A laser induced periodic surface structure (LIPSS) on graphene doped polystyrene was prepared by the means of a krypton fluoride (KrF) laser with the wavelength of 248 nm and precisely desired physico-chemical properties were obtained for the structure. Surface morphology after laser modification of polystyrene (PS) doped with graphene nanoplatelets (GNP) was studied. Laser fluence values of modifying laser light varied between 0–40 mJ·cm−2 and were used on polymeric PS substrates doped with 10, 20, 30, and 40 wt. % of GNP. GNP were incorporated into PS substrate with the solvent casting method and further laser modification was achieved with the same amount of laser pulses of 6000. Formed nanostructures with a periodic pattern were examined by atomic force microscopy (AFM). The morphology was also studied with scanning electron microscopy SEM. Laser irradiation resulted in changes of chemical composition on the PS surface, such as growth of oxygen concentration. This was confirmed with energy-dispersive X-ray spectroscopy (EDS).

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The presented paper is aimed on the plasma activation of perfluoroethylenepropylene for construction of honeycomb‐like structures on its surface by dip‐coating technique complemented with phase separation of biopolymer poly‐l‐lactid acid. Surface activation with plasma significantly improved the possibility of successful HCL pattern formation on perfluoroethylenepropylene polymer compared with pristine foil. The idea of surface pretreatment with plasma allowed us to prepare also pattern with different pore dimension, which may have a significant role for cytocompatibility enhancement and growth of specific cells such as osteoblasts. The unique combination of plasma treatment and dip‐coating technique as simple and cheap procedure was confirmed to be a significant tool for honeycomb‐like structure construction.

This article is focused on the evaluation of surface properties of polytetrafluoroethylene (PTFE) nanotextile and a tetrafluoroethylene-perfluoro(alkoxy vinyl ether) (PFA) film and their surface activation with argon plasma treatment followed with silver nanoclusters deposition. Samples were subjected to plasma modification for a different time exposure, silver deposition for different time periods, or their combination. As an alternative approach, the foils were coated with poly-L-lactic acid (PLLA) and silver. The following methods were used to study the surface properties of the polymers: goniometry, atomic force microscopy, and X-ray photoelectron microscopy. By combining the aforementioned methods for material surface modification, substrates with antibacterial properties eliminating the growth of Gram-positive and Gram-negative bacteria were prepared. Studies of antimicrobial activity showed that PTFE plasma-modified samples coated with PLLA and deposited with a thin layer of Ag had a strong antimicrobial effect, which was also observed for the PFA material against the bacterial strain of S. aureus. Significant antibacterial effect against S. aureus, Proteus sp. and E. coli has been demonstrated on PTFE nanotextile plasma-treated for 240 s, coated with PLLA, and subsequently sputtered with thin Ag layer.

This study involved the preparation and characterization of structures with a honeycomb-like pattern (HCP) formed using the phase separation method using a solution mixture of chloroform and methanol together with cellulose acetate. Fluorinated ethylene propylene modified by plasma treatment was used as a suitable substrate for the formation of the HCP structures. Further, we modified the HCP structures using silver sputtering (discontinuous Ag nanoparticles) or by adding Ag nanoparticles in PEG into the cellulose acetate solution. The material morphology was then determined using atomic force microscopy (AFM) and scanning electron microscopy (SEM), while the material surface chemistry was studied using energy dispersive spectroscopy (EDS) and wettability was analyzed with goniometry. The AFM and SEM results revealed that the surface morphology of pristine HCP with hexagonal pores changed after additional sample modification with Ag, both via the addition of nanoparticles and sputtering, accompanied with an increase in the roughness of the PEG-doped samples, which was caused by the high molecular weight of PEG and its gel-like structure. The highest amount (approx. 25 at %) of fluorine was detected using the EDS method on the sample with an HCP-like structure, while the lowest amount (0.08%) was measured on the PEG + Ag sample, which revealed the covering of the substrate with biopolymer (the greater fluorine extent means more of the fluorinated substrate is exposed). As expected, the thickness of the Ag layer on the HCP surface depended on the length of sputtering (either 150 s or 500 s). The sputtering times for Ag (150 s and 500 s) corresponded to layers with heights of about 8 nm (3.9 at % of Ag) and 22 nm (10.8 at % of Ag), respectively. In addition, we evaluated the antibacterial potential of the prepared substrate using two bacterial strains, one Gram-positive of S. epidermidis and one Gram-negative of E. coli. The most effective method for the construction of antibacterial surfaces was determined to be sputtering (150 s) of a silver nanolayer onto a HCP-like cellulose structure, which proved to have excellent antibacterial properties against both G+ and G− bacterial strains.