Search Results (14)

In this study, silver nanoparticles (Ag NPs) were synthesized on the surface of rutile-phase titanium dioxide (R-TiO₂) using a plasma-assisted technique. Comprehensive analyses were conducted to investigate the structural, morphological, optical, and electrical properties of the synthesized nanocomposites. Transmission electron microscopy (TEM) images revealed the uniform decoration of Ag NPs (average size: 29.8 nm) on the R-TiO₂ surface. X-ray diffraction (XRD) confirmed the polycrystalline nature of the samples, with decreased diffraction peak intensity indicating reduced crystallinity due to Ag decoration. The Williamson–Hall analysis showed increased crystallite size and reduced tensile strain, suggesting grain growth and stress relief. Raman spectroscopy revealed quenching and broadening of R-TiO₂ vibrational modes, likely due to increased oxygen vacancies. X-ray photoelectron spectroscopy (XPS) confirmed successful plasma-assisted deposition and the coexistence of Ag⁰ and Ag⁺ states, enhancing surface reactivity. UV-Vis spectroscopy demonstrated enhanced light absorption across the spectral range, attributed to localized surface plasmon resonance (LSPR), and a reduced optical bandgap. Dielectric properties, including dielectric constants, loss factor, and AC conductivity, were evaluated across frequencies (4–8 MHz) and temperatures (20–240 °C). The AC conductivity results indicated correlated barrier hopping (CBH) and overlapping large polaron tunneling (OLPT) as the primary conduction mechanisms. Composition-dependent dielectric behavior was interpreted through the Coulomb blockade effect. These findings suggest the potential of plasma assisted Ag NP-decorated R-TiO₂ nanostructures for photocatalysis, sensor and specific electro electrochemical systems applications. Full article

This study proposes an alternative process for obtaining ZnO/ZnS:rGO heterostructures for use in DSSCs and as promising materials for potential applications in other photonic process, such as photocatalysis and photodetection. The compound was obtained through a microwave-assisted hydrothermal method, where the electromagnetic waves and temperature were crucial points for forming ZnO, ZnO/ZnS and reducing graphene oxide (GO). The XRD, Raman, FT-IR, and FESEM results presented the structural, morphological, and chemical structures, which suggest the conversion of ZnO to ZnS for samples with higher concentrations of reduced graphene oxide (rGO). Additionally, the optical properties were analyzed through photoluminescence and UV-Vis measurements. The electrical behavior of the photoelectrodes was investigated through J-V measurements in light and dark conditions. In addition, electrochemical impedance spectroscopy (EIS) was performed and Bode phase plots were created, analyzing the recombination processes and electron lifetime. The J-V results showed that for smaller amounts of rGO, the dye-sensitized solar cells (DSSC) efficiency improved compared to the ZnO/ZnS single structure. However, it was observed that with more significant amounts of rGO, the photocurrent value decreased due to the presence of charge-trapping centers. On the other hand, the best results were obtained for the ZnO/ZnS:1% rGO sample, which showed an increase of 14.2% in the DSSC efficiency compared to the pure ZnO/ZnS photoelectrode. Full article

The controllable electrical and optical properties of two-dimensional tungsten disulfide (WS₂) attracted much attention in photocatalysis, but commercial development has been severely restricted by their restacking properties. Surfactant-assisted synthesis techniques can be considered as an effective option to break this bottleneck. In this work, the effect of surfactants including sodium dodecylbenzene sulfonate (SDBS), hexadecyltrimethylammonium bromide (CTAB), and polyvinylpyrrolidone (PVP) on the microstructure of WS₂/tourmaline composites prepared by coupled hydrothermal and calcination methods was explored. The WS₂ nanosheets were uniformly deposited on the tourmaline surface with the assistance of 1.0 mmol/L SDBS. Meanwhile, WS₂/Tour-SDBS exhibited the highest rhodamine B (RhB) degradation activity, which was 1.8 and 2.3 times higher than that of photocatalysts prepared with CTAB and PVP under the same conditions, respectively. This study provides a new tactic for the fabrication of high-performance WS₂-based composites. Full article

The removal of Cr(VI), a highly-toxic heavy metal, from industrial wastewater is a critical issue in water treatment research. Photocatalysis, a promising technology to solve the Cr(VI) pollution problem, requires urgent and continuous improvement to enhance its performance. To address this need, an electric field-assisted photocatalytic system (PCS) was proposed to meet the growing demand for industrial wastewater treatment. Firstly, we selected PAF-54, a nitrogen-rich porous organic polymer, as the PCS’s catalytic material. PAF-54 exhibits a large adsorption capacity (189 mg/g) for Cr(VI) oxyanions through hydrogen bonding and electrostatic interaction. It was then coated on carbon paper (CP) and used as the photocatalytic electrode. The synergy between capacitive deionization (CDI) and photocatalysis significantly promotes the photoreduction of Cr(VI). The photocatalytic performance was enhanced due to the electric field’s influence on the mass transfer process, which could strengthen the enrichment of Cr(VI) oxyanions and the repulsion of Cr(III) cations on the surface of PAF-54/CP electrode. In addition, the PCS system demonstrates excellent recyclability and stability, making it a promising candidate for chromium wastewater treatment. Full article

Polymorphous WO₃ micro- and nanostructures have been synthesized by the controlled Joule heating of tungsten wires under ambient conditions in a few seconds. The growth on the wire surface is assisted by the electromigration process and it is further enhanced by the application of an external electric field through a pair of biased parallel copper plates. In this case, a high amount of WO₃ material is also deposited on the copper electrodes, consisting of a few cm${}^2$ area. The temperature measurements of the W wire agrees with the values calculated by a finite element model, which has allowed us to establish the threshold density current to trigger the WO₃ growth. The structural characterization of the produced microstructures accounts for the $\gamma$-WO₃ (monoclinic I), which is the common stable phase at room temperature, along with low temperature phases, known as $\delta$-WO₃ (triclinic) on structures formed on the wire surface and $ϵ$-WO₃ (monoclinic II) on material deposited on external electrodes. These phases allow for a high oxygen vacancies concentration, which is interesting in photocatalysis and sensing applications. The results could help to design experiments to produce oxide nanomaterials from other metal wires by this resistive heating method with scaling-up potential. Full article

Constructing heterostructure within electrocatalysts proves to be an attractive approach to adjust the interfacial charge redistribution to promote the adsorption of reactive species and accelerate the charge transfer. Herein, we present the one-pot solvothermal synthesis of Ti₃C₂ supported hollow CoS₂/CoS microsphere heterostructure with uneven charge distribution as the cathodic catalyst, which displays a superior quasi-first-order degradation rate (0.031 min⁻¹) for sulfamethazine (SMT) in photo-assisted electric–Fenton (EF) process. CoS₂/CoS/Ti₃C₂ is proven to favor the 2e⁻ oxygen reduction reaction (ORR), with H₂O₂ selectivity up to 76%. The built-in potential present in the heterojunction helps to accelerate electron transfer, thus promoting the production of H₂O₂. Subsequently, H₂O₂ is rapidly activated to produce ∙OH due to the synergistic effect of Co and S. Notably, CoS₂/CoS/Ti₃C₂ exhibits enhanced photo-assisted EF (PEF) performance under light. The excellent photocatalysis properties of CoS₂/CoS/Ti₃C₂ are attributed to that the unique hollow microsphere structure of catalyst improves the light absorption, and the uneven charge distribution of CoS₂/CoS heterojunctions promotes the separation of photo-generated holes and electrons. Given the above advantages, CoS₂/CoS/Ti₃C₂ cathode delivers a high degradation rate of 98.5%, 91.8%, and 94.5% for SMT, bisphenol A, and sulfadiazine, respectively, with TOC removal efficiency of 76% for SMT with 120 min. This work provides a novel light of the design and construction of efficient PEF cathodes for the treatment of antibiotic wastewater. Full article

Herein, combining photocatalysis and Fenton oxidation, a photo-assisted Fenton system was conducted using Fe-doped Bi₄O₅Br₂ as a highly efficient photocatalyst to realize the complete degradation of Tetracycline antibiotics under visible light. It has been observed that the optimized photocatalyst 5%Fe-doped Bi₄O₅Br₂ exhibits a degradation efficiency of 100% for Tetracycline with H₂O₂ after 3 h visible-light irradiation, while a degradation percentage of 59.8% over the same photocatalyst and 46.6% over pure Bi₄O₅Br₂ were obtained without the addition of H₂O₂ (non-Fenton process). It is unambiguous that a boost photo-assisted Fenton system for the degradation of Tetracycline has been established. Based on structural analysis, it demonstrated that the Fe atoms in place of the Bi sites may result in the distortion of the local structure, which induced the occurrence of the spontaneous polarization and thus enhanced the built-in electric field. The charge separation efficiency is enhanced, and the recombination of electrons and holes is inhabited so that more charges are generated to reach the surface of the photocatalyst and therefore improve the photocatalytic degradation efficiency. Moreover, more Fe (II) sites formed on the 5%Fe-Bi₄O₅Br₂ photocatalyst and facilitated the activation of H₂O₂ to form oxidative species, which greatly enhanced the degradation efficiency of Tetracycline. Full article

The removal of pharmaceuticals from wastewater is critical due to their considerable risk on ecosystems and human health. Additionally, they are resistant to conventional chemical and biological remediation methods. Two-dimensional nanomaterials are a promising approach to face this challenge due to their combination of high surface areas, high electrical conductivities, and partially optical transparency. This review discusses the state-of-the-art concerning their use as adsorbents, oxidation catalysts or photocatalysts, and electrochemical catalysts for water treatment purposes. The bibliographic search bases upon academic databases including articles published until August 2021. Regarding adsorption, high removal capacities (>200 mg g⁻¹) and short equilibrium times (<30 min) are reported for molybdenum disulfide, metal-organic frameworks, MXenes, and graphene oxide/magnetite nanocomposites, attributed to a strong adsorbate-adsorbent chemical interaction. Concerning photocatalysis, MXenes and carbon nitride heterostructures show enhanced charge carriers separation, favoring the generation of reactive oxygen species to degrade most pharmaceuticals. Peroxymonosulfate activation via pure or photo-assisted catalytic oxidation is promising to completely degrade many compounds in less than 30 min. Future work should be focused on the exploration of greener synthesis methods, regeneration, and recycling at the end-of-life of two-dimensional materials towards their successful large-scale production and application. Full article

This article reviews the fundamental theories and reaction mechanisms of photocatalytic technologies with the assistance of electrical field for degrading multi-phase pollutants. Photo(electro)catalysis including photocatalytic oxidation (PCO) and photoelectrocatalytic oxidation (PECO) have been a potential technologies applied for the treatment of organic and inorganic compounds in the wastewaters and waste gases, which has been treated as a promising technique by using semiconductors as photo(electro)catalysts to convert light or electrical energy to chemical energy. Combining photocatalytic processes with electrical field is an option to effectively decompose organic and inorganic pollutants. Although photocatalytic oxidation techniques have been used to decompose multi-phase pollutants, developing efficient advanced oxidation technologies (AOTs) by combining photocatalysis with electrical potential is urgently demanded in the future. This article reviews the most recent progress and the advances in the field of photocatalytic technologies combined with external electrical field, including the characterization of nano-sized photo(electro)catalysts, the degradation of multi-phase pollutants, and the development of electrical assisted photocatalytic technologies for the potential application on the treatment of organic and inorganic compounds in the wastewaters and waste gases. Innovative oxidation techniques regarding photo(electro)catalytic reactions with and without oxidants are included in this review article. Full article

In the last decade, research on the synthesis and characterization of nanosized ferrites has highly increased and a wide range of new applications for these materials have been identified. The ability to tailor the structure, chemical, optical, magnetic, and electrical properties of ferrites by selecting the synthesis parameters further enhanced their widespread use. The paper reviews the synthesis methods and applications of MFe₂O₄ (M = Co, Cu, Mn, Ni, Zn) nanoparticles, with emphasis on the advantages and disadvantages of each synthesis route and main applications. Along with the conventional methods like sol-gel, thermal decomposition, combustion, co-precipitation, hydrothermal, and solid-state synthesis, several unconventional methods, like sonochemical, microwave assisted combustion, spray pyrolysis, spray drying, laser pyrolysis, microemulsion, reverse micelle, and biosynthesis, are also presented. MFe₂O₄ (M = Co, Cu, Mn, Ni, Zn) nanosized ferrites present good magnetic (high coercivity, high anisotropy, high Curie temperature, moderate saturation magnetization), electrical (high electrical resistance, low eddy current losses), mechanical (significant mechanical hardness), and chemical (chemical stability, rich redox chemistry) properties that make them suitable for potential applications in the field of magnetic and dielectric materials, photoluminescence, catalysis, photocatalysis, water decontamination, pigments, corrosion protection, sensors, antimicrobial agents, and biomedicine. Full article

The photoexcitation of suitable semiconducting materials in aqueous environments can lead to the production of reactive oxygen species (ROS). ROS can inactivate microorganisms and degrade a range of chemical compounds. In the case of heterogeneous photocatalysis, semiconducting materials may suffer from fast recombination of electron–hole pairs and require post-treatment to separate the photocatalyst when a suspension system is used. To reduce recombination and improve the rate of degradation, an externally applied electrical bias can be used where the semiconducting material is immobilised onto an electrically conducive support and connected to a counter electrode. These electrochemically assisted photocatalytic systems have been termed “photoelectrocatalytic” (PEC). This review will explain the fundamental mechanism of PECs, photoelectrodes, the different types of PEC reactors reported in the literature, the (photo)electrodes used, the contaminants degraded, the key findings and prospects in the research area. Full article

Photoelectrocatalysis is a novel technique that combines heterogeneous photocatalysis with the application of an electric field to the system through electrodes for the degradation of organic contaminants in aqueous systems, mainly of toxic dyes. The efficiency of these combined processes depends on the semiconductor properties of the catalysts, as well as on the anodic capacity of the electrode. In this study, we propose the use of active hydrotalcites in the degradation of Congo red dye through processes assisted by ultraviolet (UV) irradiation and electric current. Our research focused on evaluating the degradation capacity of Congo red by means of photolysis, catalysis, photocatalysis, electrocatalysis, and photoelectrocatalysis, as well as identifying the effect of the properties of the active hydrotalcites in these processes. The results show that a maximum degradation was reached with the photoelectrocatalysis process with active hydrotalcites and a copper anode at 6 h with 95% in a half-life of 0.36 h. The degradation is favored by the attack of the OH^• radicals under double bonds in the diazo groups where the electrode produces Cu²⁺ ions, and with the photogenerated electrons, the recombination speed of the electron–hole in the hydrotalcite catalyst is reduced until the complete degradation. Full article

Developing a photocatalyst system for solar energy conversion to electric energy or chemical energy is a topic of great interest for fundamental and practical importance. In this study, hydrogen production by a new Z-scheme photocatalysis water-splitting system was examined over Rh-doped SrTiO₃ (denoted as Rh:SrTiO₃) with Ru nanoparticle as cocatalyst for H₂ evolution and BiVO₄ photocatalyst for O₂ evolution under visible light irradiation, where Co(bpy)₃^2+/3+ was used as electron mediator. The catalysts were characterized by powder X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscopy (TEM), and Ultraviolet–visible spectroscopy. We present a fast and efficient method to synthesize Rh-doped SrTiO₃ photocatalyst via microwave-assisted hydrothermal method. Our results showed a significant effect of Ti precursor on morphology of Rh:SrTiO₃ prepared by microwave-assisted hydrothermal synthesis. The Ru/Rh:SrTiO₃ prepared by TiCl₄ precursor showed a nanoporous structure and high photocatalytic activity. The combination of Ru/Rh:SrTiO₃ with BiVO₄ achieves a high H₂ evolution rate (317 μmoL g⁻¹ h⁻¹) and O₂ evolution rate (168 μmol g⁻¹ h⁻¹) in 0.5 mM Co(bpy)₃^2+/3+ solution under visible light irradiation. Full article

TiO₂ photocatalysis is considered as an alternative to conventional disinfection processes for the inactivation of waterborne microorganisms. The efficiency of photocatalysis is limited by charge carrier recombination rates. When the photocatalyst is immobilized on an electrically conducting support, one may assist charge separation by the application of an external electrical bias. The aim of this work was to study electrochemically assisted photocatalysis with nitrogen doped titania photoanodes under visible and UV-visible irradiation for the inactivation of Escherichia coli. Aligned TiO₂ nanotubes were synthesized (TiO₂-NT) by anodizing Ti foil. Nanoparticulate titania films were made on Ti foil by electrophoretic coating (P25 TiO₂). N-doped titania nanotubes and N,F co-doped titania films were also prepared with the aim of extending the active spectrum into the visible. Electrochemically assisted photocatalysis gave higher disinfection efficiency in comparison to photocatalysis (electrode at open circuit) for all materials tested. It is proposed that electrostatic attraction of negatively charged bacteria to the positively biased photoanodes leads to the enhancement observed. The N-doped TiO₂ nanotube electrode gave the most efficient electrochemically assisted photocatalytic inactivation of bacteria under UV-Vis irradiation but no inactivation of bacteria was observed under visible only irradiation. The visible light photocurrent was only a fraction (2%) of the UV response. Full article