Film-forming Properties Research Articles

Bio-based composite film from konjac flour and dialdehyde starch: Development, properties and structural features

The development of environmental-friendly composite products from renewable resources has been considered as an excellent approach to address the negative impact of petroleum-based plastics on environment. Konjac flour (KF), as an excellent polysaccharide material, has a broad application in food field. It shows a promising future in the film field due to its excellent film-forming properties. In this work, KF was selected as primary film-forming matrix, and dialdehyde starch (DAS) as the reinforcing component. A series of KF/DAS composite films were prepared by adjusting the addition ratio of DAS component. Then, their physical and mechanical properties were characterized and analyzed. The results showed that KF/DAS composite film with 25 % DAS content exhibited the optimal mechanical properties, including tensile strength (TS) of 13.1 MPa and elongation at break (EAB) of 93.7 %, indicating that an excellent cross-linked system formed among KF and DAS utilizing the method described in this study. Furthermore, much evidences from the fourier transform infrared spectroscopy (FT-IR) and X-ray diffraction (XRD) confirmed that a strong chemical cross-linkages between DAS and KF via Schiff base and esterification reactions. Based on the thermogravimetry (TG) and scanning electron microscopy (SEM) results, KF/DAS composite films also had excellent thermal stability and a dense microstructure, although there are also changes with the DAS usage.

Development of Novel Cardanol-Derived Reactive Dispersing Agents for Bio-Based Anionic-Nonionic Waterborne Polyurethane.

This study successfully developed a bio-based, photocurable, anionic-nonionic dual-functional chain extender, and sulfonated cardanol-based polyethylene glycol (SCP), derived from renewable resources-cardanol and polyethylene glycol-for application in waterborne polyurethane dispersions (WPUDs). Utilizing SCP as a chain extender, WPUDs were prepared through a typical acetone process with poly(butylene adipate) (PBA), isophorone diisocyanate (IPDI), and ethylene diamine (EDA) at a constant NCO/OH ratio of 1:1. This research focused on the effects of polyethylene glycol molecular weight and SCP dosage on the particle size, stability, and film-forming properties of the WPUD. Optimal dispersion stability and film-forming performance were achieved with a polyethylene glycol molecular weight of 1500 and a PBA to SCP molar ratio of 4:1, yielding a particle size of 0.326 ± 0.010 μm and excellent storage stability over six months. The resulting WPU coatings exhibited a tensile strength of 11.4 MPa, which increased to 16.8 MPa after UV irradiation owing to the formation of a semi-interpenetrating network via the photopolymerization of cardanol's unsaturated side chains. UV cross-linking also enhanced water resistance, reducing the water absorption rate (WAR) from 18.68% to 4.21% and the water vapor transmission rate (WVTR) from 6.59 × 10-5 g·m⁻¹·Pa⁻¹·d⁻¹ to 2.26 × 10⁻⁵ g·m⁻¹·Pa⁻¹·d⁻¹, while also improving thermal stability. These findings demonstrate that SCP offers a sustainable and effective solution for developing high-performance WPU coatings.

Development of a Multilayer Film Including the Soluble Eggshell Membrane Fraction for the Treatment of Oral Mucosa Lesions

Background/Objectives: Oral diseases causing mucosal lesions are normally treated with local or systemic anti-inflammatory, analgesic and antimicrobial agents. The development of topical formulations, including wound-healing promoters, might speed up the recovery process, improving patients’ quality of life, and reduce the risk of deterioration in health conditions. In this study, a mucoadhesive multilayer film, including a novel biocompatible substance (solubilized eggshell membrane, SESM), was rationally designed. Methods: The SESM preparation procedure was optimized and its biological effects on cell proliferation and inflammation marker gene expression were evaluated in vitro; preformulation studies were conducted to identify the most promising polymers with film-forming properties; then, trilayer films, consisting of an outer layer including chlorhexidine digluconate as a model drug, a supporting layer and a mucoadhesive layer, incorporating SESM, were prepared using the casting method and their mechanical, adhesion and drug release control properties were evaluated. Results: SESM proved to possess a notable wound-healing capacity, inducing a wound closure of 84% in 24 h without inhibiting blood clotting. The films revealed a maximum detachment force from porcine mucosa of approx. 1.7 kPa and maximum in vivo residence time of approx. 200–240 min; finally, they released up to 98% of the loaded drug within 4 h. Conclusions: The formulated trilayer films were found to possess adequate properties, making them potentially suitable for protecting oral lesions and favoring their rapid healing, while releasing antimicrobial substances that might be beneficial in reducing the risk of bacterial infections.

Research Progress on Polysaccharide Composite Films and Coatings with Antioxidant and Antibacterial Ingredients to Extend the Shelf Life of Animal-Derived Meat

Animal-derived meat is rich in proteins and other nutrients, but is prone to spoilage during storage, including microbial contamination and fat oxidation. Therefore, there is an urgent need to find effective solutions to extend the shelf life of animal-derived meat. Polysaccharides are natural macromolecules containing multi-hydroxyl structures and functional groups, which have good solubility, film-forming properties, etc., and can form edible films. Polysaccharide films can be combined with biopolymers, nanoparticles, and natural active agents to improve their properties and enhance the antioxidant and antimicrobial activities of the films. This review summarizes the various sources of polysaccharides, such as chitosan, hyaluronic acid, sodium alginate, carrageenan, starch, and pullulan polysaccharides and their combination with different substances to extend the shelf life of animal-derived meat. This review may serve as a reference for further development of polysaccharides in animal-derived meat preservation.

Synthesis and Performance Evaluation of Multialkylated Aromatic Amide Oligomeric Surfactants as Corrosion Inhibitor/Drag Reducing Agents for Natural Gas Pipeline.

Drag reducing agents (DRAs) including amphiphiles and polymers can enhance energy efficiency and transmission volume in natural gas pipelines. However, the correlation between DRA molecular structure and drag reduction efficiency remains unclear. In this paper, the multialkylated aromatic amides (MAA) oligomeric surfactants with different numbers of amide group/n-dodecane chain (from 1 to 3) were first synthesized and characterized. Then, the potential efficiency of MAA as the corrosion inhibitors (CIs)/DRAs for natural gas pipelines was investigated by interfacial activity analysis, film-forming property test, electrochemical polarization curve measurement, and in-door loop test. The results showed that the molecular structure is the key factor influencing the performance of MAA. By increasing the number of amide group/n-dodecane chains, the interfacial activity of MAA improves greatly, thus outstandingly affecting the film-forming property of the MAA on the carbon steel sheet. For MAA-1, the formed film is too thin to cover the surface roughness, and then the corrosion inhibiting (78.64%)/drag reducing (0-2%) rates are the lowest. For MAA-3, the formed film is the thickest and smooth, thus imparting the largest corrosion inhibiting (93.88%)/drag reducing (10-14%) rates to MAA-3. For MAA-2, the formed film is thicker but not smooth, and the corrosion inhibiting (89.88%)/drag reducing (4-6%) rates are intermediate. We speculate that the structure of the MAA greatly influences the adsorption and self-assembly of MAA on the inner pipe wall and then generates different performances. This work is helpful for guiding the development of natural gas DRAs with high efficiency.

The Molecular Design and Electroluminescent Performance of Near-Infrared (NIR) Iridium(III) Complexes Bearing Isoquinoline-, Phthalazine- and Phenazine-Based Ligands.

Near-infrared (NIR) light has characteristics of invisibility to human eyes, less background interference, low light scattering, and strong cell penetration. Therefore, NIR luminescent materials have significant applications in imaging, sensing, energy, information storage and display. The development of NIR luminescent materials thus has emerged as a highly dynamic area of research in the realm of contemporary materials. To date, NIR luminescent materials are roughly divided into inorganic materials and organic materials. Compared with inorganic materials, organic NIR luminescent materials have become a hot research topic in recent years due to their rich sources, easy control of structure, simple preparation process, low cost, and good film-forming properties. Among them, iridium(III) [Ir(III)] complexes exhibit excellent properties such as thermal stability, simple synthesis, easy color modulation, short excited state lifetimes, and high brightness, thus becoming one of the ideal luminescent material systems for preparing high-quality organic light-emitting diodes. Therefore, how to obtain Ir(III) complexes with NIR emission and high efficiency through molecular design is a necessary and promising research topic. This work reviews the research progress of representative NIR Ir(III) complexes bearing isoquinoline-, phenazine-, and phthalazine-based ligands reported in recent years and introduces the design strategies and electroluminescent performances of NIR Ir(III) complexes.

Ultra-Pressurized Deposition of Hydrophobic Chitosan Surface Coating on Wood for Fungal Resistance.

Fungi (Neolentinus lepideus, Nl, and Trametes versicolor, Tv) impart wood rot, leading to economic and environmental issues. To overcome this issue, toxic chemicals are commonly employed for wood preservation, impacting the environment and human health. Surface coatings based on antimicrobial chitosan (CS) of high molar mass (145 × 105 Da) were tested as wood preservation agents using an innovative strategy involving ultra-pressurizing CS solutions to deposit organic coatings on wood samples. Before coating deposition, the antifungal activity of CS in diluted acetic acid (AcOOH) solutions was evaluated against the rot fungi models Neolentinus lepideus (Nl) and Trametes versicolor (Tv). CS effectively inhibited fungal growth, particularly in solutions with concentrations equal to or higher than 0.125 mg/mL. Wood samples (Eucalyptus sp. and Pinus sp.) were then coated with CS under ultra-pressurization at 70 bar. The polymeric coating deposition on wood was confirmed through X-ray photoelectron spectroscopy (XPS), energy dispersive X-ray spectroscopy (EDS), scanning electron microscopy (SEM) images, and water contact angle measurements. Infrared spectroscopy (FTIR) spectra of the uncoated and coated samples suggested that CS does not penetrate the bulk of the wood samples due to its high molar mass but penetrates in the surface pores, leading to its impregnation in wood samples. Coated and uncoated wood samples were exposed to fungi (Tv and Nl) for 12 weeks. In vivo testing revealed that Tv and Nl fungi did not grow on wood samples coated with CS, whereas the fungi proliferated on uncoated samples. CS of high molar mass has film-forming properties, leading to a thin hydrophobic film on the wood surface (water contact angle of 118°). This effect is mainly attributed to the high molar mass of CS and the hydrogen bonding interactions established between CS chains and cellulose. This hydrophobic film prevents water interaction, resulting in a stable coating with insignificant leaching of CS after the stability test. The CS coating can offer a sustainable strategy to prevent wood degradation, overcoming the disadvantages of toxic chemicals often used as wood preservative agents.

Synthesis and optical properties of fluorinated polyurethaneimide electro-optic waveguide polymer

Fluorinated polyurethaneimide (PUI) electro-optic waveguide polymer with polyurethane and polyimide chain segment structures was synthesized by stepwise polymerization using the synthesized amino ester oligomer pu and imide oligomer pi as monomers. Since the main chain structure of the synthesized PUI had the functionality of both polyurethane and polyimide chain segment structures, it combines the excellent thermal and film-forming properties of polyurethanes and polyimides, as well as lower optical transmission loss in the near-infrared wavelength band. The glass transition temperature (Tg) of PUI was 182 °C, and the 5% heat loss decomposition temperature was 325 °C. The PUI had good optical properties with an optical propagation loss of 1.10 dB/cm and an electro-optic (EO) coefficient (γ33) of 86 pm/V at a wavelength of 1550 nm. A Mach-Zehnder interferometric polymer waveguide EO modulator had been designed and fabricated by using the PUI as a waveguide electro-optic core layer. The prepared polymer waveguide EO modulator showed a good electro-optic modulation response at a wavelength of 1550 nm under an applied 1 kHz sinusoidal modulation signal. The results showed that the synthesized PUI met the performance requirements for the preparation of polymer optical waveguide devices and was a polymer electro-optic waveguide material with good overall performance.

Engineering high-performance and multifunctional seed coating agents from lignocellulosic components

The use of natural polymers, such as biomass, as an alternative to non-renewable polymer attracts a growing interest in sustainable agricultural production. Seed coating, an important treatment for enhancing crop performance, could be an environmentally-friendly and promising option when utilizing materials based on natural polymers. Herein, biomass-based seed coating agents derived from cellulose and lignin through a simple process were developed. Carboxymethyl cellulose was used as the primary substrate for membrane formation, supplemented with sodium lignosulfonate as an additive to enhance its mechanic and anti-UV properties. The prepared seed coating agents showed promising film-forming property, flexibility, and water retention capacity. Furthermore, these agents were effective in controlled release and anti-UV performances for pesticides encapsulated in it. Additionally, the thickness of the seed coat could be finely tuned by controlling the soaking time, and therefore resulting in an adjustable germination time. More importantly, the agents demonstrated natural degradability with nearly 80 % degradation at 60 days. It is concluded that the seed coating agents prepared provides new insight into the use of biomass-based materials in sustainable agricultural systems.

Significantly enhanced electrochemical performance of Al-Ti3C2Tx MXene synthesized from Al-Ti3AlC2 MAX phase

MXenes, a type of two-dimensional nanomaterials consisting of transition metal carbides/nitrides, have emerged as promising electrode materials for supercapacitors. Especially, Ti3C2Tx MXene prepared from Ti3AlC2 MAX phase shows great application potential in flexible supercapacitors due to its facile synthesis, excellent conductivity and film-forming property. In contrast to conventional Ti3AlC2, excessive aluminum is incorporated in the synthesis process to produce Al-Ti3AlC2. In this study, Ti3AlC2 and Al-Ti3AlC2 MAX phases are used to synthesize Ti3C2Tx and Al-Ti3C2Tx MXenes, respectively, by the same method of HF:HCl etching and LiCl intercalation. The freestanding Ti3C2Tx and Al-Ti3C2Tx film electrode is separately prepared through simple vacuum filtration. The presence of excess aluminum during the Al-Ti3AlC2 synthesis facilitates to form more homogeneous grains structure with relatively larger particle sizes and an improved stoichiometric MAX phase with a Ti:C ratio closer to 3:2. The resulting Al-Ti3C2Tx nanosheets show improved oxidation resistance with relatively uniform and larger dimensions, which facilitate the higher conductivity with slightly increased interlayer spacing for the Al-Ti3C2Tx film. Therefore, the Al-Ti3C2Tx film electrode shows more efficient ions transport and charge transfer, and thus achieves significantly enhanced capacitance (399 F g−1 at 1 A g−1) and rate performance (63.6 % retention from 1 to 10 A g−1) compared to the Ti3C2Tx film electrode (342 F g−1 at 1 A g−1, 55.6 % retention from 1 to 10 A g−1). Moreover, the Al-Ti3C2Tx-based flexible sandwiched supercapacitor also exhibits superior energy storage performance. The impressive results indicate that Al-Ti3C2Tx MXene synthesized from Al-Ti3AlC2 MAX phase possesses the great application potential in flexible supercapacitors.

Balancing PEDOT:PSS conductivity for optimal power output of p-n junction based ZnO piezoelectric nanogenerator

Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonic acid) (PEDOT:PSS), has been employed in a wide range of applications owing to its good film-forming properties, high transparency, tunable conductivity, and good thermal and environmental stability. In piezoelectric nanogenerators (PENGs), p-type PEDOT:PSS has been used to form a p-n junction with n-type ZnO nanorods, which slows down the screening of the piezoelectric polarisation to increase the generated output voltage. Optimizing the conductive property of PEDOT:PSS is therefore a potential way to improve the performance of a PENG by controlling the screening effect and internal resistance of the device. In this work, ethylene glycol (EG) is added to the PEDOT:PSS layer in a ZnO PENG to modify its conductivity. Doping with EG, induces a change in conformation of the PEDOT which transform from a coil shape to expanded-coil or linear shapes as confirmed by Raman spectroscopy. The conductivity of the PEDOT:PSS layer is enhanced and the internal resistance of the PENG device is reduced, producing a higher current output. However, at the same time, devices using higher EG doping levels produce reduced voltage output, which is related to the rapid screening of the developed polarisation. Specifically, the optimal EG content was identified at 2.5%; although this resulted in a slight 4.0% reduction in voltage output compared to undoped devices, the current output increased by 41.6%, ultimately leading to a 33.1% improvement in peak power output. Therefore, we find that a balance between reducing the device resistance, which increases current output, and supressing the screening effect, which increases voltage output, is required to produce an optimum power output from the devices.

Genus Paeonia polysaccharides: A review on their extractions, purifications, structural characteristics, biological activities, structure-activity relationships and applications.

The Paeonia genus, the most distinctive representative of the Paeoniaceae family, holds significant edible and medicinal value. Its plants are rich in chemical constituents, including polysaccharides, phenols, terpenes, and flavonoids. Among these, Paeonia polysaccharide (PPS) is a key bioactive component, exhibiting diverse biological activities such as anti-cancer, anti-depressant, anti-oxidant, anti-inflammatory, anti-bacterial, immunomodulatory activities and therapeutical effect of diabetic kidney disease. Additionally, PPS possess favorable physicochemical properties including low toxicity and high biocompatibility. Recent studies increasingly demonstrate that PPS can enhance the sensory quality of food products during processing, and confer specific functional benefits through targeted biological activities indicating substantial potential for application in the food industry. The biological activity, emulsifying capacity, and film-forming properties of PPS also render them promising additives in cosmetic formulations, suggesting opportunities for further development. Despite their potential, challenges remain, particularly in optimizing extraction and purification techniques to improve PPS yield and preserve bioactivity. Therefore, a comprehensive review of the latest research advancements and future prospects is essential to deepen the understanding and facilitate the development of PPS.

Design of novel bracket structure for falling film devolatilizer and numerical simulation of its film-forming property

The falling film devolatilizer is a new type of devolatilization equipment, which has the advantages of high film-forming efficiency and no mechanical transmission. In this study, a devolatilizer with an open falling film substrate was designed, and the film-forming performance and surface renewal performance of high viscosity fluids under the falling film structure were numerically simulated. The results indicate that the opening of the falling film substrate makes the liquid film thinner, which is beneficial for the stretching of the liquid film. The advantages of the falling film under low viscosity and high flow rate conditions are more significant. Simultaneously, four bracket structures were designed. Compared with the rectangular bracket, the renewal frequency of fan-shaped brackets can be increased by more than 20%, and the flow rate can be increased by about 10%. The improvement of the two can directly improve the falling film devolatilization performance, so as to improve the polymer polymerization degree and improve the product performance. Therefore, exploring the falling film support frame with high devolatilization performance provides a certain engineering practical significance for the design of devolatilization equipment.

Gelatin-Coated High-Sensitivity Microwave Sensor for Humidity-Sensing Applications.

In this paper, the humidity-sensing characteristics of gelatin were compared with those of poly(vinyl alcohol) (PVA) at L-band (1 ~ 2 GHz) microwave frequencies. A capacitive microwave sensor based on a defected ground structure with a modified interdigital capacitor (DGS-MIDC) in a microstrip transmission line operating at 1.5 GHz without any coating was used. Gelatin is a natural polymer based on protein sourced from animal collagen, whereas PVA is a high-sensitivity hydrophilic polymer that is widely used for humidity sensors and has a good film-forming property. Two DGS-MIDC-based microwave sensors coated with type A gelatin and PVA, respectively, with a thickness of 0.02 mm were fabricated. The percent relative frequency shift (PRFS) and percent relative magnitude shift (PRMS) based on the changes in the resonant frequency and magnitude level of the transmission coefficient for the microwave sensor were used to compare the humidity-sensing characteristics. The relative humidity (RH) was varied from 50% to 80% with a step of 10% at a fixed temperature of around 25 °C using a low-reflective temperature and humidity chamber manufactured with Styrofoam. The experiment's results show that the capacitive humidity sensitivity of the gelatin-coated microwave sensor in terms of the PRFS and PRMS was higher compared to that of the PVA-coated one. In particular, the sensitivity of the gelatin-coated microwave sensor at a low RH from 50% to 60% was much greater compared to that of the PVA-coated one. In addition, the relative permittivity of the fabricated microwave sensors coated with PVA and gelatin was extracted by using the measured PRFS and the equation was derived by curve-fitting the simulated results. The change in the extracted relative permittivity for the gelatin-coated microwave sensor was larger than that of the PVA-coated one for varying the RH.

Superior Hole Injection Material PEGDT/TPF/PVDF with p-Doping Capability for Highly Efficient Solution-Processed Organic Light-Emitting Diode.

The ability to charge injection is a key factor in determining the performance of the organic light-emitting diode (OLED) devices. Improving the work function of the anode surface via interface modification, thus lowering the hole injection barrier, stands as a crucial strategy for enhancing the performance of the OLED device. Herein, we propose an innovative p-doping hole injection material, namely, PEGDT/TPF/PVDF that exhibits excellent performance in OLED devices with the value of maximum current efficiency at 56.4 Cd A-1, maximum luminescence at 25,564 Cd m-2, and a high EQE of 19.8%. The results for PEGDT/TPF/PVDF showed good conductivity, excellent film-forming property, and high transmittance over 98% in the spectrum range of 500-700 nm. Changes in the hole-injection energy barriers observed from the surface of the anode suggest a modified anode with PEGDT/TPF/PVDF deepened the work function at a value of 0.2 eV, which dramatically improves the hole-injection properties. This work not only provides novel structural materials with exceptional hole-injection properties but also proposes a promising alternative to PEDOT/PSS.

Performance Enhancement of Polyurethane Acrylate Resin by Urushiol: Rheological and Kinetic Studies.

A natural extract, i.e., urushiol, was employed to effectively cross-link and modify commercial wet-cured polyurethane acrylic resin. Comprehensive characterization of the paint film was performed using techniques such as FTIR, SEM, and TGA. The results indicated that the incorporation of urushiol significantly increased the cross-linking density of the resin, which in turn enhanced the film-forming properties, mechanical strength, and thermal stability of the paint film. Additionally, the study discovered that under isothermal conditions, the dynamic moduli (G' and G″) of the paint film are related to the gel point frequency by a power law, aligning with the predictions of percolation theory. The application of the autocatalytic model has provided a novel approach to studying non-isothermal kinetic reactions, offering valuable insights for process optimization and further development of urushiol-based polyurethane.

The Role of Starch Incorporation into Waterborne Acrylic-Hybrid Nanoparticles for Film-Forming Applications.

The use of biopolymers as an alternative to petroleum-based polymers offers a sustainable solution with benefits such as biodegradability and unique functionalities. In this study, starch/zein bioparticles (BPs) obtained by nanoprecipitation were employed to synthesize acrylic polymer/biopolymer waterborne nanoparticles with excellent film formation capability. These hybrid nanoparticle dispersions were obtained through a semibatch emulsion polymerization using the previously synthesized BPs as seed and variable monomeric formulations composed of butyl acrylate and methyl methacrylate. A synergetic effect between acrylic and biopolymer phases was evidenced where the incorporation of BPs had a fundamental role in improving sensitive properties, such as film blocking resistance, while attaining smooth films at room temperature. These excellent film-forming properties of starch/acrylic hybrid latexes without requiring the addition of formulation agents, which depict an important benefit from an environmental viewpoint, demonstrate that they represent a promising alternative for the development of a new generation of eco-friendly binders.

Time dependent anti-corrosion and anti-scaling efficiency of polyepoxysuccinic acid inhibitor in simulated hard water

In this study, the time-dependent performance of a phosphorus-free corrosion and scale inhibitor primarily composed of polyoxyuccinic acid (PESA) and zinc salts was investigated in a laboratory-simulated hard water environment. Long-term static scale inhibition tests and corrosion rotation coupon tests were conducted under two temperature conditions, 45 °C and 80 °C, following established literature standards. Changes in water quality, scale morphology, metal corrosion status, and electrochemical impedance were monitored using calcium ion concentration analysis, optical microscopy imaging, X-ray diffraction (XRD), and electrochemical testing. The study revealed a progressive decline in the corrosion and scale inhibition efficiency of the phosphorus-free inhibitor in simulated hard water with calcium carbonate hardness levels of 300, 400, and 500 mg/L over time. Moreover, higher water hardness accelerated corrosion onset, suggesting that calcium carbonate deposition promotes metal corrosion under the experimental conditions. Density functional theory (DFT) calculations indicated that PESA chemically adsorbs onto both metal and calcite surfaces, underscoring its dual role in corrosion and scale inhibition. These findings underscore the intrinsic corrosion and scale inhibition capabilities of PESA, complementing its synergistic film-forming properties with Zn2+.

Dimeric Carbazole Core Based Dopant‐Free Hole Transport Material for n‐i‐p Planar Perovskite Solar Cell

AbstractA profitable approach for improving the stability of n‐i‐p planar perovskite solar cell (PSC) is developing dopant‐free hole transport materials (HTMs) with desirable intrinsic charge transport properties. In this work, by adopting a metal‐free catalytic intramolecular C─C coupling reaction, a carbazole dimer‐based fused‐ring is synthesized, and further developed a small molecular dopant‐free HTM abbreviated as NCz‐DM with appropriate energy level, excellent hole transport and film formation properties. Applied in n‐i‐p planar PSC, an impressive power conversion efficiency (PCE) of 24.0% is achieved, together with enhanced humidity, thermal and light stability, which is among the high level of ever‐reported results for PSCs utilizing small molecular dopant‐free HTM.

Structural and electrochromic property control of WO3 films through fine-tuning of film-forming parameters

Abstract Tungsten trioxide (WO3) films, extensively investigated for their remarkable electrochromic properties, have proven to be highly versatile in numerous applications. However, the challenge of achieving large-scale WO3 films with substantial dimensions and volumes remains a critical obstacle for industrial-scale production. Among the available techniques, magnetron sputtering stands out as the most efficient and straightforward method for the industrial preparation of WO3 films. In this comprehensive study, we meticulously explored the impact of various process parameters in magnetron sputtering on the film formation properties. By employing a controlled variable approach, we systematically investigated the influence of gas flow (Ar), sputtering pressure, power, and time. Our meticulous observations revealed that each parameter exerted distinct effects on the intricate film formation process. Careful analysis of the final dataset unequivocally demonstrated that when the sputtering conditions were meticulously optimized, the resulting films exhibited an extraordinary maximum transmittance change of 85% at a specific wavelength of 0.6 μm. Furthermore, these films showcased rapid coloring and bleaching response times, clocking in at an impressive 15 and 20 s, respectively, without any significant degradation even after undergoing 5,000 cycles. These groundbreaking findings provide invaluable insights into the intricate film formation process associated with magnetron-sputtered WO3.