Current Approach to Develop TiO2 Thin Film as Photocatalysts for Low-Density Plastic Degradation

Low-density plastic bags waste disposal is a big issue in the current scenario which gives rise to grave threats to human beings and environmental health also. Amid the various approaches applied for dealing with the problem, photocatalytic biodegradation in visible light irradiation is an advanced prospect that has received attention nowadays. The present review paper is to provide an outline of the current progress on the synthesis of titania (TiO2) thin-film photocatalysts for solid waste removal. The Photocatalysis method contains the photoinduced redox reactions in the photocatalyst which facilitates the degrading of almost organic compounds like polyethylene into carbon dioxide (CO2), water, and other substance. One of the most excellent photocatalysts which has grabbed attention in an application is titania because of its high photocatalytic activity and chemical stability. The synthesis of the photocatalyst as a thin film is a result of the unfeasible application of conventional powder photocatalyst which may cause a certain environmental hazard. The photocatalyst-coated thin film along with some environmental applications have also been reviewed. Likewise, various approaches for modifying thin-film property, film deposition techniques, and deposition on various substrates are used for the enhanced photocatalytic activity of the TiO2 thin film.

Effects of Preparation Conditions on the Efficiency of Visible-Light-Driven Hydrogen Generation Based on Cd0.25Zn0.75S Photocatalysts

Photocatalytic H2 production utilizing H2S, an industrial side-product, is regarded as an environmentally friendly process to produce clean energy through direct solar energy conversion. For this purpose, sulfide-based materials, such as photocatalysts, have been widely used due to their good solar response and high photocatalytic activity. In this work, a ZnS–CdS composite was studied, and special attention was dedicated to the influence of the preparation parameters on its H2 production activity. The ZnS–CdS composite, with an enhanced photoactivity for H2 production, was synthesized both from ammine complexes and, in a conventional way, directly from acetates at various pH values. Deviating from the traditional method, the photoactivity of ZnS–CdS prepared from ammine complexes was not affected by the pH. Besides, the hydrothermal treatment and the ammonia content strongly influenced the rate of H2 production in this system. DRS, TEM, SEM, XRD, and quantum yield measurements prove the dependence of the photoactivity of these catalysts on the structural and morphological properties determined by the preparation conditions. The promising photocatalytic efficiency achieved with the application of these ZnS–CdS catalysts, prepared without any metal deposition, encourages further investigations to enhance the rate of hydrogen generation by optimization of the reaction conditions for practical utilization.

Construction of UiO-66/Bi4O5Br2 Type-II Heterojunction to Boost Charge Transfer for Promoting Photocatalytic CO2 Reduction Performance

One of the basic challenges of CO2 photoreduction is to develop efficient photocatalysts, and the construction of heterostructure photocatalysts with intimate interfaces is an effective strategy to enhance interfacial charge transfer for realizing high photocatalytic activity. Herein, a novel UiO-66/Bi4O5Br2 heterostructure photocatalyst was constructed by depositing UiO-66 nanoparticles with octahedral morphology over the Bi4O5Br2 nanoflowers assembled from the Bi4O5Br2 nanosheets via an electrostatic self-assembly method. A tight contact interface and a built-in electric field were formed between the UiO-66 and the Bi4O5Br2, which was conducive to the photo-electrons transfer from the Bi4O5Br2 to the UiO-66 and the formation of a type-II heterojunction with highly efficient charge separation. As a result, the UiO-66/Bi4O5Br2 exhibited improved photocatalytic CO2 reduction performance with a CO generation rate of 8.35 μmol h−1 g−1 without using any sacrificial agents or noble co-catalysts. This work illustrates an applicable tactic to develop potent photocatalysts for clean energy conversion.

Synthesis of material MOFs (Fe-BTC) by mechanic-chemical method and its application in the reactive dye degradation

Nano Fe-BTC materials were successfully synthesized by mechanical chemical grinding method. Samples were characterized by X-ray difraction (XRD), Fourier-transform infrared spectroscopy (FTIR), N2 adsorption–desorption, Scanning electron microscopy (SEM), Energy-dispersive X-ray spectroscopy (EDS). SEM image of Fe-BTC-60 showed the particle size of 40–60 nm. Fe-BTC nanocomposites were tested for the photocatalytic degradation of reactive yellow 145 (RY-145) in aqueous solution. Fe-BTC composites exhibited high photocatalytic activity. Thus, at pH of 3 and high initial concentration of 100 mg RY-145/L, removal efficiency reached the value of 97.45% after 90 min of reaction.

Evaluation of photocatalytic activities in decomposition of methylene blue in aqueous solution of Mn-ZIF-8 and Mn@Zn

In the present study, manganese modified zeolitic imidazolate framework-8 (Mn-ZIF-8) and zinc-manganese bimetallic oxides (denoted as Mn@Zn), which was formed by Mn-ZIF-8 heat treatment, had been prepared and applied as photocatalysts to decompose methylene blue (MB) under UV radiation. The influence of manganese content on the structure of ZIF-8, as well as the temperature and heat treatment time of Mn-ZIF-8 material to produce Mn@Zn with high photocatalytic activity was investigated. Results showed that all Mn-ZIF-8 samples have photocatalytic activity, but the MB decomposition efficiency of Mn-ZIF-8 samples were lower than pure ZIF-8. The suitable condition for heat treatment of Mn-ZIF-8 to produce Mn@Zn with high photocatalytic activity was at 500 ºC for 5 hours. However, the MB decomposition efficiency of this sample only reached 22% after 180 minutes of UV radiation.

Oxygen-Deficient WO3/TiO2/CC Nanorod Arrays for Visible-Light Photocatalytic Degradation of Methylene Blue

At present, TiO2 is one of the most widely used photocatalytic materials. However, the narrow response range to light limits the photocatalytic performance. Herein, we reported a successful construction of self-doped R-WO3/R-TiO2/CC nanocomposites on flexible carbon cloth (CC) via electrochemical reduction to increase the oxygen vacancies (Ovs), resulting in an enhanced separation efficiency of photo-induced charge carriers. The photocurrent of R-WO3/R-TiO2/CC at −1.6 V (vs. SCE) was 2.6 times higher than that of WO3/TiO2/CC, which suggested that Ovs could improve the response to sunlight. Moreover, the photocatalytic activity of R-WO3/TiO2/CC was explored using methylene blue (MB). The degradation rate of MB could reach 68%, which was 1.3 times and 3.8 times higher than that of WO3/TiO2/CC and TiO2/CC, respectively. Furthermore, the solution resistance and charge transfer resistance of R-WO3/R-TiO2/CC were obviously decreased. Therefore, the electrochemical reduction of nanomaterials enabled a promoted separation of photogenerated electron–hole pairs, leading to high photocatalytic activity.

Controllable Synthesis of Modified Porous Anatase TiO2 with High Photocatalytic Activity

In this study, we added ZrO2 and Y2O3 to stabilize the anatase TiO2 phase at higher temperatures. Composite mesoporous TiO2/ZrO2/Y2O3 (TZY) oxides were prepared by a sol-gel method, and triblockcopolymer P123 and PEG was used as templates. The properties of the synthesized materials were characterized using X-Ray diffraction (XRD), Raman scattering, N2 adsorption/desorption, and UV-Visible spectrophotometry (UV-Vis) methods et al. The samples prepared using P123 and PEG as double-template exhibited smaller particles and a higher specific surface area than the samples prepared using P123 and PEG as single-template. Furthermore, crystal phase transition from anatase to rutile occurred later in the case of the double-template method. After introducing ZrO 2and Y2O3, the crystal phase transition and the growth of crystallites were severely suppressed. The results indicated that the RhB degradation efficiency for the double-template method was 99.24%, while the RhB degradation efficiency with TZY/P123 and TZY/PEG samples was 97.43 and 98.18%, respectively.