“…All of the tests showed that the degradation of MB followed the same pattern and the photocatalytic activity was fully sustained. This is summarized in Figure 11, which shows the decrease in the maximum absorbance peak of MB in samples over time using a logarithmic scale [80].…”
This work reports the design and characterization of functional photocatalytic coatings based on the combination of two different deposition techniques. In a first step, a poly(acrylic acid) + β-Cyclodextrin (denoted as PAA+ β-CD) electrospun fiber mat was deposited by using the electrospinning technique followed by a thermal treatment in order to provide an enhancement in the resultant adhesion and mechanical resistance. In a second step, a layer-by-layer (LbL) assembly process was performed in order to immobilize the metal oxide particles onto the previously electrospun fiber mat. In this context, titanium dioxide (TiO2) was used as the main photocatalytic element, acting as the cationic element in the multilayer LbL structure. In addition, two different metal oxides, such as tungsten oxide (WO3) and iron oxide (Fe2O3), were added into PAA anionic polyelectrolyte solution with the objective of optimizing the photocatalytic efficiency of the coating. All of the coatings were characterized by scanning electron microscopy (SEM) and atomic force microscopy (AFM) images, showing an increase in the original fiber diameter and a decrease in roughness of the mats because of the LbL second step. The variation in the wettability properties from a superhydrophilic surface to a less wettable surface as a function of the incorporation of the metal oxides was also observed by means of water contact angle (WCA) measurements. With the aim of analyzing the photocatalytic efficiency of the samples, degradation of methyl blue (MB) azo-dye was studied, showing an almost complete discoloration of the dye in the irradiated area. This study reports a novel combination method of two deposition techniques in order to obtain a functional, homogeneous and efficient photocatalytic coating.
“…All of the tests showed that the degradation of MB followed the same pattern and the photocatalytic activity was fully sustained. This is summarized in Figure 11, which shows the decrease in the maximum absorbance peak of MB in samples over time using a logarithmic scale [80].…”
This work reports the design and characterization of functional photocatalytic coatings based on the combination of two different deposition techniques. In a first step, a poly(acrylic acid) + β-Cyclodextrin (denoted as PAA+ β-CD) electrospun fiber mat was deposited by using the electrospinning technique followed by a thermal treatment in order to provide an enhancement in the resultant adhesion and mechanical resistance. In a second step, a layer-by-layer (LbL) assembly process was performed in order to immobilize the metal oxide particles onto the previously electrospun fiber mat. In this context, titanium dioxide (TiO2) was used as the main photocatalytic element, acting as the cationic element in the multilayer LbL structure. In addition, two different metal oxides, such as tungsten oxide (WO3) and iron oxide (Fe2O3), were added into PAA anionic polyelectrolyte solution with the objective of optimizing the photocatalytic efficiency of the coating. All of the coatings were characterized by scanning electron microscopy (SEM) and atomic force microscopy (AFM) images, showing an increase in the original fiber diameter and a decrease in roughness of the mats because of the LbL second step. The variation in the wettability properties from a superhydrophilic surface to a less wettable surface as a function of the incorporation of the metal oxides was also observed by means of water contact angle (WCA) measurements. With the aim of analyzing the photocatalytic efficiency of the samples, degradation of methyl blue (MB) azo-dye was studied, showing an almost complete discoloration of the dye in the irradiated area. This study reports a novel combination method of two deposition techniques in order to obtain a functional, homogeneous and efficient photocatalytic coating.
“…For example, Ce 3+ spectra in YAG were studied recently in Refs. [ 1 , 2 , 3 , 4 ]. The same Ce 3+ impurity in YAM was a subject of spectroscopic investigations in Refs.…”
In this paper, the density functional theory accompanied with linear combination of atomic orbitals (LCAO) method is applied to study the atomic and electronic structure of the Ti3+ and Ti2+ ions substituted for the host Al atom in orthorhombic Pbnm bulk YAlO3 crystals. The disordered crystalline structure of YAlO3 was modelled in a large supercell containing 160 atoms, allowing simulation of a substitutional dopant with a concentration of about 3%. In the case of the Ti2+-doped YAlO3, compensated F-center (oxygen vacancy with two trapped electrons) is inserted close to the Ti to make the unit cell neutral. Changes of the interatomic distances and angles between the chemical bonds in the defect-containing lattices were analyzed and quantified. The positions of various defect levels in the host band gap were determined.
“…The choice of the activator concentration of 2 % is explained by the following. Previous studies [17,18] have shown that 2 % Ce is the optimal concentration for YAG ceramics. The formation of radiation synthesis technology is at the very beginning.…”
The variety of applications of yttrium-aluminum garnet (YAG)-based luminescent materials and the morphology necessary for these purposes required the development of many technologies for their synthesis. All synthesis technologies used are complex. The structural phase of yttrium-aluminum garnet is formed with any technology, at temperatures exceeding 1,500 °C. The starting materials for the synthesis are metal oxides of aluminum, yttrium and other oxides for activation and modification. It seems possible to use hard radiation to form a new phase. Radiation synthesis of ceramics is realized in less than 1 s, without the use of any additives and influences.
The synthesis was carried out at the electron accelerator of the Institute of Nuclear Physics (Novosibirsk). In this work, we studied the spectral-kinetic and quantitative characteristics of luminescence for the first time obtained by the method of radiation synthesis of ceramic samples of yttrium-aluminum garnet doped with cerium with statistical processing of their values. The dependences of the reproducibility of the spectral characteristics of the luminescence of the samples on the preliminary preparation of the charge for synthesis have been investigated. Several cycles of luminophore brightness studies have been performed.
It is shown that the obtained ceramics based on yttrium-aluminum garnet doped with cerium possesses the required spectral-kinetic properties, and the efficiency of conversion of the chip radiation into luminescence is achieved, which is comparable to that available in commercial phosphors. The maximum measured values of the position of the bands are from 553.5 to 559.6 nm. Brightness values range from 4,720 to 1,960 cd/m2.
It was found that the main reason for the scatter in the characteristics of the luminescent properties of ceramics of yttrium-aluminum garnet, activated by cerium obtained by radiation assisted synthesis is the high rate of synthesis and, especially, the high rate of cooling of the samples.
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