CPCS. P-CPCS has a well-distributed porous structure containing internal and external connected water paths. Under the dual effects of the carbon flakes and porous structure, P-CPCS shows excellent photothermal conversion performance in a broad wavelength range. P-CPCS-40 achieves a high temperature of 128 °C and a rapid heating rate of 12.4 °C/s under laser irradiation (808 nm wavelength, 1.2 W/cm² power). When utilized for solar steam generation under 1 sun irradiation, P-CPCS-40 achieves 98.2% evaporation efficiency and a 1.81 kg m⁻² h⁻¹ evaporation rate. This performance means that P-CPCS-40 outperforms most other previously reported absorbers in terms of evaporation efficiency. The combination of carbon flakes, which provide a photothermal effect, and a porous polymer structure, which provides light-capturing properties, opens up a new strategy for desalination, sewage treatment, and other related fields. Full article

The urgent need to shift from non-renewable to renewable energy sources has caused widespread interest in photovoltaic technologies that allow us to harness readily available and sustainable solar energy. In the past decade, polymer solar cells (PSCs) and perovskite solar cells (Per-SCs) have gained attention owing to their low price and easy fabrication process. Charge transport layers (CTLs), transparent conductive electrodes (TCEs), and metallic top electrodes are important constituents of PSCs and Per-SCs, which affect the efficiency and stability of these cells. Owing to the disadvantages of current materials, including instability and high cost, the development of alternative materials has attracted significant attention. Owing to their more flexible physical and chemical characteristics, ternary oxides are considered to be appealing alternatives, where ATiO₃ materials—a class of ternary perovskite oxides—have demonstrated considerable potential for applications in solar cells. Here, we have employed calculations based on the density functional theory to study the structural, optoelectronic, and magnetic properties of ATiO₃ (A=Li, Na, K, Rb, and Cs) in different crystallographic phases to determine their potential as PSCs and Per-SCs materials. We have also determined thermal and elastic properties to evaluate their mechanical and thermal stability. Our calculations have revealed that KTiO₃ and RbTiO₃ possess similar electronic properties as half-metallic materials, while LiTiO₃ and CsTiO₃ are metallic. Semiconductor behavior with a direct band gap of 2.77 eV was observed for NaTiO₃, and calculations of the optical and electronic properties predicted that NaTiO₃ is the most appropriate candidate to be employed as a charge transfer layer (CTL) and bottom transparent conducting electrode (TCE) in PSCs and Per-SCs, owing to its transparency and large bandgap, whereas NaTiO₃ also provided superior elastic and thermal properties. Among the metallic and half-metallic ATiO₃ compounds, CsTiO₃ and KTiO₃ exhibited the most appropriate features for the top electrode and additional absorbent in the active layer, respectively, to enhance the performance and stability of these cells. Full article

The recombination of charge carriers at the interface between carrier transport layers such as nickel oxide (NiO_x) and the perovskite absorber has long been a challenge in perovskite solar cells (PSCs). To address this issue, we introduced a polymer additive poly(vinyl butyral) into NiO_x and subjected it to high-temperature annealing to form a void-containing structure. The formation of voids is confirmed to increase light transmittance and surface area of NiO_x, which is beneficial for light absorption and carrier separation within PSCs. Experimental results demonstrate that the incorporation of the polymer additive helped to enhance the hole conductivity and carrier extraction of NiO_x with a higher Ni³⁺/Ni²⁺ ratio. This also optimized the energy levels of NiO_x to match with the perovskite to raise the open-circuit voltage to 1.01 V. By incorporating an additional NiO_x layer beneath the polymer-modified NiO_x, the device efficiency was further increased as verified from the dark current measurement of devices. Full article

This work inspects the utilization of all-polymer solar cells (APSCs) in indoor applications under LED illumination, with a focus on boosting efficiency through simulation-based design. The study employs a SCAPS TCAD device simulator to investigate the performance of APSCs under white LED illumination at 1000 lux, with a power density of 0.305 mW/cm². Initially, the simulator is validated against experimental results obtained from a fabricated cell utilizing CD1:PBN-21 as an absorber blend and PEDOT:PSS as a hole transportation layer (HTL), where the initial measured efficiency is 16.75%. The simulation study includes an examination of both inverted and conventional cell structures. In the conventional structure, where no electron transportation layer (ETL) is present, various materials are evaluated for their suitability as the HTL. NiO emerges as the most promising HTL material, demonstrating the potential to achieve an efficiency exceeding 27%. Conversely, in the inverted configuration without an HTL, the study explores different ETL materials to engineer the band alignment at the interface. Among the materials investigated, ZnS emerges as the optimal choice, recording an efficiency of approximately 33%. In order to reveal the efficiency limitations of these devices, the interface and bulk defects are concurrently investigated. The findings of this study underscore the significance of careful material selection and structural design in optimizing the performance of APSCs for indoor applications. Full article

A passive cooling method with great potential to lower space-cooling costs, counteract the urban heat island effect, and slow down worldwide warming is radiant cooling. The solutions available frequently require complex layered structures, costly products, or a reflective layer of metal to accomplish daytime radiative cooling, which restricts their applications in many avenues. Furthermore, single-layer paints have been used in attempts to accomplish passive daytime radiative cooling, but these usually require a compact coating or only exhibit limited cooling in daytime. In our study, we investigated and evaluated in daytime the surrounding cooling outcome with aid of one layer coating composed of BaSO₄/TiO₂ microparticles in various concentrations implanted in the PVDF-HF polymers on a concrete substrate. The 30% BaSO₄/TiO₂ microparticle in the PVDF-HF coating shows less solar absorbance and excessive emissivity. The value of solar reflectance is improved by employing micro-pores in the structure of PVDF polymers without noticeable effect on thermal emissivity. The 30% BaSO₄/TiO₂/PVDF coating is accountable for the hydrophobicity and proportionate solar reflection in the UV band, resulting in efficient solar reflectivity of about 95.0%, with emissivity of 95.1% and hydrophobicity exhibiting a 117.1° water contact angle. Also, the developed coating could cool to about 5.1 °C and 3.9 °C below the surrounding temperature beneath the average solar irradiance of 900 W/m⁻². Finally, the results demonstrate that the 30% BaSO₄/TiO₂/PVDF-HF microparticle coating illustrates a typical figure of merit of 0.60 and is also capable of delivering outstanding dependability and harmony with the manufacturing process. Full article

With the growing demand for photovoltaic (PV) systems as a source of energy generation that produces no greenhouse gas emissions, effective strategies are needed to address the inherent inefficiencies of PV systems. These systems typically absorb only approximately 15% of solar energy and experience performance degradation due to temperature increases during operation. To address these issues, PV–thermal (PVT) technology, which combines PV with a thermal absorber to dissipate excess heat and convert it into additional thermal energy, is being rapidly developed. This review presents an overview of various PVT technologies designed to prevent overheating in operational systems and to enhance heat transfer from the solar cells to the absorber. The methods explored include innovative absorber designs that focus on increasing the heat transfer contact surface, using mini/microchannels for improved heat transfer contiguity, and substituting traditional metal materials with polymers to reduce construction costs while utilizing polymer flexibility. The review also discusses incorporating phase change materials for latent heat absorption and using nanofluids as coolant mediums, which offer higher thermal conductivity than pure water. This review highlights significant observations and challenges associated with absorber design, mini/microchannels, polymer materials, phase change materials, and nanofluids in terms of PV waste heat dissipation. It includes a summary of relevant numerical and experimental studies to facilitate comparisons of each development approach. Full article