Due to the numerous applications of such surfaces in energy, water, healthcare, fundamental research, and everyday activities, the fabrication of hydrophilic and superhydrophilic surfaces has gotten a lot of interest in recent years. Oil-water separation, fog collecting, lab-on-a-chip, self-cleaning, blood-plasma separation, and cell biology are some of the applications for such intensely wetted surfaces.
Deposited Molecular Structures
Many organic molecules adsorb from the solution or gas phase onto chosen solids and self-assemble into self-assembled monomolecular layers, modifying the substrate's wetting characteristics. The Langmuir-Blodgett film process may deposit monolayers and multilayers mechanically. The deposited organic layer renders the surface hydrophilic if the terminal groups are polar. The groups with the highest hydrophilicity contain -OH, -COOH, and POOH.
Furthermore, much study has been devoted to coating materials with macromolecules and biomolecules, which are particularly popular in the modification of polymers in interface with biological fluids. Albumin and heparin are two biomacromolecules that are commonly employed. Poly(ethylene glycol) and phospholipid-like macromolecules have been intensively studied among synthetic polymers.
Fig 1. Condensation and optical clarity of polyester films at high relative humidity. Left: Untreated Mylar fogs. Right: Plasma-treated superhydrophilic polyester film retains optical clarity. (Nie M, et al. 2009)
Surface Chemical Modification
The most common approaches for oxidizing polymer surfaces are plasma treatment, corona treatment, and flame treatment. Accelerated electrons hit the polymer in plasma and corona treatments, generating free radicals that form crosslinks and react with surrounding oxygen to form oxygen functional groups. Hydroxyl, peroxy, carbonyl, carbonate, ether, ester, and carboxylic acid groups are the most common polar groups formed on the surface. The polymer undergoes surface combustion during flame treatment, resulting in hydroperoxides and hydroxyl radicals. Plasma, corona, and flame treatments end with extensive surface oxidation and result in highly wettable surfaces.
UV light causes polymers to oxidize and deteriorate. UV exposure produces chain scission, cross-linking, and an increase in the density of oxygen-based polar groups on the substrate's surface, making the surface more hydrophilic.
Alkali treatment of polymers, particularly at high temperatures, can improve their surface hydrophilicity. When polymers like polyolefin and polyethylene terephthalate are etched with concentrated alkali, hydrophilic groups like hydroxyl and carboxyl are generated on the surface.
Preparation of Superhydrophilic Surfaces
Any natural or synthetic material can theoretically be chemically and mechanically roughened into a superhydrophilic surface or sub-microscopic particles that are then deposited to form a superhydrophilic coating, but only a few materials have been employed in this fashion. Titanium oxide (TiO2) and zinc oxide (ZnO) are two inorganic compounds that are extensively studied for their photogenic self-cleaning properties. Solution/suspension, inkjet printing, sol-gel processes, spin coating, and sputtering are the most common methods for depositing nanoparticle films on substrates.
Fig 2. Water remains in the shape of lenses with a contact angle of 70-80° on the TiO2-coated glass when stored in dark (a and c), but spreads completely when exposed to UV radiation (b and d). (Wang R, et al. 1997)
Polymers are also appealing materials for superhydrophilic coatings, but they typically require oxidation on their surfaces. As previously stated, several treatments that affect surface chemistry, such as surface irradiation with ion irradiation, electron beam, plasma, and corona treatment, can improve polymer surface hydrophilicity. To create the polymer superhydrophilic, the treatment must also affect the surface roughness, or the chemical treatment must be done simultaneously with surface roughening.
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