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The global trend towards conscious consumption plays an important role in consumer preferences regarding both the composition and quality of food and packaging materials, including sustainable ones. The development of biodegradable active packaging materials could reduce both the negative impact on the environment due to a decrease in the use of oil-based plastics and the amount of synthetic preservatives. This review discusses relevant functional additives for improving the bioactivity of biopolymer-based films. Addition of plant, microbial, animal and organic nanoparticles into bio-based films is discussed. Changes in mechanical, transparency, water and oxygen barrier properties are reviewed. Since microbial and oxidative deterioration are the main causes of food spoilage, antimicrobial and antioxidant properties of natural additives are discussed, including perspective ones for the development of biodegradable active packaging. [ABSTRACT FROM AUTHOR]

Increasing photon absorption by capturing light is an important way to increase the efficiency of photovoltaic devices. In this regard, the small optical band gap (Eg) and high absorption coefficient of Se-containing thin nanofilms make them ideal for next generation photovoltaic devices based on selenides. Amorphous selenium was introduced into polyamide-6 (PA 6) via a chemical synthesis in a bath and the influence of the products of its reaction with Cd2+ and Ag+ ions on the film phase composition, topographic and optical properties were evaluated. AFM data have revealed that the surface roughness of the a-Se/PA 6 composite noticeably increases compared to that of unreacted PA 6. However, at later stages of film deposition, the roughness decreases, and the thin film becomes smoother and uniform. The incorporation of solid inorganic nanoparticles into flexible polyamide network causes chain stretching, which has been confirmed by ATR-FTIR spectroscopy data. The data of X-ray diffraction analysis, depending on the stage of synthesis, showed the crystalline composition of the film with peaks of Se8, CdSe, Ag2Se and Ag, which may explain the observed optical properties. The optical properties of the composites indicate a shift in the band gap from 4.46 eV for PA 6 to 2.23–1.64 eV upon the stepwise deposition of amorphous Se, CdSe and Ag2Se. Eg is conveniently located in the visible region of solar energy, making the obtained nanofilms ideal for solar energy harvesting. [ABSTRACT FROM AUTHOR]

The aim of the research was to modify the surface of construction textiles by means of the use of thin silver oxide films, investigate the structure and optical and mechanical properties, and determine the structure, optical and mechanical properties of the aged composites. Thin films of silver oxide (Ag2O) were synthesized on a flexible PET/PVC construction textile (CT); the structural, optical, and physical properties, as well as the effect of artificial aging on these properties, were investigated. The SILAR method (successive ionic layer adsorption and reaction) was used to synthesize thin Ag2O films on the CT surface. Before the thin films were deposited, the CT surface was mechanically roughened and pretreated with acidic and alkaline solutions at an elevated temperature. XRD analysis showed that the deposited films were a polycrystalline mixed phase material consisting of Ag2O, AgO, and metallic Ag. Diffuse reflectance spectra in the ultraviolet and visible ranges (UV-Vis) were used to study the optical properties of the deposited thin films. The synthesized Ag2O/CT composites were direct-gap semiconductors (the optical band gap (Eg) was 0.89 ± 0.02 eV). Eg and refractive indices (n) increased as the aging tests were carried out. Higher Eg and n meant that the composites were a good material for optoelectronic applications. The results showed that, after modification, the structural properties and tear strength of the PET/PVC fabric remained the same while the tensile strength decreased. The same tendencies remained after artificial aging. [ABSTRACT FROM AUTHOR]

Ag–Se nanostructure films were deposited on a–Se/nylon templates by a template-engaged reaction. Firstly, amorphous selenium (a–Se) was deposited on nylon by employing the chemical bath deposition method while using H2SeO3 and Na2SO3 solutions with an increasing selenium deposition time. Then, these a–Se/nylon templates were exposed into AgNO3 solution at ambient temperature and pressure. The Ag–Se/nylon nanocomposites surface morphology, elemental and phase composition, and optical properties were monitored depending on the selenium deposition time on nylon. Scanning electron microscopy (SEM) analysis confirmed the development of a very complex surface composed of pyramidal-like sub-micron structures, agglomerates, and grid-like structures. Energy dispersive spectroscopy (EDS) proved the presence of carbon, oxygen, nitrogen, selenium, and silver. SEM/EDS cross-sectional analysis confirmed the multilayer character with different individual elemental composition in each film layer. X-ray diffraction analysis revealed a polycrystalline Ag2Se phase with or without metallic Ag. The RMS value obtained from atomic force microscopy varies from 25.82 nm to 57.04 nm. From the UV-Vis spectrophotometry, the direct optical band gaps were found to be 1.68–1.86 eV. Ag–Se/nylon composites exhibit high refractive indices in the near infrared region. [ABSTRACT FROM AUTHOR]