Photocatalytic Reaction Research Articles

A Honeycomb Layered Na2SnO3 as Novel Photocatalyst for Degradation of Rose Bengal Dye

AbstractA layered Na2SnO3 with honeycomb structure was synthesized by solid state route using sodium carbonate and tin oxide. The prepared sample was characterized by different physicochemical characterization techniques like X‐ray diffraction (XRD), field emission scanning electron microscopy (FESEM), energy dispersive X‐ray spectroscopy (EDS), X‐ray photoelectron spectroscopy (XPS), ultraviolet visible spectroscopy (UV–vis), photoluminescence spectra (PL), N2 adsorption technique (Brunauer–Emmett–Teller, electrochemical impedance spectroscopy (EIS). The photodegradation of rose bengal dye under UV light was studied. Due to honeycomb structure and high surface area of Na2SnO3, the complete degradation of rose Bengal was observed in 90 min under UV light irradiation. Results of photocatalytic dye degradation reaction demonstrated that Na2SnO3 can be employed as photocatalyst under UV light irradiation.

Hybrid magnetic nanocomposite NiFe2O4/TiO2 for Photocatalytic dye degradation and green hydrogen (H2) generation

The present paper focuses on designing and developing nanocomposites to modify their properties to increase the ability to generate hydrogen and degrade photocatalytic dyes. A nanocomposite of nickel ferrite (NiFe2O4)/Titanium dioxide (TiO2) was formulated using the sol-gel self-ignition method. X-ray diffraction (XRD) tool was adopted to analyze the structural behavior of pure nickel ferrite (NiFe2O4), pure titanium dioxide (TiO2), and nanocomposite of NiFe2O4/TiO2. XRD pattern of NiFe2O4 and TiO2 shows a monophasic nature whereas the XRD pattern of nanocomposites shows mixed phases of NiFe2O4 and TiO2. FTIR spectra confirm the formation of NiFe2O4, TiO2, and their composites with absorption bands near 400 cm-1 and 600 cm-1, 1500 cm-1. Raman spectra unveiled the presence of five active Raman modes in the case of NiFe2O4 whereas three active Raman modes are seen in TiO2. Field emission scanning electron microscopy (FE-SEM) images exposed the dense structure with spherical cluster-like morphology in the case of NiFe2O4. Energy-dispersive X-ray spectroscopy (EDX) analysis confirms the presence of all the desired elements of NiFe2O4, TiO2, and their composites in stoichiometric proportions. BET analysis of nickel ferrite NPs suggests a large surface area of the order of 31.54 m2/gm in comparison with TiO2 (19.23 m2/gm). The optical characterization was made through the UV-visible spectroscopic technique. TiO2 shows a maximum band gap of the order of 3.02 eV while NiFe2O4 shows a low band gap of the order of 1.74 eV. A typical M-H curve with saturation magnetization of the order of 27.54 emu/gm was observed for pure NiFe2O4. No magnetic properties were observed for TiO2 as it is a semiconductor. Enhancement in magnetic properties is observed with increases in NiFe2O4 content in a composite of NiFe2O4/TiO2. The photocatalytic activities were examined by degrading Methylene Blue (MB) dye under sunlight for pure nickel ferrite (NiFe2O4), pure titanium dioxide (TiO2), and a nanocomposite of NiFe2O4/TiO2. Photocatalytic hydrogen production reactions were carried out in a methanol/water solution under visible light. Consequently, the best configuration of the photocatalyst was determined as 25% wt% NiFe2O4/ TiO2 which had shown the maximum hydrogen (H2) production rate as 146.3 μmol/g/h after 8 h owing to its reduced bandgap energy and delayed e- / h+ recombination.

Adsorption Performance and Photocatalytic Activity of La-TiO2@kaolin Composites

Abstract La-TiO2@kaolin(LTK) composites were prepared via sol-gel method with kaolin, lanthanum nitrate and tetrabutyl titanate as raw materials. The samples were characterized by XRD, SEM/EDS, and UV-Vis. The visible light photocatalytic reduction activity and adsorption performance of samples for Cr(VI) were studied. The results showed that La doping can refine TiO2 grains, stabilize phase structure of anatase TiO2, and expand its absorption spectrum, thereby enhancing its photocatalytic reduction activity. Due to the composite of kaolin, the dispersion of TiO2 is improves and it is endowed with a large specific surface area lead to enhance its adsorption ability for Cr(VI). The adsorption equilibrium process of LTK for Cr(VI) conforms to the Langmuir equation model. The coupling effect of doping and composite modification improves the adsorption and visible light catalytic reduction activity of Cr(VI) over composite material samples. The adsorption-photocatalytic removal rate of LTK for Cr(VI) under visible light irradiation for 6 hours reached the highest of 96.5%. The apparent first-order kinetic constant of its photocatalytic reduction reaction was 2.6 times that of pure TiO2.

Cu‐Doped 0D Bi2WO6 Nanoparticles for Efficient Visible‐Light‐Driven Photocatalytic Tetracycline Degradation

AbstractBismuth‐based photocatalysts have been widely employed in the photocatalytic degradation of organic pollutants in wastewater. However, the lack of rational structural design and the slow generation of active free radicals have hindered its efficiency. Here, we stabilized Bi2WO6 nanoparticles by wrapping them with hydroxyl groups, introduced metal Cu doping, and underwent an annealing process to construct Cu‐BiNP nanocatalysts with exposed active sites. Under visible light irradiation, 0.03Cu‐BiNP achieved a 94.5% TC degradation efficiency, which is 15.8 times higher than the rate of bulk BiWO. The 0D structure endows Cu‐BiNP with ample opportunities for O2 adsorption and activation, and Cu atomic doping reduces the bandgap and increases the oxygen vacancy, promoting the generation of active oxygen species. This work demonstrates the rapid charge separation and activation of O2 to generate active oxygen species by 0D bismuth‐based nanocatalysts in photocatalytic oxidation reactions, providing a scalable nanocatalyst platform for TC photocatalytic degradation.

Heterophase hexagonal/orthorhombic molybdenum trioxide nanorods for photocatalytic hydrogen production

Phase engineering plays a critical role in enhancing photocatalytic performance of metal oxides. Herein, we demonstrate the phase-selective synthesis of MoO3 (hexagonal h-MoO3, orthorhombic α-MoO3, and their junction h/α-MoO3) through controlled phase transitions by adjusting annealing conditions. As evidenced with photocatalytic hydrogen evolution reaction, h/α-MoO3 (14.20 μmol/h) phase junction shows superior performance to either h-MoO3 (9.62 μmol/h) or α-MoO3 (11.31 μmol/h), with a hydrogen yield of 47.6% and 25.6% greater than that of h-MoO3 and α-MoO3 (Pt as cocatalyst), respectively. A systematic study of the chemical structure characterizations, photochemical tests, band structure analysis, and photocatalytic activity evaluation reveal that, the enhancement is attributed to the strong built-in electric field in the h/α-MoO3 phase junction, which effectively facilitates charge separation. Our findings introduce a novel strategy for improving photocatalytic performance using phase engineering.

Mn doping and ZnS nanoparticles modification on Bi2MoO6 to achieve an highly-efficient photocatalyst for TC degradation

Environmental pollution presents significant challenges to both human production and daily life. Photocatalytic technology offers a promising solution for environmental remediation, and Bi2MoO6 is widely recognized as an excellent visible light photocatalyst for the degradation of organic pollutants. Nevertheless, the high recombination rate of photogenerated charge carriers in Bi2MoO6 limits the number of charge carriers available for photocatalytic reactions, resulting in reduced photocatalytic efficiency. To overcome this limitation, we designed and synthesized a composite photocatalyst (30% ZnS/Mn0.08-Bi2MoO6). Mn-doped Bi2MoO6 nanosheets (Mn-Bi2MoO6) were prepared through a simple coprecipitation method, and ZnS nanoparticles were introduced to modify the surface, forming a ZnS/Mn-Bi2MoO6 composite photocatalyst. Experimental results demonstrated that the photocatalytic degradation rate of tetracycline using the 30% ZnS/Mn0.08-Bi2MoO6 composite increased 11.1 times and 3.7 times compared with pure Bi2MoO6 and ZnS, respectively. The formation of ZnS/Mn-Bi2MoO6 heterojunction was confirmed through XRD, XPS, SEM, and TEM analyses. Furthermore, photoelectrochemical measurements, including photocurrent, EIS, and PL, indicated that Mn doping and the ZnS nanoparticle modification significantly improved the separation and transfer efficiency of photogenerated charge carriers. DFT calculations and experimental results revealed the photocatalytic mechanism of the 30% ZnS/Mn0.08-Bi2MoO6 composite. This study provides valuable theoretical and technical insights into photocatalyst modification.

Nitrogen–oxygen vacancy and S-scheme heterostructure synergistically enhance solar photocatalysis

Introducing vacancies and constructing S-scheme heterojunctions are promising approaches for enhancing photocatalytic activity. However, the application of this synergistic strategy to realize inexpensive and efficient photocatalysts remains challenging. In this study, a straightforward hydrothermal and calcination modification strategy was used to prepare a photocatalyst in which abundant nitrogen–oxygen vacancies were coupled with a Ce-ZnO@C-g-C3N4 composite with an S-scheme heterojunction. Under sunlight irradiation, the prepared composite achieves 98.3% and 86.4% degradation of methylene blue and ciprofloxacin, with degradation rate constants of 0.3464 and 0.0893 min−1, respectively. Compared with ZnO and g-C3N4, the degradation rates of methylene blue over the composite catalyst are 34.8 and 22.7 times higher, respectively, and those of ciprofloxacin are 2.4 and 4.9 times higher, respectively. Based on a detailed examination of the catalyst structure and photoelectric properties, the high photocatalytic efficiency is attributed to nitrogen–oxygen vacancies, an enhanced surface area, and synergistic S-scheme heterojunction effects. These factors broaden the spectral range, increase the number of active sites, and facilitate efficient charge transfer, thereby enhancing the photocatalytic reaction. This system demonstrates the feasibility of integrating doping and heterojunction formation to enhance photocatalytic performance synergistically.

Dependence of photocatalytic efficiency of titania-carbon nanotube nanocomposites on optoelectrical properties and colloidal stability

The correlation of photocatalytic efficiency of titania–amorphous (nitrogen doped) carbon nanotubes (TiO2–a(N)CNT) nanocomposites with colloidal and optoelectrical properties of the photocatalysts was investigated. TiO2–aNCNT and TiO2–aCNT exhibited narrow zeta potential variation, high polydispersity index, and large agglomerate size across the pH range 1–8. Despite the poor colloidal stability, TiO2–aNCNT exhibited superior degradation for high molecular weight reactive dyes, RR 120 and Remazol brilliant blue (RBB) with 55 mg.L−1 of RR 120 mineralized under solar irradiation. The photocatalytic performance for TiO2–aNCNT and TiO2–aCNT correlated with the respective energy band gaps 3.01 and 3.14 eV, Ubarch tailing energies. Cyclic voltammetry showed a narrow peak-to-peak separation (ΔEp) of 200.7 V (vs Ag/AgCl) for TiO2–aNCNT thus confirming enhanced electron transfer kinetics. Electron impedance spectroscopy confirmed low charge transfer resistance for TiO2–aNCNT. Herein it is demonstrated that optoelectrical properties are superior in driving photocatalytic reactions.

Photocarrier relay modulating solar CO2-to-Syngas conversion

Solar-driven syngas generation by CO2 reduction provides a sustainable strategy to produce renewable fossil fuels. Nevertheless, this promising approach often suffers from tough CO2 activation, sluggish reaction kinetics and complex selectivity. Herein, we exquisitely constructed spatially directional charge transport channel over two-dimensional transition metal chalcogenide (TMC)-based heterostructure via a facile and universal electrostatic self-assembly method. Tailor-made positively charged non-conjugated insulating polymer of poly(diallyl-dimethyl-ammonium chloride) (PDDA) and negatively charged graphene oxide (GO) precursor as building blocks are controllably anchored on the TMC substrate, by which ultrathin PDDA layer is intercalated at the interface of GO and TMC. We ascertain that, in this customized sandwiched heterostructures, PDDA interim layer functions as an electron-relaying mediator, whilst graphene (GR) obtained from in-situ GO reduction during the photocatalytic reaction serves as a terminal electron-trapping reservoir, synergistically facilitating the spatially vectorial charge separation/migration over TMC, thus endowing the TMC/PDDA/GR heterostructures with conspicuously enhanced visible-light-driven photoactivity toward CO2-to-syngas conversion. Our work would inspire judicious ideas for finely modulating charge transfer over polymer-mediated photosystems and benefit our fundamental understanding of solar CO2 conversion.

Dual electric field and defect engineering induced multi-channel electron transfer for boosting photocatalytic hydrogen production on Cu2+-doped ZnMoO4/ZnIn2S4 heterojunction

Serious recombination of photogenerated carriers is the bottleneck problem of achieving high-performance photocatalytic reaction. A high efficient Cu2+-doped ZnMoO4/ZnIn2S4 (CZMOZIS) heterojunction was synthesized by hydrothermal method. The CZMOZIS heterostructure achieved hydrogen production of 11637.5 µmol g−1 within 5 h, which was 9.7 times higher than that of pure ZnIn2S4. Comprehensive characterization and theoretical calculation demonstrated that the CZMOZIS composites exhibited broad light absorption, an increased specific surface area and an optimized Gibbs free energy. The presence of oxygen vacancies in CZMOZIS composites was confirmed by X-ray photoelectron spectroscopy and high-resolution transmission electron microscopy, revealing the formation of defect levels below the conduction band (CB) of ZnMoO4. Kelvin probe force microscopy (KPFM) and Zeta potential demonstrated that the intrinsic electric field (IEF) of the CZMOZIS heterojunction was enhanced, which may be attributed to the generation of polarization electric field (PEF). The double electric field provided a robust driving force for the photogenerated carrier migration and separation. The electrons in the CB and defect levels of Cu2+-ZnMoO4 could be coupled with the holes of ZnIn2S4, thereby forming a multi-channel electron transfer. This work provides a theoretical support for promoting charge transfer to improve photocatalytic performance by dual electric field and defect engineering.

Na-doped nitride-rich carbon nitride for efficient photocatalytic NO abatement

Nitride-rich carbon nitride (C3N5) is gaining prominence as a substantial catalyst for photocatalytic reaction because of its narrow bandgap, extensive light responsiveness, and photocatalytic stability. To enhance the efficiency of photogenerated carrier separation in C3N5, we propose a strategy for Na-doped modification. Photocatalytic NO removal efficiency of C3N5/Na achieved 73.9 % under 15 % relative humidity, which is 3.5 times higher than that of C3N5. Besides, the NO removal efficiency of C3N5/Na maintained above 70 % even after six cycles under different relative humidities. Detailed analytical characterization revealed that Na doping of C3N5 not only increased its specific surface area by 5.5-fold but also modulated its energy band structure and molecular structure, leading to improved hole-carrier separation efficiency and enhancing the photocatalytic performance of C3N5/Na. ESR and reactive species trapping experiments confirmed that electrons and superoxide are the main reactive species, and modulation of the energy band structure accelerates the reaction. This work explains the effect of Na doping on C3N5 and provides a new strategy for designing efficient for photocatalytic treatment of air pollution.

Recent Advances in Visible-Light-Driven Photocatalytic Oxidation Reactions in Water.

Oxidation reactions, which represent a fundamental process in organic transformations, have consistently advanced overseveral decades. Owing to the widespread application of aqueous and photochemical synthesis, research on light-induced oxidation in water, involving radical processes, has also experienced rapid development. Recently, numerous strategies for light-induced aqueous oxidation have been ingeniously designed and developed. This review aims to discuss the notable recent advancements in this rapidly evolving field of oxidation reactions, with a focus on delving into the reaction mechanisms. It hopes to inspirethe development of aqueous photocatalytic oxidation reactions.

Eco-Friendly Concrete Solutions: The Role of Titanium Dioxide Nanoparticles in Enhancing Durability and Reducing Environmental Pollutants - A Review

Concrete is one of the key components of construction, which ensures durability and aesthetics of the building. In recent days, nanoparticles are playing an essential role in civil engineering research. The binding of nanoparticles into concrete significantly improves the mechanical and durable properties due to the nanostructure of the cementitious materials. This review paper represents the existing research data on titanium dioxide nanoparticles, when applied in the different types of concrete. The data influenced by the different research papers are presented in terms of strength and durable parameters. The most important property of titanium dioxide nanoparticle is its self-cleaning effect because of the photocatalytic reaction is also discussed. The inference from the papers shows the effect of titanium dioxide nanoparticles on correct proportion enhances the production of new material with good strength and durable properties in the construction industry. The photocatalytic action of nano titanium dioxide leads to the manufacture of self-cleaning concrete which shields the surface from environmental pollutants.

In Situ Construction of SnS2@SnO2 Heterostructure for Photo-Assisted Electrocatalysis of Oxygen Evolution Reaction.

Photo-assisted electrocatalysis has arisen as a promising approach for hydrogen generation by incorporating photocatalysts into electrocatalysts. 2D SnS2 is a photocatalyst that absorbs visible light. However, the rapid recombination of photo-generated electron-hole pairs significantly reduces the overall photocatalytic efficiency of SnS2, limiting its practical application. Thus, this study prepares an in situ heterojunction SnS2@SnO2 using a one-step hydrothermal method. The degradation efficiency of methyl orange (MO) using SnS2@SnO2 is measured, achieving a degradation rate of 92.75% within 1h, which is 1.9 times higher than that of pure SnS2. Additionally, FeNiS/SnS2@SnO2 is synthesized and exhibited significant improvements in the photo-assisted oxygen evolution reaction (OER). It achieves an overpotential of 260mV and a Tafel slope of 65.1mVdec-1 at 10mAcm-2, showing reductions of 11.8% and 31.8%, respectively, compared to FeNiS alone. These enhancements highlight the strong photo-response capability of SnS2@SnO2. Under the internal electric field of SnS2@SnO2, the photogenerated electrons in the conduction band of SnS2 quickly move toward SnO2, facilitating efficient photocatalytic reactions. FeNiS, with a lower Fermi energy level (EF), facilitates electron transfer from SnS2@SnO2 and enhances OER performance by efficiently participating in the reaction. This study paves a new path for 2D photocatalyst materials.

Chemically bonded nonmetallic LSPR S-scheme hollow heterostructure for boosting photocatalytic performance

The light absorption, mass transfer, and charges separation are essential to the efficiency of photocatalytic reaction, but constructing photocatalyst with the three excellent properties is still challenging. Herein, the interfacial Mo-S bonds and oxygen vacancy synchronously decorated MoO3-x/Zn3In2S6 (MoO3-x/ZIS) heterostructure was rationally designed and synthesized. The oxygen-defective MoO3-x nanotubes showed hollow structure and local surface plasmonic resonance (LSPR) effect, which improved mass transfer and solar light absorption. Besides, the built-in electric field and interfacial Mo-S bond provided endogenetic impetus and channels for rapid photoexcited charge carriers transfer and separation. The photocatalytic hydrogen (H2) evolution and hydrogen peroxide (H2O2) production on optimal MoO3-x/ZIS composite were 17.34 and 4.47 mmol g−1 h−1, respectively. The apparent quantum efficiency of MoO3-x/ZIS for H2 evolution at 400 nm was about 13.92 %, which was 8.09 times higher than that of ZIS. Moreover, the MoO3-x/ZIS also displayed excellent activities on the selective 5-hydroxymethylfurfural dehydrogenation. The in-situ X-ray photoelectron spectroscopy, electron paramagnetic resonance, in-situ selective photodeposition, and density functional theory calculation confirmed the S-scheme charge transfer pathway between MoO3-x and ZIS. This study provides an effective avenue for designing multifunctional photocatalysts based on the synergistic effects of chemically bonded S-scheme heterostructure and nonmetallic LSPR effect.

Photocatalytic water splitting over K3Li2Ta5O15 with a C-site-filled tungsten bronze structure and influence of metal cations at C-site on photocatalytic properties

Abstract K3Li2Ta5O15 is found as a novel photocatalyst for overall water splitting under UV light irradiation. K3Li2Ta5O15 possesses a characteristic crystal structure with Li+ ions-filled C-sites in (A1)4(A2)2C4M10O30 as the general formula of a tungsten bronze type metal oxide. Most of the reported photocatalysts with a tungsten bronze structure possess empty C-sites. K6Ta10.8O30 also possesses a C-site-filled tungsten bronze structure where C-sites are partially filled by Ta5+ ions. In diffuse reflectance spectra, K6Ta10.8O30 has an absorption edge at longer wavelength than K3Li2Ta5O15. This narrower band gap of K6Ta10.8O30 than K3Li2Ta5O15 is considered to be due to the presence of Ta5+ ions at C-sites in K6Ta10.8O30. Ta5+ ions located at 9-fold coordination C-sites with totally different surrounding environment from the 6-fold coordination M-sites will form the conduction band minimum at lower potential than those located at 6-fold coordination M-sites. The optimized K3Li2Ta5O15 shows almost the same water splitting activity with the optimized K6Ta10.8O30. Thus, it is found that the conduction band formed by Ta5+ ions at C-sites is also effective for photocatalytic reaction, being similar to that formed by Ta5+ ions at M-sites.

Multifunctional air filter with enhanced filtration, formaldehyde degradation, and antibacterial properties using PET, PDA, and RGO-TiO2

Currently, most air filters, such as polyester (PET) fiber non-woven fabric, only have a single function of particulate filtration. However, the removal of substances harmful to human health, such as volatile organic compounds (VOCs) and bacteria, is becoming increasingly important in indoor air purification. Herein, based on the biomimetic surface functionalization properties of polydopamine (PDA) and the photocatalytic degradation of organic matter and the antibacterial effect of RGO (reduced graphene oxide)-TiO2, a multifunctional NWP2/PET-PDA-RGO-TiO2(P/PPRT) filter with a sandwich structure was prepared for formaldehyde degradation, aerosol filtration, and bactericidal operation. The P/PP2R0.05T20 maintains optimal performance of photocatalytic reaction kinetics and reaches a formaldehyde degradation rate of higher than 79 % within 300 min in the 7th cycle of usage. Compared with the base subtracts, P/PP2R0.05T20 has the highest filtration efficiency of 88.57–99.18 % for 0.3–10 µm particles, respectively, and has a filtration efficiency of higher than 74 % for 0.3 µm particles in the 7th cycles of usage. The quality factor of P/PP2R0.05T20 is improved significantly due to the sandwich structure. The effect of loaded particulate on the catalyst for photocatalytic degradation of formaldehyde was also studied. It was found that the photocatalytic formaldehyde degradation rate of P/PP2R0.05T20 is about 81.8 % within 300 min under different A2 particulate load content. In addition, P/PP2R0.05T20 has a bioaerosol removal rate of higher than 98 % against E. coli. This study provides a practical approach to preparing a multifunctional air filter with the performance of aerosol filtration, photocatalytic degradation of formaldehyde, and bactericidal function using PET non-woven fabric.

The transformation of type-I La2O3/α-Bi2O3 into multi-heterojunctions during photocatalysis with enhanced photoreactivity

A small quantity of broad bandgap rare earth lanthanum oxide (La2O3) was incorporated into monoclinic bismuth oxide (α-Bi2O3) through a one-step facile calcining route to construct an efficient type-I La2O3/α-Bi2O3 heterojunction photocatalyst for pollutant degradation under UV-light irradiation. The effect of adding La2O3 on the morphology, textural, optical, photoelectrochemical, and photocatalytic properties of α-Bi2O3 was investigated. Interestingly, feeding as low as five molar percent (5 %) La2O3 could significantly increase the BET surface area and generate more h+ and •O2− for photocatalytic reaction. Moreover, the calcining-induced carbon in La2O3/α-Bi2O3 revealed a vital role in suppressing the charge carrier recombination by quickly transferring charges to the photocatalyst's surface. In particular, during the recycling process, the in-situ formed Bi2O2CO3 changes the charge carrier transferring pathway and reveals a transformation of type-I La2O3/α-Bi2O3 into multi-heterojunction of type-I and type-II. Furthermore, the formation of Bi2O2CO3 results in more active sites for the photocatalytic reaction with improved reaction kinetics. This work provides a new direction for understanding a photocatalytic system's recycling phenomena and intrinsic kinetics.

Innovations in photocatalytic trifluoromethylation: Role of heterogeneous Bi4NbO8Cl in radical generation

Photocatalytic selective trifluoromethylation reactions have garnered significant attention, particularly for their applications in pharmaceuticals, agrochemicals, and materials science. However, existing heterogeneous catalysts such as graphitic carbon nitride, CdS nanorods, and Au@ZnO core–shell nanoparticles exhibit certain limitations, including low catalytic efficiency, inadequate selectivity, and demanding reaction conditions. To address these challenges, we have developed a novel heterogeneous photocatalyst, i.e., Bi4NbO8Cl, and systematically investigated its performance in visible-light-induced hydroxytrifluoromethylation of alkenes and trifluoromethylation of (hetero)aromatics. Notably, the Bi4NbO8Cl photocatalyst exhibits remarkable stability and reusability, maintaining its performance and structural integrity over five cycles. These findings highlight the economic and practical potential of Bi4NbO8Cl, positioning it as a promising candidate for industrial applications in photocatalysis.

Effects of UV illumination on organic dye decomposition activity and antibacterial and antiviral activities of rare earth iodates

For this study, we investigated the effects of UV illumination on dye decomposition and antibacterial and antiviral activities of three rare earth iodates (Ce(IO3)4, Ce(IO3)3, and δ-La(IO3)3) that reportedly have antibacterial and antiviral activities in the dark. The objective of this study was to clarify whether bulk materials and eluted ions are involved in these activities under UV illumination. Findings indicate that Ce(IO3)3 and δ-La(IO3)3 exhibit dye degradation activity under UV illumination by a Hg-Xe lamp (7 mW/cm2), suggesting that the dye decomposition activity was caused mainly by photochemical reactions under UV with wavelengths less than 300 nm by Ce3+ and by IO3− ions eluted from the samples. The dye decomposition activity under UV illumination is expressed not only from the eluted ions but also from the bulk materials. UV illumination using a weak (0.1 mW/cm2) UV light from a black light bulb with wavelengths longer than 320 nm increased the antibacterial and antiviral activities of these materials. These results suggest that the increase in antibacterial and antiviral activities is attributable to the photocatalytic reaction of bulk materials. This study revealed that both the bulk and eluted ions are involved in these activities under UV illumination. The extent to which photochemical reactions caused by eluted ions and bulk material contribute to the decomposition activity of organic dyes and antibacterial and antiviral activities depends on the UV illumination wavelength and intensity. This study provides new insights into the use of rare earth iodates as inorganic antibacterial and antiviral materials.Graphical abstract