Materials: Food-grade platinum-cure silicone (parts A and B), zinc nitrate hexahydrate (Zn(NO₃)₂·6H₂O, 99%), ammonium chloride (NH₄Cl, 99%), 1H, 1H, 2H, 2H-perfluorodecyltriethoxysilane (PFDS, 96%) [4] .

Instrumentation: Vacuum oven, 100 mL Teflon-lined stainless-steel autoclave.

Autoclave: A 100 mL Teflon-lined stainless-steel autoclave (max. 6 MPa, ≤200˚C) was employed. Pre-use inspections ensured intact sealing rings, unobstructed vent holes, and valid rupture discs. Solution volume never exceeded 2/3 of the liner capacity; heating ramps were limited to 5 ˚C∙min⁻¹. After reaction, natural cooling to room temperature preceded opening. Operators wore heat-resistant gloves and safety goggles under a fume hood.

Vacuum oven: Operated at 80˚C and 0.08 MPa. Prior to use, oil level and transparency were verified, seals were inspected, and the pump valve was kept closed during heating to prevent backflow. After completion, the pump was switched off before gradually admitting air.

PFDS handling: PFDS is a skin and respiratory irritant; manipulations were conducted in a fume hood with nitrile gloves and a respirator. Waste liquids were collected in fluorocarbon-compatible containers for professional disposal.

To create the micro-textured silicone template, the silicone base and curing agent (1:1 w/w) were thoroughly mixed. The mixture was then degassed under vacuum for 10 minutes to remove any trapped air bubbles. This degassing step is crucial to ensure that the silicone mixture is free of any air pockets, which could interfere with the replication process. The degassed mixture was carefully poured onto a petri dish and compressed against a master mold that featured 10 µm-diameter pillars with a 15 µm pitch. This step is crucial for ensuring the accurate replication of the micro-texture from the master mold to the silicone template. After applying the mixture to the master mold, the assembly was subjected to a second degassing process for 5 minutes to further eliminate any residual air bubbles. The degassed assembly was then cured at 80˚C for 1 hour. Once the curing process was complete, the silicone template was carefully peeled off from the master mold, revealing the negatively replicated micro-texture. This micro-textured silicone template serves as the foundation for the subsequent fabrication of the superhydrophobic film ( Figure 1 ) [5] [6] .

The preparation of the nanonuclei solution began with dissolving 0.35 g of NH₄Cl in 100 mL of deionized water under magnetic stirring for 5 minutes. This step ensures that the NH₄Cl is completely dissolved in the water, forming a clear solution. Next, 0.74 g of Zn(NO₃)₂·6H₂O was added to the NH₄Cl solution, and the mixture was stirred continuously until it became clear. The addition of Zn(NO₃)₂·6H₂O is essential for the formation of zinc-based nanonuclei, which play a critical role in the subsequent hydrothermal treatment process. Core Zn(NO₃)₂ provides Zn²⁺ for nanocrystal nucleation (e.g., ZnO). NH₄Cl enables pH to fluctuate around 5 - 6 to suppress precipitation.

Formed complexes enable core-shell growth [7] . After the solution was thoroughly mixed and clarified, it was transferred to a Teflon-lined autoclave. The autoclave was then sealed and aged at room temperature for 10 hours. This aging process allows the nanonuclei to grow and form a stable solution, which is vital for the successful fabrication of the superhydrophobic film ( Figure 2 ).

The fabrication of the flexible superhydrophobic sheet involved several key steps. First, the sheets were vertically suspended in the autoclave to ensure even exposure to the hydrothermal treatment conditions. The autoclave was then sealed and heated at 85˚C for 10 hours. This hydrothermal treatment is crucial for modifying the surface of the sheets and preparing them for the subsequent silane grafting process. After the hydrothermal treatment, the sheets were carefully rinsed with deionized water to remove any residual reaction products. Next, 3 - 4 drops of PFDS were dispensed onto the lower surface of each sheet. The PFDS serves as a silane coupling agent, which is essential for grafting fluorocarbon chains onto the surface of the sheets. The container was then sealed and heated at 85˚C for 10 hours to accomplish silane self-assembly. This step forms a dense fluorocarbon layer on the surface of the sheets, significantly reducing the surface energy and enhancing the superhydrophobic properties of the film ( Figure 3 ).

The silicone mixture was prepared by combining equal weights of the silicone base (Part A) and the curing agent (Part B). This 1:1 ratio is optimal for achieving the desired mechanical properties of the silicone template. The mixture was thoroughly mixed using a mechanical stirrer to ensure uniform distribution of the curing agent within the silicone base. The mixing process was carried out for approximately 5 minutes to ensure complete homogenization. After mixing, the silicone mixture was degassed under vacuum for 10 minutes to remove any air bubbles that could affect the replication process. The degassing step is critical to ensure that the silicone mixture is free of any air pockets, which could interfere with the accurate replication of the micro-texture from the master mold.

After degassing, the silicone mixture was carefully poured onto a petri dish. The petri dish was placed on a flat surface to ensure an even distribution of the silicone mixture. The mixture was then compressed against a master mold that featured 10 µm-diameter pillars with a 15 µm pitch. The master mold was carefully aligned with the petri dish to ensure accurate replication of the micro-texture. The assembly was then subjected to a second degassing process for 5 minutes to further eliminate any residual air bubbles. This step ensures that the silicone mixture is in intimate contact with the master mold, facilitating the accurate replication of the micro-texture.

The degassed assembly was then placed in an oven and cured at 80˚C for 1 hour. The curing process is essential for solidifying the silicone mixture and ensuring that the micro-texture is accurately replicated. After curing, the silicone template was carefully peeled off from the master mold. The peeled template revealed the negatively replicated micro-texture, which is crucial for the subsequent fabrication of the superhydrophobic film. The micro-textured silicone template was then inspected under a microscope to ensure that the micro-texture was accurately replicated.

The preparation of the nanonuclei solution began with dissolving 0.35 g of NH₄Cl in 100 mL of deionized water under magnetic stirring for 5 minutes. This step ensures that the NH₄Cl is completely dissolved in the water, forming a clear solution. Next, 0.74 g of Zn(NO₃)₂·6H₂O was added to the NH₄Cl solution, and the mixture was stirred continuously until it became clear. The addition of Zn(NO₃)₂·6H₂O is essential for the formation of zinc-based nanonuclei, which play a critical role in the subsequent hydrothermal treatment process. After the solution was thoroughly mixed and clarified, it was transferred to a Teflon-lined autoclave. The autoclave was then sealed and aged at room temperature for 10 hours. This aging process allows the nanonuclei to grow and form a stable solution, which is vital for the successful fabrication of the superhydrophobic film.

The superhydrophobic film was vertically suspended in the autoclave to ensure even exposure to the hydrothermal treatment conditions. The autoclave was then sealed and heated at 85˚C for 10 hours. This hydrothermal treatment is crucial for modifying the surface of the superhydrophobic film and preparing them for the subsequent silane grafting process. After the hydrothermal treatment, the superhydrophobic film was carefully rinsed with deionized water to remove any residual reaction products. The rinsed superhydrophobic film was then inspected under a microscope to ensure that the surface modification was successful.

Next, 3 - 4 drops of PFDS were dispensed onto the lower surface of each superhydrophobic film. The PFDS serves as a silane coupling agent, which is essential for grafting fluorocarbon chains onto the surface of the superhydrophobic film. The container was then sealed and heated at 85˚C for 10 hours to accomplish silane self-assembly. This step forms a dense fluorocarbon layer on the surface of the superhydrophobic film, significantly reducing the surface energy and enhancing the superhydrophobic properties of the film. The grafted superhydrophobic film was then inspected under a microscope to ensure that the fluorocarbon layer was evenly distributed.

The superhydrophobic properties of the fabricated film were characterized by measuring the static water contact angle and sliding angle. The contact angle measurements were performed using a contact-angle goniometer (JC2000D). A droplet of deionized water was placed on the surface of the film, and the contact angle was measured using a high-resolution camera. The sliding angle was measured by tilting the film and observing the angle at which the water droplet began to slide off the surface. The measurements were repeated multiple times to ensure accuracy and reproducibility. The results showed that the film exhibited a static water contact angle of 159 ± 1˚ and a sliding angle of 3.0 ± 0.5˚ (droplet volume 5 µL). These values significantly outperform conventional rigid silica coatings, which typically have a water contact angle of approximately 150˚ and a sliding angle of around 8˚ - 10˚ [8] - [10] .

To evaluate the durability of the flexible superhydrophobic film, a series of tests were conducted, including mechanical abrasion, thermal cycling, and UV exposure of 1.5 W/m². The film maintained its superhydrophobic properties after 100 cycles of mechanical abrasion (approximately 5N for each cycle), indicating excellent mechanical stability. Additionally, the film retained its water-repellent performance after 50 thermal cycles between −20˚C and 80˚C, demonstrating good thermal stability. Furthermore, the film showed no significant degradation in superhydrophobic properties after 100 hours of UV exposure, confirming its resistance to UV aging. These results suggest that the flexible superhydrophobic film has the potential for long-term deployment in various harsh environments.

The wetting characteristics of the fabricated flexible superhydrophobic film were evaluated by measuring the static water contact angle and sliding angle. The static water contact angle was measured 5 times, eventually to be 159˚ ± 1˚ ( Figure 4 ), and the sliding angle was determined to be 3.0˚ ± 0.5˚ (droplet volume 5 µL). These values significantly outperform conventional rigid silica coatings, which typically have a water contact angle of approximately 150˚ and a sliding angle of around 8˚ - 10˚ ( Figure 5 ). The high contact angle and low sliding angle of the flexible superhydrophobic film indicate its excellent water-repellent performance. This superior performance can be attributed to the synergistic effect of the micro-/nano-binary roughness and the perfluorinated surface chemistry. The micro-textured silicone template provides the film with a rough surface structure, which increases the contact area between the water droplet and the air trapped in the micro-nanostructures, thereby reducing the surface energy of the film. The subsequent PFDS grafting forms a dense fluorocarbon layer on the surface of the film, further reducing the surface energy and enhancing the water-repellent properties.

The flexible superhydrophobic film has significant potential for various practical applications. For example, in the field of self-cleaning solar panels, the film can effectively prevent the accumulation of dust and dirt on the surface of the solar panels, thereby maintaining their high light transmittance and improving the efficiency of solar energy conversion. In the field of anti-icing aircraft coatings, the film can reduce the adhesion of ice to the aircraft surface, thereby preventing the formation of ice and ensuring the safety of aircraft flight. In the field of corrosion-resistant marine surfaces, the film can protect the surface of marine equipment from corrosion by seawater, thereby extending the service life of the equipment.