A visibly transparent radiative cooling film with self-cleaning function produced by solution processing

Freezing delay of water droplets on metallic hydrophobic surfaces in a cold environment

Heteroleptic Tin-Antimony Sulfoiodide for Stable and Lead-free Solar Cells

A durable self-cleaning superhydrophobic coating fabricated using the preset grid-spraying method

Superhydrophobic surface on Al alloy with robust durability and excellent self-healing performance

In this paper, the superhydrophobic surfaces of silicone rubber with different microstructure were directly prepared by texturing with a nanosecond fibre laser. The superhydrophobic surfaces have excellent anti-icing performance. Even at 0 °C, the superhydrophobic surface has a contact angle of ∼150° and a rolling-off angle of ∼2.5°. The superhydrophobic silicone rubber surfaces with different microstructures have obvious differences in contact behaviours with water droplets at low temperatures. The surface textured with a laser fluence of 10 J cm−2 has a larger particle size and more abundant micro-nano particles, which results in a smaller contact area with the water droplet due to greater roughness and root mean square slope. The deeper the small gaps on the superhydrophobic surface, the more time it takes for the change in contact state between the surface and the water droplets. The adhesion strength of the superhydrophobic rubber surfaces with the ice layer were smaller due to the air stored between the surfaces and the ice layer. In particular, the laser textured surface with an laser fluence of 10 J cm−2 has the lowest ice adhesion strength due to its layered micro-nano composite structure. After 30 cycles of icing and de-icing, the processed silicone rubber surface still retains excellent hydrophobicity. The superhydrophobic silicone rubber surface has important value in anti-icing and anti-pollution applications.

This work reports a facile method for fabricating superhydrophobic surface on copper plate by AgNO₃ treatment and dodecyl mercaptan modification. The as-prepared superhydrophobic copper plate presents hierarchical and rough morphology composed of nanosheets and nanoparticleformed matrix. Meanwhile, long alkyl chains are assembled onto the rough surface successfully. Consequently, the copper plate is endowed with excellent superhydrophobic performance with a water contact angle of 156.8° and a rolling angle of ca. 3°. Moreover, the superhydrophobicity has long-term durability and excellent stability. Grounded on the strong water repellence, the resultant superhydrophobic copper plate surface exhibits multi-functions. The excellent performance can be well explained by "Cushion effect" and Capillary phenomena. As a result, water and corrosive species can be prevented from contacting with the copper plate surface, and contaminants can be taken away easily by the rolling water droplets. Meanwhile, the icing process of water is delayed on the superhydrophobic surface. Therefore, the superhydrophobic copper is endued with enhanced corrosion resistance, excellent self-cleaning and anti-icing performance. We believe that this facile method provides a simple and cost-effective process to improve the properties of copper plate, and which may see practical application of the superhydrophobic materials.

Dust deposition on solar photovoltaic (PV) cells will dramatically reduce the photovoltaic power output. Self-cleaning coating may be a novel method to decrease dust deposition problems. This paper compares self-cleaning performances and mechanisms of super-hydrophobic and super-hydrophilic coating on dirt deposition decrease for solar photovoltaic cells by experimental measurement. In the process of the deposition of dust on solar cells, covering glass, coated and uncoated, is conducted under natural settling conditions. Moreover, the dust removal efficiency of the glass samples with and without coatings is studied under water spraying conditions. The wettability of different surfaces, dust deposition mass, dust removal efficiency, self-cleaning mechanisms, and transmittance of glass samples are investigated and analyzed. Under natural settling conditions, the deposition mass reduction ratio by the super-hydrophilic coating is only 8.1%, while it can reach 85.8% by the super-hydrophobic coating because of surface micro-structures and low surface energy. However, after the water spraying process, the remaining dust mass ratio for the super-hydrophobic surface is only 16.5%, while it is 18.6% for the super-hydrophilic surface. The self-cleaning mechanism of super-hydrophobic coating is that most deposited particles of dust are removed from glass samples by the rolling of liquid droplets. However, the self-cleaning mechanism of super-hydrophilic coating is the breakup of the liquid film. Therefore, both coatings can effectively reduce dust deposition under water spraying conditions. The average transmittance of super-hydrophobic and super-hydrophilic coatings after the water spraying process is 91.1% and 86.4%, respectively, while it is only 61.1% for the uncoated glass sample.

Cold Crystallization Temperature Correlated Phase Separation, Performance, and Stability of Polymer Solar Cells

Insulators, as important components in transmission lines, are prone to disturb the safe running of the power system by the ice accumulation on surfaces. Traditional anti-icing coatings are difficult to practically apply to insulators. Here, superhydrophobic (SHP) coatings were fabricated on the glass insulator surface by spraying. We studied microstructure, wettability, water droplet bouncing behavior, and anti-glaze icing properties of SHP coating. The results demonstrated that SHP coatings had micro-nano rough structures. The excellent superhydrophobicity (contact angle of 165.2° and sliding angle of 3.7°) was achieved. The water droplet was easily adhered to the surface of the glass insulators. At the same time, individual water droplets could bounce away from the surface after impacting the SHP coating. In the glaze environment, water droplets sprayed onto the SHP coating merged with each other and slid off the surface. These significantly reduce the likelihood of freezing. Furthermore, the SHP coating could dramatically delay the glaze icing and decrease the icing area. The icing weight and icicle length were smaller than glass insulators. The SHP coatings prepared in this work display great potential for the anti-icing of glass insulators.

Dust particles can adhere to surfaces, thereby decreasing the efficiency of diverse processes, such as light absorption by solar panels. It is well known that superhydrophobicity reduces the friction between water droplets and the surface, thus allowing water drops to slide/roll and detach (clean) particles from surfaces. However, the forces that attach and detach particles from surfaces during the self-cleaning mechanism and the effect of nanotextures on these forces are not fully understood. To shed light on these forces and the effect of nanotexture on them, we prepared four Si-based samples (relevant to solar panels): (1) smooth or (2) nanotextured hydrophilic surfaces and (3) smooth or (4) nanotextured hydrophobic surfaces. In agreement with previous publications, it is shown that the efficiency of particle removal increases with hydrophobicity. Furthermore, nanotexture enhances the hydrophobicity, whereby particle removal is further increased. Specifically, hydrophilic particle removal increased from ∼41%, from hydrophilic smooth Si wafers to 98% from superhydrophobic Si-based nanotextured surfaces. However, the reason for the increased particle removal is not low friction between the droplets and the superhydrophobic surfaces; it is the reduction of the adhesion force between the particle and the surface and the altered geometry of the water-particle-air line tension acting on the particles on superhydrophobic surfaces, which increases the force that can detach particles from the surfaces. The experimental methods we used and the criterion for particle removal we derived can be implemented to engineer self-cleaning surfaces using other surfaces and dust particles, exhibiting different chemistries and/or textures.

Superhydrophobic coatings with excellent self-cleaning performance have attracted significant concerns from researchers. Although various superhydrophobic coatings with prominent superhydrophobic properties have been fabricated, most developed coatings are still inadequate in pipeline scale inhibition applications. In this work, nano-silica (nano-SiO2) was modified by silane coupling of vinyltriethoxysilane (VETS) and 1H, 1H, 2H, 2H-perfluorooctyltriethoxysilane (PFTS) to prepare a superhydrophobic coating. Organosilicon of PFTS and VETS was grafted onto the surface of SiO2 for preparing the superhydrophobic coating with low surface energy, and the superhydrophobic coating was cured via poly(vinylidene fluoride) (PVDF). The results showed that the contact angle of the prepared silica-based superhydrophobic coating, denoted as VETS-PFTS@SiO2/PVDF, is 159.2°, exhibiting outstanding superhydrophobicity performance. Furthermore, the superhydrophobicity coating also showed satisfactory durability performance in 200 g load wear test after 50 cycles. Importantly, the superhydrophobic coating displayed promising mechanical durability, chemical stability performance, as well as maintained excellent superhydrophobic properties after being placed in water for 3 weeks, indicating the potential for long-term utilization. In the simulated scale inhibition test, it was found that the synthesized coating can also significantly decrease the deposition rate of CaCO3 and successfully enhance its scale inhibition performance.

Water droplets impact dynamics on laser engineered superhydrophobic ceramic surface

Tandem solar cells (TSCs), which use two or more materials to absorb sunlight, have achieved power conversion efficiencies of >25% versus 11-20% for commercialized single junction solar cell modules. The key to widespread commercialization of TSCs is to develop the wide-band, top solar cell that is both cheap to fabricate and has a high open-circuit voltage (i.e. >1V). Previous work in TSCs has generally focused on using expensive processing techniques with slow growth rates resulting in costs that are two orders of magnitude too expensive to be used in conventional solar cell modules. The objective of the PLANT PV proposal was to investigate the feasibility of using Ag(In,Ga)Se2 (AIGS) as the wide-bandgap absorber in the top cell of a thin film tandem solar cell (TSC). Despite being studied by very few in the solar community, AIGS solar cells have achieved one of the highest open-circuit voltages within the chalcogenide material family with a Voc of 949 mV when grown with an expensive processing technique (i.e. Molecular Beam Epitaxy). PLANT PV's goal in Phase I of the DOE SBIR was to (1) develop the chemistry to grow AIGS thin films via solution processing techniques to reduce costs and (2) fabricate new device architectures with high open-circuit voltage to produce full tandem solar cells in Phase II. PLANT PV attempted to translate solution processing chemistries that were successful in producing >12% efficient Cu(In,Ga)Se2 solar cells by replacing copper compounds with silver. The main thrust of the research was to determine if it was possible to make high quality AIGS thin films using solution processing and to fully characterize the materials properties. PLANT PV developed several different types of silver compounds in an attempt to fabricate high quality thin films from solution. We found that silver compounds that were similar to the copper based system did not result in high quality thin films. PLANT PV was able to deposit AIGS thin films using a mixture of solution and physical vapor deposition processing, but these films lacked the p-type doping levels that are required to make decent solar cells. Over the course of the project PLANT PV was able to fabricate efficient CIGS solar cells (8.7%) but could not achieve equivalent performance using AIGS. During the nine-month grant PLANT PV set up a variety of thin film characterization tools (e.g. drive-level capacitance profiling) at the Molecular Foundry, a Department of Energy User Facility, that are now available to both industrial and academic researchers via the grant process. PLANT PV was also able to develop the back end processing of thin film solar cells at Lawrence Berkeley National Labs to achieve 8.7% efficient CIGS solar cells. This processing development will be applied to other types of thin film PV cells at the Lawrence Berkeley National Labs. While PLANT PV was able to study AIGS film growth and optoelectronic properties we concluded that AIGS produced using these methods would have a limited efficiency and would not be commercially feasible. PLANT PV did not apply for the Phase II of this grant.

Mimicking natural superhydrophobic surfaces and grasping the wetting process: A review on recent progress in preparing superhydrophobic surfaces

Morphology control and device optimization for efficient organic solar cells